Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the American suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the UK.
| Product | Description | |
|---|---|---|
| Acetyl coenzyme A sodium salt | Acetyl coenzyme A sodium salt is an essential cofactor and carrier of acyl groups in enzymatic acetyl transfer reactions. Formed either by the oxidative decarboxylation of pyruvate in mitochondria, by the oxidation of long-chain fatty acids, or by the oxidative degradation of certain amino acids. It is a key precursor in lipid biosynthesis, and the source of all fatty acid carbons. Also a positive regulator of pyruvate carboxylase and a precursor of the neurotransmitter acetylcholine. Applications: An essential cofactor and carrier of acyl groups. Group: Coenzymes. Synonyms: Acethyl coenzyme alpha sodium salt. CAS No. 102029-73-2. Purity: ≥92%. Mole weight: 893.53. Appearance: Powder. Form: Solid. Acethyl coenzyme alpha sodium salt; Acetyl coenzyme A sodium salt; 102029-73-2. Cat No: COEC-047. |  |
| Coenzyme A sodium salt | This compound is an essential cofactor in enzymatic acetyl transfer reactions. Applications: An essential cofactor in enzymatic acetyl transfer reactions. Group: Coenzymes. Synonyms: CoA Na2. CAS No. 55672-92-9. Purity: ≥90%. Mole weight: 767.53. Appearance: Powder. Form: Solid. CoA Na2; Coenzyme A sodium salt; 55672-92-9. Cat No: COEC-003. | |
| DL-3-Hydroxy-3-methylglutaryl coenzyme A trisodium salt | DL-3-Hydroxy-3-methylglutaryl coenzyme is a trisodium salt key intermediate in the biosynthesis of cholesterol, ketone bodies and terpenes. Applications: An intermediate in biosynthesis. Group: Coenzymes. Synonyms: DL-3-Hydroxy-3-methylglutaryl coenzyme A sodium salt. CAS No. 103476-21-7. Purity: ≥95%. Mole weight: 977.62. Appearance: Crystalline. Form: Solid. DL-3-Hydroxy-3-methylglutaryl coenzyme A sodium salt; DL-3-Hydroxy-3-methylglutaryl coenzyme A trisodium salt; 103476-21-7. Cat No: COEC-042. | |
| Pentadecanoyl Coenzyme A Sodium Salt | Pentadecanoyl Coenzyme A is the derivative of Coenzyme A, which is a cofactor in enzymatic acetyl transfer reactions. It can also be used for the synthesis of substrates used for measuring acyl-CoA dehydrogenase activities, which is essential part of the investigation of patients with suspected defects in fatty acid oxidation. Synonyms: S-pentadecanoate Coenzyme A Sodium Salt; Pentadecanoyl-CoA Sodium Salt; Pentadecanethioic Acid S-Ester with Coenzyme A Sodium Salt. Molecular formula: C36H64N7O17P3S.xNa. Mole weight: 991.92. |  |
| 1,N6-Ethenoadenosine-5'-triphosphate sodium salt | N6-Ethenoadenosine-5'-triphosphate sodium salt, a compound of utmost significance in biochemical research, serves as an indispensable resource to explore the multifaceted nature of ATP, a universally acknowledged energy carrier, and its intricate involvement in diverse biological phenomena. With its distinctive configuration, it serves as an invaluable tool for investigating ATP-binding enzymes and receptors, thereby facilitating the advancement of therapeutic interventions for menacing conditions such as cancer, neurodegenerative ailments, and cardiovascular disorders. Synonyms: 1,N[6]-ethenoadenosine 5'-triphosphate, sodium salt; Disodium 3-{5-O-[hydroxy ({[ (hydroxyphosphinato) oxy]phosphinato}oxy) phosphoryl]pentofuranosyl}-3H-imidazo[2, 1-i]purine. Grades: ≥ 95% (HPLC). CAS No. 60777-99-3. Molecular formula: C12H14N5Na2O13P3. Mole weight: 575.17. | |
| 1-Naphthyl b-D-glucuronide sodium salt | 1-Naphthyl b-D-glucuronide sodium salt, an invaluable biomedicine, is employed extensively in scientific research to explore the intricate process of glucuronidation, which plays a vital role in the metabolism and elimination of a diverse array of pharmaceuticals and endogenous compounds. Acting as a versatile substrate, it facilitates the activities of glucuronosyltransferases, crucial enzymes that mediate glucuronidation reactions. Demonstrating immense utility in in vitro experiments, this product enables scientists to unravel the profound impact of glucuronidation on drug pharmacokinetics, while simultaneously facilitating the evaluation of potential drug-drug interactions. Synonyms: 1-Nap-b-D-GlcA.Na. CAS No. 83833-12-9. Molecular formula: C16H15NaO7. Mole weight: 342.28. | |
| 2,3,4,6-Tetra-O-acetyl-a-D-thiomannopyranse sodium salt | 2,3,4,6-Tetra-O-acetyl-a-D-thiomannopyranse sodium salt, a synthetic chemical entity, has been employed in the biomedical industry as a substrate to probe α-mannosidase enzymes' activity. Its application is warranted in the context of investigating α-mannosidase deficiency-mediated lysosomal storage disorders, including Niemann-Pick disease, Pompe disease, and α-mannosidosis. Such disordered states arise due to defects in lysosomal enzymes like α-mannosidase, which hinder the degradation of glycoproteins, causing their accumulation in lysosomes. Molecular formula: C14H19O9SNa. Mole weight: 386.35. | |
| 2',3'-cUMP | 2',3'-cUMP, a nucleotide analog employed in biomedical research, exhibits promise in the treatment of diverse ailments such as cancer and viral infections. By serving as either a substrate or an inhibitor of specific enzymes implicated in DNA replication and RNA synthesis, it induces modifications within cellular mechanisms. Synonyms: Uridine- 2', 3'- cyclic monophosphate, sodium salt. Grades: ≥ 97% by HPLC. CAS No. 15718-50-0. Molecular formula: C9H10N2O8P · Na. Mole weight: 328.2. | |
