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| Product | Description | |
|---|---|---|
| DNA Polymerase Alpha from Human, Recombinant | DNA polymerase alpha also known as Pol α is an enzyme complex found in eukaryotes that is involved in initiation of DNA replication. The DNA polymerase alpha complex consists of 4 subunits: POLA1, POLA2, PRIM1, and PRIM2. Group: Enzymes. Synonyms: DNA polymerase alpha; DNA polymerase; Pol &alpha. Enzyme Commission Number: EC 2.7.7.7. CAS No. 9012-90-2. DNA Polymerase. Activity: 16,835 units/mg, 5 units/ul. Storage: Store at -80°CNote: Avoid multiple freeze / thaw cycles or frequent temperature changes. Species: Human. DNA polymerase alpha; DNA polymerase; Pol &alpha. Cat No: NATE-1922. |  |
| DNA Polymerase for PAGE | DNA Polymerase for PAGE. Dna polymerase for page is purified from e. coliexpressing a cloned dna polymerase from thermus aquaticus. the enzyme consists of a single polypeptide with a molecular weight of approximately 94 kda. dna polymerase for page has 5?-3? dna polymerase activity and 5?-3? exonuclease activity. lt lacks 3?-5? exonuclease activity. this enzyme is supplied with unique buffer, and its pcr product is suitable for sds-page and agarose gel electrophoresis. Group: Cloning Enzymes. Purity: 2500U. Storage: Store at -20 ?. Cat No: CE-3004. | |
| DNA Polymerase I Klenow Fragment, Exo-Minus, Recombinant, 10X Reaction Buffer | DNA Polymerase I Klenow Fragment, Reaction Buffer (10X) supplied with D3941. Group: Molecular Biology. Grades: Molecular Biology Grade. Pack Sizes: 1ml. US Biological Life Sciences. |  Worldwide |
| DNA Polymerase I Klenow Fragment, Reaction Buffer (10X) | DNA Polymerase I Klenow Fragment, Reaction Buffer (10X) supplied with D3940. Group: Molecular Biology. Grades: Molecular Biology Grade. CAS No. 9012-90-2. Pack Sizes: 1ml. US Biological Life Sciences. | Worldwide |
| DNA Polymerase I Reaction Buffer, 10X | Reaction Buffer (10X) for D3935. Group: Molecular Biology. Grades: Molecular Biology Grade. Pack Sizes: 1ml. US Biological Life Sciences. | Worldwide |
| DNA Polymerase, Pfu, Reaction Buffer, 10X | D3935-65B1(10X Reaction Buffer): Group: Molecular Biology. Grades: Purified. Pack Sizes: 10ml, . US Biological Life Sciences. | Worldwide |
| DNA Polymerase T4 Buffer, 5X | Reaction buffer for D3943: DNA Polymerase T4, Exo-Minus. Group: Molecular Biology. Pack Sizes: 350ul. US Biological Life Sciences. | Worldwide |
| 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. | |
| HiFi DNA Polymerase | HiFi DNA Polymerase. Hifi dna polymerase contains ta dna polymerase and a proofreading 3-5 exonuclease.hifi dna polymerase provides higher specificity and higher amplification efficiency than ta dna polymerase. two different buffers are provided in the kit. hifi pcr buffer i is optimized for the amplification of genomic dna and hifi pcr buffer ii is optimized for the amplification of λdna, cdna or plasmid dna. extension rate is about 1-2 kb/min. template-independent a can be generated at the 3 end of the pcr product. amplification of genomic dna fragment up to 15 kb. Group: Cloning Enzymes. Purity: 250U; 500U. Storage: Store at -20 ?. Cat No: CE-3022. | |
| HiFi Pfu DNA Polymerase | HiFi Pfu DNA Polymerase. Hifi pfu dna polymerase is an engineered version of pfu dna polymerase with enhanced yield and higher fidelity. ehifi pfu dna polymerase possesses a proofreading 3'-5' exonuclease activity. hifi pfu dna polymerase offers high fidelity. extension rate is about 0.5 kb/min. amplification of genomic dna fragment up to 6 kb. amplification of plasmid dna fragment up to 10 kb. Group: Cloning Enzymes. Purity: 250U; 500U. Storage: Store at -20 ?. Cat No: CE-3001. | |
