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| Product | Description | |
|---|---|---|
| 1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanol Sodium Salt | Phosphatidylethanol (PEth) represents a group of glycerophospholipid homologues generated by substitution of ethanol for the lipid headgroup by the phospholipase D enzyme. Since the formation of PEth is specifically dependent on ethanol, the diagnostic specificity of PEth as an alcohol biomarker is theoretically 100%. Group: Biochemicals. Grades: Highly Purified. CAS No. 322647-55-2. Pack Sizes: 1mg, 5mg. Molecular Formula: C39H74NaO8P, Molecular Weight: 724.96. US Biological Life Sciences. |  Worldwide |
| 2'-Iodo-dADP | 2'-Iodo-dADP, a vital biochemical reagent, is widely utilized in complex investigations of nucleosides and nucleotides. Its remarkable therapeutic potential has been acknowledged due to its ability to hinder enzymes crucial in DNA synthesis and replication, creating hope for the effective cure of infectious diseases and various cancer types. Furthermore, PubMed research reveals the drug's promising potential in identifying and imaging brain tumors, opening the doors to new diagnostic avenues within medical science. Synonyms: (2'I-dADP); 2'-Iodo-2'-deoxyadenosine-5'-diphosphate, Sodium salt. Grades: ≥ 95% by HPLC. CAS No. 169968-55-2. Molecular formula: C10H14N5O9P2I (free acid). Mole weight: 537.10 (free acid). |  |
| 2-Naphthyl b-D-galactopyranoside | 2-Naphthyl b-D-galactopyranoside, a chemical compound that finds varied biomedical applications, is a substrate of choice to detect and determine the activity of galactosyl-group hydrolyzing or transferring enzymes, notably the β-galactosidase. Its essentiality in comprehending carbohydrate metabolism and the kinetics of enzymes is indisputable, and its potential in increasing diagnostic accuracy for lactose intolerance is highly promising. CAS No. 33993-25-8. Molecular formula: C16H18O6. Mole weight: 306.31. | |
| 2-O-(2-Nitrophenyl)-a-D-N-acetylneuraminic acid | 2-O-(2-Nitrophenyl)-α-D-N-acetylneuraminic acid, a synthetic organic compound utilized in the biomedical industry, serves as a substrate for sialidase enzymes and acts as a diagnostic tool for detecting sialidosis, an uncommon genetic ailment resulting from sialidase enzyme paucity. Moreover, it plays a pivotal role in the therapeutic drug development for combatting viral infections like influenza and HIV, alongside several malignancies, thus exhibiting substantial clinical significance. The efficaciousness of this compound in multiple biomedical applications remains unparalleled, driving it towards becoming an essential component in the research industry. Synonyms: ONP-a-NeuNAc. CAS No. 157707-92-1. Molecular formula: C17H22N2O11. Mole weight: 430.36. | |
| 3-Acetylumbelliferyl b-D-glucopyranoside | 3-Acetylumbelliferyl b-D-glucopyranoside is an illustrious substrate, which holds a paramount role in facilitating the enzymatic activity in glycosidases. With its discernible properties, it serves as an efficient indicator for beta-glucosidase activity. Its proficiency in elucidating Gaucher's disease has made it the cynosure of diagnostic applications. The release of a fluorescent product upon cleavage by the enzyme renders it an optimal choice for quantification and measurement of glycosidases. CAS No. 20943-16-2. Molecular formula: C17H18O9. Mole weight: 366.32. | |
| 3'-Sulpho Lewisa-BSA (3 atom spacer) | 3'-Sulpho Lewisa-BSA (3 atom spacer) is a uniquely crafted protein conjugate that is tailored for the detection of Lewis antigen in cancer cells. With its proprietary binding mechanism that homes in on the glycosyltransferase enzyme, this protein effectively paves the way for accurate measurement of the Lewis antigen levels. Distinguishing this protein from its counterparts in the market, is its 3 atom spacer designed to optimize the protein's affinity to its recognition site, thus magnifying the sensitivity and precision of assays. By exploiting the discovery that the Lewis antigen has been implicated in a spectrum of cancers such as lung, breast, ovarian, and pancreatic, this breakthrough protein holds the potential to serve as a critical diagnostic tool for cancer detection. | |
| 4-Aminobenzyl b-D-thiogalactopyranoside | 4-Aminobenzyl b-D-thiogalactopyranoside is standing as a pivotal compound, employed extensively in enzyme assay systems to gauge β-galactosidase activity within diverse biological samples. With its proficiency as an artificial substrate for the enzyme, it enables accurate measurements of the said enzymatic activity. Its broad applicability in detecting and quantifying β-galactosidase activity renders it a crucial tool in scientific research and diagnostic endeavors. Synonyms: 1-(4-Aminobenzylthio)-beta-D galactopyranose; 4-Aminobenzyl 1-Thio-beta-D-galactopryranoside; (2S,3R,4S,5R,6R)-2-[(4-aminophenyl)methylsulfanyl]-6-(hydroxymethyl)oxane-3,4,5-triol; SCHEMBL149081; 1-(4-Aminobenzylthio)-beta-dgalactopyranose; p-aminobenzyl 1-thio-beta-d-galactopyranoside; W-202473; (2S,3R,4S,5R,6R)-2-(4-aminobenzylthio)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol. CAS No. 35785-20-7. Molecular formula: C13H19NO5S. Mole weight: 301.36. | |
| 4-Aminophenyl b-D-thioglucopyranoside | 4-Aminophenyl b-D-thioglucopyranoside, a remarkable biomedicine, plays a vital role in the progress of diagnostic tools and therapeutic strategies within the scientific community. Demonstrating its prowess as a substrate analog, this compound exerts precise intervention by effectively subjugating β-D-glucosidase enzymes. Synonyms: 4-Aminophenyl 1-Thio-beta-D-glucopyranoside; (2S,3R,4S,5S,6R)-2-(4-aminophenyl)sulfanyl-6-(hydroxymethyl)oxane-3,4,5-triol; P-AMINOPHENYL-1-THIO-BETA-D-GLUCOPYRANOSIDE;(2S,3R,4S,5S,6R)-2-((4-Aminophenyl)thio)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol. CAS No. 58737-22-7. Molecular formula: C12H17NO5S. Mole weight: 287.33. | |
| 4-Chloromethyl-6,8-difluoroumbelliferyl b-D-galactopyranoside | 4-Chloromethyl-6,8-difluoroumbelliferyl b-D-galactopyranoside is a valuable compound widely used in biomedicine. It serves as a fluorogenic substrate for enzymes like β-galactosidases, aiding in the detection and analysis of various diseases. This compound is particularly beneficial for studying galactosidase activity in drug development, genetic engineering, and diagnostic applications. Its unique chemical properties make it an indispensable tool in biomedical research. CAS No. 215868-46-5. Molecular formula: C16H15ClF2O8. Mole weight: 408.74. | |
| 4-Methylumbelliferyl 2-acetamido-2-deoxy-3,6-di-O-pivaloyl-b-D-galactopyranoside | 4-Methylumbelliferyl 2-acetamido-2-deoxy-3,6-di-O-pivaloyl-b-D-galactopyranoside is a vital tool in biomedicine for studying enzyme kinetics and diagnostic purposes. This compound is used to analyze the activity of glycosidases, particularly for the detection and quantification of certain diseases and enzyme deficiencies such as Gaucher's disease. Its fluorescent properties facilitate quick and sensitive measurements, making it an indispensable tool in biomedicine research. Synonyms: 4-Methylumbelliferyl 2-Acetamido-2-deoxy-3,6-dipivaloyl-beta-D-galactopyranoside; [(3R,6S)-5-acetamido-4-(2,2-dimethylpropanoyloxy)-3-hydroxy-6-(4-methyl-2-oxochromen-7-yl)oxyoxan-2-yl]methyl 2,2-dimethylpropanoate; AKOS025295805; 4-Methylumbelliferyl 2-Acetamido-2-deoxy-3,6-dipivaloyl- beta -D-galactopyranoside; 4-Methylumbelliferyl 2-Acetamido-2-deoxy-3,6-dipivaloyl-?-D-galactopyranoside. CAS No. 849207-59-6. Molecular formula: C28H37NO10. Mole weight: 547.59. | |
