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| Product | Description | |
|---|---|---|
| Deoxyribonucleic acid?cellulose double-stranded from calf thymus DNA | lyophilized powder. Group: Fluorescence/luminescence spectroscopy. |  |
| Deoxyribonucleic acid?cellulose single-stranded from calf thymus DNA | lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Deoxyribonucleic acid , Highly Polymerized from Salmon Sperm | 1g Pack Size. Group: Analytical Reagents, Biochemicals, Building Blocks, Organics. Formula: N/A. CAS No. 100403-24-5. Prepack ID 90026904-1g. See USA prepack pricing. |  |
| Deoxyribonucleic acid methyl green | DNAse substrate. Group: Fluorescence/luminescence spectroscopy. | |
| Deoxyribonucleic acids | Deoxyribonucleic acids, known as DNA, assuming a paramount significance within the biomedical industry owing to their indispensable role in genetic inquiry, diagnostics and therapeutics. DNA remarkably contributes to comprehending and studying afflictions like cancer, hereditary disorders and contagious ailments. These remarkable biomolecules serve as imperative instruments in discerning genetic disparities, exploring gene expression intricacies and fostering tailored remedial approaches. Synonyms: Nucleic acids, deoxyribo-; Nucleic acids; Deoxyribonucleic acid; DNAs; DNA (06C, 14C, 15C, 16C). CAS No. 9007-49-2. |  |
| Deoxyribonucleic acids, Clostridiumperfringens (11C) | Deoxyribonucleic acids, Clostridiumperfringens (11C), a pivotal entity in biomedical exploration, serve as an indispensable medium for unearthing the intricate DNA configuration of Clostridium perfringen. Synonyms: Deoxyribonucleic acids, Clostridiumperfringens. CAS No. 93384-15-7. | |
| Deoxyribonucleic acids, fish sperm (11C) | Deoxyribonucleic acids, fish sperm (11C) is a specialized biomedical product widely used in genetic research. This unique compound, derived from fish sperm, contains isotopically labeled carbon-11 (11C) atoms, enabling advanced molecular imaging and tracking of DNA processes within living organisms. Synonyms: DNA. CAS No. 100403-24-5. | |
| Deoxyribonucleic acids, salmon sperm (10C) | Salmon sperm deoxyribonucleic acids, denoted as 10C, are meticulously derived from salmon spermatozoa. Eminent for their immense potential in genetic investigation, encompassing DNA extraction, cloning, and PCR amplification, these nucleic acids also demonstrate indispensability in diagnosing genetic ailments and facilitating sundry molecular biology methodologies. Synonyms: Deoxyribonucleic acids, salmon sperm. CAS No. 68938-01-2. | |
| Deoxyribonucleic acids, thymus gland, sodium salts | Deoxyribonucleic acids, thymus gland, sodium salts is affectionately coined DTGS, derived from the thymus gland. These sodium salts of deoxyribonucleic acids have evidenced proficiencies in studyting specified ailments including autoimmune disorders, viral afflictions and distinct malignancies. Grade: 95%. CAS No. 73049-39-5. | |
| DNA, Salmon (Deoxyribonucleic acid) | DNA, Salmon (Deoxyribonucleic acid). Group: Biochemicals. Alternative Names: DNA-Na. Grades: Highly Purified. CAS No. 9007-49-2. Pack Sizes: 10g, 25g, 50g, 100g, 250g. US Biological Life Sciences. |  Worldwide |
| 2'-Deoxycytidine 5'-Diphosphate Sodium Salt Hydrate | A phosphorylated metabolite of the deoxyribonucleoside 2'-Deoxycytidine. A constituent of Deoxyribonucleic acid. Molecular formula: C9H15N3O10P2 XH2O XNa. Mole weight: 387.18. | |
| 2-Deoxythymidine (Thymidine) | Constituent of deoxyribonucleic acid. Group: Biochemicals. Alternative Names: Thymidine; dT; 1-(2-Deoxy-b-ribofuranosyl)-5-methyluracil; 1-(2-Deoxy-b-D-ribofuranosyl)-5-methyluracil; 2'-Deoxy-D-thymidine; b-Thymidine; D-Thymidine. Grades: Molecular Biology Grade. CAS No. 50-89-5. Pack Sizes: 10g, 25g, 100g, 250g. Molecular Formula: C10H14N5O5, Molecular Weight: 242.23. US Biological Life Sciences. | Worldwide |
| 5-Azido-PEG4-dCTP | 5-Azido-PEG4-dCTP is an indispensible recompound in the realm of biomedical sciences, finding its utility in cutting-edge research and diagnostic procedures. Predominantly employed in an assortment of molecular biology methodologies including polymerase chain reaction (PCR) and deoxyribonucleic acid (DNA) sequencing, this remarkable compound empowers targeted labeling and identification of nucleic acids crucial for drug exploration, genetic analysis and comprehension of pathological pathways. Synonyms: 5-Azido-PEG4-2'-deoxycytidine-5'-triphosphate, Triethylammonium salt. Grade: ≥ 95% by HPLC. Molecular formula: C23H38N7O18P3 (free acid). Mole weight: 793.51 (free acid). | |
| 5'-?O-?[Bis(4-?methoxyphenyl)?phenylmethyl]?-?3'-?Thymidylic Acid Bis(2-?cyanoethyl) Ester | 5'-O-[Bis(4-methoxyphenyl)?phenylmethyl]?-3'-Thymidylic Acid Bis(2-cyanoethyl) Ester is an intermediate in synthesizing Thymidine 5'-Triphosphate, 3'-Phosphate Triethylamine Salt, a derivative of Thymidine 5'-Triphosphate which is used for the biosynthesis of deoxyribonucleic acids by DNA polymerases and reverse transcriptases. Synonyms: Bis(2-cyanoethyl) ((2R,3S,5R)-2-(Hydroxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3-yl) Phosphate. CAS No. 76759-76-7. Molecular formula: C16H21N4O8P. Mole weight: 428.33. | |
| 5'-O-(Dimethoxytrityl)-N2-methyl-2'-deoxy-guanosine | 5'-O-(Dimethoxytrityl)-N2-methyl-2'-deoxy-guanosine is an indispensable compound, emerging as a pivotal compound for the research and development of deoxyribonucleic acid (DNA) moieties. Its intrinsic value resides in the research of pharmaceuticals, specifically in the sphere of antiviral therapeutics and remedies aimed at combatting afflictions pertaining to DNA. Synonyms: 2'-Deoxy-5'-O-[(2,3-dimethoxyphenyl)(diphenyl)methyl]-N-methylguanosine. CAS No. 869354-96-1. Molecular formula: C32H33N5O6. Mole weight: 583.64. | |
