A proteolytic enzyme obtained from Streptomyces griseus.
Hydrolases that specifically cleave the peptide bonds found in PROTEINS and PEPTIDES. Examples of sub-subclasses for this group include EXOPEPTIDASES and ENDOPEPTIDASES.
A serine endopeptidase that is formed from TRYPSINOGEN in the pancreas. It is converted into its active form by ENTEROPEPTIDASE in the small intestine. It catalyzes hydrolysis of the carboxyl group of either arginine or lysine. EC 3.4.21.4.
The largest class of organic compounds, including STARCH; GLYCOGEN; CELLULOSE; POLYSACCHARIDES; and simple MONOSACCHARIDES. Carbohydrates are composed of carbon, hydrogen, and oxygen in a ratio of Cn(H2O)n.
The sum of the weight of all the atoms in a molecule.
Chromatography on non-ionic gels without regard to the mechanism of solute discrimination.
Conjugated protein-carbohydrate compounds including mucins, mucoid, and amyloid glycoproteins.
A hexose or fermentable monosaccharide and isomer of glucose from manna, the ash Fraxinus ornus and related plants. (From Grant & Hackh's Chemical Dictionary, 5th ed & Random House Unabridged Dictionary, 2d ed)
A product from the iodination of tyrosine. In the biosynthesis of thyroid hormones (THYROXINE and TRIIODOTHYRONINE), tyrosine is first iodized to monoiodotyrosine.
A strong oxidizing agent.
A superorder of CEPHALOPODS comprised of squid, cuttlefish, and their relatives. Their distinguishing feature is the modification of their fourth pair of arms into tentacles, resulting in 10 limbs.
Glucosamine is a naturally occurring amino sugar that plays a crucial role in the formation and maintenance of various tissues, particularly in the synthesis of proteoglycans and glycosaminoglycans, which are essential components of cartilage and synovial fluid in joints.

Characterization of nuclear structures containing superhelical DNA. (1/739)

Structures resembling nuclei but depleted of protein may be released by gently lysing cells in solutions containing non-ionic detergents and high concentrations of salt. These nucleoids sediment in gradients containing intercalating agents in a manner characteristic of DNA that is intact, supercoiled and circular. The concentration of salt present during isolation of human nucleoids affects their protein content. When made in I-95 M NaCl they lack histones and most of the proteins characteristic of chromatin; in 1-0 M NaCl they contain variable amounts of histones. The effects of various treatments on nucleoid integrity were investigated.  (+info)

Role of surface proteins in Vibrio cholerae attachment to chitin. (2/739)

The role of surface proteins in Vibrio cholerae attachment to chitin particles in vitro was studied. Treatment of V. cholerae O1 ATCC 14034 and ATCC 14035 with pronase E reduced the attachment of bacteria to chitin particles by 57 to 77%. A statistically significant reduction was also observed when the attachment to chitin was evaluated in the presence of homologous Sarkosyl-insoluble membrane proteins (MPs) (67 to 84%), N-acetylglucosamine (GlcNAc) (62%), the sugar that makes up chitin, and wheat germ agglutinin (40 to 56%), a lectin that binds GlcNAc. The soluble oligomers N,N'-diacetylchitobiose or N,N', N"-triacetylchitotriose caused an inhibition of 14 to 23%. Sarkosyl-insoluble MPs able to bind chitin particles were isolated and visualized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis; two of these peptides (molecular sizes, 36 and 53 kDa) specifically bind GlcNAc.  (+info)

Pronase destroys the lipopolysaccharide receptor CD14 on Kupffer cells. (3/739)

CD14 is a lipopolysaccharide (LPS) receptor distributed largely in macrophages, monocytes, and neutrophils; however, the role of CD14 in activation of Kupffer cells by LPS remains controversial. The purpose of this study was to determine if different methods used to isolate Kupffer cells affect CD14. Kupffer cells were isolated by collagenase (0.025%) or collagenase-Pronase (0.02%) perfusion and differential centrifugation using Percoll gradients and cultured for 24 h before experiments. CD14 mRNA was detected by RT-PCR from Kupffer cell total RNA as well as from peritoneal macrophages. Western blotting showed that Kupffer cells prepared with collagenase possess CD14; however, it was absent in cells obtained by collagenase-Pronase perfusion. Intracellular calcium in Kupffer cells prepared with collagenase was increased transiently to levels around 300 nM by addition of LPS with 5% rat serum, which contains LPS binding protein. This increase in intracellular calcium was totally serum dependent. Moreover, LPS-induced increases in intracellular calcium in Kupffer cells were blunted significantly (40% of controls) when cells were treated with phosphatidylinositol-specific phospholipase C, which cleaves CD14 from the plasma membrane. However, intracellular calcium did not increase when LPS was added to cells prepared by collagenase-Pronase perfusion even in the presence of serum. These cells were viable, however, because ATP increased intracellular calcium to the same levels as cells prepared with collagenase perfusion. Tumor necrosis factor-alpha (TNF-alpha) mRNA was increased in Kupffer cells prepared with collagenase perfusion 1 h after addition of LPS, an effect potentiated over twofold by serum; however, serum did not increase TNF-alpha mRNA in cells isolated via collagenase-Pronase perfusion. Moreover, treatment with Pronase rapidly decreased CD14 on mouse macrophages (RAW 264.7 cells) and Kupffer cells. These findings indicate that Pronase cleaves CD14 from Kupffer cells, whereas collagenase perfusion does not, providing an explanation for why Kupffer cells do not exhibit a CD14-mediated pathway when prepared with procedures using Pronase. It is concluded that Kupffer cells indeed contain a functional CD14 LPS receptor when prepared gently.  (+info)

