Luciferases from BACTERIA such as PHOTOBACTERIUM; VIBRIO; and PHOTORHABDUS.
The family Lampyidae, which are bioluminescent BEETLES. They contain FIREFLY LUCIFERIN and LUCIFERASES. Oxidation of firefly luciferin results in luminescence.
Luciferases from FIREFLIES, usually Photinus, that oxidizes FIREFLY LUCIFERIN to cause emission of PHOTONS.
Enzymes that oxidize certain LUMINESCENT AGENTS to emit light (PHYSICAL LUMINESCENCE). The luciferases from different organisms have evolved differently so have different structures and substrates.
A benzothaizole which is oxidized by LUCIFERASES, FIREFLY to cause emission of light (LUMINESCENCE).
A family of gram-negative bacteria whose members predominate in the bacterial flora of PLANKTON; FISHES; and SEAWATER. Some members are important pathogens for humans and animals.
INSECTS of the order Coleoptera, containing over 350,000 species in 150 families. They possess hard bodies and their mouthparts are adapted for chewing.
Emission of LIGHT when ELECTRONS return to the electronic ground state from an excited state and lose the energy as PHOTONS. It is sometimes called cool light in contrast to INCANDESCENCE. LUMINESCENT MEASUREMENTS take advantage of this type of light emitted from LUMINESCENT AGENTS.
Luciferases from RENILLA that oxidizes certain LUMINESCENT AGENTS to cause emission of PHOTONS.
Techniques used for determining the values of photometric parameters of light resulting from LUMINESCENCE.
A genus of bioluminescent marine invertebrates in the family Renillidae, order Pennatulacea, class ANTHOZOA. It contains Renilla LUCIFERASE which oxidizes coelenterazine resulting in LUMINESCENCE.
A huge subclass of mostly marine CRUSTACEA, containing over 14,000 species. The 10 orders comprise both planktonic and benthic organisms, and include both free-living and parasitic forms. Planktonic copepods form the principle link between PHYTOPLANKTON and the higher trophic levels of the marine food chains.
Organisms that live in water.
A genus of gram-negative, facultatively anaerobic, rod-shaped bacteria that are common in the marine environment and on the surfaces and in the intestinal contents of marine animals. Some species are bioluminescent and are found as symbionts in specialized luminous organs of fish.
Compound such as LUMINESCENT PROTEINS that cause or emit light (PHYSICAL LUMINESCENCE).
A genus of gram-negative bacteria existing symbiotically with nematodes of the family Heterorhabditidae (see RHABDITOIDEA). These nematodes infect a variety of soil-dwelling insects. Upon entering an insect host, the nematode releases Photorhabdus from its intestinal tract and the bacterium establishes a lethal septicemia in the insect.
The reconstitution of a protein's activity following denaturation.
The visually perceived property of objects created by absorption or reflection of specific wavelengths of light.
The extent to which an enzyme retains its structural conformation or its activity when subjected to storage, isolation, and purification or various other physical or chemical manipulations, including proteolytic enzymes and heat.
A genus of VIBRIONACEAE, made up of short, slightly curved, motile, gram-negative rods. Various species produce cholera and other gastrointestinal disorders as well as abortion in sheep and cattle.
Proteins which are involved in the phenomenon of light emission in living systems. Included are the "enzymatic" and "non-enzymatic" types of system with or without the presence of oxygen or co-factors.
Genes whose expression is easily detectable and therefore used to study promoter activity at many positions in a target genome. In recombinant DNA technology, these genes may be attached to a promoter region of interest.
The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION.
The rate dynamics in chemical or physical systems.
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.
The arrangement of two or more amino acid or base sequences from an organism or organisms in such a way as to align areas of the sequences sharing common properties. The degree of relatedness or homology between the sequences is predicted computationally or statistically based on weights assigned to the elements aligned between the sequences. This in turn can serve as a potential indicator of the genetic relatedness between the organisms.
Proteins prepared by recombinant DNA technology.
The parts of a macromolecule that directly participate in its specific combination with another molecule.

In vivo chaperone activity of heat shock protein 70 and thermotolerance. (1/8235)

Heat shock protein 70 (Hsp70) is thought to play a critical role in the thermotolerance of mammalian cells, presumably due to its chaperone activity. We examined the chaperone activity and cellular heat resistance of a clonal cell line in which overexpression of Hsp70 was transiently induced by means of the tetracycline-regulated gene expression system. This single-cell-line approach circumvents problems associated with clonal variation and indirect effects resulting from constitutive overexpression of Hsp70. The in vivo chaperone function of Hsp70 was quantitatively investigated by using firefly luciferase as a reporter protein. Chaperone activity was found to strictly correlate to the level of Hsp70 expression. In addition, we observed an Hsp70 concentration dependent increase in the cellular heat resistance. In order to study the contribution of the Hsp70 chaperone activity, heat resistance of cells that expressed tetracycline-regulated Hsp70 was compared to thermotolerant cells expressing the same level of Hsp70 plus all of the other heat shock proteins. Overexpression of Hsp70 alone was sufficient to induce a similar recovery of cytoplasmic luciferase activity, as does expression of all Hsps in thermotolerant cells. However, when the luciferase reporter protein was directed to the nucleus, expression of Hsp70 alone was not sufficient to yield the level of recovery observed in thermotolerant cells. In addition, cells expressing the same level of Hsp70 found in heat-induced thermotolerant cells containing additional Hsps showed increased resistance to thermal killing but were more sensitive than thermotolerant cells. These results suggest that the inducible form of Hsp70 contributes to the stress-tolerant state by increasing the chaperone activity in the cytoplasm. However, its expression alone is apparently insufficient for protection of other subcellular compartments to yield clonal heat resistance to the level observed in thermotolerant cells.  (+info)

Transcriptional regulation and induction of apoptosis: implications for the use of monomeric p53 variants in gene therapy. (2/8235)