| 2',3'-Dideoxyinosine-5'-monophosphate sodium salt | 2',3'-Dideoxyinosine-5'-monophosphate sodium salt, a remarkable pharmaceutical compound, emerges as a pivotal player in the battle against human immunodeficiency virus (HIV) infection. Exhibiting its prowess as an antiviral agent, this compound effectively thwarts the replication of the virus by inhibiting the reverse transcriptase enzyme. Synonyms: Didanosine 5'-monophosphate sodium salt. Molecular formula: C10H11N4O6P·Na2. Mole weight: 360.17. | |
| 25-Hydroxy-cholesterol 3-Sulfate Ester Sodium Salt-d6 | 25-Hydroxy-cholesterol 3-Sulfate Ester Sodium Salt-d6 is the isotope labelled analog of 25-Hydroxy-cholesterol 3-Sulfate Ester Sodium Salt (H825760). 25-Hydroxy-cholesterol 3-Sulfate Ester is a derivative of 4 β-Hydroxy Cholesterol (H917980), a metabolite of Cholesterol. It is formed from Cholesterol by the drug-metabolizing enzyme cytochrome P 450 3A4. A potential ligand for the nuclear receptor LXR and also a new endogenous CYP3A marker. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 1mg. Molecular Formula: C27H39D6NaO5S, Molecular Weight: 510.73. US Biological Life Sciences. |  Worldwide |
| 25-Hydroxy Vitamin D3 3-Sulfate Sodium Salt | 25-Hydroxyvitamin D3 3-Sulfate is a metabolite of 24,25-Dihydroxyvitamin D3 and 25-Hydroxyvitamin D3. Calcifediol (INN), also known as calcidiol, 25-hydroxycholecalcifero l, or 25-hydroxyvitamin D (abbreviated 25(OH)D),is a prehormone that is produced in the liver by hydroxylation of vitamin D3(cholecalciferol) by the enzyme cholecalciferol 25-hydroxylase which was isolated by Michael F. Holick. Physicians worldwide measure this metabolite to determine a patient's vitamin D status.At a typical daily intake of vitamin D3, its full conversion to calcifediol takes approximately 7 days. Calcifediol is then converted in the kidneys (by the enzyme 25(OH)D-1α-hydroxylase) into calcitriol (1,25-(OH)2D3), a secosteroid hormone that is the active form of vitamin D. It can also be converted into 24-hydroxycalcidiol in the kidneys via 24-hydroxylation. Group: Biochemicals. Alternative Names: (3 β,5Z,7E)-9,10-Secocholesta-5,7,10(19)-triene-3,25-diol 3-(Hydrogen Sulfate) Sodium Salt; 25-Hydroxyvitamin D3 3-Sulfate Sodium Salt; 25-Hydroxyvitamin D3 3 β-Sulfate Sodium Salt; Calcifediol 3-Sulfate Sodium Salt. Grades: Purified. Pack Sizes: 2.5mg. Molecular Formula: C??H??NaO?S, Molecular Weight: 502.68. US Biological Life Sciences. | Worldwide |
| 2-Aminopurine-riboside-5'-monophosphate | 2-Aminopurine-riboside-5'-monophosphate, a biochemical agent employed in scientific research, exhibits multifaceted benefits as an investigative tool. By being integrated into oligonucleotides, it enables the study of base-pair mismatches, as well as facilitating enzyme activity during nucleic acid synthesis. Furthermore, its competence in countering viral infections makes it a promising therapeutic agent. Such versatile properties have marked 2-Aminopurine-riboside-5'-monophosphate a crucial component in the field of DNA and RNA research. Synonyms: 2-Aminopurine-riboside-5'-monophosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C10H14N5O7P (free acid). Mole weight: 347.22 (free acid). | |
| 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate sodium salt | 2'-Deoxy-2'-fluoroadenosine-5'-triphosphate sodium salt, a pivotal compound in the biomedical sector, exhibits extensive utility as a substrate for diverse enzymes implicated in DNA synthesis and repair. Acclaimed for its distinct characteristics, this product finds prominence in the realm of scientific investigation and inquiry pertaining to antiviral therapeutics and disease management. Synonyms: 2'-FdATP.Na. Grades: 95%. Molecular formula: C10H15FNO12P3·xNa. Mole weight: 453.15 (free acid). | |
| 2'-Deoxy-5-hydroxymethylcytidine 5'-monophosphate sodium salt | 2'-Deoxy-5-hydroxymethylcytidine 5'-monophosphate sodium salt, a remarkable biomedicine, manifests immense potential in combating select viral infections. Mechanistically, it thwarts viral replication and diminishes viral load, largely attributed to its profound antiviral properties. Furthermore, owing to its unique pharmacological attributes, this compound aptly targets specific viral enzymes, thereby promulgating its efficacy against afflictions induced by such insidious viral strains. Molecular formula: C10H14N3Na2O8P. Mole weight: 381.19. | |
| 2'-Deoxyadenosine 5'-a-thiotriphosphate sodium salt | 2'-Deoxyadenosine 5'-a-thiotriphosphate sodium salt is a crucial tool extensively used in the biomedical industry for various research purposes. It serves as a modified nucleotide analog used in DNA sequencing, structural analyses, and enzyme kinetics studies. Additionally, it finds utility in developing antiviral drugs targeting specific viral RNA or DNA polymerases. Molecular formula: C10H12N5Na3O12P3S. Mole weight: 588.18. | |
| 2'-Deoxyadenosine 5'-O-thiophosphate sodium salt | 2'-Deoxyadenosine 5'-O-thiophosphate sodium salt symbolizes a paramount nucleotide analog extensively employed within the biomedical industry for research objectives. Research experts predominantly employ this remarkable compound to unravel the complexities surrounding DNA synthesis and repair mechanisms. Its implementation is further extended to the realm of investigating intricate enzyme kinetics and comprehending signal transduction pathways. Synonyms: 2'-Deoxyadenosine 5'-(dihydrogen phosphorothioate). CAS No. 64145-26-2. Molecular formula: C10H14N5O5PS. Mole weight: 347.29. | |