Tonic activation of presynaptic GABAB receptors in the opener neuromuscular junction of crayfish. (4/739)

Release of excitatory transmitter from boutons on crayfish nerve terminals was inhibited by (R,S)-baclofen, an agonist at GABAB receptors. Baclofen had no postsynaptic actions as it reduced quantal content without affecting quantal amplitude. The effect of baclofen increased with concentration producing 18% inhibition at 10 microM; EC50, 50% inhibition at 30 microM; maximal inhibition, 85% at 100 microM and higher. There was no desensitization, even with 200 or 320 microM baclofen. Phaclofen, an antagonist at GABAB receptors, competitively antagonized the inhibitory action of baclofen (KD = 50 microM, equivalent to a pA2 = 4.3 +/- 0.1). Phaclofen on its own at concentrations below 200 microM had no effect on release, whereas at 200 microM phaclofen itself increased the control level of release by 60%, as did 2-hydroxy-saclofen (200 microM), another antagonist at GABAB receptors. This increase was evidently due to antagonism of a persistent level of GABA in the synaptic cleft, since the effect was abolished by destruction of the presynaptic inhibitory fiber, using intra-axonal pronase. We conclude that presynaptic GABAB receptors, with a pharmacological profile similar to that of mammalian GABAB receptors, are involved in the control of transmitter release at the crayfish neuromuscular junction.  (+info)

A study of the native-denatured (N in equilibrium with D) transition in lysozyme. II. Kinetic analysis of protease digestion. (5/739)

Kinetic analyses of the protease digestion of several chemical derivatives of lysozyme [EC 3.2.1.17] showed that only the D(denatured) state of the protein is digested and that the reaction velocity is proportional to the equilibrium constant (KD) of the N in equilibrium with D transition of the protein. Alteration of the net charge of lysozyme by acetylation caused a shift of the N in equilibrium with D transition to the right (ten-fold increase in KD compared to that of native enzyme). Both the formation of a lysozyme-inhibitor complex and the introduction of a covalent bond in the lysozyme molecule restricted the transition. The magnitude of the N in equilibrium with D transition is related to the susceptibility of lysozyme to protease digestion and it is estimated that the N in equilibrium with D transition in proteins is generally important in the intracellular catabolism of proteins.  (+info)

Infection of chicken embryonic fibroblasts by measles virus: adaptation at the virus entry level. (6/739)

Measles virus (MV) has a tropism restricted to humans and primates and uses the human CD46 molecule as a cellular receptor. MV has been adapted to grow in chicken embryonic fibroblasts (CEF) and gave rise to an attenuated live vaccine. Halle and Schwarz MV strains were compared in their ability to infect both simian Vero cells and CEF. Whereas both strains infected Vero cells, only the CEF-adapted Schwarz strain was able to efficiently infect CEF. Since the expression of the human MV receptor CD46 rendered the chicken embryonic cell line TCF more permissive to the infection by the Halle MV strain, the MV entry into CEF appeared to be a limiting step in the absence of prior MV adaptation. CEF lacked reactivity with anti-CD46 antibodies but were found to express another protein allowing MV binding as an alternative receptor to CD46.  (+info)

Structural heterogeneity in the core oligosaccharide of the S-layer glycoprotein from Aneurinibacillus thermoaerophilus DSM 10155. (7/739)