The p53 tumour suppressor protein is a transcriptional activator, which can induce cell cycle arrest and apoptosis. p53 Gene mutations occur in more than 50% of all human tumours. Reintroduction of wild-type p53 but also of oligomerisation-independent p53 variants into tumour cells by gene transfer methods has been considered. We have investigated the biological properties of two carboxy-terminal deletion mutants of p53, p53 delta 300 (comprising amino acids 1-300) and p53 delta 326 (amino acids 1-326), to evaluate their potential deployment in gene therapy. Transactivation was measured in transiently transfected HeLa and SKBR3 cells. Both monomeric variants showed reduced activities compared with wild-type p53. Individual promoters were differently affected. In contrast to wild-type p53, monomeric variants were not able to induce apoptosis. We also provided wild-type p53 and p53 delta 326 with tetracycline-regulated promoters and stably introduced these constructs into Saos2 and SKBR3 cells. Upon induction, wild-type p53 expressing cells, but not p53 delta 326 expressing cells underwent apoptosis. Consistently, only wild-type p53 expressing cells accumulated p21/waf1/cip1 mRNA and protein and showed increased bax, Gadd45 and mdm2 mRNA. Neither wild-type p53 nor p53 delta 326 repressed the transcription of the IGF-1R gene in these cell lines. We conclude that the transactivation potential of monomeric, carboxy-terminally truncated p53 is not sufficient to cause induction of the endogenous target genes which trigger apoptosis.  (+info)

A strategy for enhancing the transcriptional activity of weak cell type-specific promoters. (3/8235)

Cell type- and tissue-specific promoters play an important role in the development of site-selective vectors for gene therapy. A large number of highly specific promoters has been described, but their applicability is often hampered by their inefficient transcriptional activity. In this study, we describe a new strategy for enhancing the activity of weak promoters without loss of specificity. The basic principle of this strategy is to establish a positive feedback loop which is initiated by transcription from a cell type-specific promoter. This was achieved by using a cell type-specific promoter to drive the simultaneous expression of the desired effector/reporter gene product and a strong artificial transcriptional activator which stimulates transcription through appropriate binding sites in the promoter. Using a VP16-LexA chimeric transcription factor, we show that this approach leads to a 14- to > 100-fold enhancement of both the endothelial cell-specific von Willebrand factor promoter and the gastrointestinal-specific sucrase-isomaltase promoter while maintaining approximately 30- to > 100-fold cell type specificity.  (+info)

Ligand substitution of receptor targeted DNA complexes affects gene transfer into hepatoma cells. (4/8235)

We have targeted the serpin enzyme complex receptor for gene transfer in human hepatoma cell lines using peptides < 30 amino acids in length which contain the five amino acid recognition sequence for this receptor, coupled to poly K of average chain length 100 K, using the heterobifunctional coupling reagent sulfo-LC SPDP. The number of sulfo-LC SPDP modified poly-L-lysine residues, as well as the degree of peptide substitution was assessed by nuclear magnetic resonance spectroscopy. Conjugates were prepared in which 3.5%, 7.8% or 26% of the lysine residues contained the sulfo-LC SPDP moiety. Each of these conjugates was then coupled with ligand peptides so that one in 370, one in 1039, or one in 5882 lysines were substituted with receptor ligand. Electron microscopy and atomic force microscopy were used to assess complex structure and size. HuH7 human hepatoma cells were transfected with complexes of these conjugates with the plasmid pGL3 and luciferase expression measured 2 to 16 days after treatment. All the protein conjugates in which 26% of the K residues were modified with sulfo-LC SPDP were poor gene transfer reagents. Complexes containing less substituted poly K, averaged 17 +/- 0.5 nm in diameter and gave peak transgene expression of 3-4 x 10(6) ILU/mg which persisted (> 7 x 10(5) ILU) at 16 days. Of these, more substituted polymers condensed DNA into complexes averaging 20 +/- 0.7 nm in diameter and gave five-fold less luciferase than complexes containing less substituted conjugates. As few as eight to 11 ligands per complex are optimal for DNA delivery via the SEC receptor. The extent of substitution of receptor-mediated gene transfer complexes affects the size of the complexes, as well as the intensity and duration of transgene expression. These observations may permit tailoring of complex construction for the usage required.  (+info)

Cadmium-mediated activation of the metal response element in human neuroblastoma cells lacking functional metal response element-binding transcription factor-1. (5/8235)

Metal response element-binding transcription factor-1 (MTF-1) binds specifically to metal response elements (MREs) and transactivates metallothionein (MT) gene expression in response to zinc and cadmium. This investigation contrasts the mechanism of mouse MT gene (mMT-I) promoter activation by cadmium and zinc in IMR-32 human neuroblastoma cells to determine whether MTF-1 binding to the MRE is necessary for activation by these metals. Cadmium activated a mMT-1 promoter (-150 base pairs) luciferase reporter 20-25-fold through a MRE-dependent mechanism. In contrast, zinc had little effect on the mMT-1 luciferase reporter. IMR-32 cells lacked MRE binding activity, and treatment with zinc in vitro or in vivo did not generate a MTF-1. MRE complex, suggesting that IMR-32 cells lack functional MTF-1. Overexpression of mMTF-1 regenerated a zinc-mediated induction of the MRE without affecting cadmium activation. Because no other transition metals tested activated the MRE, this effect appeared to be cadmium-specific. These data demonstrate that in IMR-32 human neuroblastoma cells, zinc and cadmium can use independent mechanisms for activation of the mMT-I promoter and cadmium-mediated MRE activation is independent of MTF-1 and zinc.  (+info)

Gene expression and chromatin organization during mouse oocyte growth. (6/8235)