| 2-Ethynyl-ATP (2-EATP) | 2-Ethynyl-ATP (2-EATP), a modified nucleotide, finds its utility in enzymatic assays intended to scrutinize ATP-binding proteins, namely kinases and phosphatases. It also serves as a powerful instrument to investigate ATP-dependent enzymes implicated in numerous pathological conditions, viz. cancer and neurological disorders. Synonyms: 2-Ethynyl-adenosine-5'-triphosphate, Sodium salt. Grades: ≥ 90% by HPLC, contains approx. 6% 2-Ethynyl-ADP. Molecular formula: C12H16N5O13P3. Mole weight: 531.2. | |
| 2H,5H-Pyrano[4,3-b]pyranyl Mupirocin Methyl Ester | 2H,5H-Pyrano[4,3-b]pyranyl Mupirocin Methyl Ester is an intermediate in the synthesis of 2H,5H-Pyrano[4,3-b]pyranyl Mupirocin Sodium Impurity (P840550), which also a mupirocin (M794000) impurity. The rearrangement isomer of Mupirocin is prepared using an enzyme-catalyzed, selective deesterification. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 1mg. Molecular Formula: C27H46O9. 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'-Iodo-dAMP | 2'-Iodo-dAMP, a nucleotide analogue renowned for inhibiting DNA polymerases and viral enzymes, has been extensively studied for its antiviral potential against a host of viruses, encompassing herpes simplex virus and HIV. Additionally, this product has found widespread use in the synthesis of oligonucleotides employed in gene therapy and drug discovery, exhibiting an immense capacity for ground-breaking research in the realm of science. Synonyms: (2'I-dAMP); 2'-Iodo-2'-deoxyadenosine-5'-monophosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C10H13N5O6PI (free acid). Mole weight: 457.12 (free acid). | |
| 2-Naphthyl-Beta-D-Glucuronide Sodium Salt | 2-Naphthyl-Beta-D-Glucuronide Sodium Salt is a highly significant compound applied in the realm of compound, assuming an indispensable role in the exploration of drug metabolism and detoxification. Operating as a crucial substrate for the enzyme glucuronidase, it profoundly facilitates the investigative examination of glucuronidation pathways. Its prominence becomes particularly eminent when studying the ramifications of pharmaceuticals and their metabolites on glucuronidation processes. | |
| 2'-O-Methyluridine-5'-triphosphate sodium salt | 2'-O-Methyluridine-5'-triphosphate sodium salt is a crucial reagent widely used in the field of biomedicine. It plays a vital role as a substrate for various enzymes involved in cellular processes. This product is commonly utilized in research related to RNA synthesis, RNA modification, and RNA labeling. Additionally, it serves as a key component in studies involving antiviral drug development and understanding certain diseases at the molecular level. Synonyms: 2'OMe-UTP Na. Molecular formula: C10H17N2O15P3·xNa. Mole weight: 498.17 (free acid). | |
| (2S,4R)-1-(tert-Butoxycarbonyl)-4-(tosyloxy)pyrrolidine-2-carboxylic Acid | (2S,4R)-1-(tert-Butoxycarbonyl)-4-(tosyloxy)pyrrolidine-2-carboxylic Acid is an intermediate in the synthesis of Fosinopril-d5 Sodium Salt (F727803), the labeled analogue of Fosinopril Sodium Salt (F727800), a phosphinic acid containing angiotensin converting enzyme (ACE) inhibitor. Antihypertensive. Group: Biochemicals. Grades: Highly Purified. CAS No. 96314-28-2. Pack Sizes: 500mg, 5g. Molecular Formula: C17H23NO7S, Molecular Weight: 385.43. US Biological Life Sciences. | Worldwide |
| 4H-Furo[2,3-c]pyranyl Mupirocin Sodium Impurity | 4H-Furo[2,3-c]pyranyl Mupirocin Sodium Impurity is an impurity of Mupirocin, which is a carboxylic acid bacteriostatic/bactericidal antibiotic. Uses: Mupirocin (m794000) impurity. the rearrangement isomer of mupirocin is prepared using an enzyme-catalyzed, selective deesterification. Synonyms: [2R-[2α(1S*, 2S*, 3S*), 3aβ, 6α(E), 7β, 7aα]]-9-[[4-[2-(1, 3-Dihydroxy-2-methylbutyl)hexahydro-7-hydroxy-4H-furo[3, 2-c]pyran-6-yl]-3-methyl-1-oxo-2-butenyl]oxy]nonanoic Acid Monosodium Salt. CAS No. 116182-43-5. Molecular formula: C26H43NaO9. Mole weight: 522.60. | |
| 4-Methylumbelliferyl 2-acetamido-2-deoxy-b-D-galactopyranoside-4-sulfate sodium salt | 4-Methylumbelliferyl 2-acetamido-2-deoxy-b-D-galactopyranoside-4-sulfate sodium salt is a compound of remarkable chemical intricacy, primarily employed as a substrate for the discernment of enzyme activity and the probing of diverse biochemical mechanismsl. Its wide-ranging utility extends to the investigation of enzymes implicated in afflictions including lysosomal storage disorders and bacterial infections. Molecular formula: C18H20NNaO11S. Mole weight: 481.41. | |
| 4-Methylumbelliferyl 2-Acetamido-2-deoxy-β-D-galactopyranoside, 4-Sulfate Sodium Salt | This sodium salt compound, 4-Methylumbelliferyl 2-Acetamido-2-deoxy-β-D-galactopyranoside sulfate, is utilized in biomedicine for its ability to detect lysosomal enzymes involved in the diagnosis of lysosomal storage diseases. It acts as a fluorogenic substrate, aiding in the identification and characterization of specific enzymes implicated in diseases such as Gaucher's disease and GM1 gangliosidosis. Grades: 96%. Molecular formula: C18H20NNaO11S. Mole weight: 481.41. | |
