Substrats d'enzymes

<p>A non-metabolizable allolactose analogue, widely used in molecular biology for overexpression of recombinant proteins from inducible systems under the control of lac promoter. IPTG binds to the LacI repressor and causes its release from the lac operator, allowing gene expression to take place. Present in vectors of pGEX, pGEM-T, pET, pRSET, pMAL class and others.</p>

<p>5-(Pentafluorobenzoylamino)fluoroscein di-b-D-galactopyranoside, commonly referred as PFB-FDG or PFB-FDGal, is a cell-permeable enzyme substrate for β-galactosidase used in live cell imaging assays. After cleavage, 5-(pentafluorobenzoylamino)fluorescein (PFB-F) is released, generating a green fluorescence (Em ~520 nm)) of a higher intensity than fluorescein. Its main use is for bacterial detection (e.g. E. coli LacZ assays), but also for flow cytometry analytical assays.</p>

<p>Crimson-Gal (Crimson-beta-D-galactopyranoside) is a chromogenic indicator for beta-galactosidase activity. The colorless product is cleaved by lactose-utilizing bacteria in liquid media or on agar plates and yields a crimson colored precipitate. Crimson-Gal can also be used as detecting agent for beta-galactosidase activity in reporter gene assays or for identification of positive transformants on agar plates when using the α-complementation approach. Read more in the Application Notes.</p>

<p>Chromogenic substrate targeting lipase, C8 esterase</p>

<p>4-Nitrophenyl 5-O-trans-feruloyl-alpha-L-arabinofuranoside is a chromogenic substrate for alpha-L-arabinofuranosidase. Upon hydrolysis, para-nitrophenol is released yielding a yellowish colour. 4-Nitrophenyl 5-O-trans-feruloyl-alpha-L-arabinofuranoside is used in different applications such as the Plant cell wall degradation assays, bacterial enzyme profiling</p>

<p>Applications It was found in the root bark of Punica granatum L., Punicaceae. Used as a enzyme substrate.<br>References Hunt, R., et al.: J. Pharm. Pharmacol., 22, 29S (1970), Hashimoto, T., et al.: Plant Physiol., 100, 836 (1992), Boswell, H., et al.: Phytochemistry, 52, 855 (1999),<br></p>

<p>Applications A histochemical substrate for a-N-acetyl-galactosaminidase.<br>References Zhu, et al.: Gene, 137, 309 (1994)<br></p>

<p>Applications (S)-ETHYL 2,6-DIISOCYANATOHEXANOATE (cas# 45172-15-4) is a useful research chemical.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>Applications p-Nitrophenyl α-D-Glucopyranoside is a substrate for α-glucosidase inhibitor.<br>References O'Neill, R., et al.: J. Biol. Chem., 264, 20430 (1989), Carpita, N., et al.: Plant J., 3, 1 (1993), Henrissat, B., et al.: Biochem. J., 293, 781 (1993), Nakai, H., et al.: Biochimie, 89, 49 (2007) ,<br></p>

<p>Stability Hygroscopic<br>Applications Protected Glucopyranosiduronic Acid.<br></p>

<p>Aldol 496 acetate is a chromogenic substrate for the enzyme Aldolase. It is also used as a ligand to detect the presence of Aldolase in biological fluids and tissues. This product is designed for Food testing, Diagnostics, Chromogenic substrate, Staining, Enzyme substrate, Bioluminescence, Fluorogenic substrate, Chemiluminescence, and Culture media. Aldol 496 acetate is an organic chemical with high purity and high quality.</p>

<p>Aldol® 515 propionate is a chromogenic substrate that is used as a reagent in food testing, diagnostics, and environmental testing. It reacts with an enzyme to form a fluorescent product that can be detected with a spectrophotometer. The substrate has been shown to have high purity and high quality.</p>

<p>2-Dodecylresorufin is a fluorescent probe that reacts with the hydroxyl radicals in the cell, which are generated by the enzyme superoxide dismutase. 2-Dodecylresorufin can be used to measure reactive oxygen species (ROS) and ROS-induced cellular damage. It is also used to study oxidative stress in vitro. The chemical structure of 2-dodecylresorufin contains a linker arm that provides a reversible linkage to the cell surface, allowing for extracellular measurements of reactive oxygen species (ROS). This compound has been shown to have high reactivity, making it useful for studying population dynamics and fluorescent techniques.</p>

<p>2-Nitrophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside is a chromogenic substrate used to detect and measure the activity of glycosidase enzymes. Glycosidases are enzymes that hydrolyze glycosidic bonds in carbohydrates, and are produced by many organisms. The substrate is cleaved by glycosidase to release a chromophore, which can be quantified via spectrophotometry analysis. 2-Nitrophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside is widely used in various applications, including enzyme kinetics studies, inhibitor screening, and the detection of NAGase activity in biological samples, such as serum, urine, and cell lysates. It is also used for the identification and characterization of glycosidases in microorganisms and the study of glycosylation-related processes in cells and tissues.</p>