Mouse oocytes can be classified according to their chromatin organization and the presence [surrounded nucleolus (SN) oocytes] or absence [nonsurrounded nucleolus (NSN) oocytes] of a ring of Hoechst-positive chromatin around the nucleolus. Following fertilization only SN oocytes are able to develop beyond the two-cell stage. These studies indicate a correlation between SN and NSN chromatin organization and the developmental competence of the female gamete, which may depend on gene expression. In the present study, we have used the HSP70.1Luc transgene (murine HSP70.1 promoter + reporter gene firefly luciferase) to analyze gene expression in oocytes isolated from ovaries of 2-day- to 13-week-old females. Luciferase was assayed on oocytes after classification as SN or NSN type. Our data show that SN oocytes always exhibit a higher level of luciferase activity, demonstrating a higher gene expression in this category. Only after meiotic resumption, metaphase II oocytes derived from NSN or SN oocytes acquire the same level of transgene expression. We suggest that the limited availability of transcripts and corresponding proteins, excluded from the cytoplasm until GVBD in NSN oocytes, could explain why these oocytes have a lower ability to sustain embryonic development beyond the two-cell stage at which major zygotic transcription occurs. With this study we have furthered our knowledge of epigenetic regulation of gene expression in oogenesis.  (+info)

UV-A-induced decrease in nuclear factor-kappaB activity in human keratinocytes. (7/8235)

Previous reports have demonstrated an increase in nuclear factor-kappaB (NF-kappaB) activity in response to UV radiation. These studies have essentially focused on the DNA-damaging fraction of solar UV radiation (UV-B and UV-C). In contrast, the effects of UV-A radiation (320-400 nm) on NF-kappaB are not well known. In this study, we present evidence that UV-A radiation induces a marked decrease in NF-kappaB DNA-binding activity in NCTC 2544 human keratinocytes. In addition, NCTC 2544 keratinocytes pretreated with UV-A fail to respond to NF-kappaB inducers. Moreover, UV-A radiation induces a decrease in NF-kappaB-driven luciferase reporter gene expression in NCTC 2544 keratinocytes. The expression of the gene encoding IkappaBalpha (IkappaB is the NF-kappaB inhibitor), which is closely associated with NF-kappaB activity, is also reduced (3-fold) upon UV-A treatment. Our results indicate that the UV-A-induced decrease in NF-kappaB DNA-binding activity is associated with a decrease in the levels of the p50 and p65 protein subunits. This is the first evidence that an oxidative stress, such as UV-A radiation, may induce a specific decrease in NF-kappaB activity in mammalian cells, probably through degradation of NF-kappaB protein subunits. These findings suggest that UV-A could modulate the NF-kappaB-dependent gene expression.  (+info)

Modulation of human airway smooth muscle proliferation by type 3 phosphodiesterase inhibition. (8/8235)

Elevation in cell cAMP content can inhibit mitogenic signaling in cultured human airway smooth muscle (HASM) cells. We studied the effects of the type 3-selective phosphodiesterase inhibitor siguazodan, the type 4-selective phosphodiesterase inhibitor rolipram, and the nonselective inhibitor 3-isobutyl-1-methylxanthine (IBMX) on proliferation of cultured HASM cells. At concentrations selective for the type 3 phosphodiesterase isoform, siguazodan inhibited both [3H]thymidine incorporation (IC50 2 microM) and the increase in cell number (10 microM; 64% reduction) induced by platelet-derived growth factor-BB (20 ng/ml). These effects were mimicked by IBMX. At concentrations selective for type 4 phosphodiesterase inhibition, rolipram was without effect. A 20-min exposure to siguazodan and rolipram did not increase whole cell cAMP levels. However, in HASM cells transfected with a cAMP-responsive luciferase reporter (p6CRE/Luc), increases in cAMP-driven luciferase expression were seen with siguazodan (3.9-fold) and IBMX (16.5-fold). These data suggest that inhibition of the type 3 phosphodiesterase isoform present in airway smooth muscle results in inhibition of mitogenic signaling, possibly through an increase in cAMP-driven gene expression.  (+info)

Luciferases are enzymes that catalyze the light-emitting reaction in bioluminescent organisms. Bacterial luciferases are specifically derived from luminous bacteria and are composed of two components: a heterodimeric enzyme (luciferase) and a small fatty aldehyde, typically decanal. The enzyme catalyzes the oxidation of the aldehyde in the presence of molecular oxygen, reduced flavin mononucleotide (FMNH2), and long-chain fatty acids, resulting in the formation of the corresponding acid and light emission. This light-emitting reaction is often used in various biochemical and biological applications, such as reporter gene assays, bioluminescent imaging, and biosensors.

I'm sorry for any confusion, but "fireflies" is not a term used in medical definitions. Fireflies are actually insects (beetles) that produce a chemical reaction in their bodies to create light, a phenomenon known as bioluminescence. There is no medical context or definition associated with the term "fireflies."

Luciferases are enzymes that catalyze the emission of light by a chemical reaction. Firefly luciferase is a specific type of luciferase that is found in fireflies and certain other insects. This enzyme catalyzes the oxidation of luciferin, a molecule that produces light when it is oxidized. The reaction also requires ATP (adenosine triphosphate) and oxygen. The light produced by this reaction is bioluminescence, which is light that is produced by a living organism. Firefly luciferase is widely used in research for a variety of purposes, including the detection of specific molecules and the study of gene expression.

Luciferases are a class of enzymes that catalyze the oxidation of their substrates, leading to the emission of light. This bioluminescent process is often associated with certain species of bacteria, insects, and fish. The term "luciferase" comes from the Latin word "lucifer," which means "light bearer."

The most well-known example of luciferase is probably that found in fireflies, where the enzyme reacts with a compound called luciferin to produce light. This reaction requires the presence of oxygen and ATP (adenosine triphosphate), which provides the energy needed for the reaction to occur.