| 4-Methylumbelliferyl 3,6-Di-O-benzoyl-β-D-galactopyranoside | 4-Methylumbelliferyl 3,6-Di-O-benzoyl-β-D-galactopyranoside, a highly specialized biomedicine compound, exemplifies an invaluable tool for evaluating and quantifying β-galactosidase activity. Its multifaceted utilization spans a myriad of research endeavors and diagnostic protocols to unveil the intricacies surrounding the expression and functionality of this pivotal enzyme. By shedding light on the physiological and pathological dimensions intertwined with β-galactosidase-related disorders, notably lysosomal storage diseases, this product unfurls boundless avenues for comprehensive comprehension in scientific spheres. Grades: 98%. Molecular formula: C30H26O10. Mole weight: 546.52. | |
| 4-Methylumbelliferyl b-D-xylopyranoside | 4-Methylumbelliferyl b-D-xylopyranoside, an indispensable entity in the realm of biomedical science, serves as an invaluable resource. Functioning primarily as a substrate for esteemed b-xylosidase enzymes, it additionally assumes the role of a luminescent indicator in the investigation of carbohydrate metabolism. Through its implementation, the comprehensive assessment and identification of diverse medicinal compounds and afflictions linked to b-xylosidase activity can be efficiently accomplished, thereby significantly contributing to the advancement of cutting-edge research and diagnostic endeavors. Synonyms: 4-MU-b-D-Xyl; 2H-1-Benzopyran-2-one, 4-methyl-7-(b-D-xylopyranosyloxy)-; 4-Methyl-7-(beta-D-xylopyranosyloxy)-2H-1-benzopyran-2-one; 4-methyl-7-(((2S,3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)-2H-chromen-2-one. Grades: ≥98%. CAS No. 6734-33-4. Molecular formula: C15H16O7. Mole weight: 308.28. | |
| 4-Methylumbelliferyl phosphate bis(cyclohexylammonium) salt | 4-Methylumbelliferyl phosphate bis(cyclohexylammonium) salt, known for its pivotal importance in the field of biomedicine, serves as an invaluable biomolecular reagent. Within enzyme assays, this compound exhibits an exceptional capability to gauge the activity of alkaline phosphatase, a prominent enzyme intricately involved in numerous vital cellular processes. Consequently, it stands as an invaluable substrate employed in diagnostic assessments, enabling the detection and assessment of alkaline phosphatase's presence and functionality. Remarkably high levels of purity are maintained, ensuring the utmost precision and dependability in biochemical investigations. Synonyms: 4-Methylumbelliferyl phosphate bis(cyclohexylammonium) salt; cyclohexanamine; (4-methyl-2-oxochromen-7-yl) dihydrogen phosphate; 4-Methylumbelliferyl phosphate bis (cyclohexylammonium) salt; 4-Methylumbelliferyl phosphate, bis(cyclohexylammonium)salt; cyclohexanamine hemi(4-methyl-2-oxo-2H-chromen-7-yl phosphate); 4-METHYLUMBELLIFERYL PHOSPHATE,BIS(CYCLOHEXYLAMMONIUM) SALT. CAS No. 128218-53-1. Molecular formula: C10H9O6P.2C6H13N. Mole weight: 454.50. | |
| 4-Methylumbelliferyl propionate | 4-Methylumbelliferyl propionate, an invaluable biomedical tool, serves as a substrate in studying enzyme kinetics and inhibition, aiding researchers and diagnosticians in comprehending the intricate processes underlying numerous disorders and medical advancements. Synonyms: 4-Mu-Propionate Propionic acid-4-methylumbelliferyl ester. CAS No. 3361-13-5. Molecular formula: C13H12O4. Mole weight: 232.23. | |
| 4-Nitrophenyl 3,4-O-isopropylidene-a-D-galactopyranoside | 4-Nitrophenyl 3,4-O-isopropylidene-α-D-galactopyranoside, a fundamental compound within the biomedical sector, holds immense value for diverse research and diagnostic practices. With its capability to facilitate the examination and modulation of α-D-galactopyranoside-associated mechanisms and compounds like enzymes, receptors, and carbohydrates, this reagent stands as an indispensable resource. Its remarkable adaptability renders it an exemplary instrument in the field of drug innovation, catering to the treatment of ailments characterized by α-D-galactopyranoside remnants. Synonyms: 4-Nitrophenyl 3,4-O-isopropylidene-a-D-galactopyranoside; (3As,4R,6R,7R,7aR)-4-(hydroxymethyl)-2,2-dimethyl-6-(4-nitrophenoxy)-4,6,7,7a-tetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-7-ol; p-Nitrophenyl3,4-O-Isopropylidene-alpha-D-galactopyranoside; DTXSID80512595; W-202237; 4-Nitrophenyl 3,4-O-(1-methylethylidene)-alpha-D-galactopyranoside. CAS No. 29781-32-6. Molecular formula: C15H19NO8. Mole weight: 341.31. | |
| 4-Nitrophenyl a-D-maltopentaoside | 4-Nitrophenyl α-D-maltopentaoside, a crucial biomedical compound, illuminates the realm of enzymatic reactions and carbohydrate metabolism. Undertaking the role of a glycosidase substrate, it unfurls opportunities to unravel the intricacies of these enzymes' activity. This invaluable resource thrives not only in diagnostic tool and drug development but also in deciphering ailments intertwined with carbohydrate metabolism disorders. Synonyms: PG5. CAS No. 66068-38-0. Molecular formula: C36H55NO28. Mole weight: 949.81. | |
| 4-Nitrophenyl b-D-mannopyranoside | 4-Nitrophenyl b-D-mannopyranoside, a biomedical compound, plays a pivotal role in advancing diagnostic tools and therapeutic strategies for specific diseases through cutting-edge research and development. It finds extensive utilization in the exploration of enzyme activity, particularly in the realm of carbohydrate metabolism, offering valuable insights into the intricate interplay between enzymes and substrates. Synonyms: PNP-mannoside. CAS No. 35599-02-1. Molecular formula: C12H15NO8. Mole weight: 301.25. | |
| 5'-Biotin-A-Monophosphate | 5'-Biotin-A-Monophosphate, a biomedicine product, serves as an essential substrate for the enzyme adenosine deaminase. It enables the comprehensive study of adenosine metabolism in various tissues and cells. Apart from this, 5'-Biotin-A-Monophosphate is an effective tool in developing diagnostic kits for adenosine deaminase deficiency and equally monitoring the progress of enzyme replacement therapy. Synonyms: 5'-Biotin-AMP. Grades: ≥90% by AX-HPLC. Molecular formula: C26H41N8O9PS. Mole weight: 672.70. | |
| 5-Bromo-3-indolyl nonanoate | 5-Bromo-3-indolyl nonanoate is a compound commonly used in research and diagnostic applications acting as a substrate for enzymes such as β-galactosidase, enabling the visualization and detection of reporter gene expression in cellular pathways. This compound is especially valuable in studying gene expression in diseases like cancer, neurodegenerative disorders and cardiovascular conditions. Synonyms: Blue-nonanoate. CAS No. 133950-70-6. Molecular formula: C17H22BrNO2. Mole weight: 352.27. | |
| 5-Bromo-6-chloro-3-indolyl acetate | 5-Bromo-6-chloro-3-indolyl acetate, a chemical compound widely utilized in the biomedical sector, assumes a paramount role in enzymatic assays within academic and scientific circles. Its primary function involves the detection and quantification of β-galactosidase, an indispensable enzyme intrinsic to numerous pharmaceuticals, malignancies, pathogens, and hereditary abnormalities. In research and diagnostic domains, this highly efficacious substrate guarantees dependable and precise outcomes, thereby exemplifying its quintessential significance. Synonyms: 5-Bromo-6-chloro-3-indoxyl 3-acetate. CAS No. 102185-48-8. Molecular formula: C10H7BrClNO2. Mole weight: 288.52. | |
