Enzymes which catalyze the hydrolases of ester bonds within DNA. EC 3.1.-.
Cytoplasmic proteins that bind estradiol, migrate to the nucleus, and regulate DNA transcription.
Cyclohexane ring substituted by one or more ketones in any position.
Enzyme systems composed of two subunits and requiring ATP and magnesium for endonucleolytic activity; they do not function as ATPases. They exist as complexes with modification methylases of similar specificity listed under EC 2.1.1.72 or EC 2.1.1.73. The systems recognize specific short DNA sequences and cleave a short distance, about 24 to 27 bases, away from the recognition sequence to give specific double-stranded fragments with terminal 5'-phosphates. Enzymes from different microorganisms with the same specificity are called isoschizomers. EC 3.1.21.5.
Enzyme systems containing three different subunits and requiring ATP, S-adenosylmethionine, and magnesium for endonucleolytic activity to give random double-stranded fragments with terminal 5'-phosphates. They function also as DNA-dependent ATPases and modification methylases, catalyzing the reactions of EC 2.1.1.72 and EC 2.1.1.73 with similar site-specificity. The systems recognize specific short DNA sequences and cleave at sites remote from the recognition sequence. Enzymes from different microorganisms with the same specificity are called isoschizomers. EC 3.1.21.3.
Cytoplasmic proteins that bind estrogens and migrate to the nucleus where they regulate DNA transcription. Evaluation of the state of estrogen receptors in breast cancer patients has become clinically important.
The 17-beta-isomer of estradiol, an aromatized C18 steroid with hydroxyl group at 3-beta- and 17-beta-position. Estradiol-17-beta is the most potent form of mammalian estrogenic steroids.
One of the Type II site-specific deoxyribonucleases (EC 3.1.21.4). It recognizes and cleaves the sequences C/CGG and GGC/C at the slash. HpaII is from Haemophilus parainfluenzae. Several isoschizomers have been identified. EC 3.1.21.-.
Enzyme systems containing a single subunit and requiring only magnesium for endonucleolytic activity. The corresponding modification methylases are separate enzymes. The systems recognize specific short DNA sequences and cleave either within, or at a short specific distance from, the recognition sequence to give specific double-stranded fragments with terminal 5'-phosphates. Enzymes from different microorganisms with the same specificity are called isoschizomers. EC 3.1.21.4.
A semisynthetic derivative of PODOPHYLLOTOXIN that exhibits antitumor activity. Teniposide inhibits DNA synthesis by forming a complex with topoisomerase II and DNA. This complex induces breaks in double stranded DNA and prevents repair by topoisomerase II binding. Accumulated breaks in DNA prevent cells from entering into the mitotic phase of the cell cycle, and lead to cell death. Teniposide acts primarily in the G2 and S phases of the cycle.
A ubiquitous casein kinase that is comprised of two distinct catalytic subunits and dimeric regulatory subunit. Casein kinase II has been shown to phosphorylate a large number of substrates, many of which are proteins involved in the regulation of gene expression.
Addition of methyl groups. In histo-chemistry methylation is used to esterify carboxyl groups and remove sulfate groups by treating tissue sections with hot methanol in the presence of hydrochloric acid. (From Stedman, 25th ed)
A fibrillar collagen found predominantly in CARTILAGE and vitreous humor. It consists of three identical alpha1(II) chains.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.

Telomeric repeats on small polydisperse circular DNA (spcDNA) and genomic instability. (1/2461)

Small polydisperse circular DNA (spcDNA) is a heterogeneous population of extrachromosomal circular molecules present in a large variety of eukaryotic cells. Elevated amounts of total spcDNA are related to endogenous and induced genomic instability in rodent and human cells. We suggested spcDNA as a novel marker for genomic instability, and speculated that spcDNA might serve as a mutator. In this study, we examine the presence of telomeric sequences on spcDNA. We report for the first time the appearance of telomeric repeats in spcDNA molecules (tel-spcDNA) in rodent and human cells. Restriction enzyme analysis indicates that tel-spcDNA molecules harbor mostly, if not exclusively, telomeric repeats. In rodent cells, tel-spcDNA levels are higher in transformed than in normal cells and are enhanced by treatment with carcinogen. Tel-spcDNA is also detected in some human tumors and cell lines, but not in others. We suggest, that its levels in human cells may be primarily related to the amount of the chromosomal telomeric sequences. Tel-spcDNA may serve as a unique mutator, through specific mechanisms related to the telomeric repeats, which distinguish it from the total heterogeneous spcDNA population. It may affect telomere dynamics and genomic instability by clastogenic events, alterations of telomere size and sequestration of telomeric proteins.  (+info)

A 43-nucleotide RNA cis-acting element governs the site-specific formation of the 3' end of a poxvirus late mRNA. (2/2461)

The 3' ends of late mRNAs of the ati gene, encoding the major component of the A-type inclusions, are generated by endoribonucleolytic cleavage at a specific site in the primary transcript [Antczak et al., (1992), Proc. Natl. Acad. Sci. USA 89, 12033-12037]. In this study, sequence analysis of cDNAs of the 3' ends of ati mRNAs showed these mRNAs are 3' polyadenylated at the RNA cleavage site. This suggests that ati mRNA 3' end formation involves cleavage of a late transcript, with subsequent 3' polyadenylation of the 5' cleavage product. The RNA cis-acting element, the AX element, directing orientation-dependent formation of these mRNA 3' ends, was mapped to a 345-bp AluI-XbaI fragment. Deletion analyses of this fragment showed that the boundaries of the AX element are within -5 and +38 of the RNA cleavage site. Scanning mutagenesis showed that the AX element contains at least two subelements: subelement I, 5'-UUUAU downward arrowCCGAUAAUUC-3', containing the cleavage site ( downward arrow), separated from the downstream subelement II, 5'-AAUUUCGGAUUUGAAUGC-3', by a 10-nucleotide region, whose composition may be altered without effect on RNA 3' end formation. These features, which differ from those of other elements controlling RNA processing, suggest that the AX element is a component of a novel mechanism of RNA 3' end formation.  (+info)

A randomly amplified polymorphic DNA marker specific for the Bacillus cereus group is diagnostic for Bacillus anthracis. (3/2461)