Luciferases have important applications in scientific research, particularly in the development of sensitive assays for detecting gene expression and protein-protein interactions. By labeling a protein or gene of interest with luciferase, researchers can measure its activity by detecting the light emitted during the enzymatic reaction. This allows for highly sensitive and specific measurements, making luciferases valuable tools in molecular biology and biochemistry.

Firefly luciferin is not a medical term, but a biological term used to describe a compound involved in bioluminescence, specifically in fireflies.

Luciferin is a molecule that can produce light when it reacts with oxygen in the presence of an enzyme called luciferase and adenosine triphosphate (ATP), which is a source of energy in cells. In fireflies, this reaction occurs in specialized cells within the lantern organ of the insect, producing the characteristic glowing light.

While not directly related to medical terminology, bioluminescence and its underlying mechanisms have been studied for potential applications in medical research, such as developing sensitive biosensors for detecting various biological molecules or monitoring cellular processes.

Vibrionaceae is a family of Gram-negative, facultatively anaerobic, rod-shaped bacteria that are commonly found in aquatic environments. The bacteria are known for their ability to produce endotoxins and exotoxins, which can cause illness in humans and animals. Some members of this family are capable of causing foodborne illnesses, wound infections, and gastrointestinal diseases.

The most well-known genus within Vibrionaceae is Vibrio, which includes several species that are significant human pathogens. For example, Vibrio cholerae is the causative agent of cholera, a severe diarrheal disease that can lead to dehydration and death if left untreated. Other notable Vibrio species that can cause illness in humans include Vibrio parahaemolyticus and Vibrio vulnificus, which are often associated with raw or undercooked seafood consumption and wound infections, respectively.

Proper food handling, cooking, and hygiene practices can help prevent Vibrionaceae infections. People with weakened immune systems, chronic liver disease, or iron overload disorders may be at higher risk of severe illness from Vibrio infections and should take extra precautions to avoid exposure.

"Beetles" is not a medical term. It is a common name used to refer to insects belonging to the order Coleoptera, which is one of the largest orders in the class Insecta. Beetles are characterized by their hardened forewings, known as elytra, which protect their hind wings and body when not in use for flying.

There are many different species of beetles found all over the world, and some can have an impact on human health. For example, certain types of beetles, such as bed bugs and carpet beetles, can cause skin irritation and allergic reactions in some people. Other beetles, like the Colorado potato beetle, can damage crops and lead to economic losses for farmers. However, it is important to note that most beetles are not harmful to humans and play an essential role in ecosystems as decomposers and pollinators.

Luminescence is not a term that has a specific medical definition. However, in general terms, luminescence refers to the emission of light by a substance that has absorbed energy. This phenomenon can occur in some medical contexts, such as in medical imaging techniques like bioluminescence imaging (BLI) and chemiluminescence immunoassays (CLIA).

In BLI, genetically modified organisms or cells are used to produce light at specific wavelengths that can be detected and measured. This technique is often used in preclinical research to study biological processes such as gene expression, cell proliferation, and metastasis.

In CLIA, an enzymatic reaction produces light that is used to detect and quantify the presence of a specific analyte or target molecule. This technique is commonly used in clinical laboratories for the detection of various biomarkers, such as hormones, drugs, and infectious agents.

Therefore, while luminescence is not a medical term per se, it has important applications in medical research and diagnostics.

Luciferases are enzymes that catalyze light-emitting reactions. They are named after the phenomenon of luciferin, a generic term for the light-emitting compound, being oxidized by the enzyme luciferase in fireflies. The reaction produces oxyluciferin, carbon dioxide, and a large amount of energy, which is released as light.

Renilla luciferase, specifically, is a type of luciferase that comes from the sea pansy, Renilla reniformis. It catalyzes the oxidation of coelenterazine, a substrate derived from green algae, to produce coelenteramide, carbon dioxide, and light. The reaction takes place in the presence of oxygen and magnesium ions.

Renilla luciferase is widely used as a reporter gene in molecular biology research. A reporter gene is a gene that produces a protein that can be easily detected and measured, allowing researchers to monitor the activity of other genes or regulatory elements in a cell. In this case, when the Renilla luciferase gene is introduced into cells, the amount of light emitted by the enzyme reflects the level of expression of the gene of interest.

Luminescent measurements refer to the quantitative assessment of the emission of light from a substance that has been excited, typically through some form of energy input such as electrical energy or radiation. In the context of medical diagnostics and research, luminescent measurements can be used in various applications, including bioluminescence imaging, which is used to study biological processes at the cellular and molecular level.

Bioluminescence occurs when a chemical reaction produces light within a living organism, often through the action of enzymes such as luciferase. By introducing a luciferase gene into cells or organisms, researchers can use bioluminescent measurements to track cellular processes and monitor gene expression in real time.

Luminescent measurements may also be used in medical research to study the properties of materials used in medical devices, such as LEDs or optical fibers, or to develop new diagnostic tools based on light-emitting nanoparticles or other luminescent materials.

In summary, luminescent measurements are a valuable tool in medical research and diagnostics, providing a non-invasive way to study biological processes and develop new technologies for disease detection and treatment.

"Renilla" is not a medical term itself, but it refers to a genus of bioluminescent marine organisms called sea pansies. These organisms produce a greenish-blue light through a chemical reaction that involves a protein called "Renilla reniformis luciferase." This enzyme can be used in medical research as a reporter gene, allowing the detection and measurement of gene expression or protein interaction within cells.

Therefore, when you see "Renilla" mentioned in a medical context, it is likely referring to this specific luciferase enzyme or its use in scientific experiments.

Copepoda is a subclass of small crustaceans found in various aquatic environments, including marine and freshwater. They are typically characterized by a segmented body with a distinct head and thorax, and they have a pair of antennae, mandibles, and maxillules used for feeding. Copepods are important members of the zooplankton community and serve as a significant food source for many larger aquatic organisms, such as fish and whales. Some copepod species can also be parasitic, infecting various marine animals, including fish, crustaceans, and mammals.