| 5-Bromo-6-chloro-3-indolyl phosphate p-toluidine salt | 5-Bromo-6-chloro-3-indolyl phosphate p-toluidine salt, an indispensable compound in biomedical investigation, exhibits its aptitude to discern alkaline phosphatase activity. This entity facilitates the elucidation of said enzyme within biological specimens, thereby contributing to the discernment of diverse maladies and anomalous phosphatase activity. Moreover, this product assumes a pivotal function in manifold endeavors concerning drug exploration and diagnostic undertakings. Synonyms: Magenta phosphate p-toludine salt. CAS No. 6769-80-8. Molecular formula: C8H5BrClNO4P.C7H10N. Mole weight: 433.63. | |
| 5-Carboxy-UTP | 5-Carboxy-UTP, a nucleotide analog renowned for its versatility and efficacy, is a highly sought-after compound in the realm of biomedicine. Widely employed in the study of RNA processing enzymes and the regulation of RNA metabolism, this exquisite molecule exhibits remarkable potential for the identification of RNA modifications and the creation of diagnostic tools capable of combating notorious afflictions such as cancer and viral infections. Synonyms: 5-Carboxyuridine-5'-Triphosphate; 5-caUTP. Grades: ≥95% by AX-HPLC. Molecular formula: C10H15N2O17P3. Mole weight: 528.1. | |
| 5-Propargylamino-ddUTP - ATTO-Rho101 | 5-Propargylamino-ddUTP - ATTO-Rho101, a fluorescent nucleotide utilized in the cancer diagnostics investigations, possesses exclusive chemical architecture that renders it appropriate for the assignment of labels, identification, and quantitative analysis of the cancer progression-related enzymes and cellular functions. Its enormous sensitivity and specificity portray its importance in identifying the underlying biochemical pathways of cancer for developing potential therapeutic targets. Synonyms: 5-Propargylamino-2',3'-dideoxyuridine-5'-triphosphate, labeled with ATTO Rho101, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C49H55N6O16P3 (free acid). Mole weight: 1076.29 (free acid). | |
| 6,8-Difluoro-4-methylumbelliferyl b-D-cellotetraoside | 6,8-Difluoro-4-methylumbelliferyl b-D-cellotetraoside is a compound used for studying cellulase enzymes involved in the degradation of cellulose, a key component of plant cell walls. It acts as a substrate, releasing a fluorogenic compound upon enzymatic cleavage, enabling analysis of cellulase activity. It aids in understanding cellulose metabolism and can be used in various research and diagnostic applications related to cellulosic materials and cellulose-degrading enzymes. Molecular formula: C34H46F2O23. Mole weight: 860.71. | |
| 6-Chloro-3-indolyl a-D-galactopyranoside | 6-Chloro-3-indolyl α-D-galactopyranoside is a biochemical compound used in the compound industry. It acts as a substrate for the detection of β-galactosidase enzyme activity. This enzymatic reaction is widely utilized in diagnostics and research, providing valuable information about lac gene expression and cellular processes. Synonyms: 6-Chloro-3-indolyl alpha-D-galactopyranoside; 6-Chloro-3-indolyl-alpha-D-galactopyranoside; (2R,3R,4S,5R,6R)-2-[(6-CHLORO-1H-INDOL-3-YL)OXY]-6-(HYDROXYMETHYL)OXANE-3,4,5-TRIOL; (2R,3R,4S,5R,6R)-2-((6-Chloro-1H-indol-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; Salmon alpha-Gal; 6-Chloro-3-indolyl a-D-galactopyranoside; SCHEMBL284849; DTXSID401259204; MFCD02683908; AKOS026674402; 6-Chloro-3-indoxyl alpha-D-galactopyranoside; 6-Chloro-3-indoxyl-alpha-D-galactopyranoside; 6-Chloro-3-indolyl alpha -D-galactopyranoside; C-4995; 6-Chloro-1H-indol-3-yl alpha-D-galactopyranoside; A-D-GALACTOPYRANOSIDE,6-CHLORO-1H-INDOL-3-YL; 6-Chloro-3-indolyl alpha-D-galactopyranoside, >=98.0% (HPLC); (2R,3R,4S,5R,6R)-2-(6-chloro-1H-indol-3-yloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol. CAS No. 198402-61-8. Molecular formula: C14H16ClNO6. Mole weight: 329.73. | |
| 6-Chloro-3-indoxyl-3-acetate | 6-Chloro-3-indoxyl-3-acetate is an extraordinary biomedical compound, extensively employed in cutting-edge research and diagnostics. Flaunting its exquisite nature, this exceptional substrate exhilarates numerous enzymes, specifically β-galactosidase, effectively unraveling the enigmatic maze of lacZ gene expression. Synonyms: 6-chloro-1H-indol-3-yl acetate;(6-chloro-1H-indol-3-yl) acetate; 6-Chloro-3-indoxyl-3-acetate; 1H-Indol-3-ol,6-chloro-,3-acetate;1H-Indol-3-ol, 6-chloro-, 3-acetate. CAS No. 114305-99-6. Molecular formula: C10H8ClNO2. Mole weight: 209.63. | |
| 6-Chloro-3-indoxyl nonanoate | 6-Chloro-3-indoxyl nonanoate is an essential biochemical recompound, finding extensive employment in enzymatic assays to facilitate the precise identification and quantification of targeted enzymes within diverse biological systems. Possessing a distinctive chemical arrangement, this compound serves as a catalyst for investigations concerning drug metabolism, protein functionality and diagnostic methodologies for diseases. Synonyms: Salmon-nonanoate. CAS No. 133950-72-8. Molecular formula: C17H22ClNO2. Mole weight: 307.81. | |
| 6-Methoxy-2-naphthalene carboxaldehyde | 6-Methoxy-2-naphthalene carboxaldehyde is used as a diagnostic reagent in tumor studies involving aldehyde dehydrogenase enzymes. In addition it is used in organic synthesis reactions forming fluorescent substrates for inhibition studies relating to hypertension and vascular inflammation. Group: Biochemicals. Alternative Names: 2-Methoxy-6-naphthalene carboxaldehyde; 6-Methoxy-2-naphthaldehyde; 6-Methoxy-2-naphthalene carboxaldehyde; MONAL 62. Grades: Highly Purified. CAS No. 3453-33-6. Pack Sizes: 25g. US Biological Life Sciences. | Worldwide |
| 7-Propargylamino-7-deaza-dATP - ATTO-700 | 7-Propargylamino-7-deaza-dATP - ATTO-700, a fluorescent dye, finds application in biomedical research to identify DNA replication, protein-DNA interactions, and enzyme activity. Moreover, it is a highly effective tool in diagnostic applications to detect infectious diseases like HIV, hepatitis B and C, and influenza. Synonyms: 7-Deaza-7-propargylamino-2'-deoxyadenosine-5'-triphosphate, labeled with ATTO 700, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C14H20N5O12P3- ATTO 700 (free acid). Mole weight: 1090.26 (free acid). | |
| 7-Propargylamino-7-deaza-ddGTP - ATTO-Rho11 | 7-Propargylamino-7-deaza-ddGTP - ATTO-Rho11, a fluorescent nucleotide analog, is an invaluable biomedical research tool. With its ability to serve as a substrate for DNA replication and repair enzymes, it enables studies of these vital processes. Additionally, its potential for use in diagnostic tools offers great promise for its application in cancer research, where aberrant DNA replication and repair are all too common. Synonyms: 7-Deaza-7-propargylamino-2',3'-dideoxyguanosine-5'-triphosphate, labeled with ATTO Rho11, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C49H57N8O15P3 (free acid). Mole weight: 1090.31 (free acid). | |
| 8-[(6-Amino)hexyl]-amino-adenosine-2',5'-bisphosphate - ATTO-465 | 8-[(6-Amino)hexyl]-amino-adenosine-2',5'-bisphosphate - ATTO-465 is a fluorescently labeled derivative of ATP analog that is widely used in biochemical and cellular studies. It is a useful tool for monitoring the activity of enzymes involved in ATP hydrolysis and lipid signaling pathways. Additionally, this product is commonly employed for calcium ion detection, receptor-ligand binding assays, and diagnostic purposes in the field of biomedicine. Synonyms: 8-[(6-Amino)hexyl]-amino-adenosine-2',5'-bisphosphate, labeled with ATTO 465, Triethylammonium salt. Grades: ≥ 95% by HPLC. Molecular formula: C33H44N10O11P2 (free acid). Mole weight: 818.71 (free acid). | |