The surface layer glycoprotein of Aneurinibacillus thermoaerophilus DSM 10155 has a total carbohydrate content of 15% (by mass), consisting of O-linked oligosaccharide chains. After proteolytic digestion of the S-layer glycoprotein byPronase E and subsequent purification of the digestion products by gel permeation chromatography, chromatofocusing and high-performance liquid chromatography two glycopeptide pools A and B with identical glycans and the repeating unit structure -->4)-alpha-l-Rha p -(1-->3)-beta-d- glycero -d- manno -Hep p -(1--> (Kosma et al., 1995b, Glycobiology, 5, 791-796) were obtained. Combined evidence from modified Edman-degradation in combination with liquid chromatography electrospray mass-spectrometry and nuclear magnetic resonance spectroscopy revealed that both glycopeptides contain equal amounts of the complete core structure alpha-l-Rha p -(1-->3)-alpha-l-Rha p -(1-->3)-beta-d-Gal p NAc-(1-->O)-Thr/Ser and the truncated forms alpha-l-Rha p -(1-->3)-beta-d-Gal p NAc-(1-->O)-Thr/Ser and beta-d-Gal p NAc-(1-->O)-Thr/Ser. All glycopeptides possessed the novel linkage types beta-d-Gal p NAc-(1-->O)-Thr/Ser. The different cores were substituted with varying numbers of disaccharide repeating units. By 300 MHz proton nuclear magnetic resonance spectroscopy the complete carbohydrate core structure of the fluorescently labeled glyco-peptide B was determined after Smith-degradation of its glycan chain. The NMR data confirmed and complemented the results of the mass spectroscopy experiments. Based on the S-layer glycopeptide structure, a pathway for its biosynthesis is suggested.  (+info)

Interaction of secreted nascent chains with surrounding membrane in Bacillus subtilis. (8/739)

To determine the length of secreted nascent polypeptide chain that is surrounded by membrane, we digested labeled nascent chains protruding from protoplasts of Bacillus subtilis with Pronase and isolated the residual ribosome-attached chains from the membrane-polysome fraction. Gel chromatography revealed a sharp major peak that had been protected by membrane plus bound ribosomes. The ribosomes themselves protected half as great a length. Because no free chain between the ribosome and the membrane was detected by Pronase treatment, the difference between the two protected lengths should measure the length protected by the membrane. More accurate measurements of these lengths, obtained by dansylation of the exposed NH2 terminus of the isolated fragments, yielded a difference of 21 amino acids. This value corresponds to an extended chain of 75 A, which is approximately the thickness of the bacterial cell membrane. We earlier presented evidence that bacterial ribosomes are attached to membrane solely by their secreted chain. The present results further show that after loss of the extracellular segment of the chain its attachment persists, at 37 degrees as well as 0 degrees C. These findings suggest that the chain does not slip through a passive membrane but is actively held within a channel.  (+info)

Pronase is not a medical term itself, but it is a proteolytic enzyme mixture derived from the bacterium Streptomyces griseus. The term "pronase" refers to a group of enzymes that can break down proteins into smaller peptides and individual amino acids by hydrolyzing their peptide bonds.

Pronase is used in various laboratory applications, including protein degradation, DNA and RNA isolation, and the removal of contaminating proteins from nucleic acid samples. It has also been used in some medical research contexts to study protein function and structure, as well as in certain therapeutic settings for its ability to break down proteins.

It is important to note that pronase is not a drug or a medical treatment itself but rather a laboratory reagent with potential applications in medical research and diagnostics.

Peptide hydrolases, also known as proteases or peptidases, are a group of enzymes that catalyze the hydrolysis of peptide bonds in proteins and peptides. They play a crucial role in various biological processes such as protein degradation, digestion, cell signaling, and regulation of various physiological functions. Based on their catalytic mechanism and the specificity for the peptide bond, they are classified into several types, including serine proteases, cysteine proteases, aspartic proteases, and metalloproteases. These enzymes have important clinical applications in the diagnosis and treatment of various diseases, such as cancer, viral infections, and inflammatory disorders.

Trypsin is a proteolytic enzyme, specifically a serine protease, that is secreted by the pancreas as an inactive precursor, trypsinogen. Trypsinogen is converted into its active form, trypsin, in the small intestine by enterokinase, which is produced by the intestinal mucosa.

Trypsin plays a crucial role in digestion by cleaving proteins into smaller peptides at specific arginine and lysine residues. This enzyme helps to break down dietary proteins into amino acids, allowing for their absorption and utilization by the body. Additionally, trypsin can activate other zymogenic pancreatic enzymes, such as chymotrypsinogen and procarboxypeptidases, thereby contributing to overall protein digestion.

Carbohydrates are a major nutrient class consisting of organic compounds that primarily contain carbon, hydrogen, and oxygen atoms. They are classified as saccharides, which include monosaccharides (simple sugars), disaccharides (double sugars), oligosaccharides (short-chain sugars), and polysaccharides (complex carbohydrates).