'Aquatic organisms' are living beings that inhabit bodies of water, such as oceans, seas, lakes, rivers, and ponds. This group includes a wide variety of species, ranging from tiny microorganisms like plankton to large marine mammals like whales. Aquatic organisms can be divided into several categories based on their specific adaptations to their environment, including:

1. Plankton: small organisms that drift with the water currents and include both plants (phytoplankton) and animals (zooplankton).
2. Nekton: actively swimming aquatic organisms, such as fish, squid, and marine mammals.
3. Benthos: organisms that live on or in the bottom of bodies of water, including crustaceans, mollusks, worms, and some types of algae.
4. Neuston: organisms that live at the air-water interface, such as certain species of insects and small fish.

Aquatic organisms play a critical role in maintaining the health and balance of aquatic ecosystems, providing food and habitat for other species, and contributing to global nutrient cycling and climate regulation.

"Photobacterium" is a genus of Gram-negative, facultatively anaerobic bacteria that are capable of producing light, a phenomenon known as bioluminescence. These bacteria are commonly found in marine environments and are often associated with fish and other sea creatures. They are typically rod-shaped and can exist as free-living organisms or as symbiotic partners within host organisms. Photobacterium species are known to produce a variety of enzymes and metabolites that have potential applications in biotechnology and medicine. However, some strains of Photobacterium can cause infections in humans, particularly in individuals with weakened immune systems.

Luminescent agents, also known as optical imaging agents or fluorescent contrast agents, are substances that emit light upon excitation with external energy sources such as ultraviolet or visible light. In the medical field, these agents are often used in diagnostic and research applications, particularly in medical imaging techniques like fluorescence imaging and bioluminescence imaging.

Luminescent agents can be divided into two main categories: organic and inorganic. Organic luminescent agents include small molecules, dyes, and proteins such as green fluorescent protein (GFP), while inorganic luminescent agents include nanoparticles like quantum dots and upconversion nanoparticles.

These agents are used to enhance the contrast between healthy and diseased tissues or cells, allowing for better visualization of specific structures or processes within the body. They have been used in various medical applications such as cancer detection, atherosclerosis imaging, stem cell tracking, and gene expression analysis. However, it is important to note that the use of luminescent agents in medical imaging requires careful consideration of their potential toxicity, biocompatibility, and pharmacokinetics.

*Photorhabdus* is a genus of gram-negative, bioluminescent bacteria that are symbiotic with certain species of entomopathogenic nematodes (nematodes that infect and kill insects). These bacteria are found in the gut of the nematodes and are released into the insect host when the nematode infects it. The bacteria produce toxins and other virulence factors that help to kill the insect and provide a nutrient-rich environment for the nematodes to reproduce. After reproduction, the nematodes and *Photorhabdus* bacteria work together again to seek out a new insect host. Some species of *Photorhabdus* have also been shown to have potential as biological control agents for certain insect pests.

Protein renaturation is the process of restoring the native, functional structure of a protein that has been denatured due to exposure to external stressors such as changes in temperature, pH, or the addition of chemical agents. Denaturation causes proteins to lose their unique three-dimensional structure, which is essential for their proper function. Renaturation involves slowly removing these stressors and allowing the protein to refold into its original configuration, restoring its biological activity. This process can be facilitated by various techniques, including dialysis, dilution, or the addition of specific chemical chaperones.

In the context of medical terminology, 'color' is not defined specifically with a unique meaning. Instead, it generally refers to the characteristic or appearance of something, particularly in relation to the color that a person may observe visually. For instance, doctors may describe the color of a patient's skin, eyes, hair, or bodily fluids to help diagnose medical conditions or monitor their progression.

For example, jaundice is a yellowing of the skin and whites of the eyes that can indicate liver problems, while cyanosis refers to a bluish discoloration of the skin and mucous membranes due to insufficient oxygen in the blood. Similarly, doctors may describe the color of stool or urine to help diagnose digestive or kidney issues.

Therefore, 'color' is not a medical term with a specific definition but rather a general term used to describe various visual characteristics of the body and bodily fluids that can provide important diagnostic clues for healthcare professionals.

Enzyme stability refers to the ability of an enzyme to maintain its structure and function under various environmental conditions, such as temperature, pH, and the presence of denaturants or inhibitors. A stable enzyme retains its activity and conformation over time and across a range of conditions, making it more suitable for industrial and therapeutic applications.

Enzymes can be stabilized through various methods, including chemical modification, immobilization, and protein engineering. Understanding the factors that affect enzyme stability is crucial for optimizing their use in biotechnology, medicine, and research.

"Vibrio" is a genus of Gram-negative, facultatively anaerobic, curved-rod bacteria that are commonly found in marine and freshwater environments. Some species of Vibrio can cause diseases in humans, the most notable being Vibrio cholerae, which is the causative agent of cholera, a severe diarrheal illness. Other pathogenic species include Vibrio vulnificus and Vibrio parahaemolyticus, which can cause gastrointestinal or wound infections. These bacteria are often transmitted through contaminated food or water and can lead to serious health complications, particularly in individuals with weakened immune systems.

Luminescent proteins are a type of protein that emit light through a chemical reaction, rather than by absorbing and re-emitting light like fluorescent proteins. This process is called bioluminescence. The light emitted by luminescent proteins is often used in scientific research as a way to visualize and track biological processes within cells and organisms.

One of the most well-known luminescent proteins is Green Fluorescent Protein (GFP), which was originally isolated from jellyfish. However, GFP is actually a fluorescent protein, not a luminescent one. A true example of a luminescent protein is the enzyme luciferase, which is found in fireflies and other bioluminescent organisms. When luciferase reacts with its substrate, luciferin, it produces light through a process called oxidation.