| Acid Blue 40 | Acid Blue 40, also known as C.I. Acid Blue 40 or Solvent Blue 40, is a synthetic anionic dye belonging to the triphenylmethane family. It is an important component in the synthesis of many other dyes and has a wide variety of applications in various industries. Uses: Acid blue 40 has many scientific applications, including use in the field of medical diagnostics. it is used in the detection of certain proteins and enzymes, as well as in the detection of bacteria and other microorganisms. it is also used in the study of cell metabolism, as it can be used to measure the activity of certain enzymes. additionally, it is used to detect the presence of certain hormones and other metabolites in biological samples. Group: Acid dyes. Alternative Names: C.I. Acid Blue 40;2-Anthracenesulfonic acid, 4-((4-(acetylamino)phenyl)amino)-1-amino-9,10-dihydro-9,10-dioxo-, sodium salt (1:1). CAS No. 6424-85-7. Molecular formula: C22H16N3NaO6S. Mole weight: 473.43. Appearance: Powder. IUPACName: sodium 4-(4-acetamidoanilino)-1-amino-9,10-dioxoanthracene-2-sulfonic acid. Canonical SMILES: CC (=O)NC1=CC=C (C=C1)NC2=CC (=C (C3=C2C (=O)C4=CC=CC=C4C3=O)N)S (=O) (=O)[O-]. [Na+]. ECNumber: 229-190-5. Catalog: ACM6424857-1. |  |
| a-D-Glucose-1-phosphate dipotassium salt hydrate | a-D-Glucose-1-phosphate dipotassium salt hydrate is a vital compound in biomedicine utilized for various purposes. This product is commonly used in the treatment of glycogen storage diseases and as a substrate for enzyme reactions involved in glycolysis and glycogenesis. With its hygroscopic property, it serves as an essential component in research and diagnostic applications. Synonyms: Cori Ester Dipotassium Salt. CAS No. 5996-14-5. Molecular formula: C6H11K2O9P.H2O. Mole weight: 336.32 (anhydrous). | |
| ADPS | It is a novel Trinder's reagent used as a water-soluble reagent for the determination of hydrogen peroxide by enzyme spectrophotometry, and is widely used in diagnostic detection and biochemical test. Synonyms: N-Ethyl-N-(3-sulfopropyl)-3-methoxyaniline sodium salt; 3-[Ethyl(3-methoxyphenyl)amino]-1-propanesulfonic Acid Sodium Salt; N-Ethyl-N-(3-sulfopropyl)-m-anisidine Sodium Salt. Grades: ≥ 95 %. CAS No. 82611-88-9. Molecular formula: C12H18NNaO4S. Mole weight: 295.33. | |
| Amino-Functionalized Magnetic Nanoparticles(5mg/mL,0.5-0.6μm) | The surface of the super paramagnetic Fe3O4 nanoparticle is covalently functionalized with rich primary aliphatic amino groups, and can be used for further functionalization. Uses: Amino group functionalized magnetic nanoparticles can be used in diagnostic immunoassay, gene transfection, biomolecule separation, cell separation, enzyme immobilization, drug delivery, and biomedical imaging. Group: Nanospheres. |  |
| AMPPD disodium salt | AMPPD is a chemiluminescent enzyme substrate applied in clinical diagnostics. Synonyms: Lumigen PPD; 3-(4-Methoxyspiro[1,2-dioxetane-3,2'-tricyclo[3.3.1.1(3,7)]decan]-4-yl)phenol dihydrogen phosphate disodium salt. CAS No. 124951-96-8. Molecular formula: C18H21Na2O7P. Mole weight: 426.3. | |
| Angiotensin 1/2 (5-7) acetate | The precursor angiotensinogen is cleaved by renin to form angiotensin I. Angiotensin I is hydrolyzed by angiotensin-converting enzyme (ACE) to form the biologically active angiotensin II. Angiotensin II has been investigated for the treatment, basic science, and diagnostic of Hypertension, Renin Angiotensin System, and Idiopathic Membranous Nephropathy. Molecular formula: C19H31N5O6. Mole weight: 425.49. | |
| beta-Gal-TEG-N3 | beta-Gal-TEG-N3 is a biomedical product that plays a critical role in the field of drug delivery and diagnostics. It is commonly used as a linker molecule for the conjugation of beta-galactosidase enzymes to various drugs and imaging agents. This enables targeted delivery and localization of therapeutic and diagnostic substances for the treatment and detection of specific diseases, including cancers and genetic disorders. Molecular formula: C12H23N3O8. Mole weight: 337.33. | |
| Carboxyl-Functionalized Magnetic Nanoparticles(5mg/mL,0.5-0.6μm) | The surface of the super paramagnetic Fe3O4 nanoparticle is covalently functionalized with rich carboxyl groups, and can be used for further functionalization. Uses: Carboxyl functionalized magnetic nanoparticles can be used in the area of diagnostic immunoassay, gene transfection, biomolecule separation, cell separation, enzyme immobilization, drug delivery, and biomedical imaging. Group: Nanospheres. | |
| Chemically modified Aspergillus niger Glucose Oxidase | Oxidoreductase that catalyzes the conversion of D-glucose to D-glucono-1,5-lactone which hydrolyzes spontanously to gluconate. Take advantage of the enhanced liquid stability. Rely on the proven diagnostic quality of this product. Applications: Use glucose oxidase (god), chemically modified for the determination of α-amylase and d-glucose or o2. Group: Enzymes. Synonyms: glucose oxyhydrase; corylophyline; penatin; glucose aerodehydrogenase; microcid; β-D-glucose oxidase; D-glucose oxidase; D-glucose-1-oxidase; β-D-glucose:quinone oxidoreductase; glucose oxyhydrase; deoxin-1; GOD; GOx; notatin; glucose oxidase. GOD. Mole weight: 79 kD. Activity: >20 U/mg lyophilizate. Stability: At +2 to +8°C within specification range for 12 months. Store dry. Appearance: Yellowish white lyophilizate. Source: Aspergillus niger. EC 1.1.3.4; glucose oxyhydrase; corylophyline; penatin; glucose aerodehydrogenase; microcid; β-D-glucose oxidase; D-glucose oxidase; D-glucose-1-oxidase; β-D-glucose:quinone oxidoreductase; glucose oxyhydrase; deoxin-1; GOD; 9001-37-0; glucose oxidase enzyme; GOx; notatin; glucose oxidase. Cat No: DIA-285. |  |
| Chemically modified Cholesterol Oxidase from Brevibacterium species | Oxidoreductase that catalyzes the interconversion of cholesterol to cholest-4-en-3-one. Rely on the proven diagnostic quality of this product. Applications: Use cholesterol oxidase in diagnostic tests for the determination of cholesterol in combination with cholesterol esterase. Group: Enzymes. Synonyms: Cholesterol-O2 oxidoreductase; 3 beta-Hydroxy steroid oxidoreductase; 3β-hydroxysteroid: oxygen oxidoreductase; cholesterol: oxygen oxidoreductase; cholesterol oxidase. CHOD. Mole weight: 60 kD (native and SDS). Activity: 10-20 U/mg lyophilizate. Stability: At -15 to -25°C within specification range for 12 months. Store dry. Protect from light. Appearance: Yellow lyophilizate. Storage: No decrease in activity over 6 weeks at +35°C. Source: Brevibacterium species. Cholesterol-O2 oxidoreductase; 3 beta-Hydroxy steroid oxidoreductase; 3β-hydroxysteroid: oxygen oxidoreductase; cholesterol: oxygen oxidoreductase; cholesterol oxidase; EC 1.1.3.6. Cat No: DIA-284. | |
| Chemically modified Cucurbita species Ascorbate Oxidase | Oxidoreductase that oxidizes ascorbic acid to dehydroascorbate. Take advantage of the improved stability in liquid reagents. Rely on the proven diagnostic quality of this product. Applications: Use ascorbate oxidase, chemically modified, in a variety of diagnostic tests to eliminate the interference of ascorbic acid, since ascorbic acid interferes with the trinder reaction that is widely used for the colorimetric determination of analytes. it is useful in liquid as well as dry chemistry test, e.g., for the determination of uric acid, lactate or creatinine. Group: Enzymes. Synonyms: ascorbase; ascorbic acid oxidase; ascorbate oxidase; ascorbic oxidase; ascorbate dehydrogenase; L-ascorbic acid oxidase; AAO; L-ascorbate: O2 oxidoreductase; AA oxidase; L-ascorbate oxidase. AAO. Mole weight: Approximately 140 kD. Activity: >180 U/mg lyophilizate (+37°C, L-ascorbate); Specific activity (+37°C): >1,800 U/mg protein. Stability: At -15 to -25°C within specification range for 12 months. Store dry. Keep tightly sealed. Appearance: Turquoise lyophilizate. Source: Cucurbita species. ascorbase; ascorbic acid oxidase; ascorbate oxidase; ascorbic oxidase; ascorbate dehydrogenase; L-ascorbic acid oxidase; AAO; L-ascorbate: O2 oxidoreductase; AA oxidase; EC 1.10.3.3; 9029-44-1; L-ascorbate oxidase. Cat No: DIA-283. | |