Aiming to develop a DNA marker specific for Bacillus anthracis and able to discriminate this species from Bacillus cereus, Bacillus thuringiensis, and Bacillus mycoides, we applied the randomly amplified polymorphic DNA (RAPD) fingerprinting technique to a collection of 101 strains of the genus Bacillus, including 61 strains of the B. cereus group. An 838-bp RAPD marker (SG-850) specific for B. cereus, B. thuringiensis, B. anthracis, and B. mycoides was identified. This fragment included a putative (366-nucleotide) open reading frame highly homologous to the ypuA gene of Bacillus subtilis. The restriction analysis of the SG-850 fragment with AluI distinguished B. anthracis from the other species of the B. cereus group.  (+info)

X-chromosome inactivation patterns do not implicate asymmetric splitting of the inner cell mass in the aetiology of twin-twin transfusion syndrome. (4/2461)

The aetiology of twin-twin transfusion syndrome (TTTS) is unclear. We investigated the hypothesis that monochorionic (MC) pregnancies with TTTS are associated with differences in the timing and symmetry of twinning compared to MC twin pregnancies without TTTS. DNA was extracted from the umbilical cord vessels of 26 female MC twins, 14 with and 12 without TTTS on serial antenatal ultrasound. X-inactivation patterns were determined by DNA digestion with Hhal and Hpall followed by polymerase chain reaction for a polymorphic trinucleotide repeat in the androgen receptor gene. Products were quantified by densitometry and results compared to those in peripheral blood samples of adult female controls. The median degree of non-random inactivation was similar in MC twins with TTTS, in MC twins without TTTS, and in adult controls. The percentage of individuals with skewed (> or =30/70%) inactivation patterns was no different in MC twins with TTTS compared to those without TTTS, and was similar to adult controls using either enzyme technique. In conclusion we found no difference in the degree or frequency of non-random X-inactivation patterns in TTTS. X-inactivation patterns do not appear to be a useful tool for studying the symmetry of inner cell mass splitting in monochorionic twins.  (+info)

Comparison of large restriction fragments of Mycobacterium avium isolates recovered from AIDS and non-AIDS patients with those of isolates from potable water. (5/2461)

We examined potable water in Los Angeles, California, as a possible source of infection in AIDS and non-AIDS patients. Nontuberculous mycobacteria were recovered from 12 (92%) of 13 reservoirs, 45 (82%) of 55 homes, 31 (100%) of 31 commercial buildings, and 15 (100%) of 15 hospitals. Large-restriction-fragment (LRF) pattern analyses were done with AseI. The LRF patterns of Mycobacterium avium isolates recovered from potable water in three homes, two commercial buildings, one reservoir, and eight hospitals had varying degrees of relatedness to 19 clinical isolates recovered from 17 patients. The high number of M. avium isolates recovered from hospital water and their close relationship with clinical isolates suggests the potential threat of nosocomial spread. This study supports the possibility that potable water is a source for the acquisition of M. avium infections.  (+info)

Requirement of ATM in phosphorylation of the human p53 protein at serine 15 following DNA double-strand breaks. (6/2461)

Microinjection of the restriction endonuclease HaeIII, which causes DNA double-strand breaks with blunt ends, induces nuclear accumulation of p53 protein in normal and xeroderma pigmentosum (XP) primary fibroblasts. In contrast, this induction of p53 accumulation is not observed in ataxia telangiectasia (AT) fibroblasts. HaeIII-induced p53 protein in normal fibroblasts is phosphorylated at serine 15, as determined by immunostaining with an antibody specific for phosphorylated serine 15 of p53. This phosphorylation correlates well with p53 accumulation. Treatment with lactacystin (an inhibitor of the proteasome) or heat shock leads to similar levels of p53 accumulation in normal and AT fibroblasts, but the p53 protein lacks a phosphorylated serine 15. Following microinjection of HaeIII into lactacystin-treated normal fibroblasts, lactacystin-induced p53 protein is phosphorylated at serine 15 and stabilized even in the presence of cycloheximide. However, neither stabilization nor phosphorylation at serine 15 is observed in AT fibroblasts under the same conditions. These results indicate the significance of serine 15 phosphorylation for p53 stabilization after DNA double-strand breaks and an absolute requirement for ATM in this phosphorylation process.  (+info)

Isolation of Enterococcus faecalis clinical isolates that efficiently adhere to human bladder carcinoma T24 cells and inhibition of adhesion by fibronectin and trypsin treatment. (7/2461)

The adherence of Enterococcus faecalis strains to human T24 cells was examined by scanning electron microscopy. Five highly adhesive strains were identified from 30 strains isolated from the urine of patients with urinary tract infections. No efficiently adhesive strains were found among the 30 strains isolated from the feces of healthy students. The five isolated strains also adhered efficiently to human bladder epithelial cells. Analysis of restriction endonuclease-digested plasmid DNAs and chromosome DNAs showed that the five strains were different strains isolated from different patients. The adhesiveness of these strains was inhibited by treatment with fibronectin or trypsin, implying that a specific protein (adhesin) on the bacterial cell surface mediates adherence to fibronectin on the host cell surfaces, and the adhesin differs from the reported adhesins.  (+info)

A new CYP2A6 gene deletion responsible for the in vivo polymorphic metabolism of (+)-cis-3,5-dimethyl-2-(3-pyridyl)thiazolidin-4-one hydrochloride in humans. (8/2461)

(+)-Cis-3,5-dimethyl-2-(3-pyridyl)thiazolidin-4-one hydrochloride (SM-12502) is a newly developed drug as a platelet-activating factor receptor antagonist. The disposition of SM-12502 was investigated in plasma from 28 healthy Japanese volunteers after a single i.v. administration of SM-12502. Three of 28 subjects were phenotyped as poor metabolizers (PMs). Genomic DNAs from three extensive metabolizers or three PMs of SM-12502 were analyzed by Southern blot analysis with CYP2A6 cDNA as a probe. DNAs from three PMs digested with SacI and SphI showed novel restriction fragment length polymorphisms (RFLPs); one type without 4.5- and 2.6-kb fragments and a weak density of a 6.4-kb fragment (E-type), and the other type without 7.1- and 5.5-kb restriction fragments (C'-type) as compared with three extensive metabolizers, respectively. The deletional restriction fragments specific to three PMs in SacI- and SphI-RFLPs were identified as CYP2A6. Using polymerase chain reaction-RFLP analyses of the gene from the three PMs, we found that the exon 1, exon 8, and exon 9 in CYP2A6 were absent. A new RFLP characterized by SacI and SphI was found to be due to the entire gene deletion of the three exons and was associated with the decreased metabolism of SM-12502. This study demonstrates a new deletional allele in the human CYP2A6 gene responsible for the poor metabolic phenotype of SM-12502.  (+info)

Deoxyribonucleases (DNases) are a group of enzymes that cleave, or cut, the phosphodiester bonds in the backbone of deoxyribonucleic acid (DNA) molecules. DNases are classified based on their mechanism of action into two main categories: double-stranded DNases and single-stranded DNases.