| 4-Nitrophenyl 2-acetamido-2-deoxy-b-D-glucopyranoside-6-sulfate sodium salt | 4-Nitrophenyl 2-acetamido-2-deoxy-b-D-glucopyranoside-6-sulfate sodium salt is a highly specialized and potent compound, acting as an exquisite substrate for the discerning enzymes intricately connected to lysosomal storage disorders. Synonyms: Sodium ((2R,3S,4R,5R,6S)-5-acetamido-3,4-dihydroxy-6-(4-nitrophenoxy)tetrahydro-2H-pyran-2-yl)methyl sulfate; sodium; [(2R,3S,4R,5R,6S)-5-acetamido-3,4-dihydroxy-6-(4-nitrophenoxy)oxan-2-yl]methyl sulfate. CAS No. 467446-91-9. Molecular formula: C14H17N2O11S.Na. Mole weight: 444.35. | |
| 4-Thio-ethyl-UTP | 4-Thio-ethyl-UTP, a compound extensively utilized in biomedical research, particularly in the field of RNA splicing and editing, is an immensely versatile alternative substrate to UTP, especially when investigating the function of RNA editing enzymes. Its exclusive selectivity for specific RNA sequences further enhances its usefulness, rendering it an essential tool for studying cancer and genetic disorders. Synonyms: 4-Thio-ethyl-uridine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C11H19N2O14P3S (free acid). Mole weight: 528.26 (free acid). | |
| 4-Thio-UDP | 4-Thio-UDP, in the realm of compound industry, standing as a prominent biochemical compound of significant usage. Exhibiting itself as a substrate for multifarious enzymes governing intricate cellular processes, it has garnered attention due to its potential therapeutic implications concerning nucleotide metabolism and signaling pathways. Its paramountcy in research pertaining to cancer, neurodegenerative disorders and immune system impairments remains undeniable. Synonyms: 4-Thio-uridine-5'-diphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C9H14N2O11P2S (free acid). Mole weight: 420.22 (free acid). | |
| 5-Bromo-3-indolyl b-D-galactopyranoside-6-sulfate sodium salt | 5-Bromo-3-indolyl β-D-galactopyranoside-6-sulfate sodium salt is an extensively researched and academically significant compound, serving as a chromogenic substrate, widely adopted for the discernment of b-galactosidase enzyme function. Recognized for its unrivaled prowess, this cutting-edge compound substantially contributes to the comprehensive comprehension of gene expression, regulation and meticulously scrutinizes biological samples. Molecular formula: C14H15BrNNaO9S. Mole weight: 476.23. | |
| 5-Bromo-4-chloro-1H-indol-3-yl phosphate sodium | Sodium 5-bromo-4-chloro-1H-indol-3-yl phosphate is commonly used as a substrate for phosphatase assays in biochemistry and molecular biology. This compound is converted by phosphatases to a yellow compound that can be easily measured spectrophotometrically or fluorometrically. Furthermore, it has been used as a useful reagent in enzyme-catalyzed reactions and a tool for studying signal transduction pathways. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 102185-33-1. Pack Sizes: 100 mg; 250 mg. Product ID: HY-W045537. |  |
| 5-Bromo-4-chloro-3-indolyl b-D-glucuronide sodium salt trihydrate | 5-Bromo-4-chloro-3-indolyl β-D-glucuronide sodium salt trihydrate is a valuable biochemical reagent widely used in the biomedical industry. It acts as a substrate for enzymes like β-glucuronidase, aiding in the detection and quantification of enzyme activity in various biological samples. This compound is especially helpful in studying drug metabolism, toxicity, and certain diseases such as liver disorders and cancer. Synonyms: X-Glucuronide trihydrate X-GlcA Na. CAS No. 370100-64-4. Molecular formula: C14H12BrClNNaO7.3H2O. Mole weight: 498.64. | |
| 5-Bromo-6-chloro-3-indolyl phosphate disodium salt monohydrate | 5-Bromo-6-chloro-3-indolyl phosphate disodium salt monohydrate is a crucial recompound within the biomedical sector, serving as an indispensable tool for conducting enzymatic assays. Its utilization facilitates the exploration of diverse cellular mechanisms by enabling the detection of alkaline phosphatase. This compound assumes particular significance in the realm of drug exploration and development as it greatly facilitates the identification and screening of potential enzyme inhibitors. Synonyms: Magenta phosphate sodium salt. CAS No. 404366-59-2. Molecular formula: C8H4BrClNO4PNa2.H2O. Mole weight: 388.45. | |
| 5-Bromo-dUMP | 5-Bromo-dUMP is a highly active inhibitor of thymidylate synthase, serving as a pivotal component in hindering the catalytic ability of this vital enzyme involved in the research and development of DNA. Its efficacious employment as an antitumor compound against diverse malignancies proficiently impedes the generation of DNA, thus efficaciously curbing the proliferation of malignant cells inherent to cancerous growths. Synonyms: (5Br-dUMP); 5-Bromo-2'-deoxyuridine-5'-monophosphate, Sodium salt. Grades: ≥ 95% by HPLC. CAS No. 6666-38-2. Molecular formula: C9H12N2O8PBr (free acid). Mole weight: 387.08 (free acid). | |
| 5'-CMPS | 5'-CMPS is a potent, competitive inhibitor that regulates enzymes. It can interact with cytidine-5'-monophosphate. Synonyms: Cytidine- 5'- O- monophosphorothioate, sodium salt. Grades: ≥ 97% by HPLC. CAS No. 47151-76-8. Molecular formula: C9H14N3O7PS (free acid). Mole weight: 339.3 (free acid). | |
| 5'-dIMPS | 5'-dIMPS is a potent, competitive inhibitor that regulates enzymes. It can interact with 2'-deoxyinosine-5'-monophosphate. Synonyms: 2'- Deoxyinosine- 5'- O- monophosphorothioate, sodium salt. Grades: ≥ 97% by HPLC. CAS No. 771477-45-3. Molecular formula: C10H13N4O6PS (free acid). Mole weight: 348.3 (free acid). | |