| Chemically modified Glycerol-3-phosphate Oxidase from E. coli | Recombinant oxidoreductase that catalyzes the interconversion of glycerol 3-phosphate to dihydroxyacetone phosphate. Take advantage of the enhanced liquid stability of this enzyme. Rely on the proven diagnostic quality of this product. Applications: Use glycerol-3-phosphate oxidase in diagnostic tests for the determination of triglycerides together with glycerol kinase and lipoprotein lipase. Group: Enzymes. Synonyms: glycerol-3-phosphate oxidase; sn-glycerol-3-phosphate: oxygen 2-oxidoreductase; glycerol phosphate oxidase; glycerol-1-phosphate oxidase; glycerol phosphate oxidase; L-alpha-glycerophosphate oxidase; alpha-glycerophosphate oxidase; L-alpha-glycerol-3-phos. Glycerol-3-phosphate oxidase. Mole weight: 75 kD (SDS-PAGE); 74 kD (gel filtration, Sephadex G 150). Activity: >10 U/mg lyophilizate (+37°C, L-α-glycerol phosphate); Specific activity (+25°C): >40 U/mg protein. Stability: At +2 to +8°C within specification range for 12 months. Store dry. Appearance: Green yellow amorphous lyophilizate. Source: E. coli. glycerol-3-phosphate oxidase; EC 1.1.3.21; sn-glycerol-3-phosphate: oxygen 2-oxidoreductase; glycerol phosphate oxidase; glycerol-1-phosphate oxidase; glycerol phosphate oxidase; L-alpha-glycerophosphate oxidase; alpha-glycerophosphate oxidase; L-alpha-glycerol-3-phosphate oxidase. Cat No: DIA-287. | |
| Chemically modified Porcine L-Lactate Dehydrogenase | Dehydrogenase that catalyzes the interconversion of L(+)-lactate to pyruvate. Take advantage of the enhanced liquid stability of this enzyme. Rely on the proven diagnostic quality of this product. Applications: Use l-lactate dehydrogenase (l-ldh), chemically modified, in a variety of diagnostic tests for the removal of pyruvate in determinations working with nadh (i.e., triglycerides, lipase, aldolase, aminotransferases, glutamate dehydrogenase). Group: Enzymes. Synonyms: lactic acid dehydrogenase; L-lactic dehydrogenase; L-lactic acid dehydrogenase; lactate dehydrogenase; L-lactate dehydrogenase; L-LDH; LAD; LD; Lactate. LDH. Activity: >25 U/mg lyophilizate; >150 U/mg protein. Stability: At +2 to +8°C within specification range for 12 months. Appearance: White lyophilizate. Source: Porcine heart. Species: Porcine. EC 1.1.1.27; 9001-60-9; lactic acid dehydrogenase; L (+)-nLDH; L-(+)-lactate dehydrogenase; L-lactic dehydrogenase; L-lactic acid dehydrogenase; lactate dehydrogenase; lactate dehydrogenase NAD-dependent; lactic dehydrogenase; NAD-lactate dehydrogenase; L-lactate dehydrogenase; (S)-Lactate:NAD+ oxidoreductase; L-LDH; LAD; LD; Lactate. Cat No: DIA-279. | |
| Chemically modified Pseudomonas species Cholesterol Esterase | Hydrolase that splits fatty acids from sterols. Take advantage of the enhanced stability of this enzyme in liquid reagents. Rely on the proven diagnostic quality of this product. Applications: Use cholesterol esterase, chemically modified in diagnostic tests for the determination of cholesterol in combination with cholesterol oxidase. Group: Enzymes. Synonyms: cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; sterol esterase; CE. Cholesterol Esterase. Mole weight: ~129 kD. Activity: >10 U/mg lyophilizate; >100 U/mg protein. Stability: At +2 to +8°C within specification range for 12 months. Store dry. Appearance: Brownish lyophilizate. Source: Pseudomonas species. cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; EC 3.1.1.13; 9026-00-0; sterol esterase; CE. Cat No: DIA-281. | |
| Chemically modified Pseudomonas species Lipoprotein Lipase | Enzyme that hydrolyzes triglycerides into three free fatty acids and glycerol. Take advantage of the enhanced liquid stability of this enzyme. Rely on the proven diagnostic quality of this product. Applications: Use lipoprotein lipase in diagnostic tests for the determination of triglycerides together with glycerol kinase and glycerol-3-phosphate dehydrogenase. Group: Enzymes. Synonyms: Lipoprotein lipase; LPL; Clearing factor lipase; Diacylglycerol lipase; Diglyceride lipase. LPL. Mole weight: 47 kD. Activity: >10 U/mg lyophilizate. Stability: At +2 to +8°C within specification range for 12 months. Store dry. Appearance: Brownish lyophilizate. Source: Pseudomonas species. Lipoprotein lipase; LPL; EC 3.1.1.34; Clearing factor lipase; Diacylglycerol lipase; Diglyceride lipase. Cat No: DIA-282. | |
| Choline Kinase (Crude Enzyme) | Choline kinase (also known as CK,ChoK and choline phosphokinase) is an enzyme which catalyzes the first reaction in the choline pathway for phosphatidylcholine (PC) biosynthesis. This reaction involves the transfer of a phosphate group from adenosine triphosphate (ATP) to choline in order to form phosphocholine. Thus, the two substrates of this enzyme are ATP and choline, whereas its two products are adenosine diphosphate (ADP) and O-phosphocholine. Choline kinase requires magnesium ions (+2) as a cofactor for this reaction. This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with an alcohol grou... CHKA and CHKB and are only active in their homodimeric, heterodimeric and oligomeric forms. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Biotechnology; diagnostics; drug development; medicine. Group: Enzymes. Synonyms: Choline Kinase (phosphorylating); choline phosphokinase; choline-ethanolamine kinase. Enzyme Commission Number: EC 2.7.1.32. CAS No. 9026-67-9. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. Choline Kinase (phosphorylating); choline phosphokinase; choline-ethanolamine kinase. Pack: 100ml. Cat No: NATE-1825. | |
| Creatine Kinase MB Isoenzyme Type-1 from Human, Recombinant | The three isoenzymes (MM, MB, and BB) are found in muscle, cardiac and brain tissues. These recombinant proteins are ideal for calibrating diagnostic instruments and researching neuromuscular diseases. Creatine Kinases can be used for indications in many neuromuscular applications. These disorders include cardiac disease, mitochondrial disorders, inflammatory myopathies, myasthenia, polymyositis, McArdle's disease, NMJ disorders, muscular dystrophy, ALS, hypo and hyperthyroid disorders, central core disease, acid maltase deficiency, myoglobinuria, rhabdomyolysis, motor neuron diseases, rheumatic diseases, and other that create elevated or reduced levels of Creat... in elisa. the ckmbiti is purified by proprietary chromatographic techniques. Group: Enzymes. Synonyms: Creatine Kinase MB Isoenzyme Type-I; Creatine Kinase MB Isoenzyme Type-1; CKMBITI; CKMBI; CKMB; CKMBT1. Purity: Greater than 95.0% as determined by (a) Analysis by RP-HPLC. (b) Analysis by SDS-PAGE. CK. Activity: 500 IU/mg. Stability: CKMBITI although stable at 15°C for 7 days, should be stored below -18°C. Please prevent freeze-thaw cycles. Appearance: Sterile Filtered colourless liquid formulation. Source: Pichia Pastoris. Species: Human. Creatine Kinase MB Isoenzyme Type-I; Creatine Kinase MB Isoenzyme Type-1; CKMBITI; CKMBI; CKMB; CKMBT1. Cat No: NATE-0818. | |