Double-stranded DNases cleave both strands of the DNA duplex, while single-stranded DNases cleave only one strand. These enzymes play important roles in various biological processes, such as DNA replication, repair, recombination, and degradation. They are also used in research and clinical settings for applications such as DNA fragmentation analysis, DNA sequencing, and treatment of cystic fibrosis.

It's worth noting that there are many different types of DNases with varying specificities and activities, and the medical definition may vary depending on the context.

Estradiol receptors are a type of nuclear receptor protein that are activated by the hormone 17-β estradiol, which is a form of estrogen. These receptors are found in various tissues throughout the body, including the breasts, uterus, ovaries, prostate, and brain.

There are two main types of estradiol receptors, known as ERα and ERβ. Once activated by estradiol, these receptors function as transcription factors, binding to specific DNA sequences in the nucleus of cells and regulating the expression of target genes. This process plays a critical role in the development and maintenance of female sex characteristics, as well as in various physiological processes such as bone metabolism, cognitive function, and cardiovascular health.

Abnormalities in estradiol receptor signaling have been implicated in several diseases, including breast and endometrial cancers, osteoporosis, and neurological disorders. As a result, estradiol receptors are an important target for the development of therapies aimed at treating these conditions.

Cyclohexanones are organic compounds that consist of a cyclohexane ring (a six-carbon saturated ring) with a ketone functional group (-CO-) attached to it. The general structure is C6H11CO. They can be found in various natural sources, including essential oils and certain plants, but many cyclohexanones are also synthesized for use in the chemical industry.

Cyclohexanones are important intermediates in the production of various chemicals, such as nylon and other synthetic fibers, resins, and perfumes. One of the most common cyclohexanones is cyclohexanone itself, which is a colorless liquid with an odor reminiscent of peppermint or acetone. It is used in the production of adipic acid, a precursor to nylon.

Like other ketones, cyclohexanones can undergo various chemical reactions, such as reduction, oxidation, and condensation. However, due to the cyclic structure of cyclohexanones, they also exhibit unique reactivity patterns that are exploited in organic synthesis.

Deoxyribonucleases, Type III Site-Specific are a type of enzyme that cleaves DNA at specific sequences. They are also known as restriction endonucleases and are found in bacteria, where they play a role in the defense against foreign DNA, such as that from viruses. These enzymes recognize and bind to specific sites on the DNA molecule, and then cut the phosphodiester bonds between the sugar and phosphate groups of the DNA backbone, resulting in double-stranded breaks at the recognition site. The ends of the cleaved DNA molecules are often "sticky" or complementary to each other, allowing for the joining of DNA fragments from different sources through a process called ligation.

Type III restriction enzymes are unique because they require two recognition sites in close proximity to each other on the same DNA molecule in order to cleave the DNA. They also have both endonuclease and methyltransferase activities, which allows them to modify their own recognition site to prevent self-destruction.

These enzymes are widely used in molecular biology research for various purposes such as cloning, genome editing, and DNA fingerprinting.

Deoxyribonucleases, Type I Site-Specific are a group of enzymes that cleave the phosphodiester bonds in the DNA backbone at specific recognition sites. They are also known as restriction endonucleases or restriction enzymes. These enzymes play a crucial role in the restriction modification system, which provides bacterial and archaeal cells with a defense mechanism against foreign DNA, such as that of bacteriophages (viruses that infect bacteria).

Type I site-specific deoxyribonucleases are complex multifunctional enzymes composed of several subunits. They have three main activities: sequence-specific double-stranded DNA cleavage, ATP-dependent DNA translocation, and methylation of recognition sites. These enzymes recognize specific palindromic sequences in the DNA (usually 4-8 base pairs long) and cleave the phosphodiester bond at a defined distance from the recognition site, often resulting in staggered cuts that leave overhanging single-stranded ends.

Type I restriction enzymes require magnesium ions as cofactors for their endonuclease activity and ATP for their translocase activity. They are generally less specific than other types of restriction enzymes (Types II and III) since they cleave DNA within a broader range around the recognition site, rather than at fixed positions.

The restriction-modification system consists of two components: a restriction endonuclease (such as Type I deoxyribonucleases) that cuts foreign DNA at specific sites and a methyltransferase that modifies the host's DNA by adding methyl groups to the same recognition sites, protecting it from cleavage. This system allows the cell to distinguish between its own DNA and foreign DNA, providing an effective defense mechanism against invading genetic elements.

In summary, Deoxyribonucleases, Type I Site-Specific are restriction endonucleases that recognize specific sequences in double-stranded DNA and cleave the phosphodiester bonds at defined distances from the recognition site. They play a critical role in the bacterial and archaeal defense system against foreign DNA by selectively degrading invading genetic elements while sparing the host's methylated DNA.

Estrogen receptors (ERs) are a type of nuclear receptor protein that are expressed in various tissues and cells throughout the body. They play a critical role in the regulation of gene expression and cellular responses to the hormone estrogen. There are two main subtypes of ERs, ERα and ERβ, which have distinct molecular structures, expression patterns, and functions.

ERs function as transcription factors that bind to specific DNA sequences called estrogen response elements (EREs) in the promoter regions of target genes. When estrogen binds to the ER, it causes a conformational change in the receptor that allows it to recruit co-activator proteins and initiate transcription of the target gene. This process can lead to a variety of cellular responses, including changes in cell growth, differentiation, and metabolism.

Estrogen receptors are involved in a wide range of physiological processes, including the development and maintenance of female reproductive tissues, bone homeostasis, cardiovascular function, and cognitive function. They have also been implicated in various pathological conditions, such as breast cancer, endometrial cancer, and osteoporosis. As a result, ERs are an important target for therapeutic interventions in these diseases.

Estradiol is a type of estrogen, which is a female sex hormone. It is the most potent and dominant form of estrogen in humans. Estradiol plays a crucial role in the development and maintenance of secondary sexual characteristics in women, such as breast development and regulation of the menstrual cycle. It also helps maintain bone density, protect the lining of the uterus, and is involved in cognition and mood regulation.

Estradiol is produced primarily by the ovaries, but it can also be synthesized in smaller amounts by the adrenal glands and fat cells. In men, estradiol is produced from testosterone through a process called aromatization. Abnormal levels of estradiol can contribute to various health issues, such as hormonal imbalances, infertility, osteoporosis, and certain types of cancer.