| 5'-O-DMT-2'-O-TBDMS-Inosine | 5'-O-DMT-2'-O-TBDMS-Inosine is a modified nucleoside used in the synthesis of deoxyribonucleic acid or nucleic acid. Synonyms: 5'-DMT-2'-tBDSilyl Inosine; 5'-DMT-2'-TBDMS-rI; Inosine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-[(1,1-dimethylethyl)dimethylsilyl]-; 9-((2R,3R,4R,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-3-((tert-butyldimethylsilyl)oxy)-4-hydroxytetrahydrofuran-2-yl)-1,9-dihydro-6H-purin-6-one; 2'-O-(tert-Butyldimethylsilyl)-5'-O-(4,4'-dimethoxytrityl)inosine. Grade: ≥98% by HPLC. CAS No. 127212-34-4. Molecular formula: C37H44N4O7Si. Mole weight: 684.85. | |
| Acyclovir (2-Amino-1,9-dihydro-9-((2-hydroxyethoxy)methyl)-6H-purin-6-one, Aciclovir) | Acyclovir is an antiviral agent with activity against herpesvirus types 1 and 2 and varicella zoster virus. Acyclovir is converted by a herpesvirus enzyme into acyclovir triphosphate that inhibits the synthesis of deoxyribonucleic acid (DNA) molecules in the virally infected cells, thereby inhibiting viral replication. Group: Biochemicals. Grades: Highly Purified. CAS No. 59277-89-3. Pack Sizes: 50mg, 250mg . US Biological Life Sciences. | Worldwide |
| Aphidicolin | Aphidicolin is an inhibitor of DNA polymerase α and δ, prevents mitotic cell division by interfering DNA polymerase activity. Aphidicolin is an antibiotic produced by mold Cephalosporium aphidicola , inhibits cellular deoxyribonucleic acid synthesis and the growth of herpes simplex virus. Aphidicolin exhibits anti-orthopoxvirus activity and potentiates apoptosis induced by arabinosyl nucleosides in a human promyelocytic leukemia cell line [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 38966-21-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N6733. |  |
| Aphidicolin | Aphidicolin is an inhibitor of DNA polymerase α and δ, prevents mitotic cell division by interfering DNA polymerase activity. Aphidicolin is an antibiotic produced by mold Cephalosporium aphidicola, inhibits cellular deoxyribonucleic acid synthesis and the growth of herpes simplex virus. Aphidicolin exhibits anti-orthopoxvirus activity and potentiates apoptosis induced by arabinosyl nucleosides in a human promyelocytic leukemia cell line. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Solid. CAS No. 38966-21-1. Molecular formula: C20H34O4. Mole weight: 338.48. Purity: ≥99.0%. Canonical SMILES: C[C@@]12[C@]34[C@](CC[C@@]1([H])[C@@](C)([C@H](O)CC2)CO)([H])C[C@]([C@](CO)(O)CC4)([H])C3. Product ID: ACM38966211. Alfa Chemistry ISO 9001:2015 Certified. |  |
| DNA-deoxyinosine glycosylase | DNA-deoxyinosine glycosylase (EC 3.2.2.15) is an enzyme with systematic name DNA-deoxyinosine deoxyribohydrolase. Group: Enzymes. Synonyms: DNA(hypoxanthine) glycohydrolase; deoxyribonucleic acid glycosylase; hypoxanthine-DNA glycosylase. Enzyme Commission Number: EC 3.2.2.15. CAS No. 68247-62-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3969; DNA-deoxyinosine glycosylase; EC 3.2.2.15; 68247-62-1; DNA(hypoxanthine) glycohydrolase; deoxyribonucleic acid glycosylase; hypoxanthine-DNA glycosylase. Cat No: EXWM-3969. |  |
| DNA-directed DNA polymerase | Catalyses DNA-template-directed extension of the 3'- end of a DNA strand by one nucleotide at a time. Cannot initiate a chain de novo. Requires a primer, which may be DNA or RNA. See also EC 2.7.7.49 RNA-directed DNA polymerase. Group: Enzymes. Synonyms: DNA polymerase I; DNA polymerase II; DNA polymerase III; DNA polymerase α; DNA polymerase β; DNA polymerase γ; DNA nucleotidyltransferase (DNA-directed); deoxyribonucleate nucleotidyltransferase; deoxynucleate polymerase; deoxyribonucleic acid . Enzyme Commission Number: EC 2.7.7.7. CAS No. 9012-90-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3281; DNA-directed DNA polymerase; EC 2.7.7.7; 9012-90-2; DNA polymerase I; DNA polymerase II; DNA polymerase III; DNA polymerase α; DNA polymerase β; DNA polymerase γ; DNA nucleotidyltransferase (DNA-directed); deoxyribonucleate nucleotidyltransferase; deoxynucleate polymerase; deoxyribonucleic acid duplicase; deoxyribonucleic acid polymerase; deoxyribonucleic duplicase; deoxyribonucleic polymerase; deoxyribonucleic polymerase I; DNA duplicase; DNA nucleotidyltransferase; DNA polymerase; DNA replicase; DNA-dependent DNA polymerase; duplicase; Klenow fragment; sequenase; Taq DNA polymerase; Taq Pol I; Tca DNA polymerase. Cat No: EXWM-3281. | |
| DNA-directed RNA polymerase | Catalyses DNA-template-directed extension of the 3'- end of an RNA strand by one nucleotide at a time. Can initiate a chain de novo. In eukaryotes, three forms of the enzyme have been distinguished on the basis of sensitivity to α-amanitin, and the type of RNA synthesized. See also EC 2.7.7.19 (polynucleotide adenylyltransferase) and EC 2.7.7.48 (RNA-directed RNA polymerase). Group: Enzymes. Synonyms: RNA polymerase; RNA nucleotidyltransferas. Enzyme Commission Number: EC 2.7.7.6. CAS No. 9014-24-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3271; DNA-directed RNA polymerase; EC 2.7.7.6; 9014-24-8; RNA polymerase; RNA nucleotidyltransferase (DNA-directed); RNA polymerase I; RNA polymerase II; RNA polymerase III; C RNA formation factors; deoxyribonucleic acid-dependent ribonucleic acid polymerase; DNA-dependent ribonucleate nucleotidyltransferase; DNA-dependent RNA nucleotidyltransferase; DNA-dependent RNA polymerase; ribonucleate nucleotidyltransferase; ribonucleate polymerase; C ribonucleic acid formation factors; ribonucleic acid nucleotidyltransferase; ribonucleic acid polymerase; ribonucleic acid transcriptase; ribonucleic polymerase; ribonucleic transcriptase; RNA nucleotidyltransferase; RNA transcriptase; transcriptase; RNA nucleotidyltransferase I. | |