| D-Amino Acid Oxidase (Crude Enzyme) | D-Amino Acid Oxidase (DAAO; also DAO, OXDA, DAMOX) is a peroxisomal enzyme containing FAD as cofactor that is expressed in a wide range of species from yeasts to human. It is not present in plants or in bacteria which instead use D-amino acid dehydrogenase. Its function is to oxidize D-amino acids to the corresponding imino acids, producing ammonia and hydrogen peroxide. DAAO is a candidate susceptibility gene and together with G72 may play a role in the glutamatergic mechanisms of schizophrenia. Risperidone andsodium benzoate are inhibitors of DAAO. DAAO is used as a biocatalyst in several biotechnological applications, such as the oxidation of cephalosporin C, the deracem...n may use the morpheein model of allosteric regulation. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Biotechnology; industry; drug development; medicine; pharmacology; analysis; diagnostics; synthesis. Group: Enzymes. Synonyms: ophio-amino-acid oxidase; L-amino acid:O 2 oxidoreductase; new yellow enzyme. Enzyme Commission Number: EC 1.4.3.3. CAS No. 9000-88-8. DAAO. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. ophio-amino-acid oxidase; L-amino acid:O 2 oxidoreductase; new yellow enzyme. Pack: 100ml. Cat No: NATE-1807. | |
| Dnp-Pro-Leu-Gly-Leu-Trp-Ala-DArg-NH2 | Dnp-Pro-Leu-Gly-Leu-Trp-Ala-DArg-NH2, a peptide utilized for biological research, is an exemplary agent for evaluating proteolytic activity and inhibitor effects. Notably, its potential in disease treatment, encompassing cancer and inflammation, has put it at the forefront of therapeutic development. In addition to its promising therapeutic properties, Dnp-Pro-Leu-Gly-Leu-Trp-Ala-DArg-NH2 may serve as a vital diagnostic tool for identifying pertinent enzymes within biological samples, providing otherwise unattainable insights for investigative purposes. Synonyms: N-(2,4-DINITROPHENYL)-PRO-LEU-GLY-LEU-TRP-ALA-D-ARG AMIDE; MMP SUBSTRATE, FLUOROGENIC; 360 MMP FRET SUBSTRATE I; DNP-PRO-LEU-GLY-LEU-TRP-ALA-D-ARG-NH2; DNP-PLGLWAR-NH2; N-(2,4-dinitrophenyl)-pro-leu-gly-leu-*trp-ala-D-. Grades: 98%. CAS No. 121282-17-5. Molecular formula: C45H64N14O11. Mole weight: 977.08. | |
| EC 1.1.1.47 | EC 1.1.1.47. Synonyms: glucose dehydrogenase F. bacillus mega-terium;Dehydrogenase, glucose;GLUCOSE DEHYDROGENASE THERMOPLASMA,*ACID OPHILUM REC;BETA-D-GLUCOSE: NADP+ 1-OXIDOREDUCTASE;GLUCOSE DEHYDROGENASE;GLUCOSE DEHYDROGENASE, NADP DEPENDENT;GDH;EC 1.1.1.47. CAS No. 9028-53-9. Product ID: CDF4-0056. Category: Enzyme Preparations. Product Keywords: Food Ingredients; Enzyme Preparations; EC 1.1.1.47; CDF4-0056; 9028-53-9; 232-836-9; 9028-53-9. Purity: 0.99. Color: White. EC Number: 232-836-9. Physical State: Powder. Storage: -20°C. Application: Diagnostics and cofactor regeneration of NAD(P)H in reductive processes. Product Description: This product has been enhanced for energy efficiency and waste prevention when used in biofuel cell research. |  |
| EDA-m7GDP - ATTO-Rho6G | EDA-m7GDP - ATTO-Rho6G, a fluorescent-labeled probe, offers a valuable tool for exploring RNA capping enzymes and unraveling the intricacies of mRNA formation. With the capacity to identify factors integral to vital processes such as mRNA processing, translation initiation, and immune evasion, this discreet yet powerful resource is a must-have for any researcher seeking to expand knowledge in drug target discovery, drug development, and viral infection diagnostics. Synonyms: 2'/3'-O-(2-Aminoethyl-carbamoyl)-7-methyl-guanosine-5'-diphosphate, labeled with ATTO Rho6G, Triethylammonium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C45H56N10O15P2(free acid). Mole weight: 1038.34 (free acid). | |
| Epoxy-Functionalized Magnetic Nanoparticles(30mg/mL,0.5-0.6μm) | The surface of the super paramagnetic Fe3O4 nanoparticle is covalently functionalized with rich carboxyl groups, and can be used for further functionalization. Uses: Epoxy functionalized magnetic nanoparticles can be used in the area of diagnostic immunoassay, gene transfection, biomolecule separation, cell separation, enzyme immobilization, drug delivery, and biomedical imaging. Group: Nanospheres. | |
| Glucose Dehydrogenase, Recombinant | In enzymology, a glucose 1-dehydrogenase (EC 1.1.1.47) is an enzyme that catalyzes the chemical reaction:beta-D-glucose + NAD (P)+? D-glucono-1,5-lactone + NAD (P)H + H+. The 3 substrates of this enzyme are beta-D-glucose, NAD+, and NADP+, whereas its 4 products are D-glucono-1,5-lactone, NADH, NADPH, and H+. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. Applications: Gdh can be used as the raw material enzyme in clinic diagnostic of blood glucose. Group: Enzymes. Synonyms: EC 1.1.1.47; D-glucose dehydrogenase (NAD (P)+); hexose phosphate dehydrogenase; β-D-glucose:NAD (P)+ 1-oxidoreductase; glucose 1-dehydrogenase; Glucose dehydrogenase; 9028-53-9. Enzyme Commission Number: EC 1.1.1.47. CAS No. 9028-53-9. Purity: 90% (SDS-PAGE test). Mole weight: About 28kDa (SDS-PAGE detection). Activity: About 200U/mg. Appearance: White powder, lyophilized. Storage: 4°C, store at -20°C for long-term preservation. Form: Freeze dried powder. EC 1.1.1.47; D-glucose dehydrogenase (NAD (P)+); hexose phosphate dehydrogenase; β-D-glucose:NAD (P)+ 1-oxidoreductase; glucose 1-dehydrogenase; Glucose dehydrogenase; 9028-53-9. Cat No: NATE-1139. | |
| Glutamate Dehydrogenase from Thermophilic Bacterium, recombinant | GDH is an oxidoreductase enzyme which relates carbon and nitrogen metabolism. It catalyzes the reduction of α-ketoglutarate and ammonia to L-glutamate and vice versa. This enzyme is a robust and ideal candidate for research use, and industrial applications in the diagnostics and food industries. Group: Enzymes. Synonyms: glutamate dehydrogenase; glutamic dehydrogenase; glutamate dehydrogenase (NAD+); glutamate oxidoreductase; glutamic acid dehydrogenase; L-glutamate dehydrogenase; NAD+-dependent glutamate dehydrogenase; NAD+-dependent glutamic dehyd. Enzyme Commission Number: EC 1.4.1.2. CAS No. 9001-46-1. GLDH. Mole weight: 270 kDa; Homohexameric ( 45 kDa per subunit). Activity: > 90 U/mg protein. Storage: at -20 °C. Form: Lyophilized powder. Source: E. coli. Species: Thermophilic Bacterium. glutamate dehydrogenase; glutamic dehydrogenase; glutamate dehydrogenase (NAD+); glutamate oxidoreductase; glutamic acid dehydrogenase; L-glutamate dehydrogenase; NAD+-dependent glutamate dehydrogenase; NAD+-dependent glutamic dehydrogenase; NAD+-glutamate dehydrogenase; NAD+-linked glutamate dehydrogenase; NAD+-linked glutamic dehydrogenase; NAD+-specific glutamic dehydrogenase; NAD+-specific glutamate dehydrogenase; NAD+:glutamate oxidoreductase; NADH-linked glutamate dehydrogenase; GLDH; EC 1.4.1.2. Cat No: NATE-1701. | |
| Glutamate Dehydrogenase (NAD(P)) from E.coli, Recombinant | Glutamate dehydrogenase (GLDH) is an enzyme, present in most microbes and the mitochondria of eukaryotes, as are some of the other enzymes required for urea synthesis, that converts glutamate to α-ketoglutarate, and vice versa. In animals, the produced ammonia is usually used as a substrate in the urea cycle. Typically, the α-ketoglutarate to glutamate reaction does not occur in mammals, as glutamate dehydrogenase equilibrium favours the production of ammonia and α-ketoglutarate. Applications: Use recombinant glutamate dehydrogenase in diagnostic tests for the determination of ammonia, urea, l-glutamate, glutamate pyruvate transaminase and leucine aminopeptidase. Group: Enzymes. Synonyms: glu. CAS No. 9029-12-3. GLDH. Mole weight: ~2 200 kD for the associated enzyme with 8 subunits; 280 kD for one subunit. Activity: >80 U/mg. Stability: At +2 to +8°C within specification range for 12 months. Store dry. Appearance: White lyophilizate. Source: E.coli. glutamate dehydrogenase (NADP+); glutamic dehydrogenase; dehydrogenase; glutamate (nicotinamide adenine dinucleotide (phosphate)); glutamic acid dehydrogenase; L-glutamate dehydrogenase; L-glutamic acid dehydrogenase; NAD(P)-glutamate dehydrogenase; NAD(P)H-dependent glutamate dehydrogenase; glutamate dehydrogenase (NADP); EC 1.4.1.4; GLDH. Cat No: NATE-0981. | |