Monosaccharides, such as glucose, fructose, and galactose, are the simplest form of carbohydrates. They consist of a single sugar molecule that cannot be broken down further by hydrolysis. Disaccharides, like sucrose (table sugar), lactose (milk sugar), and maltose (malt sugar), are formed from two monosaccharide units joined together.

Oligosaccharides contain a small number of monosaccharide units, typically less than 20, while polysaccharides consist of long chains of hundreds to thousands of monosaccharide units. Polysaccharides can be further classified into starch (found in plants), glycogen (found in animals), and non-starchy polysaccharides like cellulose, chitin, and pectin.

Carbohydrates play a crucial role in providing energy to the body, with glucose being the primary source of energy for most cells. They also serve as structural components in plants (cellulose) and animals (chitin), participate in various metabolic processes, and contribute to the taste, texture, and preservation of foods.

Molecular weight, also known as molecular mass, is the mass of a molecule. It is expressed in units of atomic mass units (amu) or daltons (Da). Molecular weight is calculated by adding up the atomic weights of each atom in a molecule. It is a useful property in chemistry and biology, as it can be used to determine the concentration of a substance in a solution, or to calculate the amount of a substance that will react with another in a chemical reaction.

Gel chromatography is a type of liquid chromatography that separates molecules based on their size or molecular weight. It uses a stationary phase that consists of a gel matrix made up of cross-linked polymers, such as dextran, agarose, or polyacrylamide. The gel matrix contains pores of various sizes, which allow smaller molecules to penetrate deeper into the matrix while larger molecules are excluded.

In gel chromatography, a mixture of molecules is loaded onto the top of the gel column and eluted with a solvent that moves down the column by gravity or pressure. As the sample components move down the column, they interact with the gel matrix and get separated based on their size. Smaller molecules can enter the pores of the gel and take longer to elute, while larger molecules are excluded from the pores and elute more quickly.

Gel chromatography is commonly used to separate and purify proteins, nucleic acids, and other biomolecules based on their size and molecular weight. It is also used in the analysis of polymers, colloids, and other materials with a wide range of applications in chemistry, biology, and medicine.

Glycoproteins are complex proteins that contain oligosaccharide chains (glycans) covalently attached to their polypeptide backbone. These glycans are linked to the protein through asparagine residues (N-linked) or serine/threonine residues (O-linked). Glycoproteins play crucial roles in various biological processes, including cell recognition, cell-cell interactions, cell adhesion, and signal transduction. They are widely distributed in nature and can be found on the outer surface of cell membranes, in extracellular fluids, and as components of the extracellular matrix. The structure and composition of glycoproteins can vary significantly depending on their function and location within an organism.

Mannose is a simple sugar (monosaccharide) that is similar in structure to glucose. It is a hexose, meaning it contains six carbon atoms. Mannose is a stereoisomer of glucose, meaning it has the same chemical formula but a different structural arrangement of its atoms.

Mannose is not as commonly found in foods as other simple sugars, but it can be found in some fruits, such as cranberries, blueberries, and peaches, as well as in certain vegetables, like sweet potatoes and turnips. It is also found in some dietary fibers, such as those found in beans and whole grains.

In the body, mannose can be metabolized and used for energy, but it is also an important component of various glycoproteins and glycolipids, which are molecules that play critical roles in many biological processes, including cell recognition, signaling, and adhesion.

Mannose has been studied as a potential therapeutic agent for various medical conditions, including urinary tract infections (UTIs), because it can inhibit the attachment of certain bacteria to the cells lining the urinary tract. Additionally, mannose-binding lectins have been investigated for their potential role in the immune response to viral and bacterial infections.

Monoiodotyrosine (MIT) is a thyroid hormone precursor that is formed by the iodination of the amino acid tyrosine. It is produced in the thyroid gland as part of the process of creating triiodothyronine (T3) and thyroxine (T4), which are active forms of thyroid hormones. MIT itself does not have significant biological activity, but it plays a crucial role in the synthesis of more important thyroid hormones.

Periodic acid is not a medical term per se, but it is a chemical reagent that is used in some laboratory tests and staining procedures in the field of pathology, which is a medical specialty.

Periodic acid is an oxidizing agent with the chemical formula HIO4 or H5IO6. It is often used in histology (the study of the microscopic structure of tissues) to perform a special staining technique called the periodic acid-Schiff (PAS) reaction. This reaction is used to identify certain types of carbohydrates, such as glycogen and some types of mucins, in tissues.

The periodic acid first oxidizes the carbohydrate molecules, creating aldehydes. These aldehydes then react with a Schiff reagent, which results in a pink or magenta color. This reaction can help pathologists identify and diagnose various medical conditions, such as cancer, infection, and inflammation.