| 5'-dUMPS | 5'-dUMPS is a potent, competitive inhibitor that regulates enzymes. It can interact with 2'-deoxypyrimidine-5'- monophosphate. Synonyms: 2'- Deoxyuridine- 5'- O- monophosphorothioate, sodium salt. Grades: ≥ 97 % by HPLC. CAS No. 205379-91-5. Molecular formula: C9H13N2O7PS (free acid). Mole weight: 324.3 (free acid). | |
| 5-Iodo-3-indolyl-b-D-galactopyranoside-6-sulfate sodium salt | 5-Iodo-3-indolyl-b-D-galactopyranoside-6-sulfate sodium salt is a compound commonly used in the biomedical industry for staining and detecting galactosidase activity in cells and tissues. It offers high sensitivity and specificity allowing for the identification and analysis of cells expressing the enzyme. Molecular formula: C14H15INNaO9S. Mole weight: 523.24. | |
| 5-Methyl-dCMP | 5-Methyl-dCMP, a modified nucleotide utilized in DNA and RNA synthesis, offers potential applications in cancer therapy due to its ability to destabilize cancer cell DNA and inhibit cell proliferation upon incorporation. Acting as a substrate for the DNA polymerase enzyme, it integrates into DNA synthesis. Its implications extend beyond traditional nucleotides, presenting new possibilities in the realm of genetic research. Synonyms: 5-Methyl-2'-deoxycytidine-5'-monophosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C10H16N3O7P (free acid). Mole weight: 321.22 (free acid). | |
| 5'-PuMP | 5'-PuMP is a potent, competitive inhibitor that regulates enzymes. It can interact with adenosine-5'-monophosphate. Synonyms: Purine riboside- 5'- O- monophosphate, sodium salt. Grades: ≥ 97% by HPLC. CAS No. 13484-60-1. Molecular formula: C10H13N4O7P (free acid). Mole weight: 332.2 (free acid). | |
| 5'-TMPS | 5'-TMPS is a potent, competitive inhibitor that regulates enzymes. It can interact with thymidine-5'-monophosphate. Synonyms: Thymidine- 5'- O- monophosphorothioate, sodium salt. Grades: ≥ 97% by HPLC. CAS No. 15548-51-3. Molecular formula: C10H15N2O7PS (free acid). Mole weight: 338.3 (free acid). | |
| 5'-UMPS | 5'-UMPS is a potent, competitive inhibitor that regulates enzymes. It can interact with uridine-5'-monophosphate. Synonyms: Uridine- 5'- O- monophosphorothioate, sodium salt. Grades: ≥ 95% by HPLC. CAS No. 15548-52-4. Molecular formula: C9H13N2O8PS (free acid). Mole weight: 340.3 (free acid). | |
| 6-Benzoyl-2-naphthylphosphate disodium salt | 6-Benzoyl-2-naphthylphosphate disodium salt, an indispensable asset in the field of biomedicine, serves as a formidable suppressor of alkaline phosphatase. As a pivotal enzyme implicated in diverse metabolic mechanisms, the inhibition of this enzyme assumes paramount significance. Synonyms: 6-benzoyl-2-naphthyl phosphate disodium; disodium; (6-benzoylnaphthalen-2-yl) phosphate; Sodium 6-benzoylnaphthalen-2-yl phosphate. CAS No. 74144-43-7. Molecular formula: C17H11Na2O5P. Mole weight: 372.22. | |
| 6-Chloro-GTP | 6-Chloro-GTP is a highly significant compound, playing a pivotal role due to its exceptional antiviral attributes which effectively impede viral replication. By selectively targeting viral RNA research and development-associated enzymes, this remarkable compound showcasing an outstanding inhibitory effect. Promisingly, it finds extensive application in studying various viral infections like hepatitis C and respiratory syncytial virus (RSV). Synonyms: (6Cl-GTP); 6-Chloro-guanosine-5'-triphosphate, Sodium salt; 2-Amino-6-chloro-9-(β-D-ribofuranosyl)-purine. Grades: ≥ 95% by HPLC. Molecular formula: C10H15N5O13P3Cl (free acid). Mole weight: 541.62 (free acid). | |
| 6-Fluo-10-NAD? | 6-Fluo-10-NAD? is a fluorescent analogue of β-NAD+ (λexc494 nm, λem517 nm) used as a non-radioactive alternative to radio-labelled β-NAD+ for research on enzymes requiring β-NAD+. Synonyms: β- Nicotinamide- N6- (2- (6- [fluoresceinyl]aminohexanoyl) aminoethyl) adenine dinucleotide, sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C50H53N9O21P2 (free acid). Mole weight: 1178 (free acid). | |
| 7-CH-5'-AMP / 5'-TuMP | 7-CH-5'-AMP is a potent, competitive inhibitor that regulates enzymes. It can interact with adenosine-5'-monophosphate. Synonyms: 7- Deazaadenosine- 5'- O- monophosphate, sodium salt. Grades: ≥ 97% by HPLC. CAS No. 16719-46-3. Molecular formula: C11H15N4O7P (free acid). Mole weight: 346.2 (free acid). | |
| 8-[(4-Amino)butyl]-amino-ATP | 8-[(4-Amino)butyl]-amino-ATP is a remarkable biomedical compound assuming the role of an enzyme cofactor in an array of intricate cellular mechanisms. Synonyms: 8-[(4-Amino)butyl]-amino-adenosine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. CAS No. 162473-99-6. Molecular formula: C14H26N7O13P3 (free acid). Mole weight: 593.32 (free acid). | |
| 8-[(6-Amino)hexyl]-amino-adenosine-2',5'-bisphosphate | 8-[(6-Amino)hexyl]-amino-adenosine-2',5'-bisphosphate, a chemical compound widely implemented in biomedicine as both a substrate and inhibitor of enzymes primarily involved in nucleic acid metabolism, demonstrates promising utility in exploring the impact of different drugs and ailments, viz., cancer, on the functioning of DNA and RNA processing. Synonyms: 8-[(6-Amino)hexyl]-amino-adenosine-2',5'-bisphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C16H29N7O10P2 (free acid). Mole weight: 541.39 (free acid). | |