| Glycerol-3-phosphate Oxidase from E. coli, Recombinant | Recombinant oxidoreductase that catalyzes the interconversion of glycerol 3-phosphate to dihydroxyacetone phosphate. Rely on the proven diagnostic quality of this product. Applications: Use glycerol-3-phosphate oxidase in diagnostic tests for the determination of triglycerides together with glycerol kinase and lipoprotein lipase. Group: Enzymes. Synonyms: glycerol-3-phosphate oxidase; sn-glycerol-3-phosphate: oxygen 2-oxidoreductase; glycerol phosphate oxidase; glycerol-1-phosphate oxidase; glycerol phosphate oxidase; L-alpha-glycerophosphate oxidase; alpha-glycerophosphate oxidase; L-alpha-glycerol-3-phosphate oxidase; GPO. CAS No. 9046-28-0. Glycerol-3-phosphate oxidase. Mole weight: 75 kD (SDS-PAGE); 74 kD (gel filtration, Sephadex G 150). Activity: >90 U/mg lyophilizate (+37°C). Stability: At +2 to +8°C within specification range for 12 months. Store dry. Appearance: Greenish yellow lyophilizate. Source: E. coli. glycerol-3-phosphate oxidase; EC 1.1.3.21; sn-glycerol-3-phosphate: oxygen 2-oxidoreductase; glycerol phosphate oxidase; glycerol-1-phosphate oxidase; glycerol phosphate oxidase; L-alpha-glycerophosphate oxidase; alpha-glycerophosphate oxidase; L-alpha-glycerol-3-phosphate oxidase. Cat No: DIA-286. | |
| Hexokinase from Yeast, chemically modified | A hexokinase is an enzyme that phosphorylates hexoses (six-carbon sugars), forming hexose phosphate. In most organisms, glucose is the most important substrate of hexokinases, and glucose-6-phosphate the most important product. Hexokinase can transfer an inorganic phosphate group from ATP to a substrate. Hexokinases should not be confused with glucokinase, which is a specific isoform of hexokinase. While other hexokinases are capable of phosphorylating several hexoses, glucokinase acts with a 50-fold lower substrate affinity and its only hexose substrate is glucose. Recombinant enzyme that converts hexose to hexose-6-phosphate. take advantage of the improved stability in liquid reagents. rely on the proven diagnostic quality of this product. Applications: Use hexokinase in diagnostic tests for blood glucose using the hexokinase method and for the determination of creatine kinase. Group: Enzymes. Synonyms: hexokinase type . Hexokinase. Mole weight: 57 kD (SDS-PAGE). Activity: > 40 U/mg lyophilizate. Stability: At +2 to +8°C within specification range for 18 months. Store dry. Appearance: White lyophilizate. Source: Yeast. hexokinase type IV glucokinase; hexokinase D; hexokinase type IV; hexokinase (phosphorylating); ATP-dependent hexokinase; glucose ATP phosphotransferase; hexokinase; ATP:D-hexose 6-phosphotransferase. Cat No: NATE-0989. | |
| Lactose | Lactose is a type of sugar found in milk and milk products. It is composed of two simple sugar molecules, glucose and galactose, joined together by a chemical bond. Lactose is broken down in the body by the enzyme lactase, which is produced in the small intestine. Uses: 1. food industry: lactose is widely used as a sweetener and bulking agent in the production of baked goods, confectionery, and dairy products. 2. pharmaceutical industry: lactose is a common excipient in the manufacture of tablets and capsules as it helps to bind drugs together and provide them with their desired physical properties. 3. medical industry: lactose is used in diagnostic tests for lactose intolerance and the determination of small intestinal transit time. 4. agriculture: lactose is used as a nutritional supplement in animal feed to increase milk production and improve weight gain in young animals. 5. chemical industry: lactose is used as a raw material in the production of lactic acid, which is used in a range of industrial applications, including the production of biodegradable plastics. Group: Sugars and derivatives. Alternative Names: Galβ1, 4Glc. CAS No. 63-42-3. Molecular formula: C12H22O11. Mole weight: 342.3. Appearance: white, odorless, and crystalline powder. Purity: 0.98. IUPACName: (2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol. Canonical SMILES: C (C1C (C (C (C ( | |
| L-Glutamate Decarboxylase (Crude Enzyme) | Glutamate decarboxylase or glutamic acid decarboxylase (GAD) is an enzyme that catalyzes the decarboxylation of glutamate to GABA and CO 2. In mammals, GAD exists in two isoforms encoded by two different genes - GAD1 and GAD2. These isoforms are GAD67 and GAD65 with molecular weights of 67 and 65 kDa, respectively. GAD1 and GAD2 are expressed in the brain where GABA is used as a neurotransmitter, GAD2 is also expressed in the pancreas. At least two more forms, GAD25 and GAD44 (embryonic; EGAD) are described in the developing brain. They are coded by the alternative transcripts of GAD1, I-80 and I-86: GAD25 is coded by both, GAD44 - only by I-80.This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Medicine; synthesis; diagnostics; food industry. Group: Enzymes. Synonyms: L-glutamic acid. Enzyme Commission Number: EC 4.1.1.15. CAS No. 9024-58-2. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. L-glutamic acid decarboxylase; L-glutamic decarboxylase; cysteic acid decarboxylase; L-glutamate α-decarboxylase; aspartate 1-decarboxylase; aspartic α-decarboxylase; L-aspartate-α-decarboxylase; γ-glutamate decarboxylase; L-glutamate 1-carboxy-lyase. Pack: 100ml. Cat No: NATE-1846. | |
| L-Glutamate Dehydrogenase (Crude Enzyme) | Glutamate dehydrogenase (GLDH) is an enzyme, present in most microbes and the mitochondria of eukaryotes, as are some of the other enzymes required for urea synthesis, that converts glutamate to α-ketoglutarate, and vice versa. In animals, the produced ammonia is usually used as a substrate in theurea cycle. Typically, the α-ketoglutarate to glutamate reaction does not occur in mammals, as glutamate dehydrogenase equilibrium favours the production of ammonia and α-ketoglutarate. Glutamate dehydrogenase also has a very low affinity for ammonia (high Michaelis constant of about 1 mM), and therefore toxic levels of ammonia would have to be present in the bo...; diagnostics. Group: Enzymes. Synonyms: glutamic dehydrogenase; glutamate dehydrogenase (NAD); glutamate oxidoreductase; glutamic acid dehydrogenase; L-glutamate dehydrogenase; NAD-dependent glutamate dehydrogenase; NAD-dependent glutamic dehydrogenase; NAD-glutamate dehydrogenase; NAD-linked glutamate dehydrogenase; NAD-linked glutamic dehydrogenase; NAD-specific glutamic dehydrogenase; NAD-specific glutamate dehydrogenase; NAD:glutamate oxidoreductase; NADH-linked glutamate dehydrogenase. Enzyme Commission Number: EC 1.4.1.2. CAS No. 9001-46-1. GLDH. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 mo | |