Deoxyribonuclease HpaII, also known as HpaII endonuclease or simply HpaII, is an enzyme that cleaves double-stranded DNA at the recognition site 5'-CCGG-3'. It is a type of restriction endonuclease that is isolated from the bacterium Haemophilus parainfluenzae. The 'H' and the 'pa' in HpaII stand for Haemophilus parainfluenzae, and the Roman numeral II indicates that it was the second such enzyme to be discovered from this bacterial species.

The HpaII enzyme cuts the DNA strand between the two Gs in the recognition site, leaving a 5'-overhang of two unpaired cytosines on the 3'-end of each cleaved strand. This specificity makes it useful for various molecular biology techniques, such as genetic fingerprinting, genome mapping, and DNA sequencing.

It is worth noting that HpaII is sensitive to methylation at the internal cytosine residue within its recognition site. If the inner cytosine in the 5'-CCGG-3' sequence is methylated (i.e., 5-methylcytosine), HpaII will not cut the DNA at that site, which can be exploited for epigenetic studies and DNA methylation analysis.

Deoxyribonucleases, Type II Site-Specific are a type of enzymes that cleave phosphodiester bonds in DNA molecules at specific recognition sites. They are called "site-specific" because they cut DNA at particular sequences, rather than at random or nonspecific locations. These enzymes belong to the class of endonucleases and play crucial roles in various biological processes such as DNA recombination, repair, and restriction.

Type II deoxyribonucleases are further classified into several subtypes based on their cofactor requirements, recognition site sequences, and cleavage patterns. The most well-known examples of Type II deoxyribonucleases are the restriction endonucleases, which recognize specific DNA motifs in double-stranded DNA and cleave them, generating sticky ends or blunt ends. These enzymes are widely used in molecular biology research for various applications such as genetic engineering, cloning, and genome analysis.

It is important to note that the term "Deoxyribonucleases, Type II Site-Specific" refers to a broad category of enzymes with similar properties and functions, rather than a specific enzyme or family of enzymes. Therefore, providing a concise medical definition for this term can be challenging, as it covers a wide range of enzymes with distinct characteristics and applications.

Teniposide is a synthetic podophyllotoxin derivative, which is an antineoplastic agent. It works by interfering with the DNA synthesis and function of cancer cells, leading to cell cycle arrest and apoptosis (programmed cell death). Teniposide is primarily used in the treatment of acute lymphoblastic leukemia (ALL) and other malignancies in children. It is often administered through intravenous infusion and is typically used in combination with other chemotherapeutic agents.

The medical definition of Teniposide can be stated as:

Teniposide, chemically known as (4'-demethylepipodophyllotoxin 9-[4,6-O-(R)-benzylidene-α-L-glucopyranoside]), is a semi-synthetic podophyllotoxin derivative with antineoplastic activity. It inhibits DNA topoisomerase II, leading to the formation of DNA-topoisomerase II cleavable complexes, G2 arrest, and apoptosis in cancer cells. Teniposide is primarily used in the treatment of acute lymphoblastic leukemia (ALL) and other malignancies in children, often administered through intravenous infusion and typically used in combination with other chemotherapeutic agents.

Casein Kinase II (CK2) is a serine/threonine protein kinase that is widely expressed in eukaryotic cells and is involved in the regulation of various cellular processes. It is a heterotetrameric enzyme, consisting of two catalytic subunits (alpha and alpha') and two regulatory subunits (beta).

CK2 phosphorylates a wide range of substrates, including transcription factors, signaling proteins, and other kinases. It is known to play roles in cell cycle regulation, apoptosis, DNA damage response, and protein stability, among others. CK2 activity is often found to be elevated in various types of cancer, making it a potential target for cancer therapy.

Methylation, in the context of genetics and epigenetics, refers to the addition of a methyl group (CH3) to a molecule, usually to the nitrogenous base of DNA or to the side chain of amino acids in proteins. In DNA methylation, this process typically occurs at the 5-carbon position of cytosine residues that precede guanine residues (CpG sites) and is catalyzed by enzymes called DNA methyltransferases (DNMTs).

DNA methylation plays a crucial role in regulating gene expression, genomic imprinting, X-chromosome inactivation, and suppression of repetitive elements. Hypermethylation or hypomethylation of specific genes can lead to altered gene expression patterns, which have been associated with various human diseases, including cancer.

In summary, methylation is a fundamental epigenetic modification that influences genomic stability, gene regulation, and cellular function by introducing methyl groups to DNA or proteins.

Collagen Type II is a specific type of collagen that is a major component of the extracellular matrix in articular cartilage, which is the connective tissue that covers and protects the ends of bones in joints. It is also found in other tissues such as the vitreous humor of the eye and the inner ear.

Collagen Type II is a triple helix molecule composed of three polypeptide chains that contain a high proportion of the amino acids proline and hydroxyproline. This type of collagen provides structural support and elasticity to tissues, and it also plays a role in the regulation of cell behavior and signaling.

Collagen Type II is a target for autoimmune responses in conditions such as rheumatoid arthritis, where the immune system mistakenly attacks the body's own collagen, leading to joint inflammation and damage. It is also a common component of various dietary supplements and therapies used to support joint health and treat osteoarthritis.

Molecular sequence data refers to the specific arrangement of molecules, most commonly nucleotides in DNA or RNA, or amino acids in proteins, that make up a biological macromolecule. This data is generated through laboratory techniques such as sequencing, and provides information about the exact order of the constituent molecules. This data is crucial in various fields of biology, including genetics, evolution, and molecular biology, allowing for comparisons between different organisms, identification of genetic variations, and studies of gene function and regulation.