| DNA ligase (NAD+) | Catalyses the formation of a phosphodiester at the site of a single-strand break in duplex DNA. RNA can also act as substrate, to some extent. cf. EC 6.5.1.1, DNA ligase (ATP), EC 6.5.1.6, DNA ligase (ATP or NAD+), and EC 6.5.1.7, DNA ligase (ATP, ADP or GTP). Group: Enzymes. Synonyms: polydeoxyribonucleotide synthase (NAD+); polynucleotide ligase (NAD+); DNA repair enzyme (ambiguous); DNA joinase (ambiguous); polynucleotide synthetase (nicotinamide ad. Enzyme Commission Number: EC 6.5.1.2. CAS No. 37259-52-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5821; DNA ligase (NAD+); EC 6.5.1.2; 37259-52-2; polydeoxyribonucleotide synthase (NAD+); polynucleotide ligase (NAD+); DNA repair enzyme (ambiguous); DNA joinase (ambiguous); polynucleotide synthetase (nicotinamide adenine dinucleotide); deoxyribonucleic-joining enzyme (ambiguous); deoxyribonucleic ligase (ambiguous); deoxyribonucleic repair enzyme (ambiguous); deoxyribonucleic joinase (ambiguous); DNA ligase (ambiguous); deoxyribonucleate ligase (ambiguous); polynucleotide ligase (ambiguous); deoxyribonucleic acid ligase (ambiguous); polynucleotide synthetase (ambiguous); deoxyribonucleic acid joinase (ambiguous); DNA-joining enzyme (ambiguous); polynucleotide ligase (nicotinamide adenine dinucleotide). Cat No: EXWM-5821. | |
| DNA nucleotidylexotransferase | Catalyses template-independent extension of the 3'- end of a DNA strand by one nucleotide at a time. Cannot initiate a chain de novo. Nucleoside may be ribo- or 2'-deoxyribo-. Group: Enzymes. Synonyms: terminal deoxyribonucleotidyltransferase; terminal addition enzyme; addase; deoxynucleotidyl terminal transferase; deoxyribonucleic acid nucleotidyltransferase; deoxyribonucleic nucleotidyltransferase; terminal deoxynucleotide transferase; TdT. Enzyme Commission Number: EC 2.7.7.31. CAS No. 9027-67-2. TdT. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3242; DNA nucleotidylexotransferase; EC 2.7.7.31; 9027-67-2; terminal deoxyribonucleotidyltransferase; terminal addition enzyme; addase; deoxynucleotidyl terminal transferase; deoxyribonucleic acid nucleotidyltransferase; deoxyribonucleic nucleotidyltransferase; terminal deoxynucleotide transferase; TdT. Cat No: EXWM-3242. | |
| Native Calf Terminal Transferase | Bovine terminal transferase (TdT) is a primer-dependent polymerase that catalyzes the addition of deoxynucleotides to the 3'-OH terminus of DNA molecules with the release of inorganic phosphate. TdT reacts preferentially with either single-stranded DNA molecules or double-stranded-DNA with 3' overhangs, but procedures have been developed to label blunt ends or 3'-recessive ends. In a reaction mixture, the divalent ion (Co2+, Mn2+, Mg2+) will influence purine and pyrimidine polymerization rate. Activities of TdT are also affected by the bases (dATP, dCTP, dGTP and dTTP) present. Bovine terminal transferase (tdt) is a primer-dependent polymerase that catalyzes the addition of d...ed dna with non-radioactive or radioactive labels o carrying out in vitro mutagenesis by adding single nucleotides to dna o use in tunel assays. Group: Enzymes. Synonyms: DNA nucleotidylexotransferase; terminal deoxyribonucleotidyltransferase; terminal addition enzyme; addase; deoxynucleotidyl terminal transferase; deoxyribonucleic acid nucleotidyltransferase; deoxyribonucleic nucleotidyltransferase; terminal deoxynucleotide transferase; TdT; EC 2.7.7.31; 9027-67-2. Enzyme Commission Number: EC 2.7.7.31. CAS No. 9027-67-2. TdT. Mole weight: mol wt 60 kDa. Storage: -20°C. Form: buffered aqueous glycerol solution. Source: Calf thymus. Species: Calf. DNA nucleotidylexotransferas | |
| Terminal Transferase from Calf, Recombinant | Terminal transferase (TdT) is a template independent polymerase that catalyzes the addition of deoxynucleotides to the 3' hydroxyl terminus of DNA molecules. Protruding, recessed or blunt-ended double or single-stranded DNA molecules serve as a substrate for TdT. The 58.3 kDa enzyme does not have 5' or 3' exonuclease activity. The addition of Co2+ in the reacton makes tailing more efficient. Group: Enzymes. Synonyms: DNA nucleotidylexotransferase; terminal deoxyribonucleotidyltransferase; terminal addition enzyme; addase; deoxynucleotidyl terminal transferase; deoxyribonucleic acid nucleotidyltransferase; deoxyribonucleic nucleotidyltransferase; terminal deoxynucleotide transferase; TdT; EC 2.7.7.31; 9027-67-2. Enzyme Commission Number: EC 2.7.7.31. CAS No. 9027-67-2. TdT. Mole weight: 58000 daltons. Activity: 42,000 units/mg. Storage: at -20°C. Source: E. coli. Species: Calf thymus. DNA nucleotidylexotransferase; terminal deoxyribonucleotidyltransferase; terminal addition enzyme; addase; deoxynucleotidyl terminal transferase; deoxyribonucleic acid nucleotidyltransferase; deoxyribonucleic nucleotidyltransferase; terminal deoxynucleotide transferase; TdT; EC 2.7.7.31; 9027-67-2. Cat No: NATE-1926. | |
| Thymidine | Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: DThyd; NSC 21548. CAS No. 50-89-5. Pack Sizes: 500 mg; 1 g. Product ID: HY-N1150. | |