| L-Lactate Dehydrogenase from Porcine, Recombinant | A lactate dehydrogenase (LDH or LD) is an enzyme found in nearly all living cells (animals, plants, and prokaryotes). LDH catalyzes the conversion of pyruvate to lactate and back, as it converts NADH to NAD+ and back. A dehydrogenase is an enzyme that transfers a hydride from one molecule to another. Applications: High purity l-lactate dehydrogenase (porcine) for use in research, biochemical enzyme assays and in vitro diagnostic analysis. Group: Enzymes. Synonyms: EC 1.1.1.27; 9001-60-9; lactic acid dehydrogenase; L (+)-nLDH; L- (+)-lactate dehydrogenase; L-lactic dehydrogenase; L-lactic acid dehydrogenase; lactate dehydrogenase; lactate dehydrogenase NAD-dependent; lactic dehydrogenase; NAD-lactate dehydrogenase; L-lactate dehydrogenase; (S)-Lactate:NAD+ oxidoreductase; L-LDH; LAD; LD; Lactate. Enzyme Commission Number: EC 1.1.1.27. CAS No. 9001-60-9. Activity: ~ 330 U/mg. Storage: > 2 years at 4°C. Form: In 3.2 M ammonium sulphate. Source: Porcine. EC 1.1.1.27; 9001-60-9; lactic acid dehydrogenase; L (+)-nLDH; L- (+)-lactate dehydrogenase; L-lactic dehydrogenase; L-lactic acid dehydrogenase; lactate dehydrogenase; lactate dehydrogenase NAD-dependent; lactic dehydrogenase; NAD-lactate dehydrogenase; L-lactate dehydrogenase; (S)-Lactate:NAD+ oxidoreductase; L-LDH; LAD; LD; Lactate. Cat No: NATE-1105. | |
| MADB | It is a novel Trinder's reagent used as a water-soluble reagent for the determination of hydrogen peroxide by enzyme spectrophotometry, and is widely used in diagnostic detection and biochemical test. Synonyms: N,N-Bis(4-sulfobutyl)-3,5-dimethylaniline disodium salt; Sodium 4,4'-((3,5-dimethylphenyl)azanediyl)bis(butane-1-sulfonate). Grades: ≥95%. CAS No. 209518-16-1. Molecular formula: C16H25NNa2O6S2. Mole weight: 437.48. | |
| Mannitol Dehydrogenase (Crude Enzyme) | This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD + or NADP + as acceptor. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Diagnostics; biotechnology. Group: Enzymes. Synonyms: MTD; NAD-dependent mannitol dehydrogenase. Enzyme Commission Number: EC 1.1.1.255. CAS No. 144941-29-7. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. MTD; NAD-dependent mannitol dehydrogenase. Pack: 100ml. Cat No: NATE-1796. | |
| Mant-XDP | Mant-XDP, a fluorescent probe, is a tool of promise utilized for monitoring MMPs' activity, enzymes that instigate tissue degradation underlying several diseases claiming countless lives. As a diagnostic tool, it shows sufficient prospects for use in conditions, ranging from cancer to rheumatoid arthritis, while simultaneously illuminating its potential therapeutic applications. Synonyms: 2'/3'-O-(N-Methyl-anthraniloyl)-xanthosine-5'-diphosphate, Triethylammonium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C18H21N5O13P2(free acid). Mole weight: 577.33 (free acid). | |
| N6-(6-Amino)hexyl-dATP - ATTO-540Q | N6-(6-Amino)hexyl-dATP - ATTO-540Q emerges as a potent fluorescent enzyme substrate, having various applications in drug discovery, diagnostics and DNA-based assays. Synonyms: N; -(6-Amino)hexyl-2'-deoxyadenosine-5'-triphosphate, labeled with ATTO 540Q, Triethylammonium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C16H29N6O12P3- ATTO 540Q (free acid). Mole weight: 1130.36 (free acid). | |
| N-Acetyl-3-iodo-L-tyrosine hemihydrate | N-Acetyl-3-iodo-L-tyrosine hemihydrate, a chemical reagent with notable significance in studying enzyme inhibitors and protein synthesis, is widely utilized in the medical research community to develop promising drug therapies for thyroid disorders and cancers. Such compounds may also be used to synthesize radioiodinated compounds, essential in the realm of medical imaging and diagnostics. Uses: Thyronine analog. Synonyms: L-Tyrosine, N-acetyl-3-iodo-, hydrate (2:1). CAS No. 23277-49-8. Molecular formula: C22H26I2N2O9. Mole weight: 716.3. | |
| Native Acremonium sp. Ascorbate Oxidase | In enzymology, a L-ascorbate oxidase (EC 1.10.3.3) is an enzyme that catalyzes the chemical reaction:2 L-ascorbate + O2<-> 2 dehydroascorbate + 2 H2O. Thus, the two substRates of this enzyme are L-ascorbate and O2, whereas its two products are dehydroascorbate and H2O. This enzyme belongs to the family of oxidoreductases, specifically those acting on diphenols and related substances as donor with oxygen as acceptor. This enzyme participates in ascorbate metabolism. It employs one cofactor, copper. Applications: This enzyme is useful for avoidance from interference of ascorbic acid on diagnostic assay such as blood, uric acid, tg, tc and creatinine. Group: Enzymes. Synonyms: ascorbase; ascorbic acid oxidase; ascorbate oxidase; ascorbic oxidase; ascorbate dehydrogenase; L-ascorbic acid oxidase; AAO; L-ascorbate:O2 oxidoreductase;. Enzyme Commission Number: EC 1.10.3.3. CAS No. 9029-44-1. AAO. Mole weight: 80 kDa?gel filtration?. Activity: > 200 U/mg. Appearance: Light blue amorphous powder, lyophilized. Storage: Storage at ?20°C in the presence of a desiccant is recommended. Form: Freeze dried powder. Source: Acremonium sp. ascorbase; ascorbic acid oxidase; ascorbate oxidase; ascorbic oxidase; ascorbate dehydrogenase; L-ascorbic acid oxidase; AAO; L-ascorbate:O2 oxidoreductase; AA oxidase; EC 1.10.3.3; L-ascorbate oxidase. Cat No: NATE-0864. | |
| Native Bacillus sp. Monoglyceride Lipase | In enzymology, an acylglycerol lipase (EC 3.1.1.23) is an enzyme that catalyzes a chemical reaction that uses water molecules to break the glycerol monoesters of long-chain fatty acids. This enzyme belongs to the family of hydrolases, specifically those acting on carboxylic ester bonds. This enzyme participates in glycerolipid metabolism. Is an enzyme produced by microorganisms. this product shall be used for a diagnostics reagent. Applications: Useful for enzymatic determiantion of triglyceride. Group: Enzymes. Synonyms: EC 3.1.1.23; acylglycerol lipase; glycerol-ester acylhydrolase; monoacylglycerol lipase; monoacylglycerolipase; monoglyceride lipase; monoglyceride hydrolase; fatty acyl monoester lipase; monoacylglycerol hydrolase; monoglyceridyllipase; monoglyceridase. Enzyme Commission Number: EC 3.1.1.23. CAS No. 9040-75-9. Monoglyceride lipase. Mole weight: 20 kDa (gel filtration). Activity: > 20 U/mg. Appearance: White powder. Storage: Storage at-20°C in the presence of a desiccant is recommended. Form: Freeze dried powder. Source: Bacillus sp. EC 3.1.1.23; acylglycerol lipase; glycerol-ester acylhydrolase; monoacylglycerol lipase; monoacylglycerolipase; monoglyceride lipase; monoglyceride hydrolase; fatty acyl monoester lipase; monoacylglycerol hydrolase; monoglyceridyllipase; monoglyceridase. Cat No: NATE-0455. | |
| Native Bacillus stearothermophilius NAD Synthetase | In enzymology, a NAD+ synthase (EC 6.3.1.5) is an enzyme that catalyzes the chemical reaction:ATP + deamido-NAD+ + NH3<-> AMP + diphosphate + NAD+. The 3 substrates of this enzyme are ATP, deamido-NAD+, and NH3, whereas its 3 products are AMP, diphosphate, and NAD+. This enzyme belongs to the family of ligases, specifically those forming carbon-nitrogen bonds as acid-D-ammonia (or amine) ligases (amide synthases). This enzyme participates in nicotinate and nicotinamide metabolism and nitrogen metabolism. Is an enzyme produced by microorganisms. this product shall be used for a diagnostics reagent. Applications: Useful for enzymatic determination of atp, ammonia, urea or creatinine. it is also suitable for enzymatic cycling method. Group: Enzymes. Synonyms: EC 6.3.1.5; 9032-69-3; NAD+ synthetase; NAD+ synthase; nicotinamide adenine dinucleotide synthetase; diphosp. Enzyme Commission Number: EC 6.3.1.5. CAS No. 9032-69-3. NAD Synthetase. Mole weight: 50 kDa (gel filtration); 25 kDa (SDS-PAGE). Activity: > 1 U/mg. Appearance: White powder. Storage: Storage at-20°C in the presence of a desiccant is recommended. Form: Freeze dried powder. Source: Bacillus stearothermophilius. EC 6.3.1.5; 9032-69-3; NAD+ synthetase; NAD+ synthase; nicotinamide adenine dinucleotide synthetase; diphosphopyridine nucleotide synthetase. Cat No: NATE-0471. | |
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