Decapodiformes is a taxonomic order of marine cephalopods, which includes squids, octopuses, and cuttlefish. The name "Decapodiformes" comes from the Greek words "deca," meaning ten, and "podos," meaning foot, referring to the fact that these animals have ten limbs.

However, it is worth noting that within Decapodiformes, octopuses are an exception as they only have eight arms. The other members of this order, such as squids and cuttlefish, have ten appendages, which are used for locomotion, feeding, and sensory perception.

Decapodiformes species are known for their complex behaviors, sophisticated communication systems, and remarkable adaptations that enable them to thrive in a variety of marine habitats. They play important ecological roles as both predators and prey in the ocean food chain.

Glucosamine is a natural compound found in the body, primarily in the fluid around joints. It is a building block of cartilage, which is the tissue that cushions bones and allows for smooth joint movement. Glucosamine can also be produced in a laboratory and is commonly sold as a dietary supplement.

Medical definitions of glucosamine describe it as a type of amino sugar that plays a crucial role in the formation and maintenance of cartilage, ligaments, tendons, and other connective tissues. It is often used as a supplement to help manage osteoarthritis symptoms, such as pain, stiffness, and swelling in the joints, by potentially reducing inflammation and promoting cartilage repair.

There are different forms of glucosamine available, including glucosamine sulfate, glucosamine hydrochloride, and N-acetyl glucosamine. Glucosamine sulfate is the most commonly used form in supplements and has been studied more extensively than other forms. While some research suggests that glucosamine may provide modest benefits for osteoarthritis symptoms, its effectiveness remains a topic of ongoing debate among medical professionals.