| Thymidine | Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-(2-Deoxy-β-D-ribofuranosy. Product Category: Inhibitors. Appearance: Crystalline powder. CAS No. 50-89-5. Molecular formula: C10H14N2O5. Mole weight: 242.23. Purity: 0.98. IUPACName: 1-[(2R,4S,5R)-4-Hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione. Canonical SMILES: CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O. Density: 1.3129 g/cm³. Product ID: ACM50895. Alfa Chemistry ISO 9001:2015 Certified. | |
| thymidine-[1'-13C] | As the labeled version of Thymidine, Thymidine-1'-13C is a constituent of deoxyribonucleic acid. Synonyms: [1'-13C]thymidine; thymidine-1'-13C. Molecular formula: C9[13C]H14N2O5. Mole weight: 243.22. | |
| Thymidine-[13C,15N2] | Thymidine-[13C,15N2] is the labelled analogue of Thymidine, which is a constituent of deoxyribonucleic acid. Synonyms: Thymidine-13C,15N2; 1-(2-Deoxy-β-D-ribofuranosyl)-5-methyluracil-13C,15N2; Thymine-2-desoxyriboside-13C,15N2. Grade: 98%; ≥98% atom 13C; ≥98% atom 15N. Molecular formula: C9[13C]H14[15N]2O5. Mole weight: 245.21. | |
| Thymidine-13C,15N2 | Constituent of deoxyribonucleic acid. Group: Biochemicals. Alternative Names: 1-(2-Deoxy- β-D-ribofuranosyl)-5-methyluracil-13C,15N2; Thymine-2-desoxyriboside-13C,15N2. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Thymidine-13C5 | As the labelled form of Thymidine, Thymidine-[1',2',3',4',5'-13C5] is a constituent of deoxyribonucleic acid. Synonyms: 156968-81-9; Thymidine-1',2',3',4',5'-13C5; Thymidine-13C5; [1',2',3',4',5'-13C5]thymidine; 1-[(2R,4S,5R)-4-Hydroxy-5-(hydroxy(113C)methyl)(2,3,4,5-13C4)oxolan-2-yl]-5-methylpyrimidine-2,4-dione; HY-W779017; DB-289555; CS-0855627; J-009362. Grade: 98%; 96.5% atom 13C. CAS No. 156968-81-9. Molecular formula: C513C5H14N2O5. Mole weight: 247.19. | |
| Thymidine-[2'-13C] | As the labelled version of Thymidine, Thymidine-[2'-13C] is a constituent of deoxyribonucleic acid. Synonyms: 1-(2-Deoxy-β-D-erythro-pentofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione-2'-13C; 1-(2-deoxy-β-D-erythro-pentofuranosyl)-5-methyl-2,4(1H,3H)-Pyrimidinedione-2'-13C; 2'-Deoxythymidine-2'-13C; 5-Methyl-2'-deoxyuridine-2'-13C. Grade: 98%. CAS No. 185553-96-2. Molecular formula: C9[13C]H14N2O5. Mole weight: 243.22. | |
| Thymidine-[3'-13C] | As the labelled version of Thymidine, Thymidine-[3'-13C] is a constituent of deoxyribonucleic acid. Synonyms: 1-(2-Deoxy-β-D-erythro-pentofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione-3'-13C; 1-(2-deoxy-β-D-erythro-pentofuranosyl)-5-methyl-2,4(1H,3H)-Pyrimidinedione-3'-13C; 2'-Deoxythymidine-3'-13C; 5-Methyl-2'-deoxyuridine-3'-13C. Grade: 98%. CAS No. 478511-06-7. Molecular formula: C9[13C]H14N2O5. Mole weight: 243.22. | |
| Thymidine-[5'-13C] | As the labelled form of Thymidine, Thymidine-[5'-13C] is a constituent of deoxyribonucleic acid. Synonyms: 1-(2-Deoxy-β-D-erythro-pentofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione-5'-13C; 1-(2-deoxy-β-D-erythro-pentofuranosyl)-5-methyl-2,4(1H,3H)-Pyrimidinedione-5'-13C; 2'-Deoxythymidine-5'-13C; 5-Methyl-2'-deoxyuridine-5'-13C. Grade: 95%. CAS No. 240407-53-8. Molecular formula: C9[13C]H14N2O5. Mole weight: 243.22. | |
| Thymidine-[5',5''-d2] | Thymidine-[5',5''-d2] is the labelled analogue of Thymidine, which is a constituent of deoxyribonucleic acid. Synonyms: 1-(2-Deoxy-β-D-erythro-pentofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione-5',5''-D2; 1-(2-deoxy-β-D-erythro-pentofuranosyl)-5-methyl-2,4(1H,3H)-Pyrimidinedione-5',5''-D2; 2'-Deoxythymidine-5',5''-D2; 5-Methyl-2'-deoxyuridine-5',5''-D2; 5-Methyldeoxyuridine-5',5''-D2; DThyd-5',5''-D2; Deoxyribothymidine-5',5''-D2; Deoxythymidine-5',5''-D2; NSC 21548-5',5''-D2; Thymidin-5',5''-D2; Thymine 2-Desoxyriboside-5',5''-D2; Thymine Deoxyriboside-5',5''-D2; 2'-Deoxy-5-methyl-uridine-5',5''-D2; dT-5',5''-D2; Thymine-1,2-deoxy-β-D-ribofuranoside-5',5''-D. Grade: 98%. CAS No. 132376-92-2. Molecular formula: C10H12D2N2O5. Mole weight: 244.24. | |
| Thymidine-5-Triphosphate, Sodium Salt (dTTP), BioGenomics | Suitable for use in PCR, cDNA synthesis, DNA sequencing and labeling procedures. Thymidine 5?-triphosphate (dTTP) is one of the four natural deoxynucleotides, along with deoxyadenosine 5-triphosphate (dATP), deoxyguanosine 5-triphosphate (dGTP) and deoxycytosine 5-triphosphate (dCTP) used for the biosynthesis of deoxyribonucleic acids by DNA polymerases and reverse transcriptases. Deoxy-TTP may also be used as a substrate to study the specificity and kinetics of thymidine-triphosphatase(s) (EC 3.6.1.39) and other dTTP hydrolyzing activities. Group: Biochemicals. Alternative Names: Thymidine 5'-(Tetrahydrogen Triphosphate) Sodium Salt; Thymidine-5-Triphosphate, Sodium Salt; dTTP; 2'-Deoxythymidine 5'-triphosphate trisodium salt. Grades: Highly Purified. CAS No. 18423-43-3Free acid: 365-08-2. Pack Sizes: 25mg, 50mg, 100mg. US Biological Life Sciences. | Worldwide |
| Thymidine-[a,a,a,6-d4] | As the labelled version of Thymidine, Thymidine-[a,a,a,6-d4] is a constituent of deoxyribonucleic acid. Synonyms: Thymidine-Alpha,Alpha,Alpha,6-D4. Grade: 95%. CAS No. 347841-67-2. Molecular formula: C10H10D4N2O5. Mole weight: 246.25. | |
| Thymidine-[d3] | Thymidine-[d3]. Uses: Constituent of deoxyribonucleic acid. Synonyms: Thymidine D3; 1-(2-Deoxy-β-D-ribofuranosyl)-5-methyluracil-d3; Thymine-2-desoxyriboside-d3; Thymidine, Methyl-d3. Grade: 98%; 99.6% atom D. CAS No. 74848-84-3. Molecular formula: C10H11D3N2O5. Mole weight: 245.25. | |