| KD Plus DNA Polymerase | KD Plus DNA Polymerase. Kd plus dna polymerase is a genetically modified high fidelity dna polymerase. this enzyme provides higher amplification capability than traditional pfu dna polymerase and fast amplification speed equal to taq dna polymerase (1 kb/min). due to strong 3-5 exonuclease activity, this enzyme offers 108-fold fidelity as compared to taq dna polymerase. amplification of genomic dna fragment up to 15 kb. amplification of plasmid dna fragment up to 20 kb. Group: Cloning Enzymes. Purity: 100U; 200U. Storage: Store at -20 ?. Cat No: CE-3019. | |
| KOD DNA Polymerase from Thermococcus kodakaraensis, Recombinant | KOD is a high fidelity thermostable DNA polymerase that amplifies target DNA up to 6 kbp with superior accuracy and yield for PCR applications. The enzyme's 3'?5' exonuclease-dependent proofreading activity results in a lower PCR mutation frequency than any other commercially available DNA polymerase. The elongation rate and processivity are 5 times and 10 to 15 times higher, respectively, than for Pfu DNA polymerase, resulting in highly accurate and robust yield, in a short reaction time. Higher fidelity than pfu dna polymerase--excellent for cloninggreater yield--extension speed is 2x faster than taq dna polymerase and 5x faster than pfu dna polymerasehigher processivity--sequential nucleotide polymerization is 10- to 15-fold greater than pfu and tli dna polymerasesamplifies plasmid and lambda dna templates up to 6 kbpamplifies genomic dna templates up to 2 kbpno truncated amplification products. Group: Enzymes. Purity: > 90% homogeneous by SDS-PAGE. DNA Polymerase. Storage: at -20°C. Source: E. coli. Species: Thermococcus kodakaraensis. KOD DNA polymease; DNA polymease; KOD. Cat No: NATE-1632. | |
| Monoclonal Anti-DNA polymerase ? p125 antibody produced in rat | ~1.0 mg/mL, purified immunoglobulin, buffered aqueous solution. Group: Fluorescence/luminescence spectroscopy. |  |
| Monoclonal Anti-DNA polymerase ? p50 antibody produced in rat | ~1.0 mg/mL, clone PDK 7B4, purified immunoglobulin, buffered aqueous solution. Group: Fluorescence/luminescence spectroscopy. | |
| Pfu DNA Polymerase | Pfu DNA Polymerase. Pfu dna polymerase is a fast, high fidelity and high processivity hot start dna polymerase. extension rate is about 2-4 kb/min. amplification of genomic dna fragment up to 15 kb. amplification of plasmid dna fragment up to 20 kb. Group: Cloning Enzymes. Purity: 250U; 500U. Storage: Store at -20 ?. Cat No: CE-3015. | |
| Phi29 DNA Polymerase | Phi29 DNA Polymerase. This product is a 74.4 kda purified recombinant protein inducibly expressed in e. coli carrying the φ29 dna polymerase gene. with high sensitivity and great synthesis ability, it can be used for whole genome amplification from a single cell. it possesses 3'?5' proofreading exonuclease activity to ensure high fidelity of resulting dna. its properties of multiple strand displacement and processive synthesis allow >10 kb lengths of amplification products from genome or plasmid dna, and enable rolling-circle replication of circular dna. · isothermal amplification. · high fidelity; high efficiency; high sensitivity; high yield. · random primers or specific n9 primers can be used. Group: DNA Modifying Enzymes. Purity: 250U; 5*250U. Storage: Store at -20°C. Cat No: ME-4001. | |