<p>4-Trifluoromethylumbelliferyl a-D-N-acetylneuraminic acid is a fluorescent chemiluminescent substrate that is used in the detection of beta-galactosidase activity. Beta-galactosidase catalyzes the hydrolysis of 4-trifluoromethylumbelliferyl a-D-N-acetylneuraminic acid to form 4-trifluoromethylumbelliferone and D-galactose, which emits light at approximately 480 nm. This reaction can be detected by fluorescence spectrophotometry using a fluorometer or photometer. 4TFUNA is not toxic, does not inhibit enzymes, and has been tested for toxicity and mutagenicity using bacteria and mammalian cells.</p>

<p>4-Methylumbelliferyl 3,4,6-tri-O-acetyl-2-deoxy-2-trifluoroacetamido-b-D-glucopyranoside is a fluorogenic substrate specifically designed for the detection and quantification of hexosaminidase enzymes. Upon cleavage by the target enzyme, it generates a bright fluorescent signal facilitating the investigation of enzyme activity, screening of inhibitors, and diagnostics.</p>

<p>Green fluorescent cationic dye</p>

<p>2-Nitrophenyl 2,3,4-tri-O-acetyl-beta-D-xylopyranoside is a chromogenic substrate used to detect the enzymatic activity of xylosidase. After cleavage, the nitrophenyl moiety is released exhibiting a light yellowish color. 2-Nitrophenyl 2,3,4-tri-O-acetyl-beta-D-xylopyranoside is used in bacterial hemicellulose metabolism assays.</p>

<p>4-Methylumbelliferyl 3-O-(α-L-fucopyranosyl)-β-D-galactopyranoside is an organic compound that is used as a radioactive marker for DNA. It can be synthesized in the laboratory and its use allows for the tracking of DNA molecules. The production of this marker is achieved by recombinant expression of the gene encoding the enzyme β-D-galactosidase, which hydrolyzes 4-methylumbelliferyl β-D-galactopyranoside to release 4-methylumbelliferone and α-L-fucopyranose. The enzyme uses UDP glucose as a cofactor to catalyse the reaction. This product has been isolated from Corynebacterium glutamicum, with recombinant expression vectors used to produce it in host cells such as Escherichia coli or Corynebacterium glutamicum. It has been found that</p>

<p>6,8-Difluoro-4-methylumbelliferyl b-D-glucuronide is a chemiluminescent substrate for the enzyme glucuronidase. The compound has been shown to be stable in the presence of a wide range of pHs and temperatures. It can be used in applications such as diagnostics, culture media and food testing. 6,8-Difluoro-4-methylumbelliferyl b-D-glucuronide has a high purity level and can be used as an indicator for other compounds such as acetaminophen or ibuprofen.</p>

<p>2-Nitrophenyl 2,3-di-O-acetyl-b-D-xylopyranoside is a chromogenic substrate used to assay the activity of xylosidase enzymes. It is hydrolyzed by xylosidase to yield a yellow-colored product, 2-nitrophenol, which absorbs light at 405 and 410 nm. This substrate is used in research to study the function of xylosidase enzymes and their role in various biological processes. It is also used in diagnostic tests for the detection of xylosidase activity in different microorganisms, including bacteria and fungi.</p>

<p>4-Methylumbelliferyl acetate is a fluorescent compound that can be used to measure the activity of cytochrome P450 enzymes. The fluorescence intensity of 4-methylumbelliferyl acetate increases when it reacts with substrates and inhibitors in vitro. This chemical has been shown to inhibit the enzyme cyclooxygenase in rat liver microsomes, which may lead to blood disorders. It also inhibits coumarin derivatives and human pathogens, such as erythromycin-resistant Staphylococcus aureus (MRSA). 4-Methylumbelliferyl acetate is used as a substrate for polymerase chain reaction (PCR) analysis because it is not susceptible to hydrolysis by esterases.</p>

<p>Resorufin benzyl ether is a chemical compound that can be used as a substrate for cytochrome P450. It has been shown to inhibit the activity of epoxide hydrolase, an enzyme involved in the metabolism of endoperoxides. Resorufin benzyl ether has also been found to inhibit cytochrome P450 enzymes, which are responsible for oxidative metabolism of xenobiotics. This compound has been shown to have a high affinity for mouse monoclonal antibody and is used in immunoassays to detect mouse antibodies. Resorufin benzyl ether is used in biochemical assays and polymerase chain reactions (PCRs) as a fluorescence marker. In addition, this compound is used in model systems to study enzyme activities such as recombinant cytochrome p450 and protein oxidation by reactive oxygen species (ROS).</p>