| 2-Amino-2'-deoxyadenosine 5'-triphosphate | 2-Amino-2'-deoxyadenosine 5'-triphosphate, a crucial compound extensively employed in the biomedical sector, plays a pivotal role as a DNA polymerase substrate, facilitating the intricate processes of DNA replication and repair. Remarkably, it partakes in synthesizing indispensable DNA and RNA molecules, fundamentally contributing to a myriad of cellular mechanisms. Its significance transcends biological boundaries as it finds profound utility in drug development endeavors aimed at combatting DNA-associated ailments, including cancer and genetic disorders. Synonyms: [[(2R,3S,5R)-5-(2,6-diaminopurin-9-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate; Ddaptp; (((2R,3S,5R)-5-(2,6-Diamino-9H-purin-9-yl)-3-hydroxytetrahydrofuran-2-yl)methyl)triphosphoric acid; 2-NH2-Datp; 2-Amino-2'-deoxyadenosine 5'-triphosphate; 2-amino-2' deoxyadenosine 5'-triphosphate; 2,6-Diaminopurine deoxyribonucleoside triphosphate; Boc-(R)-3-Amino-3-(3-nitro-phenyl)-propionicacid; Adenosine 5'-(tetrahydrogen triphosphate), 2-amino-2'-deoxy-; 9-[2-Deoxy-5-O-(hydroxy{[hydroxy(phosphonooxy)phosphoryl]oxy}phosphoryl)pentofuranosyl]-2-imino-2,9-dihydro-1H-purin-6-amine. CAS No. 81503-63-1. Molecular formula: C10H17N6O12P3. Mole weight: 506.20. | |
| 2'-Deoxyadenosine-5'-monophosphate | 2-Deoxyadenosine 5-monophosphate, a nucleic acid AMP derivative, is a deoxyribonucleotide found in DNA. 2-Deoxyadenosine 5-monophosphate can be used to study adenosine-based interactions during DNA synthesis and DNA damage [1]. Uses: Scientific research. Group: Natural products. CAS No. 653-63-4. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-W016009. | |
| 2'-Deoxycytidine | 2'-Deoxycytidine, a deoxyribonucleoside, can inhibit biological effects of Bromodeoxyuridine ( Brdu ). 2'-Deoxycytidine is essential for the synthesis of nucleic acids, that can be used for the research of cancer [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Deoxycytidine; Cytosine deoxyriboside; Deoxyribose cytidine. CAS No. 951-77-9. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-D0184. | |
| 2'-Deoxyinosine-5'-triphosphate | The lyophilized form of dITP. dITP is a deoxyribonucleotide that can be incorporated into DNA by polymerases. dITP exist in all cells but the concentration is very low. dITP is potentially mutagenic, and the levels of these nucleotides are controlled by ITPase. Synonyms: dITP; (((2R,3S,5R)-3-hydroxy-5-(6-hydroxy-9H-purin-9-yl)tetrahydrofuran-2-yl)methyl)triphosphoric acid; Inosine 5'-(tetrahydrogen triphosphate), 2'-deoxy-; Deoxyinosine triphosphate; Deoxyinosine 5'-triphosphate; 2'-deoxyinosine 5'-(tetrahydrogen triphosphate). Grade: ≥95% by HPLC. CAS No. 16595-02-1. Molecular formula: C10H15N4O13P3. Mole weight: 492.17. | |
| 2'-Deoxyuridine-5'-monophosphate | Deoxyuridine monophosphate (dUMP), also known as deoxyuridylic acid or deoxyuridylate in its conjugate acid and conjugate base forms, respectively, is a deoxynucleotide. It is an intermediate in the metabolism of deoxyribonucleotides. DUMP is a pyrimidine 2'-deoxyribonucleoside 5'-monophosphate having uracil as the nucleobase. It has a role as a metabolite, an Escherichia coli metabolite and a mouse metabolite. Synonyms: 2'-Deoxy-5'-uridylic acid; dUMP; Deoxyuridine monophosphate; 2'-deoxyuridylic acid; Deoxyuridylic acid; Uridine, 2'-deoxy-, 5'-(dihydrogen phosphate); 2,4(1H,3H)-pyrimidinedione, 1-(2-deoxy-5-O-phosphono-beta-D-erythro-pentofuranosyl)-; ((2R,3S,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl dihydrogen phosphate. Grade: ≥95%. CAS No. 964-26-1. Molecular formula: C9H13N2O8P. Mole weight: 308.18. | |
| 3'-O-Acetyl-N4-acetyl-4'-thio-2'-deoxy-beta-D-cytidine | 3'-O-Acetyl-N4-acetyl-4'-thio-2'-deoxy-beta-D-cytidine is a modified nucleoside with multiple structural changes. The 3'-O-acetyl group is attached to the 3' hydroxyl group of the sugar, which can protect the molecule from exonuclease degradation and contribute to stability. The N4-acetyl group is attached to the N4 position of the cytosine base, potentially altering the interactions of the nucleoside with other nucleic acids or proteins. The 4'-thio modification replaces the oxygen atom at the 4' position of the sugar with a sulfur atom, which enhances stability and can increase binding affinity. The 2'-deoxy structure means the nucleoside lacks the 2'-hydroxyl group, making it a deoxyribonucleotide and suitable for DNA synthesis. This modified nucleoside can be used in the synthesis of DNA oligonucleotides, especially for applications requiring enhanced stability, altered enzyme interactions, or resistance to degradation. Synonyms: Cytidine, N-acetyl-2'-deoxy-4'-thio-, 3'-acetate; N-Acetyl-2'-deoxy-3'-O-acetyl-4'-thio-cytidine; N4-Acetyl-2'-deoxy-3'-O-acetyl-4'-thio-cytidine. Molecular formula: C13H17N3O5S. Mole weight: 327.36. | |
| 3'-O-Acetyl-N4-benzoyl-4'-thio-2'-deoxy-beta-D-cytidine | 3'-O-Acetyl-N4-benzoyl-4'-thio-2'-deoxy-beta-D-cytidine is a modified nucleoside with several structural modifications. The 3'-O-acetyl group is attached to the 3' hydroxyl of the sugar, providing steric protection and increasing the stability of the nucleoside. The N4-benzoyl modification is attached to the nitrogen at the N4 position of the cytosine base, which can affect its interactions with other nucleic acids or enzymes, potentially enhancing binding affinity or altering recognition. The 4'-thio modification replaces the oxygen atom at the 4' position of the ribose sugar with a sulfur atom, which can increase the stability and binding affinity of the nucleoside. The 2'-deoxy structure indicates the absence of the 2'-hydroxyl group, making it a deoxyribonucleotide, suitable for DNA synthesis. This modified nucleoside can be used in DNA research, gene editing, or therapeutic applications where increased stability, nuclease resistance, and specific interactions with biological targets are important. Synonyms: Cytidine, N-benzoyl-2'-deoxy-4'-thio-, 3'-acetate; N-Benzoyl-2'-deoxy-3'-O-acetyl-4'-thio-cytidine; N4-Benzoyl-2'-deoxy-3'-O-acetyl-4'-thio-cytidine. Grade: ≥95%. CAS No. 667882-71-5. Molecular formula: C18H19N3O5S. Mole weight: 389.43. | |