Luminescent proteins have many applications in research, including as reporters for gene expression, as markers for protein-protein interactions, and as tools for studying the dynamics of cellular processes. They are also used in medical imaging and diagnostics, as well as in the development of new therapies.

A "reporter gene" is a type of gene that is linked to a gene of interest in order to make the expression or activity of that gene detectable. The reporter gene encodes for a protein that can be easily measured and serves as an indicator of the presence and activity of the gene of interest. Commonly used reporter genes include those that encode for fluorescent proteins, enzymes that catalyze colorimetric reactions, or proteins that bind to specific molecules.

In the context of genetics and genomics research, a reporter gene is often used in studies involving gene expression, regulation, and function. By introducing the reporter gene into an organism or cell, researchers can monitor the activity of the gene of interest in real-time or after various experimental treatments. The information obtained from these studies can help elucidate the role of specific genes in biological processes and diseases, providing valuable insights for basic research and therapeutic development.

An amino acid sequence is the specific order of amino acids in a protein or peptide molecule, formed by the linking of the amino group (-NH2) of one amino acid to the carboxyl group (-COOH) of another amino acid through a peptide bond. The sequence is determined by the genetic code and is unique to each type of protein or peptide. It plays a crucial role in determining the three-dimensional structure and function of proteins.

In the context of medicine and pharmacology, "kinetics" refers to the study of how a drug moves throughout the body, including its absorption, distribution, metabolism, and excretion (often abbreviated as ADME). This field is called "pharmacokinetics."

1. Absorption: This is the process of a drug moving from its site of administration into the bloodstream. Factors such as the route of administration (e.g., oral, intravenous, etc.), formulation, and individual physiological differences can affect absorption.

2. Distribution: Once a drug is in the bloodstream, it gets distributed throughout the body to various tissues and organs. This process is influenced by factors like blood flow, protein binding, and lipid solubility of the drug.

3. Metabolism: Drugs are often chemically modified in the body, typically in the liver, through processes known as metabolism. These changes can lead to the formation of active or inactive metabolites, which may then be further distributed, excreted, or undergo additional metabolic transformations.

4. Excretion: This is the process by which drugs and their metabolites are eliminated from the body, primarily through the kidneys (urine) and the liver (bile).

Understanding the kinetics of a drug is crucial for determining its optimal dosing regimen, potential interactions with other medications or foods, and any necessary adjustments for special populations like pediatric or geriatric patients, or those with impaired renal or hepatic function.

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.

In genetics, sequence alignment is the process of arranging two or more DNA, RNA, or protein sequences to identify regions of similarity or homology between them. This is often done using computational methods to compare the nucleotide or amino acid sequences and identify matching patterns, which can provide insight into evolutionary relationships, functional domains, or potential genetic disorders. The alignment process typically involves adjusting gaps and mismatches in the sequences to maximize the similarity between them, resulting in an aligned sequence that can be visually represented and analyzed.

Recombinant proteins are artificially created proteins produced through the use of recombinant DNA technology. This process involves combining DNA molecules from different sources to create a new set of genes that encode for a specific protein. The resulting recombinant protein can then be expressed, purified, and used for various applications in research, medicine, and industry.

Recombinant proteins are widely used in biomedical research to study protein function, structure, and interactions. They are also used in the development of diagnostic tests, vaccines, and therapeutic drugs. For example, recombinant insulin is a common treatment for diabetes, while recombinant human growth hormone is used to treat growth disorders.

The production of recombinant proteins typically involves the use of host cells, such as bacteria, yeast, or mammalian cells, which are engineered to express the desired protein. The host cells are transformed with a plasmid vector containing the gene of interest, along with regulatory elements that control its expression. Once the host cells are cultured and the protein is expressed, it can be purified using various chromatography techniques.

Overall, recombinant proteins have revolutionized many areas of biology and medicine, enabling researchers to study and manipulate proteins in ways that were previously impossible.

In the context of medical and biological sciences, a "binding site" refers to a specific location on a protein, molecule, or cell where another molecule can attach or bind. This binding interaction can lead to various functional changes in the original protein or molecule. The other molecule that binds to the binding site is often referred to as a ligand, which can be a small molecule, ion, or even another protein.

The binding between a ligand and its target binding site can be specific and selective, meaning that only certain ligands can bind to particular binding sites with high affinity. This specificity plays a crucial role in various biological processes, such as signal transduction, enzyme catalysis, or drug action.

In the case of drug development, understanding the location and properties of binding sites on target proteins is essential for designing drugs that can selectively bind to these sites and modulate protein function. This knowledge can help create more effective and safer therapeutic options for various diseases.