| RNA-directed DNA polymerase | Catalyses RNA-template-directed extension of the 3'- end of a DNA strand by one deoxynucleotide at a time. Cannot initiate a chain de novo. Requires an RNA or DNA primer. DNA can also serve as template. See also EC 2.7.7.7 DNA-directed DNA polymerase. Group: Enzymes. Synonyms: DNA nucleotidyltransferase (RNA-directed); reverse transcriptase; revertase; RNA-dependent deoxyribonucleate nucleotidyltransferase; RNA revertase; RNA-dependent DNA polymerase; RNA-instructed DNA polymerase; RT. Enzyme Commission Number: EC 2.7.7.49. CAS No. 9068-38-6. RT. 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-3261; RNA-directed DNA polymerase; EC 2.7.7.49; 9068-38-6; DNA nucleotidyltransferase (RNA-directed); reverse transcriptase; revertase; RNA-dependent deoxyribonucleate nucleotidyltransferase; RNA revertase; RNA-dependent DNA polymerase; RNA-instructed DNA polymerase; RT. Cat No: EXWM-3261. | |
| Speed Pfu DNA Polymerase | Speed Pfu DNA Polymerase. Speed pfu dna polymerase is a hot start, high fidelity and high processivity dna polymerase. speed pfu dna polymerase has an extension rate of up to 6 kb/min. speed pfu dna polymerase has high extension rate, fidelity, and amplification efficiency. extension rate is about 2-6 kb/min. amplification of genomic dna fragment up to 15 kb. amplification of plasmid dna fragment up to 20 kb. Group: Cloning Enzymes. Purity: 250U; 500U. Storage: Store at -20 ?. Cat No: CE-3016. | |
| TA DNA Polymerase | TA DNA Polymerase. Ta dna polymerase is a mixture of taq dna polymerase with a proofreading 3-5 exonuclease. the fidelity is equal to hifi pfu dna polymerase. the yield is equal to that from taq dna polymerase. it is more suitable for high fidelity ta cloning. ta dna polymerase offers 18-fold fidelity as compared to taq dna polymerase. extension rate is about 1-2 kb/min. template-independentacan be generated at the 3end of the pcr product. amplification of genomic dna fragment up to 8 kb. Group: Cloning Enzymes. Purity: 250U; 500U. Storage: Store at -20 ?. Cat No: CE-3024. | |
| Taq DNA polymerase | Taq DNA polymerase is a thermostable DNA polymerase that can be used in PCR [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2304873-37-6. Pack Sizes: 500 U. Product ID: HY-E70086. |  |
| Taq DNA Polymerase | Taq DNA Polymerase. Taq dna polymerase is purified from e. coli expressing a cloned dna polymerase from thermus aquaticus. the enzyme consists of a single polypeptide with a molecular weight of approximately 94 kda. taq dna polymerase has 5?-3? dna polymerase activity and 5?-3? exonuclease activity. it lacks 3?-5? exonuclease activity. taq dna polymerase is suitable for routine amplification. pcr products are unsuitable for page. extension rate is about 1-2 kb/min. template-independent a can be generated at the 3? end of the pcr product. amplification of genomic dna fragment up to 4 kb. Group: Cloning Enzymes. Purity: 500U; 2500U. Storage: Store at -20 ?. Cat No: CE-3003. | |
| 1-(2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl)6-methylpurine | 1-(2'-Deoxy-2'-fluoro-b-D-arabinofuranosyl)6-methylpurine, a remarkable antiviral compound, demonstrates its efficacy in combatting herpes simplex and varicella-zoster viruses. Through its robust inhibition of viral DNA polymerase, this agent dismantles viral replication processes, thereby alleviating associated symptoms. With its exceptional selectivity towards viral enzymes, this therapeutic option proves to be a commendable approach for managing viral infections among affected individuals. Synonyms: 6-Methylpurine-2'-deoxy-2'-fluoro-beta-D-arabinoriboside. Grade: ≥95%. CAS No. 2095417-72-2. Molecular formula: C11H13FN4O3. Mole weight: 268.24. |  |