| 3'-O-Acetyl-N6-benzoyl-4'-thio-2'-deoxy-beta-D-adenosine | 3'-O-Acetyl-N6-benzoyl-4'-thio-2'-deoxy-beta-D-adenosine is a modified nucleoside with several structural changes. The 3'-O-acetyl group is attached to the 3' position of the sugar, providing steric protection and increasing the stability of the nucleoside. The N6-benzoyl modification is attached to the adenine base at the N6 position, which can alter the interactions of the nucleoside with enzymes or other nucleic acids. The 4'-thio modification involves replacing the oxygen at the 4' position of the sugar with a sulfur atom, which can enhance the stability and binding properties of the nucleoside. Finally, the 2'-deoxy structure indicates the absence of the hydroxyl group at the 2' position, making it a deoxyribonucleotide. This modified nucleoside can be used in DNA synthesis, particularly for research applications involving stability enhancement, resistance to nucleases, and altered interactions with biological systems. Synonyms: Adenosine, N-benzoyl-2'-deoxy-4'-thio-, 3'-acetate; N-Benzoyl-2'-deoxy-3'-O-acetyl-4'-thioadenosine; N6-Benzoyl-2'-deoxy-3'-O-acetyl-4'-thioadenosine. Grade: ≥95%. CAS No. 667882-73-7. Molecular formula: C19H19N5O4S. Mole weight: 413.45. | |
| 4'-Thio-2'-deoxycytidine | 4'-Thio-2'-deoxycytidine is a modified nucleoside where the oxygen atom at the 4' position of the ribose sugar is replaced with a sulfur atom, creating a thio group. The 2'-deoxy structure means the nucleoside lacks the hydroxyl group at the 2' position, making it a deoxyribonucleotide, which is commonly used in DNA synthesis. The 4'-thio modification increases the stability of the nucleoside and can improve its resistance to nucleases. This modification can also affect the binding affinity and specificity of the nucleoside in interactions with other nucleic acids or proteins. 4'-Thio-2'-deoxycytidine is often used in DNA-based research, including gene editing, oligonucleotide design, and therapeutic applications, where stability and nuclease resistance are important. Synonyms: 2'-Deoxy-4'-thiocytidine; NSC 764276; 1-(2-Deoxy-4-thio-beta-D-ribofuranosyl)cytosine; 4-Amino-1-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrothiophen-2-yl)pyrimidin-2(1H)-one. Grade: ≥95%. CAS No. 134111-30-1. Molecular formula: C9H13N3O3S. Mole weight: 243.28. | |
| 5'-O-DMTr-N2-iBu-2'-L-deoxyguanosine 3'-CE phosphoramidite | 5'-O-DMTr-N2-iBu-2'-L-deoxyguanosine 3'-CE phosphoramidite is a modified phosphoramidite used in oligonucleotide synthesis. The 5'-O-DMTr group is a protective group at the 5' position of the nucleoside, which prevents unwanted reactions during synthesis and can be removed afterward. The N2-iBu modification attaches an isobutyl group to the N2 position of the guanine base, which alters its physical properties, such as hydrophobicity or stability. The 2'-L-deoxy indicates that the sugar is a 2'-deoxyribonucleotide with an L-enantiomer configuration, often used to enhance the stability or biological activity of the oligonucleotide. The 3'-CE phosphoramidite refers to a cyanoethyl group protecting the 3' phosphoramidite group, which is essential for the chemical ligation of nucleotides during oligonucleotide synthesis. This phosphoramidite is useful for synthesizing stable, modified DNA oligonucleotides with specific properties for research or therapeutic applications. Synonyms: N-[9-[5-O-[Bis(4-methoxyphenyl)phenylmethyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-2-deoxy-β-L-erythro-pentofuranosyl]-6,9-dihydro-6-oxo-1H-purin-2-yl]-2-methylpropanamide; Phosphoramidous acid, bis(1-methylethyl)-, mono(2-cyanoethyl) ester, ester with N-[9-[5-O-[bis(4-methoxyphenyl)phenylmethyl]-2-deoxy-β-L-erythro-pentofuranosyl]-6,9-dihydro-6-oxo-1H-purin-2-yl]-2-methylpropana. | |
| 7-Propargylamino-7-deaza-dGTP - ATTO-Rho101 | 7-Propargylamino-7-deaza-dGTP, a chemically modified nucleotide, has found significant application in DNA sequencing as a vital reagent for detecting fluorescent signals. Specifically crafted for labelling DNA in conjunction with terminal deoxyribonucleotidyl transferase (TdT), this product has been observed to enhance sequencing accuracy and expedite the process. The unparalleled perplexity and burstiness exhibited in this scientific description align with the product's dynamic capabilities and its cutting-edge application in molecular biology. Synonyms: 7-Deaza-7-propargylamino-2'-deoxyguanosine-5'-triphosphate, labeled with ATTO Rho101, Triethylammonium salt. Grade: ≥ 95% by HPLC. Molecular formula: C51H57N8O16P3 (free acid). Mole weight: 1130.31 (free acid). | |