Luciferases can be produced in the lab through genetic engineering for a number of purposes. Luciferase genes can be ... "X-Shining Thermostable Luciferase". Gould SJ, Subramani S (November 1988). "Firefly luciferase as a tool in molecular and cell ... In the luciferase reaction, light is emitted when luciferase acts on the appropriate luciferin substrate. Photon emission can ... Luciferase can act as an ATP sensor protein through biotinylation. Biotinylation will immobilize luciferase on the cell-surface ...
Firefly luciferase is a 62 kDa protein that catalyzes the production of light. In the presence of MgATP and molecular oxygen, ... Crystal structure of firefly luciferase throws light on a superfamily of adenylate-forming enzymes.. Conti, E., Franks, N.P., ... Firefly luciferase shows extensive sequence homology with a number of enzymes that utilize ATP in adenylation reactions. ...
In the DLR™ Assay, the activities of firefly and Renilla luciferases are measured sequentially from a single sample. ... The Dual-Luciferase® Reporter (DLR™) Assay System provides an efficient means of performing two reporter assays. ... Nano-Glo® Luciferase Assay System. Add-mix-measure assay for NanoLuc® Luciferase with >2 hour half-life in most applications. ... The pGL4 Luciferase Reporter Vectors are designed for use with the DLR™ Assay Systems. A Renilla luciferase vector with ...
The Luciferase Quantum Dot in the vaccine. 11/24/20. 8. SHOCK AS ITS REVEALED AN ENZYME CALLED LUCIFERASE IS WHAT MAKES BILL ... Luciferase in vaccines and Chat GPT. 10/13/23. 2. SHOCKING - Bioluminescent LUCIFERASE Material Found In COVID Vaccine. 10/17/ ... Re: Luciferase in the vaccine--Coincidence?. Also, credit to the poster James Brownlow. Here is a link to the definition of ... Luciferase in the vaccine--Coincidence?. A Christian forum called Five Doves posts letters weekly about whats going on. Just ...
In the DLR™ Assay, the activities of firefly and Renilla luciferases are measured sequentially from a single sample. ... The Dual-Luciferase® Reporter (DLR™) Assay System provides an efficient means of performing two reporter assays. ... Nano-Glo® Luciferase Assay System. Add-mix-measure assay for NanoLuc® Luciferase with >2 hour half-life in most applications. ... The pGL4 Luciferase Reporter Vectors are designed for use with the DLR™ Assay Systems. A Renilla luciferase vector with ...
Luciferase Is Okay For Research After All Suspicion that a popular enzyme used in biomedical studies might have adverse ... Firefly luciferase, a luminescence-inducing enzyme, is often engineered into cells to facilitate imaging in studies on the ... This close resemblance has raised concerns that luciferase-engineered cells could have adverse effects on metabolism and thus ... experimental artifacts that might invalidate some of the many studies-estimated to number about 30,000-in which luciferase has ...
"Luciferases" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH (Medical Subject ... This graph shows the total number of publications written about "Luciferases" by people in Harvard Catalyst Profiles by year, ... Transfection, Spinfection, Exofection, and Luciferase Assays for Analysis of CCN Genes Expression Mechanism. Methods Mol Biol. ... Enzymes that oxidize certain LUMINESCENT AGENTS to emit light (PHYSICAL LUMINESCENCE). The luciferases from different organisms ...
Browse Addgenes collection of luciferase plasmids used for assays of transcriptional regulation and biosensors. ... Luciferase-pcDNA3. Firefly. CMV. Mammalian expression of firefly luciferase. William Kaelin. 21375. pHIV-Luciferase. Firefly. ... Highlights of Luciferase Tools in our Collection. Modified/Novel Luciferases. *AkaLuc: A modified firefly luciferase engineered ... pCMV-IRES-Renilla Luciferase-IRES-Gateway-Firefly Luciferase (pIRIGF). Firefly/Renilla. Creation ORF-Firefly luciferase gene ...
The widely used coelenterazine-powered Renilla luciferase was discovered over 40 years ago, but the oxidative mechanism by ... Structures of ancestral and extant luciferases complexed with the substrate-like analogue azacoelenterazine or a reaction ... Structural and biochemical studies of an ancestral enzyme with dual dehalogenase and luciferase activity ... providing insights that will guide the engineering of next-generation luciferase-luciferin pairs for ultrasensitive optical ...
Gaussia Luciferase and Cypridina Luciferase are the brightest commercially available luciferases, enabling the user to detect ... The first generation of luciferase reporters developed were based on Firefly Luciferase (FLuc). Insect luciferases, including ... Later, a marine luciferase from the sea pansy Renilla reniformis was isolated. Renilla Luciferase (RLuc), like most marine ... Gaussia Luciferase. Naturally secreted from the deep sea copepod Gaussia princeps (3) (Figure 1), Gaussia Luciferase (GLuc) was ...
Luciferase. Luciferase produces blue/green light through the oxidation of reduced flavin mononucleotide and a long chain ... lux A and lux B code for the components of luciferase lux CDE codes for a fatty acid reductase complex that makes the fatty ... Team:Cambridge/ProjectBioluminescence/Luciferase/WikiGeneticsLuxCDABE. From 2010.igem.org. Revision as of 15:28, 19 July 2010 ...
lux A and lux B code for the components of luciferase lux CDE codes for a fatty acid reductase complex that makes the fatty ... Luciferase produces blue/green light through the oxidation of reduced flavin mononucleotide (a standard biomolecule) and a long ... Team:Cambridge/ProjectBioluminescence/Luciferase/WikiGeneticsLuxCDABE. From 2010.igem.org. (Difference between revisions) ...
... luciferase activity in whole cell producing a very strong flash signal which decays rapidly.Features of the Firefly Luciferase ... The Thermo Scientific Pierce Firefly Luciferase Flash Assay Kit provides reagents to measure Red firefly ... Versatile luciferases: microplate luminometers and flash luciferase assays. For Research Use Only. Not for use in diagnostic ... Features of the Firefly Luciferase Flash Assay Kit:. • Highly sensitive detection of firefly luciferase activity. • Use with ...
Displays a graphical map based on nucleotide sequence data labeled with restriction enzymes, plasmid features, ORFs (theoretical open reading frames) and primers. Hovering over data labels will display additional information (e.g. cut site). To select a portion of sequence, click one location on the plasmid and then a second location to display the sequence between the two locations.. ...