... at the U.S. National Library of Medicine Medical Subject Headings (MeSH) Portal: Biology v t e (EC 3.4.24, All stub ... Pronase is under investigation as a way to improve image quality in gastroscopy by thinning the mucus in advance. Proteinase K ... Pronase is a commercially available mixture of proteases isolated from the extracellular fluid of Streptomyces griseus. ...
"Destruction of Sodium Conductance Inactivation in Squid Axons Perfused with Pronase". J. Gen. Physiol. 62 (4): 375-391. doi: ...
The Ge3 epitope is encoded by exon 3. It is sensitive to trypsin but resistant to chymotrypsin, papain and pronase. It is ... pronase and neuraminidase. The relatively rare Leach phenotype is due either to a deletion in exons 3 and 4 or to a frameshift ... It is located within exon 2 and is sensitive to trypsin and papain but resistant to chymotrypsin and pronase. ...
Enzymes such as pronase and most effectively proteinase K from Tritirachium album degrade PLA. Four possible end-of-life ...
ZD uses a digestive enzyme like pronase which makes it a chemical drilling method. The chemicals used in ZD may have a damaging ...
... (EC 3.4.24.31, pronase component, Streptomyces griseus neutral proteinase, actinase E, SGNPI) is an enzyme. This ...
Agramont became an agricultural engineer and served as the national director of Productora Nacional de Semillas (PRONASE). ...
What is left is digested cellular content mixed with tissue; pronase/DNAse is added to clean up dead cellular material as well ...
The researchers found that in the absence of pronase, the system was only able to release less than 20% of its cargo in 24 ... The trigger for this system was the presence of a lysosomal proteolytic enzyme (protease), in this case, pronase. ... hours, however, in the presence of pronase, there was a 90% release of cargo within 5 hours. Within the topic of gated drug ...
... pronase, and hydrogenase, among others. The efficacy of these enzymes depends on the type of plastic being degraded. ...
Pronase)". Journal of Biochemistry. 104 (3): 451-6. PMID 3149277. Komiyama T, Bigler TL, Yoshida N, Noda K, Laskowski M (June ...
... while the innermost is sensitive to cellulase and pronase. Around the outside of the cell membrane is the bacterial cell wall. ...
This suggested a physical, tethered mechanism for inactivation as the pronase was inferred to degrade the channel blocker and ... showing that internal treatment with pronase disrupted the inactivation phenomenon. ...
Her cell fusion technique was successful where others had failed due to the choice to remove the zona pellucida with pronase ...
... pronase or alpha-chymotrypsin. There are about 40 known variants in the MNS blood group system. These have arisen largely as a ...
... or pronase, before agitating the tissue to release the cells into suspension. Alternatively, pieces of tissue can be placed in ...
... (EC 3.4.21.81, Streptomyces griseus protease B, pronase B, serine proteinase B, Streptomyces griseus proteinase ...
More specifically, the law proposes: The creation of a National Program for Sustainable Energy Use (PRONASE), which targets ...
... pronase MeSH D08.811.277.656.300.760.733 - protease la MeSH D08.811.277.656.300.760.787 - subtilisins MeSH D08.811.277.656. ... pronase MeSH D08.811.277.656.300.480.827 - thermolysin MeSH D08.811.277.656.300.760 - serine endopeptidases MeSH D08.811. ... pronase MeSH D08.811.277.656.675.374.827 - thermolysin MeSH D08.811.277.656.675.555 - metalloexopeptidases MeSH D08.811.277.656 ...
It is also marketed as a combination drug with cromoglicic acid as Frenal Compositum, in combination with pronase as Isopal P, ...
... alone or after an initial short pre-incubation phase with pronase (0.2% - 1%). Cell yield after enzymatic digestion of the ...
Pronase at the U.S. National Library of Medicine Medical Subject Headings (MeSH) Portal: Biology v t e (EC 3.4.24, All stub ... Pronase is under investigation as a way to improve image quality in gastroscopy by thinning the mucus in advance. Proteinase K ... Pronase is a commercially available mixture of proteases isolated from the extracellular fluid of Streptomyces griseus. ...
It is intended to be used in combination with Biocares Pronase enzyme concentrate of the Carezyme III: Pronase Kit for IHC and ... Pronase Buffer is provided in a ready-to-use format. ... Pronase Buffer quantity. Add to cart. SKU: PRB957H Categories: ... Pronase Buffer is provided in a ready-to-use format. It is intended to be used in combination with Biocares Pronase enzyme ... concentrate of the Carezyme III: Pronase Kit for IHC and ISH procedures. ...
Eistraining (10 EUR pro Nase). Eistraining (10 EUR pro Nase) 27. September 2014. 19:30. - 21:00. ...
Pronase digestion of the purified heavy chains and subsequent end labeling with fluorescein isothiocyanate produced ...
The proteins were removed with pronase treatment. The remaining non-proteinaceous component was not stained by Coomassie blue ...
Ancillary studies: C4d negative, pronase studies negative for masked Ig. Chronicity grade: moderate (total renal chronicity ...
Pronase E : 0.15% Carbonate-Phosphate buffer. (see reference) Spielman, A. , Mody, I. , Brand, J. , Whitney, G. , MacDonald, J ...
Pronase; Dako) for the Chlamydiaceae antibody and repeated microwave treatment in citrate buffer (ChemMate; Dako) for the ...
Hosts and donors were dechorionated using Pronase, then arranged within the wells of a custom-molded agarose plate at ... then dechorionated using Pronase (Roche). At the 256-512 cell stage, watchmakers forceps were used to excise the animal ...