... (EC 3.1.21.4, type II restriction enzyme) is an enzyme. This enzyme catalyses the ... Type+II+site-specific+deoxyribonuclease at the U.S. National Library of Medicine Medical Subject Headings (MeSH) Portal: ... following chemical reaction Endonucleolytic cleavage of DNA to give specific double-stranded fragments with terminal 5'- ...
These site-specific deoxyribonucleases catalyse the endonucleolytic cleavage of DNA to give specific double-stranded fragments ... XhoI is a type II restriction enzyme EC that recognise the double-stranded DNA sequence CTCGAG and cleaves after C-1. Type II ...
... deoxyribonucleases, type i site-specific MeSH D08.811.277.352.335.350.300.260 - deoxyribonucleases, type ii site-specific MeSH ... deoxyribonucleases, type i site-specific MeSH D08.811.277.352.355.325.300.260 - deoxyribonucleases, type ii site-specific MeSH ... deoxyribonucleases, type i site-specific MeSH D08.811.150.280.260 - deoxyribonucleases, type ii site-specific MeSH D08.811. ... deoxyribonuclease hpaii MeSH D08.811.277.352.335.350.300.270 - deoxyribonucleases, type iii site-specific MeSH D08.811.277.352. ...
... (pronounced "Hin D Three") is a type II site-specific deoxyribonuclease restriction enzyme isolated from Haemophilus ... Unlike type I restriction enzymes, type II restriction endonucleases perform very specific cleaving of DNA. Type I restriction ... at sites other than their recognition site whereas type II restriction enzymes cleave only at their specific recognition site. ... Despite the uncertainty concerning the structure-catalysis relationship of type II endonucleases, site-directed mutagenesis of ...
What was then needed was a tool that would cut DNA at specific sites, rather than at random sites along the length of the ... In the late 1960s, scientists Stuart Linn and Werner Arber isolated examples of the two types of enzymes responsible for phage ... They are further subcategorized as deoxyribonucleases and ribonucleases. The former acts on DNA, the latter on RNA. ... endonucleases like RuvC resolve Holliday junctions into two separate dsDNAs by cleaving the junctions at two symmetrical sites ...
... type I site-specific deoxyribonuclease EC 3.1.21.4: type II site-specific deoxyribonuclease EC 3.1.21.5: type III site-specific ... deoxyribonuclease V EC 3.1.21.8: T4 deoxyribonuclease II * EC 3.1.21.9: T4 deoxyribonuclease IV * EC 3.1.21.10: crossover ... deoxyribonuclease I EC 3.1.4.6: Now EC 3.1.22.1, deoxyribonuclease II EC 3.1.4.7: Now EC 3.1.31.1, micrococcal nuclease EC 3.1. ... deoxyribonuclease II EC 3.1.22.2: Aspergillus deoxyribonuclease K1 EC 3.1.22.3: now EC 3.1.21.7 EC 3.1.22.4: crossover junction ...
Two specific types of nucleic acid, DNA and RNA, are common to all living organisms, serving to encode the genetic information ... The two sister chromatids are ultimately separated from each other into two different cells during mitosis or meiosis. site- ... Compare deoxyribonuclease. ribonucleic acid (RNA) A polymeric nucleic acid molecule composed of a series of ribonucleotides ... restriction site A short, specific sequence of nucleotides (typically 4 to 8 bases in length) that is reliably recognized by a ...
Restriction endonucleases (restriction enzymes) are divided into three categories, Type I, Type II, and Type III, according to ... Type I can cleave at random sites of about 1000 base pairs or more from the recognition sequence and it requires ATP as source ... An example of a Type I restriction endonuclease.: 64 Furthermore, there exist DNA/RNA non-specific endonucleases, such as those ... such as deoxyribonuclease I, cut DNA relatively nonspecifically (without regard to sequence), while many, typically called ...
The LACTB2 protein has a metallo β-lactamase (MBL) fold, with two zinc ions in the active site. The metallo beta-lactamases ... A tumor-specific LACTB2-NCOA2 fusion originating from intra-chromosomal rearrangement of chromosome 8 has been identified at ... Enforced expression of wild-type NCOA2 but not the LACTB2-NCOA2 fusion protein impaired the pro-tumorigenic phenotypes of CRC ... deoxyribonucleases (DNases) and other metabolic enzymes MBL ribonucleases are responsible for RNA processing, generating the 3 ...
Each type of exonuclease has a specific type of function or requirement. Exonuclease I breaks apart single-stranded DNA in a 3 ... RNA polymerase II is known to be in effect during transcriptional termination; it works with a 5' exonuclease (human gene Xrn2 ... ISBN 978-0-12-122723-4. Lehman IR, Nussbaum AL (August 1964). "The deoxyribonucleases of Escherichia Coli. V. on the ... end of yeast 5.8S rRNA is generated by exonucleases from an upstream cleavage site". EMBO J. 13 (10): 2452-63. doi:10.1002/j. ...
"Cell-type-specific characteristics modulate the transduction efficiency of adeno-associated virus type 2 and restrain infection ... It can also infect non-dividing cells and has the ability to stably integrate into the host cell genome at a specific site ( ... On the "left side" of the genome there are two promoters called p5 and p19, from which two overlapping messenger ribonucleic ... deoxyribonuclease-resistant AAV particles. With regard to gene therapy, ITRs seem to be the only sequences required in cis next ...
The two main types of DNase found in animals are known as deoxyribonuclease I (DNase I) and deoxyribonuclease II (DNase II). ... Website Deoxyribonuclease I from Sigma-Aldrich Solutions website Deoxyribonuclease I, active site from InterPro Website (CS1 ... are very sequence-specific. Other DNases cleave only double-stranded DNA, others are specific for single-stranded molecules, ... Deoxyribonuclease II (DNase II) is also known as acid deoxyribonuclease because it has optimal activity in the low pH ...
There are specific genes that were found to be crucial in the different biofilm growth stages. Two of these genes include rocD ... bacteriophage typing, spa locus typing, and SCCmec typing are often conducted more than others. With these methods, it can be ... The nasal region has been implicated as the most important site of transfer between dogs and humans. S. aureus is one of the ... Deoxyribonuclease, which breaks down the DNA, protects S. aureus from neutrophil extracellular trap-mediated killing. S. aureus ...
... deoxyribonuclease S1, Aspergillus nuclease S1, Neurospora crassa single-strand specific endonuclease, S1 nuclease, single- ... The first two zincs activate the attacking water in hydrolysis whilst the third zinc ion stabilizes the leaving oxyanion. ... Additionally, the side chain of tryptophan located in the cavity in the active site and its backbone supports the action one of ... "An extracellular S1-type nuclease of marine fungus Penicillium melinii". Marine Biotechnology. 14 (1): 87-95. doi:10.1007/ ...