| 8-Azido-ADP | 8-Azido-ADP is a renowned nucleotide analogue, profoundly disrupting a spectrum of enzymes engaged in DNA replication and repair. Synonyms: 8-Azido-adenosine-5'-diphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C10H14N8O10P2 (free acid). Mole weight: 468.21 (free acid). | |
| 8-Azido-ATP | 8-Azido-ATP is a synthetic form of ATP that contains an azide group. This molecule has been used extensively in chemical biology to study ATP-binding proteins and enzymes. By introducing an azide group into the ATP molecule, researchers can use click chemistry to attach probes or tags to specific sites in the ATP-binding pocket. This has been useful for identifying new drug targets and studying the mechanism of ATP-dependent processes. Synonyms: 8-Azido-adenosine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. CAS No. 81380-25-8. Molecular formula: C10H15N8O13P3 (free acid). Mole weight: 548.19 (free acid). | |
| 8-CPT-cAMP | 8-CPT-cAMP is an activator of cAMP- and cGMP-dependent protein kinase and of Epac. It has an improved membrane permeability, phosphodiesterase stability and selectivity for site B of cAK type II. Uses: Enzyme inhibitors. Synonyms: 8- (4- Chlorophenylthio)adenosine- 3', 5'- cyclic monophosphate, sodium salt. Grades: ≥ 99% by HPLC. CAS No. 93882-12-3. Molecular formula: C16H14ClN5O6PS · Na. Mole weight: 493.8. | |
| 8-Iodo-GTP | 8-Iodo-GTP, a modified nucleotide, serves as a guanine nucleotide-binding proteins (G proteins) substrate for biochemical research. Its highly selective incorporation into G proteins allows for the investigation of their interactions with enzymes and receptors. Furthermore, researchers have studied its potential efficacy in the treatment of cancer. Synonyms: (8I-GTP); 8-Iodo-guanosine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. CAS No. 1071796-43-4. Molecular formula: C10H15N5O14P3I (free acid). Mole weight: 649.07 (free acid). | |
| 8-Oxo-dGDP | 8-Oxo-dGDP, a nucleotide analog, serves as a substrate for DNA polymerases and as a regulator for those enzymes associated with DNA repair in biochemical studies. Furthermore, it is employed to explore the involvement of oxidative stress in cancer and neurodegenerative diseases, such as Alzheimer's and Parkinson's. Synonyms: 8-Oxo-2'-deoxyguanosine-5'-diphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C10H15N5O11P2 (free acid). Mole weight: 443.20 (free acid). | |
| 8-Trifluoromethyl-ADP | 8-Trifluoromethyl-ADP is a nucleoside diphosphate that plays a crucial role in energy metabolism. It serves as a substrate for enzymes involved in the synthesis of ATP, which is a key currency of cellular energy. Additionally, it is also used in research to study the regulation of various ion channels and transporters, as well as to investigate signal transduction pathways implicated in a variety of diseases such as cancer and neurological disorders. Synonyms: 8-Trifluoromethyl-adenosine-5'-diphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C11H14N5O10P2F3 (free acid). Mole weight: 495.20 (free acid). | |
| Acacia | Acacia is available as white or yellowish-white thin flakes, spheroidal tears, granules, powder, or spray-dried powder. It is odorless and has a bland taste. Synonyms: Acaciae gummi; acacia gum; arabic gum; E414; gum acacia; gummi africanum; gum arabic; gummi arabicum; gummi mimosae; talhagum. CAS No. 9000-5-1. Product ID: PE-0462. Category: Emulsifying Agents; Stabilizing Agents; Suspending Agents; Tablet Binder; Viscosity-increasing Agents. Product Keywords: Binder Excipients; Emulsifier Excipients; Stabilizers; Suspending Agents; PE-0462; Acacia; Emulsifying Agents; Stabilizing Agents; Suspending Agents; Tablet Binder; Viscosity-increasing Agents; ; 9000-5-1. UNII: 5C5403N26O. Grade: Pharmceutical Excipients. Administration route: Oral; buccal or sublingual. Dosage Form: Oral preparations and buccal or sublingual tablets. Stability and Storage Conditions: Aqueous solutions are subject to bacterial or enzymatic degradation but may be preserved by initially boiling the solution for a short time to inactivate any enzymes present; microwave irradiation can also be used.Aqueous solutions may also be preserved by the addition of an antimicrobial preservative such as 0.1% w/v benzoic acid, 0.1% w/v sodium benzoate, or a mixture of 0.17% w/v methylparaben and 0.03% propylparaben. Powdered acacia should be stored in an airtight container in a cool, dry place. Source and Preparation: Acacia is the dried gummy exudate obtained from |  |
| Acetyl xylan esterase from Bacillus subtilis, Recombinant | In enzymology, an acetylxylan esterase (EC 3.1.1.72) is an enzyme that catalyzes a chemical reaction, the deacetylation of xylans and xylo-oligosaccharides. This enzyme belongs to the family of hydrolases, specifically those acting on carboxylic ester bonds. Group: Enzymes. Synonyms: Acetylxylan esterase; EC 3.1.1.72; 188959-24-2; 9000-82-2. Enzyme Commission Number: EC 3.1.1.72. CAS No. 188959-24-2;9000-82-2. Purity: >90% as judged by SDS-PAGE. Acetylxylan esterase. Mole weight: 28.0 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus subtilis. Acetylxylan esterase; EC 3.1.1.72; 188959-24-2; 9000-82-2. Cat No: NATE-1534. | |