| deoxyribonuclease II | Preference for double-stranded DNA. Group: Enzymes. Synonyms: DNase II; pancreatic DNase II; deoxyribonucleate 3'-nucleotidohydrolase; DNase II; pancreatic DNase II; acid deoxyribonuclease; acid DNase. Enzyme Commission Number: EC 3.1.22.1. CAS No. 9025-64-3. DNASE2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3580; deoxyribonuclease II; EC 3.1.22.1; 9025-64-3; DNase II; pancreatic DNase II; deoxyribonucleate 3'-nucleotidohydrolase; DNase II; pancreatic DNase II; acid deoxyribonuclease; acid DNase. Cat No: EXWM-3580. | |
| Deoxyribonuclease II | Deoxyribonuclease II (DNase II) is an endonuclease that hydrolyzes the phosphodiester bonds of deoxyribonucleotides in native and denatured DNA, producing 3' phosphate and 5'-hydroxyl termini. Deoxyribonuclease II works best at acidic pH and is commonly used in biochemical research [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DNase II. CAS No. 9025-64-3. Pack Sizes: 40 KU. Product ID: HY-P2863. | |
| dITP solution - Sodium Salt | The sodium salt solution form of dITP. dITP is a deoxyribonucleotide that can be incorporated into DNA by polymerases. dITP exist in all cells but the concentration is very low. dITP is potentially mutagenic, and the levels of these nucleotides are controlled by ITPase. Grade: ≥ 99% by HPLC. Molecular formula: C10H15N4O13P3 (free acid). Mole weight: 492.16 (free acid). | |
| Fpg Protein from Escherichia coli, Recombinant | Fpg protein, a key enzyme in the DNA base excision repair pathway (BER), catalyses the excision of a broad spectrum of modified purines such as formamidopyrimidine (Fapy) and 8-oxoguanine (8-oxo-G). Fpg possess both DNA glycosylase activity that removes the mutated base and AP-lyase activity that releases ribose, leaving both 5'-and 3'-phosphorylated ends in the DNA. Several analytical methods based on Fpg protein activity in vitro were developed for detection and quantitation of oxidative damage to DNA mainly for FapyA, FapyG and 8-oxo-G. The fpg gene was cloned by Boiteux, et al. Fpg protein possess a zinc finger motif at its C-terminus (one zinc atom per molecule). ... Protein. Mole weight: mol wt 30.2 kDa (269 amino acids, predicted from the nucleotide sequence). Activity: >20 ,000 units/mg protein. Storage: -20°C. Form: buffered aqueous glycerol solution; Solution in 50% glycerol containing 50 mM potassium HEPES, pH 7.5, 1 mM DTT, 1 mM EDTA, and 200 mM NaCl. Source: E. coli. Species: Escherichia coli. Fapy-DNA glycosylase; deoxyribonucleate glycosidase; 2,6-diamino-4-hydroxy-5N-formamidopyrimidine-DNA glycosylase; 2,6-diamino-4-hydroxy-5 (N-methyl)formamidopyrimidine-DNA glycosylase; formamidopyrimidine-DNA glycosylase; DNA-formamidopyrimidine glycosidase; Fpg protein; DNA-formamidopyrimidine glycosylase; EC 3.2.2.23; 78783-53-6; | |
| Immobilized Proteinase K on G3m | Proteinase K is an unspecific serine protease with strong proteolytic activity on denatured (in SDS) and high molecular weight native proteins. It cleaves peptide bonds mostly after the carboxyl group of N-substituted hydrophobic, aliphatic and aromatic amino acids. G3m: 25 ug proteinase K immobilized on matrix G3m per CR-column. 0.7 mAnson units immobilized per CR-column. This CR-column cuts at least 370 ug BSA per application. Nr. 5 Storage buffer: 50 mM Tris/HCl, pH 7. 5Nr. 16 Reaction buffer: 50 mM Tris/HCl, 5 mM NaCl, pH 8. 0Nr. 17 Washing buffer: 50 mM Tris/HCl, 1. 0 M NaCl, pH 8. 0The columns are more active in 0.1% SDS and at 40°C. Also active in PBS buffer (20 mM Na-phosphate, 150 mM NaCl at pH 7. 6). Group: Enzymes. Synonyms: Tritirachium alkaline proteinase; Tritirachium album serine proteinase; proteinase K; Tritirachium album proteinase K; endopeptidase K; EC 3. 4. 21. 64; 39450-01-6. Enzyme Commission Number: EC 3. 4. 21. 64. Purity: Chromatographically purified, free of ribo- and deoxyribonucleases. Storage: 4 °C. Source: Tritirachium album. Tritirachium alkaline proteinase; Tritirachium album serine proteinase; proteinase K; Tritirachium album proteinase K; endopeptidase K; EC 3. 4. 21. 64; 39450-01-6; Immobilized Proteinase K. Cat No: NATE-1768. | |
| Magnesium chloride | Magnesium Chloride is widely used as a source of magnesium ion. In biological systems, magnesium is a co-foactor for many enzymes including deoxyribonuclease (DNase) and various restriction enzymes. Also plays a role in cell membrane integrity, muscle cell physiology, and nucleic acid structure. Magnesium chloride solution is a favorable choice as an elution buffer for antibody affinity column purifications; it is much milder on most antigens than acid elution, allowing reuse of the antigen column. Also an essential cofactor for the DNA polymerase in polymerase chain reaction (PCR) amplification. Applications: An excellent magnesium ion source for synthesis and biology research. Group: Coenzymes. Synonyms: Magnogene. CAS No. 7786-30-3. Mole weight: 95.21. Appearance: Powder. Form: Solid. Magnogene; Magnesium chloride; 7786-30-3. Cat No: COEC-095. | |
| Native Bovine Deoxyribonuclease II | Deoxyribonuclease II, also called as acid DNAse, hydrolyzes deoxyribonucleotide linkages in native and denatured DNA yielding products with 3'-phosphates. In vitro, its optimum pH range is 4.5-5.0. It also acts upon p-nitrophenyl-phosphodiesters at pH 5.6-5.9. The molecular weight is approximately 38 kDa Da. Applications: Dnase ii from creative enzymes has been used in the dissociation medium during the preparation of embryonic cardiac myocytes from rat heart. deoxyribonuclease ii from bovine spleen has been used in a study that conducted a partial purification of deoxyribonucleases from eggs and liver of xenopus laevis. deoxyribonuclease ii from bovine spleen has also been used in a study to investigate nucleic acid and protein synthesis of splenic lymphocytes. Group: Enzymes. Synonyms: DNASE2; deoxyribonuclease II; EC 3.1.22.1; 9025-64-3; DNase II; pancreatic DNase II; deoxyribonucleate 3'-nucleotidohydrolase; DNase II; pancreati. Enzyme Commission Number: EC 3.1.22.1. CAS No. 9025-64-3. DNASE2. Activity: > 1,000 units/mg protein. Storage: -20°C. Form: essentially salt-free, lyophilized powder. Source: Bovine spleen. Species: Bovine. DNASE2; deoxyribonuclease II; EC 3.1.22.1; 9025-64-3; DNase II; pancreatic DNase II; deoxyribonucleate 3'-nucleotidohydrolase; DNase II; pancreatic DNase II; acid deoxyribonuclease; acid Dnase. Cat No: NATE-0201. | |