At these sites, the two interact through a series of weak, non-covalent bonds. The main source of bonds comes from hydrogen ... The two can be separated quite easily and often are during replication and transcription. Specific remodeling proteins are ... The digestion of chromatin DNA at regularly spaced sites by a nuclear deoxyribonuclease". Biochem. Biophys. Res. Commun. 52 (2 ... Numerous reports show a link between age-related diseases, birth defects, and several types of cancer with disruption of ...
... like other type II restriction endonucleases, often requires divalent metals as cofactors to catalyze DNA cleavage. Two-metal ... The two metal ions (A and B) are 4.1 apart from each other in the active site and are in-line with these residues. In general, ... Deoxyribonuclease+BamHI at the U.S. National Library of Medicine Medical Subject Headings (MeSH) 5 crystal structures[dead link ... Because of its ability to recognize specific DNA sequence and cleave by a nuclease, BamHI carries various importances in ...
However, it requires two base pairs at one cleavage site, and the other cleavage site of double-stranded DNA should have more ... Deoxyribonuclease IV is a type of deoxyribonuclease that has both an exonucleolytic and an endonucleolytic activity. It ... DNase IV does not recognize specific sequences on DNA for non-staggered cleavage. ... Friedberg EC, Hadi SM, Goldthwait DA (November 1969). "Endonuclease II of Escherichia coli. II. Enzyme properties and studies ...
... which may include cellular recognition of specific or non-specific attachment sites on a surface, nutritional cues, or in some ... A study showed that the type of current used made no difference to the bioelectric effect. Biofilms can also be harnessed for ... This was supported mainly with the fact that the two most abundantly produced molecules by the immune system also support ... Enzymes that degrade the biofilm extracellular matrix, such as dispersin B and deoxyribonuclease, may contribute to biofilm ...
There are two different sites at which the tRNA-intron endonuclease cleaves the intron, the 5′- and 3′-splice sites. At the 5' ... All four structures are maintained by two specific interactions. The first interaction is between the β strands of two nearby ... Four types of archaeal tRNA-intron lyase structures have been identified: α4, α′2, (αβ)2, and 𝜀2. ... XK deoxyribonucleases". Protein Science. 10 (3): 656-660. doi:10.1110/ps.37101. PMC 2374129. PMID 11344334. Messmore JM, Fuchs ...
For CS Type II patients who have little neural growth after birth, the lifespan is significantly decreased to 7 years after ... which follows to finding at least one mutation at a specific locus per one million gametes. DNA is the only biologic molecule ... deoxyribonuclease (apurinic or apyrimidinic); E. coli endonuclease III; phage-T4 UV endonuclease; Micrococcus luteus UV ... The enzyme DNA-(apurinic or apyrimidinic site) lyase, also referred to as DNA-(apurinic or apyrimidinic site) 5'- ...
... with sharp peaks and valleys of coverage suggestion that it may preferentially initiate packaging at specific sites in the ... The two best studied GTAs (RcGTA and BaGTA) randomly package all of the DNA in the cell, with no overrepresentation of GTA- ... Different GTA types have originated independently from viruses in several bacterial and archaeal lineages. These cells produce ... insensitive to deoxyribonuclease, and not associated with phage production. Because of its presumed function it was named gene ...
In single-end sequencing, there is only one read per fragment (i.e., RPM = FPM). In paired-end sequencing, there are two reads ... This can uncover the existence of rare cell types within a cell population that may never have been seen before. For example, ... RNA-Seq data has been used to infer genes involved in specific pathways based on Pearson correlation, both in plants and ... RNA Isolation: RNA is isolated from tissue and mixed with Deoxyribonuclease (DNase). DNase reduces the amount of genomic DNA. ...
The digestion of chromatin DNA at regularly spaced sites by a nuclear deoxyribonuclease". Biochemical and Biophysical Research ... CAD is synthesized with the help of ICAD (inhibitor of CAD), which works as a specific chaperone for CAD and is found complexed ... Apoptosis can be initiated by a myriad of different mechanisms in different cell types, and the kinetics of these events vary ... The linker sites are the only parts of the DNA strand that are exposed and thus accessible to CAD. Degradation of nuclear DNA ...
Hartley JL, Temple GF, Brasch MA (November 2000). "DNA cloning using in vitro site-specific recombination". Genome Research. 10 ... and expression of two novel human genes similar to deoxyribonuclease I". Genomics. 42 (3): 507-513. doi:10.1006/geno.1997.4748 ... The accumulation of DNaseX has been detected in all premalignant and malignant tumor types examined to date. The accumulation ... Deoxyribonuclease-1-like 1 is an enzyme that in humans is encoded by the DNASE1L1 gene. It is also known as DNaseX due to its ...
It contains two exons that span about 25 kb of genomic DNA. The Se locus encodes a specific fucosyltransferase that is ... Human Proteome Project Launch website~ https://web.archive.org/web/20110726163128/http://www.hupo.org/research/hpp/HPP_legrain_ ... encoding protein Deoxyribonuclease II, lysosomal DPF1: encoding protein D4, zinc and double PHD fingers family 1 EID2: ETV2: ... P/Q type, alpha 1A subunit (Familial hemiplegic migraine Type I). Gene map locus 19p13 COMP: Cartilage oligomeric matrix ...
Sakano K, Oikawa S, Hasegawa K, Kawanishi S (November 2001). "Hydroxyurea induces site-specific DNA damage via formation of ... of the exogenous DNA into the cells may require proteins that are involved in the assembly of type IV pili and type II ... Lacks S, Greenberg B, Neuberger M (June 1974). "Role of a deoxyribonuclease in the genetic transformation of Diplococcus ... The uptake of DNA is generally non-sequence specific, although in some species the presence of specific DNA uptake sequences ...
It has been shown in mice that in certain conditions neutrophils have a specific type of migration behaviour referred to as ... II. The influence of sodium and potassium ions]". Tsitologiia. 47 (6): 554-558. PMID 16708849. Zilionis R, Engblom C, Pfirschke ... Neutrophils are recruited to the site of injury within minutes following trauma and are the hallmark of acute inflammation; ... March 2015). "Coronary neutrophil extracellular trap burden and deoxyribonuclease activity in ST-elevation acute coronary ...