| Acetyl xylan esterase from Ruminococcus flavefaciens, Recombinant | In enzymology, an acetylxylan esterase (EC 3.1.1.72) is an enzyme that catalyzes a chemical reaction, the deacetylation of xylans and xylo-oligosaccharides. This enzyme belongs to the family of hydrolases, specifically those acting on carboxylic ester bonds. Group: Enzymes. Synonyms: Acetylxylan esterase; EC 3.1.1.72; 188959-24-2; 9000-82-2. Enzyme Commission Number: EC 3.1.1.72. CAS No. 188959-24-2;9000-82-2. Purity: >90% as judged by SDS-PAGE. Acetylxylan esterase. Mole weight: 27.2 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Ruminococcus flavefaciens. Acetylxylan esterase; EC 3.1.1.72; 188959-24-2; 9000-82-2. Cat No: NATE-1533. | |
| Acetyl xylan esterase from Thermotoga maritima, Recombinant | In enzymology, an acetylxylan esterase (EC 3.1.1.72) is an enzyme that catalyzes a chemical reaction, the deacetylation of xylans and xylo-oligosaccharides. This enzyme belongs to the family of hydrolases, specifically those acting on carboxylic ester bonds. Group: Enzymes. Synonyms: Acetylxylan esterase; EC 3.1.1.72; 188959-24-2; 9000-82-2. Enzyme Commission Number: EC 3.1.1.72. CAS No. 188959-24-2;9000-82-2. Purity: >90% as judged by SDS-PAGE. Acetylxylan esterase. Mole weight: 39.2 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Thermotoga maritima. Acetylxylan esterase; EC 3.1.1.72; 188959-24-2; 9000-82-2. Cat No: NATE-1535. | |
| Acid Black 234 | Acid Black 234 is a water-soluble azo dye that belongs to the family of synthetic dyes. It is widely used in the textile, leather, and paper industries for dyeing and printing purposes. AB234 is also used as a pH indicator, inks, and colorants in cosmetics, food, and pharmaceutical products. Uses: Acid black 234 has been extensively studied for its potential applications in various scientific fields. in the field of environmental science, acid black 234 is used as a tracer dye to study the transport and fate of pollutants in soil and water. acid black 234 is also used in the field of biotechnology as a substrate for the detection of enzyme activity. in the field of medicine, acid black 234. Group: Acid dyes. Alternative Names: 4-Amino-3- [2- [4- [ [ [4- [2- (2, 4-diaminophenyl) diazenyl] phenyl] sulfonyl] amino] phenyl] diazenyl] -5-hydroxy-6- (2-phenyldiazenyl) -2, 7-naphthalenedisulfonic acid sodium salt;Acid Black 234;C.I. 30027;Black NB;2, 7-Naphthalenedisulfonic acid, 4-amino-3-[[4-[[[4-[. CAS No. 157577-99-6. Molecular formula: C34H26N10Na2O9S3. Mole weight: 860.8. Appearance: Black Powder. IUPACName: disodium; 4-amino-3- [ [4- [ [4- [ (2, 4-diaminophenyl) diazenyl] phenyl] sulfonylamino] phenyl] diazenyl] -5-hydroxy-6-phenyldiazenylnaphthalene-2, 7-disulfonate. Canonical SMILES: C1=CC=C (C=C1)N=NC2=C (C3=C (C (=C (C=C3C=C2S (=O) (=O)[O-])S (=O) (=O)[O-])N=NC4=CC=C (C=C4)NS (=O) (=O)C5=CC=C (C=C5)N=NC6=C (C=C (C=C6)N |  |
| 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. | |
| Acid Brown 4 | Acid Brown 4 is a widely used chemical reagent in laboratory experiments. It has been used for many years in biochemical, physiological, and medical research. Uses: Acid brown 4 is used in a variety of scientific research applications. it is used as an enzyme inhibitor, a fluorescent probe, a chromogenic reagent, and a fluorescent label. it has also been used in immunological assays, in the study of protein-protein interactions, and in the study of dna-protein interactions. Group: Acid dyes. Alternative Names: Acid Brown 4;Acid brown 4 (C.I. 14805). CAS No. 5858-51-5. Molecular formula: C16H12N3O4SNa. Mole weight: 365.33. Appearance: Powder. Purity: 0.98. IUPACName: sodium;6-[(4-aminophenyl)diazenyl]-5-hydroxynaphthalene-1-sulfonate. Canonical SMILES: C1=CC2=C (C=CC (=C2O)N=NC3=CC=C (C=C3)N)C (=C1)S (=O) (=O)[O-]. [Na+]. ECNumber: 227-492-1. Catalog: ACM5858515. | |
| Acid Red 336 | Acid Red 336 is a water-soluble dye that belongs to the azo dye family. It is a red to brown powder that has excellent color fastness and stability. It is also known as C.I. Acid Red 336. Uses: Acid red 336 is widely used in scientific research as a staining agent for various biological samples. it is used to stain cells, tissues, and proteins for microscopic analysis. acid red 336 is also used in the study of dna and rna by staining them to visualize their structure and location. it is also used in the study of enzymes and their activity. Group: Acid dyes. Alternative Names: Acid Red 336;C.I.Acid red 336;Red N-2RBL. CAS No. 12239-11-1. Molecular formula: C20H13N2NaO5S. Mole weight: 416.382. Appearance: Powder. IUPACName: sodium;(4E)-4-[(2-hydroxynaphthalen-1-yl)hydrazinylidene]-3-oxonaphthalene-1-sulfonate. Canonical SMILES: C1=CC=C2C (=C1)C=CC (=C2NN=C3C4=CC=CC=C4C (=CC3=O)S (=O) (=O)[O-])O. [Na+]. Catalog: ACM12239111. | |
| Adenosine 5'-diphosphate sodium salt | Adenosine 5'-diphosphate sodium salt is an adenine nucleotide that is phosphorylated into ATP by ATPase. This phosphorylation is a key part of cellular homeostatis as it allows for energy storage and is involved in nucleic acid metabolism. ADP affects platelet activation through its interaction with ADP receptors P2Y1, P2Y12 and P2X1. Upon its conversion to adenosine by ecto-ADPases, platelet activation is inhibited via adenosine receptors. Applications: An adenine nucleotide. Group: Coenzymes. Synonyms: ADP. CAS No. 20398-34-9. Purity: ≥95%. Mole weight: 427.2. Appearance: Powder. Form: Solid. ADP; Adenosine 5'-diphosphate sodium salt; 20398-34-9. Cat No: COEC-077. | |