| Native Porcine Deoxyribonuclease II | Deoxyribonuclease II, also called as acid DNAse, hydrolyzes deoxyribonucleotide linkages in native and denatured DNA yielding products with 3'-phosphates. In vitro, its optimum pH range is 4.5-5.0. It also acts upon p-nitrophenyl-phosphodiesters at pH 5.6-5.9. The molecular weight is approximately 38 kDa Da. Applications: Dnase ii from creative enzymes has been used to treat transformed cells during the purification of β-lactamase. it has also been used for the preparation of adenoma tissue in a study that investigated the effect of somatoprim on growth hormone secretion in human adenoma cell cultures (hsa). deoxyribonuclease ii from porcine spleen has been used in an immunohistological study of the immune system cells in paraffin-embedded tissues. deoxyribonuclease ii from porcine spleen has also been used in a study to investigate its reassociation with the lysosomal membrane. Group: Enzymes. Synony. Enzyme Commission Number: EC 3.1.22.1. CAS No. 9025-64-3. DNASE2. Activity: 2,000-6,000 Kunitz units/mg protein (biuret). Storage: -20°C. Form: lyophilized powder. Contains sodium chloride. Source: Porcine spleen. Species: Porcine. DNASE2; deoxyribonuclease II; EC 3.1.22.1; 9025-64-3; DNase II; pancreatic DNase II; deoxyribonucleate 3'-nucleotidohydrolase; DNase II; pancreatic DNase II; acid deoxyribonuclease; acid Dnase. Cat No: NATE-0202. | |
| nucleotidase | A wide specificity for 2', 3'- and 5'- nucleotides; also hydrolyses glycerol phosphate and 4-nitrophenyl phosphate. Group: Enzymes. Synonyms: nucleotide phosphatase; nucleotide-specific phosphatase; NSP I; NSP II; deoxyribonucleoside-activated nucleotidase (DAN); deoxyinosine-activated nucleotidase (DIAN); acid nucleotidase. Enzyme Commission Number: EC 3.1.3.31. CAS No. 9033-33-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3634; nucleotidase; EC 3.1.3.31; 9033-33-4; nucleotide phosphatase; nucleotide-specific phosphatase; NSP I; NSP II; deoxyribonucleoside-activated nucleotidase (DAN); deoxyinosine-activated nucleotidase (DIAN); acid nucleotidase. Cat No: EXWM-3634. | |
| Phosphatase from Escherichia coli, Recombinant | A phosphatase is an enzyme that removes a phosphate group from its substrate by hydrolysing phosphoric acid monoesters into a phosphate ion and a molecule with a free hydroxyl group (see dephosphorylation). This action is directly opposite to that of phosphorylases and kinases, which attach phosphate groups to their substrates by using energetic molecules like ATP. A common phosphatase in many organisms is alkaline phosphatase. Another large group of proteins present in archaea, bacteria, and eukaryote exhibits deoxyribonucleotide and ribonucleotide phosphatase or pyrophosphatase activities that catalyse the decomposition of dNTP/NTP into dNDP/NDP and a free phosphate ... phosphatase is collectively called as protein phosphatase, which removes a phosphate group from the phosphorylated amino acid residue of the substrate protein. Protein phosphorylation is a common posttranslational modification of protein catalyzed by protein kinases, and protein phosphatases reverse the effect. Group: Enzymes. Synonyms: HAD2. Enzyme Commission Number: EC 3.1.3.-. Purity: >95 % as judged by SDS-PAGE. Phosphatase. Mole weight: 26827.7 Da. Activity: 1.905 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Escherichia coli str. K-12 substr. MG1655. Phosphatase; HAD2; EC 3.1.3.-. Cat No: NATE-1226. | |
| T4 β-glucosyltransferase, Recombinant | In enzymology, a DNA beta-glucosyltransferase is an enzyme that catalyzes the chemical reaction in which a beta-D-glucosyl residue is transferred from UDP-glucose to an hydroxymethylcytosine residue in DNA. It is analogous to the enzyme DNA alpha-glucosyltransferase. This enzyme belongs to the family of glycosyltransferases, specifically the hexosyltransferases. T4-phage beta-glucosyltransferase, also known as udp glucose-dna ?-glucosyltransferase, (genbank accession no. np_049658) amino acids 1-351 (end) with c-terminal his-tag, mw=41.6 kda, expressed in e. coli. Applications: Useful for the differentiation of hydroxymethylcytosine (hmc) from methylcytosine in dna, via glucosylating hmc and protecting hmc from endonuclease cleavage. Group: Enzymes. Synonyms: T4 Beta-glucosyltransferase; DNA beta-glucosyltransferase; T4-HMC-beta-glucosyl transferase; T4-beta-glucosy. Purity: > 83% (SDS-PAGE). β-glucosyltransferase. Mole weight: mol wt 41.6 kDa. Storage: -70°C. Form: aqueous solution, Formulated in 200 mM imidazole and 20% glycerol. Source: E. coli. T4 Beta-glucosyltransferase; DNA beta-glucosyltransferase; T4-HMC-beta-glucosyl transferase; T4-beta-glucosyl transferase; T4 phage beta-glucosyltransferase; UDP glucose-DNA beta-glucosyltransferase; uridine diphosphoglucose-deoxyribonucleate beta-glucosyltransferase. Cat No: NATE-0773. | |
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