Crystal structure of the thermostable Japanese Firefly Luciferase complexed with High-energy intermediate analogue ... Structural basis for the spectral difference in luciferase bioluminescence.. Nakatsu, T., Ichiyama, S., Hiratake, J., Saldanha ... In fact, a single amino acid substitution in luciferase changes the emission colour from yellow-green to red. Although the ... Here we report the crystal structures of wild-type and red mutant (S286N) luciferases from the Japanese Genji-botaru (Luciola ...
Recombinant Lucia Luciferase Protein is a positive control for luciferase reporter assays. It can be used as an internal ... A coelenterazine luciferase encoded by a synthetic gene. ... Lucia luciferase Gene Lucia luciferase Reporter Gene in ... A coelenterazine luciferase encoded by a synthetic gene. Recombinant Lucia Luciferase Protein is a positive control for ... Recombinant Lucia Luciferase Protein. Recombinant Lucia. Unit size. Cat. code. Docs. Qty. Price. ...
1.13.12.B5: Arachnocampa luciferase. This is an abbreviated version!. For detailed information about Arachnocampa luciferase, ...
Comparison of standard Renilla-type luciferase with a new engineered luciferase variant.. ... Unlike HLDs, which belong to the family of α/β hydrolases (EC 3.8.1.5) the RLuc luciferase is cofactor-independent ... We expect that this newly gained knowledge will enable rational engineering of novel luciferases and luciferins with fine-tuned ... This project aimed to employ in-lab reconstructed dual-function (dehalogenase/luciferase) ancestral enzyme (ancHLD-RLuc) to ...
5x Firefly Luciferase Lysis Buffer is concentrated lysis buffer designed for use with our Firefly Luciferase Assay Kits in ... Firefly Luciferase Assay Kit 2.0. Flash-type firefly luciferase assay kit.. 30075. Firefly Luciferase Assay Kit (Lyophilized). ... Renilla Luciferase Assay Kit 2.0. Flash-type Renilla luciferase assay kit.. 99912. 5X Passive Lysis Buffer. Extra lysis buffer ... Dual-Luciferase® Assay System (Firefly & Renilla). E1910, E1960, E1980. Firefly & Renilla Luciferase Single Tube Assay Kit. ...
... please contact luciferase assay. Other Luciferase products are available in stock. Specificity: Luciferase Category: Quantum ... Human IgG antibody Laboratories manufactures the luciferase quantum dot reagents distributed by Genprice. The Luciferase ...
DR CARRIE MADEJ, "LUCIFERASE, THE ANTICHRIST BEAST SYSTEM & THE LINE IS BEING DRAWN" ... TRADCATKNIGHT: NEW! SPECIAL GUEST VIDEO INTERVIEW: OCTOBER 23: DR CARRIE MADEJ, "LUCIFERASE, THE ANTICHRIST BEAST SYSTEM & THE ... https://tradcatknight.org/2020/10/23/new-special-guest-video-interview-october-23-dr-carrie-madej-luciferase-the-antichrist- ...
Tag: dual luciferase. Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome. *. ...
ATP Cell Viability Luciferase Assay A highly sensitive firefly luciferase cell based assay for quantifying ATP in cell cultures ... Bioluminescent Firefly Luciferase Assays. Firefly luciferase is a widely used bioluminescent reporter for studying gene ... 2) Firefly Luciferase (CS224520): 5 X 200 µ. 3) ATP Assay Buffer (CS224521): 1 X 10 mL. 4) ATP, 2µM (CS224522): 1 X 100 µL ... This kit takes advantage of Firefly luciferases use of ATP to oxidize D-Luciferin and the resulting production of light in ...
US-5418155-A chemical patent summary.
Structural and biochemical studies of an ancestral enzyme with dual dehalogenase and luciferase activity ... which catalyses both dehalogenase and luciferase reactions. Insertion-deletion (InDel) backbone mutagenesis of Anc(HLD-RLuc) ... network model highlights the importance of the conformational flexibility of a loop-helix fragment of Renilla luciferases for ... and fragment transplantation resulting in greater catalysis and longer glow-type bioluminescence of the ancestral luciferase. ...
Non-denaturing optimization of purification for mutant luciferase and human diaphorase produced 4.1 and 2.6 mg/ml, respectively ... and two proteins firefly mutant red-emitter luciferase, and human DT-diaphorase proteins by altering these variables on ... Non-denaturing optimization of purification for mutant luciferase and human diaphorase produced 4.1 and 2.6 mg/ml, respectively ... and two proteins firefly mutant red-emitter luciferase, and human DT-diaphorase proteins by altering these variables on ...
We characterized these viruses by comparing luciferase activity to virus production, and validated luciferase activity as an ... High-throughput, luciferase-based reverse genetics systems for identifying inhibitors of Marburg and Ebola viruses.. ... two distinct screening platforms based on MARV and EBOV reverse genetics systems that express secreted Gaussia luciferase (gLuc ... two distinct screening platforms based on MARV and EBOV reverse genetics systems that express secreted Gaussia luciferase (gLuc ...
Luciferase gene-loaded CS-Qdots as self-illuminating probes for specif… ... Luciferase gene-loaded CS-Qdots as self-illuminating probes for specific hepatoma imaging GET ALL OF THE COVID-19 / 2020 CHAOS ... Luciferase gene-loaded CS-Qdots as self-illuminating probes for specific h… ... Whats In the Vaccines? , Luciferase gene-loaded CS-Qdots as self-illuminating probes for specific hepatoma imaging ...
LuminoCell: a versatile and affordable platform for real-time monitoring of luciferase-based reporters. by Lucie Nesvadbová on ... Luciferase reporter assays represent a simple and sensitive experimental system in cell and molecular biology to study multiple ... Therefore, we aimed to develop a small, affordable luminometer allowing continuous measurement of luciferase activity, designed ... and portable luminometer capable of real-time monitoring in-cell luciferase activity. The LuminoCell costs $40, requires less ...
EF1a-Luciferase (firefly) -2A-GFP from GenTarget. Cat Number: LVP1060. UK & Europe Distribution. ... EF1a-Luciferase (firefly) -2A-GFP , LVP1060 GenTarget EF1a-Luciferase (firefly) -2A-GFP , LVP1060. (No reviews yet) Write a ... Decrease Quantity of EF1a-Luciferase (firefly) -2A-GFP , LVP1060 Increase Quantity of EF1a-Luciferase (firefly) -2A-GFP , ... EF1a-Luciferase (firefly) -2A-GFP , LVP1060 , GenTarget. Description:. Pre-made lentiviral particles co-express firefly ...

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