... site-directed mutagenesis - site-specific recombination - Slc22a21 - slot blot - SNP - Slc22a21 - SMCR2 - snRNA - snRNP - ... Fragile site, folic acid type, rare, fra(2)(q13) - Fragile X syndrome - frameshift mutation - fructose 5-dehydrogenase - ... Na+-transporting two-sector ATPase - NADH:ubiquinone reductase (Na+-transporting) - native gel - nematode Her-1 - ... deoxyribonuclease (DNase) - deoxyribonucleic acid - deoxyribonucleotide - deoxyuridine phosphorylase - diabetes mellitus - ...
direct repeat Any two or more repetitions of a specific sequence of nucleotides occurring in the same orientation (i.e. in ... homologous recombination A type of genetic recombination in which nucleotide sequences are exchanged between two similar or ... integron A mobile genetic element consisting of a gene cassette containing the gene for a site-specific recombinase, integrase- ... deoxyribonuclease (DNase) Any of a class of nuclease enzymes which catalyze the hydrolytic cleavage of phosphodiester bonds in ...
MALDI-TOF (Matrix-assisted laser desorption/ionization - time of flight) is a specific type of mass spectrometry that is able ... tissue biopsies from a normally sterile site, fluid from a normally sterile site (like a joint), dental, abscess, abdominal or ... Streaking these two organisms perpendicular to each other on a blood agar plate will yield a "bow-tie" clearing of the blood ... DNase agar is used to test whether a microbe can produce the exoenzyme deoxyribonuclease (DNase), which hydrolyzes DNA. Methyl ...
Type II site-specific deoxyribonuclease (EC 3.1.21.4, type II restriction enzyme) is an enzyme. This enzyme catalyses the ... Type+II+site-specific+deoxyribonuclease at the U.S. National Library of Medicine Medical Subject Headings (MeSH) Portal: ... following chemical reaction Endonucleolytic cleavage of DNA to give specific double-stranded fragments with terminal 5- ...
DNA Restriction-Modification Enzymes - Deoxyribonucleases, Type II Site-Specific PubMed MeSh Term *Overview ... DNA Restriction-Modification Enzymes - Deoxyribonuclease BamHI PubMed MeSh Term * DNA Restriction-Modification Enzymes - ... DNA Restriction-Modification Enzymes - Deoxyribonuclease HindIII PubMed MeSh Term * DNA Restriction-Modification Enzymes - ...
CTGCAG-specific type II deoxyribonucleases * Deoxyribonucleases, Type II Site-Specific Grants and funding * AG036871/AG/NIA NIH ...
Deoxyribonucleases, Type II Site-Specific [D08.811.277.352.335.350.300.260]. *Deoxyribonuclease EcoRI [D08.811.277.352.335.350. ... Deoxyribonucleases, Type II Site-Specific [D08.811.277.352.355.325.300.260]. *Deoxyribonuclease EcoRI [D08.811.277.352.355.325. ... One of the Type II site-specific deoxyribonucleases (EC 3.1.21.4). It recognizes and cleaves the sequence G/AATTC at the slash ... This graph shows the total number of publications written about "Deoxyribonuclease EcoRI" by people in this website by year, ...
Deoxyribonucleases, Type II Site-Specific / genetics* * Diabetes Mellitus, Type 1 / drug therapy ... Background: Type 1 diabetes (T1D) is an autoimmune disease mediated by T-helper (Th) cells. Additionally, the immune system ... VDR FokI polymorphism is associated with a reduced T-helper cell population under vitamin D stimulation in type 1 diabetes ... 2 Department of Internal Medicine I, Division of Endocrinology, Diabetes and Metabolism, University Hospital Frankfurt, Germany ...
Deoxyribonucleases, Type II Site-Specific/metabolism * Electrophoresis, Gel, Pulsed-Field * Extracellular Matrix Proteins/ ...
Deoxyribonucleases, Type II Site-Specific. *Deoxyribonuclease EcoRI. *DNA Restriction Enzymes. Citation. APA ... Recently, two cloned segments of human X-chromosome DNA have been described which detect structural alterations within or near ... but is probably located between independent sites of mutation which yield DMD. The breakpoints of some deletions are delineated ...
Deoxyribonucleases, Type II Site-Specific * Directed Molecular Evolution * Endodeoxyribonucleases * Escherichia Coli * Gene ...
Type II site-specific deoxyribonuclease activity GO:0009036 * ribonuclease IX activity GO:0033896 ...
type Ii site-specific deoxyribonuclease subunit S 3553_sll6098-sacB ATGGCGATCGCCAGCCGAGCAGGTC… Fic family protein ... type II toxin-antitoxin system VapC family toxin 3418_ssl5095-sacB ATGACTAATTCAGCAACCCAAGGTC… type II toxin-antitoxin system ... two-component sensor histidine kinase 3497_slr6042-sacB ATGCAAAACCGGATCATTGTTCAGG… efflux RND transporter periplasmic adaptor ... two-component response regulator 3496_slr6041-sacB ATGCAGAACAATAGATTATTCAATC… ...
Deoxyribonucleases, Type II Site-Specific [D08.811.150.280.260] * Deoxyribonuclease BamHI [D08.811.150.280.260.240] ... Deoxyribonucleases, Type II Site-Specific [D08.811.277.352.335.350.300.260] * Deoxyribonuclease BamHI [D08.811.277.352.335.350. ... Deoxyribonucleases, Type II Site-Specific [D08.811.277.352.355.325.300.260] * Deoxyribonuclease BamHI [D08.811.277.352.355.325. ... One of the Type II site-specific deoxyribonucleases (EC 3.1.21.4). It recognizes and cleaves the sequence G/GATCC at the slash ...
Deoxyribonucleases, Type II Site-Specific. *Device Removal. *Diabetes Mellitus, Type 2. *Diagnosis, Differential ...
CONCLUSION: A novel StyI restriction enzyme can be used to confirm the commonest type of Hb G-Philadelphia. DNA sequencing ... RESULTS: Twenty-two cases (78.6%) of 28 cases amplified were tested positive for Hb G-Philadelphia by StyI restriction ... Sequencing of the six negative cases revealed two cases of Hb G-Philadelphia with C→A mutation in codon 68 in α2 globin gene, ... plus one case each of Hb G-Norfolk Hb Stanleyville-II, Hb Matsue-Oki and Hb Mizushi. ...
... indicated that recombination between transfecting DNAs occurred concomitantly with DNA replication but that the two processes ... conclude that the dramatic expansion of recombination activities in the cytoplasm of poxvirus-infected cells is virus specific ... Deoxyribonucleases, Type II Site-Specific, DNA, Viral, Densitometry, Transfection, Nucleic Acid Hybridization, Virus ... Cookies on this website We use cookies to ensure that we give you the best experience on our website. If you click Accept all ...
First, we typed 80 patients suffering from severe sepsis and 153 healthy individuals and found no association of the -308 ... Adult, Aged, Alleles, Animals, Cell Line, Deoxyribonucleases, Type II Site-Specific, Gene Deletion, Heterozygote, Homozygote, ... Cookies on this website We use cookies to ensure that we give you the best experience on our website. If you click Accept all ... First, we typed 80 patients suffering from severe sepsis and 153 healthy individuals and found no association of the -308 ...