| Adenosine-5'-[-(propargyl)]triphosphate sodium salt | Adenosine-5'-[-(propargyl)]triphosphate sodium salt, a pivotal biomolecular entity, holds utmost significance in combating cardiovascular ailments. Operating as a substrate for diverse cellular energy metabolic enzymes, it expedites the amalgamation of adenosine triphosphate (ATP). This compound, characterized by its distinctive propargyl modification, manifests profound implications in pharmaceutical exploration and scholarly investigations. Its primary focus gravitates towards adenosine receptors and metabolic cascades, rendering it an invaluable component within the realm of drug discovery and scientific scrutiny. Molecular formula: C13H18N5O13P3. Mole weight: 545.23. | |
| Adenosine 5'-triphosphate (sodium salt) | Adenosine 5'-Triphosphate, disodium salt is a p2 purinergic (P2X and P2Y) agonist that increases Ca2+-activated K+ channel activity. It has been found to induce a release of prostoglandin D2 and histamine from rat peritoneal mast cells in a dose-dependent manner. Applications: A p2 purinergicagonist. Group: Coenzymes. Synonyms: ATP disodium salt. CAS No. 987-65-5. Purity: ≥98%. Mole weight: 551.14. Appearance: Powder. Form: Solid. ATP disodium salt; Adenosine 5'-Triphosphate, disodium salt; 987-65-5. Cat No: COEC-004. | |
| ADP - lyophilized | ADP - lyophilized is a pharmaceutical compound used in the biomedical industry for the analysis of enzyme activity as well as the investigation of energy metabolism and cellular signaling pathways. With its lyophilized formulation, this compound is designed to improve stability and facilitate reconstitution. Synonyms: Adenosine-5'-diphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C10H15N5O10P2 (free acid). Mole weight: 427.20 (free acid). | |
| 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. | |
| Alcohol dehydrogenase from E. coli, Recombinant | Alcohol dehydrogenases (ADH) are a group of dehydrogenase enzymes that occur in many organisms and facilitate the interconversion between alcohols and aldehydes or ketones with the reduction of nicotinamide adenine dinucleotide (NAD+ to NADH). In Humans and many other animals, they serve to break down alcohols that otherwise are toxic, and they also participate in geneRation of useful aldehyde, ketone, or alcohol groups during biosynthesis of various metabolites. In yeast, plants, and many bacteria, some alcohol dehydrogenases catalyze the opposite reaction as part of fermentation to ensure a constant supply of NAD+. Applications: High purity recombinant alcohol dehyd...l dehydrogenase; yeast alcohol dehydrogenase; EC 1.1.1.1. Enzyme Commission Number: EC 1.1.1.1. CAS No. 9031-72-5. Alcohol dehydrogenase. Mole weight: ~ 38,642 Da. Activity: 6.7 U/mg protein at pH 8.5 and 25°C. Storage: Store at 4°C. Do not store the enzyme in presence of sodium azide. Form: In 3.2 M ammonium sulphate. Source: E. coli. aldehyde reductase; ADH; alcohol dehydrogenase (NAD); aliphatic alcohol dehydrogenase; ethanol dehydrogenase; NAD-dependent alcohol dehydrogenase; NAD-specific aromatic alcohol dehydrogenase; NADH-alcohol dehydrogenase; NADH-aldehyde dehydrogenase; primary alcohol dehydrogenase; yeast alcohol dehydrogenase; EC 1.1.1.1. Cat No: NATE-0803. | |
| Alginate lyase from Saccharophagus degradans, Recombinant | In enzymology, a poly (beta-D-mannuronate) lyase (EC 4.2.2.3) is an enzyme that catalyzes the chemical reaction:Eliminative cleavage of polysaccharides containing beta-D-mannuronate residues to give oligosaccharides with 4-deoxy-alpha-L-erythro-hex-4-enopyranuronosyl groups at their ends. This enzyme belongs to the family of lyases, specifically those carbon-oxygen lyases acting on polysaccharides. This enzyme participates in fructose and mannose metabolism. Group: Enzymes. Synonyms: alginate lyase I; alginate lyase; alginase I; alginase II; alginase; poly (β-D-1,4-mannuronide) lyase; EC 4.2.2.3. Enzyme Commission Number: EC 4.2.2.3. CAS No. 9024-15-1. Purity: >90% as judged by SDS-PAGE. Alginate lyase. Mole weight: 31.7 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Saccharophagus degradans. alginate lyase I; alginate lyase; alginase I; alginase II; alginase; poly (β-D-1,4-mannuronide) lyase; EC 4.2.2.3. Cat No: NATE-1545. | |
| Alginic Acid Calcium Salt | Calcium alginate is a water-insoluble, gelatinous, cream-coloured substance that can be created through the addition of aqueous calcium chloride to aqueous sodium alginate. Calcium alginate is also used for entrapment of enzymes and forming artificial seeds in plant tissue culture.Alginate is the term usually used for the salts of alginic acid, but it can also refer to all the derivatives of alginic acid and alginic acid itself; in some publications the term algin is used instead of alginate. Alginate is present in the cell walls of brown algae as the calcium, magnesium and sodium salts of alginic acid. Group: Heterocyclic organic compound. Alternative Names: Sodium alginate, Landalgine, Nouralgine, Pectalgine, Algiline, Calginate, Combinace, Duckalgin, Kaltostat, Kelcosol, Protanal, Protatek, Amnucol, Halltex, Kelacid, Kelsize, Keltone, Lamitex, Manucol, Manutex. CAS No. 9005-35-0. Molecular formula: C36H42Ca3O36. Mole weight: 398.316680 [g/mol]. Appearance: Gelatinous, cream coloured substance. Purity: 0.96. IUPACName: 6-(2-carboxy-4,5-dihydroxy-6-methoxyoxan-3-yl)oxy-4,5-dihydroxy-3-methoxyoxane-2-carboxylic acid. Catalog: ACM9005350. | |
Our database is helping our users find suppliers everyday.