<p>Colchicine fluorescein is the fluorogenic form of colchicine. It is used for staining assembly of tubulin. Colchicine-site inhibitors (abbrevated as CBSIs) disrupt tubulin polymerization. Colchicine fluorescein serves as a probe to study the binding of colchicine to tubulin, as the colchicine binding site is a promising target for discovering novel antitumour agents.</p>

<p>D-Ile-Pro-Arg p-nitroanilide dihydrochloride is a chromogenic substrate commonly used in research to assess the activity of various enzymes. It has been utilized in studies related to thrombin inhibition, enzyme assays of protease enzymes, activation and enzymatic activity analysis of Factor VII-activating protease, and as a substrate for measuring glandular kallikrein activity. This substrate has been employed in assays to study the amidolytic activity of enzymes such as thrombin, plasma kallikrein, plasmin, and other proteases.</p>

<p>Aldol® 470 L-pyroglutamic acid amide is a chromogenic and fluorogenic enzyme substrate used for detection of pyrrolidonyl peptidase (PYRase) activity. The colorless enzyme substrate is cleaved by PYRase-producing bacteria grown in liquid or solid media, yielding orange color. In addition, green fluorescence is generated when a suitable matrix is present, such as, the surface of cellulose acetate filters, polypropylene tubes or microplates, and polyethylene vials. Aldol® 470 L-pyroglutamic acid amide is suitable for use under aerobic and anaerobic conditions.</p>

<p>Aldol® 450 acetate is an enzyme substrate that is used in the detection of aldolase activity. Aldol® 450 acetate has been shown to be a useful alternative to the traditional bioluminescence and chemiluminescence methods for detecting aldolase activity. It has also been shown to be effective as a fluorogenic substrate for detecting aldolase activity in food products. Aldol® 450 acetate can be conjugated with other compounds, such as ligands and dyes, to enable it to detect different enzymes.<br>Aldol® 450 acetate has an absorption maximum at 450 nm and fluoresces blue-green under longwave UV light excitation. It is soluble in water and exhibits excellent stability at high temperatures (up to 50°C) and pH (1-14).</p>

<p>3-Indolyl b-D-cellotrioside is a chemiluminescent substrate that is used for the detection of bacterial activity. 3-Indolyl b-D-cellotrioside reacts with hydrogen peroxide to produce light, which can be detected by luminometers. This product can be used in diagnostic tests to detect the presence of bacteria in food, water, and other samples. It has been shown to have excellent performance characteristics and high purity and quality.</p>

<p>4-Nitrophenyl 2-O-(2,3,4-tri-O-acetyl-a-L-fucopyranosyl)-6-O-benzoyl-3,4-O-isopropylidene a D galactopyranoside is an analog of galactose that binds to the DNA and regulates gene expression. This compound has been shown to be able to regulate gene expression levels in cells. 4NP2B6OB was used as a probe for microarray analysis of gene expression profiles from environmental samples. It was found that 4NP2B6OB could be used as a probe for the identification of genes in high density arrays.</p>

<p>4-Nitrophenyl 6-O-(a-D-glucopyranosyl)-a-D-glucopyranoside is an advanced chromogenic pNP enzyme substrate that delivers unparalleled performance in enzymatic assays. This high-quality substrate is specifically designed for studying glycosidases and other enzymes involved in carbohydrate metabolism. Our 4-Nitrophenyl 6-O-(a-D-glucopyranosyl)-a-D-glucopyranoside is synthesized with the highest quality materials to provide incredible accuracy and reliability in your research applications.</p>

<p>Histamine (Scombrotoxin) fish poisoning is the most frequent cause of fish poisoning incidents today. Cymit Quimica's BCM®; Histamine-producingbacteria Broth (C-0450) is a growth medium for the detection of histamine-producing bacteria in food and water samples. The medium contains an indicator that turns orange to red due to metabolites released by histidine decarboxylase.</p>

<p>4-Nitrophenyl 2,3-di-O-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)-4,6-benzylidene-b-D-glucopyranoside is a high purity, high quality 4nitrophenol derivative that is used as a food testing substrate. It is also used for the detection of fluorescence in environmental testing. This product can be conjugated with ligands for use in diagnostic assays.</p>

<p>Resorufin pentyl ether is a drug transporter that can be used as an experimental model for studying the effects of chemical pesticides on humans. Resorufin pentyl ether inhibits energy metabolism and inhibits hepatic p450 activity and polymerase chain reaction in hepatocyte-like cells in vitro. It has been shown to inhibit the enzyme activities of rat liver p450s and human cytochrome P450 3A4 (CYP3A4) at physiological levels. Resorufin pentyl ether has also been shown to be toxic in mice, with toxicity studies showing an LD50 of 4.5 mg/kg after oral administration. This drug is not active against bacteria or fungi, but it is able to inhibit protein synthesis in model systems containing mouse monoclonal antibodies or calf thymus DNA.</p>