Type II Site-Specific:genetics, Female, Fetal Growth Retardation:genetics, Fetus:anatomy & histology, Genotype, Gestational Age ... Journal Article 2008; 29(4): 493-499 PubMed PMID: 18766139 Citation Keywords: Adult, Blood Flow Velocity, Deoxyribonucleases, ... Factor II positive subjects (n=47) had a mean factor II activity of 127.96%+/-21.37. F-II activity among carriers (heterozygous ... F-V activity among wild type (n=41), F-V Leiden heterozygous (n=169) and F-V Leiden homozygous (n=8) were 92.93%+/-16.17, 87.02 ...
regulation of Type III site-specific deoxyribonuclease activity GO:0032086 * positive regulation of telomeric loop formation ... positive regulation of mating type switching by positive regulation of transcription from RNA polymerase II promoter ... positive regulation of mating type switching by regulation of transcription from RNA polymerase II promoter ... positive regulation of mating type switching by transcription from RNA polymerase II promoter ...
Deoxyribonucleases, Type II Site-Specific. * DNA Repair. * DNA Replication. * DNA, Kinetoplast. * Molecular Sequence Data ... Login to edit your profile (add a photo, awards, links to other websites, etc.) ...
Deoxyribonucleases - Deoxyribonuclease HindIII * Deoxyribonucleases - Deoxyribonucleases, Type II Site-Specific * Diagnostic ... DNA Restriction-Modification Enzymes - Deoxyribonuclease HindIII * DNA Restriction-Modification Enzymes - Deoxyribonucleases, ... Endonucleases - Deoxyribonuclease HindIII * Endonucleases - Deoxyribonucleases, Type II Site-Specific * Genetic Phenomena - ...
... and is probably related to Tris-dependent site-specific cleavage of the DNA (19). Nondegradative PFGE was only achieved by ... Six patients had received aerosolized deoxyribonuclease. Two patients had received oral corticosteroids, and four had received ... identical to the type-strain M. abscessus ATCC 19977T), -5a (differing from ATCC 19977T by 5 nt, and identical to the reference ... Three samples (3.2%) from two water supply points tested positive for rapidly growing mycobacteriua (M. mucogenicum, two ...
type I site-specific deoxyribonuclease complex type II site-specific deoxyribonuclease complex ... type III site-specific deoxyribonuclease complex type IV site-specific deoxyribonuclease complex ... BRENDA uses cookies to anonymously track site statistics, and to enhance the user expericence. By clicking the "Accept" button ...
Type III site-specific deoxyribonuclease. 8e-08. 57.4. NC_018867:10238:60407. 60407. 63490. 3084. Dehalobacter sp. CF ... Type III site-specific deoxyribonuclease. 1e-10. 66.6. NC_004631:948054:970921. 970921. 973881. 2961. Salmonella enterica subsp ... Type III site-specific deoxyribonuclease. 9e-14. 77.4. NC_010170:4463000:4489211. 4489211. 4492216. 3006. Bordetella petrii, ... Type III site-specific deoxyribonuclease. 1e-10. 66.6. NC_013411:2191514:2205716. 2205716. 2208670. 2955. Geobacillus sp. ...
... where it causes site-specific recombination of the LoxP sites resulting in KO of the CXCR4 gene (Figure 1A). For animal ... these data indicate that the CXCL12/CXCR4 axis plays an important role in the shift from type 1 to type 2 immune response ... Cell viability (,70% cells alive) and concentration were assessed by the Countess II Cell Counter (Invitrogen) to ensure the ... and deoxyribonuclease I (0.1 mg/mL; Sigma-Aldrich) for 30 minutes at 37°C. Afterward, the cell suspension was filtered ...
Due to the specific chromatin landscapes in different tissue types, distinct ranges of OCF values were accordingly observed in ... two plasma samples collected in a 12-month interval showed decreased accessibility of AR binding sites, reflecting the androgen ... particularly of deoxyribonuclease 1-like 3 (DNASE1L3) [58,59]. DNASE1L3 and DNASE1 are the most abundant DNases in mammalian ... Zhong, S.; He, X.; Bar-Joseph, Z. Predicting tissue specific transcription factor binding sites. BMC Genom. 2013, 14, 796. [ ...
Details on mammalian cell type (if applicable):. Blood of two male donors.. Additional strain / cell type characteristics:. not ... Type of assay:. mammalian erythrocyte micronucleus test. Specific details on test material used for the study:. The test ... Welcome to the ECHA website. This site is not fully supported in Internet Explorer 7 (and earlier versions). Please upgrade ... in two separate experiments. A treat and plate procedure was used for all treatments in this study as deoxyribonuclease, ...
Type III Site Specific Deoxyribonucleases 59% * Horizontal Gene Transfer 39% * Endonucleases 35% ... Evidence for type III restriction and modification systems in Mycoplasma pulmonis. Dybvig, K., Cao, Z., French, C. T. & Yu, H. ... Type three secretion system-mediated escape of Burkholderia pseudomallei into the host cytosol is critical for the activation ... The Bordetella type III secretion system effector BteA contains a conserved N-terminal motif that guides bacterial virulence ...
By using this website, you agree to our Terms and Conditions, Your US state privacy rights, Privacy statement and Cookies ... By generating a two-dimensional map of the data using the dimensionality reduction algorithm t-SNE for each tumor sample, we ... C The population percentage of all immune cell types in tumor tissues and paratumor tissues. D Heatmap showing the population ... 20 µg/mL deoxyribonuclease I) to generate single-cell suspensions. An average of 1-3 × 106 cells were prepared and stained ...
Type I site-specific deoxyribonuclease. 90.33. 0.8105. 97. sll7001 Putative transposase [ISY391e(partial copy): 166 - 1298]. ... Photosystem II core light harvesting protein. 16.12. 0.8846. 15. slr1068 Hypothetical protein. 16.97. 0.9055. ...
B. subtilis YtpP and TrxA Wild-Type Gene Design and Site-Directed Mutagenesis. B. subtilis YtpP (B. subtilis subsp. subtilis ... Find support for a specific problem in the support section of our website. ... The first two criteria are based on analogy to the well-characterized glutaredoxin and mycoredoxin. Two potential candidates, ... 50 μg/mL deoxyribonuclease I (DNase I Bovine pancreas-Sigma) and 10 mM MgCl2). Following resuspension, the cells were sonicated ...
On the basis of whole-transcriptome analyses, we identify many genes that are expressed in a sex- or life stage-specific manner ... The functions of deoxyribonuclease II in immunity and development. DNA Cell Biol. 27, 223-228 (2008). ... This is because it is in intimate contact with host tissue and because it is home to two specialized cellular structures-the ... celiac disease and type 1 diabetes), as well as for two likely immune-unrelated complex traits (height and body mass index). ...

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