Figure 7 MALDI-TOF spectra of amino acid-SG adducts in pronase digests of rHSA (A) and amino acid-SG adducts in pronase digests ... Both trypsin and pronase digested samples were heat inactivated at 60°C for 30 min and centrifuged at 17,000 × g for 20 min ... The pronase digests were analyzed on the MALDI-TOF mass spectrometer using the same matrix and sample preparation detailed ... Our ability to detect Lys-, Cys-, and His-SG adducts in pronase/aminopeptidase digests of serum from patients exposed to S. ...
Ovaries were subjected to more gentle treatment with pronase solution (1 mg/ml of Pronase E, Sigma) in AdDF+++ with ROCK ... a For organoid derivation oviducts and ovaries were separated and subjected to collagenase or pronase treatment, respectively. ...
Structure of the O-glycosidically linked carbohydrate units of fetuin
Pro naše děti a mámy Pro naše děti a mámy http://www.knihcentrum.cz/pro-nase-deti-a-mamy ...
Benefit of pronase in image quality during EUS.. Han JP; Hong SJ; Moon JH; Lee GH; Byun JM; Kim HJ; Choi HJ; Ko BM; Lee MS. ... 4. Effect of pronase as mucolytic agent on imaging quality of magnifying endoscopy.. Kim GH; Cho YK; Cha JM; Lee SY; Chung IK. ... Effect of pronase premedication on narrow-band imaging endoscopy in patients with precancerous conditions of stomach.. Cha JM; ... Effects of premedication with Pronase for endoscopic ultrasound of the stomach: A randomized controlled trial.. Wang GX; Liu X ...
The effect of using Premedication of simethicone/pronase with or without Postural Change on Visualization of the Mucosa before ...
sensitive to trypsin, chmotrypsin, ficin, pronase, papain, and bromelain. Homo Sapiens. *Homo Sapiens ...
... isolated hippocampi were dissociated with Pronase E (0.5 mg/ml) and thermolysin (0.5 mg/ml) in HBSS (in mm: 130 NaCl, 10 HEPES ...
Pronase E from Streptomyces griseus min. 5.0 DMC-U/mg lyophil.. * Proteinase K from Tritirachium album solution 20 mg solid/ml ...
... and NHANES samples were prepared by performing a protein digestion using pronase to release the chlorinated tyrosine biomarkers ...
Alb was isolated and subject to a pronase digestion and the digest treated to isolate MDI-lysine and acetyl-MDI-lysine ...
HA preparation from umbilical cord (1 μg/ml) was digested with 150 U/ml hyaluronidase (HYAL) or pronase for 30 minutes followed ... HA preparation from umbilical cord (1 μg/ml) was digested with 150 U/ml hyaluronidase (HYAL) or pronase for 30 minutes followed ... The HA preparation used was treated with hyaluronidase or pronase before being added to the culture. Hyaluronidase treatment, ... but not pronase treatment, abolished the anti-osteoclastogenic activity of HA (Fig. 2A). We also examined other HA preparations ...
At 8 h postfertilization (hpf), embryos were dechorionated with Pronase enzyme and incubated with 5 μM Regorafenib containing ...
All prices presented are US list price for sale to clients in the Domestic US only. Please see your international distributor for country specific pricing. For a full list of international distributors, click here. ...
https://www.rybsvaz.cz/beta/index.php/1111-opereni-rybozravi-predatori-aneb-nejen-kormoran-velky-je-ptaci-hrozbou-pro-nase-ryby ...
C under agitation in GBSS containing 0.5 g/L collagenase IV and 0.5 g/L pronase (MilliporeSigma). Cells were then passed ...
1 mg mL-1 Pronase was added to biotin-labeled tubulin, and left for 1 h at 37 °C.. This mixture was added to avidin solution, ...
Prior to antibody incubation, some strips were treated for 1 h with either Pronase E (Sigma, 1 mg ml−1 in 50 mM Tris-HCl, pH ... Pronase treatment of the transferred proteins of P. cinnamomi abolished antibody binding; treatment with periodate did not (Fig ... Lanes c and d show strips pretreated with Pronase and periodate, respectively, before antibody incubations. Positions of ... Lanes c and d show strips pretreated with Pronase and periodate, respectively, before antibody incubations. Positions of ...
  • Briefly, calibrators, quality controls, a matrix blank, blind QCs, and NHANES samples were prepared by performing a protein digestion using pronase to release the chlorinated tyrosine biomarkers. (cdc.gov)
  • The thyroid hormone content of 1 capsule or tablet of herbal medicine, measured following Pronase digestion and ethanol extraction, was approximately 1 g of triiodothyronine and 3 to 4 g of thyroxine. (second-opinions.co.uk)
  • Immunofluorescence on frozen tissue presented false negative for kappa light chain, as ultimately proven by paraffin-embedded tissue after pronase digestion. (bvsalud.org)
  • Use of paraffin-embedded tissue after pronase digestion and immunoelectron microscopy is beneficial to improve the sensitivity of diagnosis. (bvsalud.org)
  • ¹⁴C-AFB₁ spiked corn sample (1 μCi/kg, original AFB₁ = 7500 ng/g) was subjected to sequential isolation and separation procedures (CH₂Cl₂, and CH₃OH extraction, followed by acetic acid and NaOH treatment or Pronase E digestion) to determine the distribution of ammonia/aflatoxin reaction products. (arizona.edu)
  • and 19% with acid-base treatment or Pronase digestion. (arizona.edu)
  • The final matrix following either the acid-base treatment or Pronase digestion contained 37% of the added radioactivity. (arizona.edu)
  • Pronase is a commercially available mixture of proteases isolated from the extracellular fluid of Streptomyces griseus. (wikipedia.org)
  • Enzymatic treatment with proteolytic enzymes (i.e. pepsin, trypsin or pronase) has been performed to expose the masked antigens. (enzolifesciences.com)
  • Pronase is a mixture of several nonspecific endo- and exoproteases that digest proteins down to single amino acids. (haoranbio.com)
  • Mintz instead removed the protective layer by treating the embryos with pronase, a mixture of enzymes designed to degrade the zona pellicula , causing minimal damage to the embryo. (asu.edu)
  • The tissue was soaked in pronase for two hours to remove mucus and fixed with 10% formalin before SICM investigation. (parksystems.com)
  • Mucus was removed from colon tissue surfaces with pronase treatment. (parksystems.com)
  • Destruction of sodium conductance inactivation in squid axons perfused with pronase. (xenbase.org)
  • Thin-layer chromatography of dinitrophenyl derivatives prepared from Pronase-digested microsomal protein and sodium dodecyl sulfate-polyacrylamide disc gel electrophoresis of solubilized microsomes indicated that the radiolabeled products were covalently bound to amino acid residues of microsomal protein. (aspetjournals.org)
  • This study aimed to confirm whether pre-procedure oral administration of pronase could improve the diagnostic performance of Lugol chromoendoscopy in high-risk patients being screened for early ESCC. (bvsalud.org)
  • The diagnostic performance of Lugol chromoendoscopy had improved with the use of pronase (area under the curve = 0.85 vs. 0.69, P = 0.019), accompanied by an increased sensitivity (86.67% vs. 47.62%, P = 0.004). (bvsalud.org)
  • CONCLUSIONS: Pre-procedure oral administration of pronase significantly increased the detection rate of early ESCC and optimized the diagnostic performance of Lugol chromoendoscopy, which should be recommended during routine endoscopic screening for early ESCC in high-risk patients. (bvsalud.org)
  • Raney nickel desulfunization of Pronase hydrolysates released several HCP metabolites that were apparently bound to sulfur-containing amino acids such as cysteine and homocysteine. (aspetjournals.org)
  • We observed that P- and E-selectin bound to pronase-sensitive ligands on murine monocytic WEHI-3 cells and murine neutrophils, indicating that the ligands for both selectins are glycoproteins. (ashpublications.org)
  • 2H5 and KM93 bound to pronase-resistant structures, indicating that the mAbs did not identify selectin ligands. (ashpublications.org)
  • The researchers also found that an antibody specific for the R2 domain labeled filaments before, but not after, pronase treatment. (alzforum.org)
  • The activity of SMAL was sensitive to pronase and heating at 100(DEGREES)C for 30 minutes but insensitive to RNase. (etsu.edu)
  • To determine if the R3 and R4 domains were necessary and sufficient to form the core, they treated their filament samples with pronase, which is known to remove all but the cores of tau fibrils. (alzforum.org)
  • Pronase is under investigation as a way to improve image quality in gastroscopy by thinning the mucus in advance. (wikipedia.org)
  • Pronase is a mixture of proteolytic enzymes that cause the complete hydrolysis of proteins. (themasterchemistry.com)
  • The sequencing of albumin-adduct tryptic peptides and the analysis of pronase/aminopeptidase digests demonstrated that lysyl, cysteinyl, and histidyl residues are involved in the formation of these adducts. (nih.gov)
  • 15. Premedication with pronase or N-acetylcysteine improves visibility during gastroendoscopy: an endoscopist-blinded, prospective, randomized study. (nih.gov)
  • TRIAL REGISTRATION: Pronase improves efficacy of Lugol chromoendoscopy screening on esophageal cancerous lesions (NCT02030769). (bvsalud.org)
  • 1. Efficacy and safety of using premedication with simethicone/Pronase during upper gastrointestinal endoscopy examination with sedation: A single center, prospective, single blinded, randomized controlled trial. (nih.gov)
  • 13. Determination of the optimal time for premedication with pronase, dimethylpolysiloxane, and sodium bicarbonate for upper gastrointestinal endoscopy. (nih.gov)
  • Pronase is under investigation as a way to improve image quality in gastroscopy by thinning the mucus in advance. (wikipedia.org)
  • 16. Benefit of pronase in image quality during EUS. (nih.gov)
  • 3. The effect of using Premedication of simethicone/pronase with or without Postural Change on Visualization of the Mucosa before Endoscopy: A prospective, double blinded, randomized controlled trial. (nih.gov)
  • 4. Effect of pronase as mucolytic agent on imaging quality of magnifying endoscopy. (nih.gov)
  • RESULTS: Pre-procedure oral administration of pronase improved mucosal visibility during Lugol chromoendoscopy (P = 0.008). (bvsalud.org)
  • This study aimed to confirm whether pre-procedure oral administration of pronase could improve the diagnostic performance of Lugol chromoendoscopy in high-risk patients being screened for early ESCC. (bvsalud.org)
  • Patients were randomly assigned (1:1) to groups with or without (control group) pronase administration. (bvsalud.org)
  • CONCLUSIONS: Pre-procedure oral administration of pronase significantly increased the detection rate of early ESCC and optimized the diagnostic performance of Lugol chromoendoscopy, which should be recommended during routine endoscopic screening for early ESCC in high-risk patients. (bvsalud.org)
  • In the Tanguay zebrafish toxicity testing workflow, the early life stage embryos are routinely staged and the chorions are enzymatically removed using pronase (63.6 mg/ml, 3.5 U/mg) at 4 hours post fertilization (hpf) with a custom automated dechorionator (Mandrell et al. (nih.gov)