| 1-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)cytosine (2'-FANA-C) | 1-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)cytosine (2'-FANA-C) is a constructed synthetic analogue of nucleoside, possessing the potent capability of antineoplastic activity. The disruption of DNA synthesis via the inhibition of DNA polymerase, it utilises specifically in the research of solid neoplasms. Grade: ≥ 97%. | |
| 1-(2-Deoxy-4-thio-α-D-erythro-pentofuranosyl)thymine | 1-(2-Deoxy-4-thio-α-D-erythro-pentofuranosyl)thymine is a remarkable nucleoside analog possessing potent antiviral and antitumor properties. This compound efficaciously hampers the progress of HIV-1 reverse transcriptase and DNA polymerases. Piercing through the intricacies, its structural resemblance to thymidine empowers it to impede DNA replication, thus holding paramount potential in mitigating viral replication and repressing malignant neoplasms. Synonyms: 1-(2-Deoxy-4-thio-alpha-D-erythro-pentofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione; 1-[(2S,4S,5R)-4-Hydroxy-5-(hydroxymethyl)tetrahydrothiophen-2-yl]-5-methyl-pyrimidine-2,4-dione. Grade: 95%. CAS No. 134111-35-6. Molecular formula: C10H14N2O4S. Mole weight: 258.30. | |
| 1-((2R,3S,4S,5R)-3-Fluoro-4-hydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione | 1-((2R,3S,4S,5R)-3-Fluoro-4-hydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione is an efficacious pharmaceutical compound that has been extensively studied to treat viral infections caused by herpes simplex virus (HSV), varicella-zoster virus (VZV), and cytomegalovirus (CMV). The remarkable feature of this drug is its ability to effectively inhibit viral DNA polymerase, thereby halting viral replication and preventing spread. As nucleoside analogue, it is a preferred choice for combination therapy to achieve superior antiviral potency. The exquisite chemical structure of this compound enables it to bind to the viral polymerase in a unique manner, conferring its remarkable therapeutic benefit. Molecular formula: C10H13FN2O5. Mole weight: 260.22. | |
| 1-(3'-O-Methyl-b-D-xylofuranosyl)cytosine | 1-(3'-O-Methyl-b-D-xylofuranosyl)cytosine, a formidable antiviral compound, has garnered significant attention in combating various viral infections. Its mechanism of action revolves around impeding the replication of viral genetic material by selectively hindering viral DNA polymerases. Remarkably, this agent has showcased exceptional efficacy against herpesviruses and poxviruses, thereby establishing itself as a paramount weapon in battling viral maladies. | |
| 1-[(5E)-3-O-[(Bis-diisopropylamino)(2-cyanoethoxy)phosphino]-5,6-dideoxy-6-(diethoxyphosphinyl)-2-O-(2-methoxyethyl)-β-D-ribo-hex-5-enofuranosyl]uracil | 1-[(5E)-3-O-[(Bis-diisopropylamino)(2-cyanoethoxy)phosphino]-5,6-dideoxy-6-(diethoxyphosphinyl)-2-O-(2-methoxyethyl)-β-D-ribo-hex-5-enofuranosyl]uracil - a remarkable pharmaceutical compound known for its potency against viral infections. Deemed an anti-DNA virus agent, this unique product is effective against formidable pathogens like herpes simplex virus (HSV), varicella-zoster virus (VZV), and even the notorious human immunodeficiency virus (HIV). By restraining viral DNA polymerase, it deftly curtails virus replication, ultimately conferring unparalleled therapeutic benefits. Grade: ≥95%. Molecular formula: C26H44N4O10P2. Mole weight: 634.60. | |
| 1-(alpha-L-Threofuranosyl)thymine | 1-(alpha-L-Threofuranosyl)thymine is an analogue nucleoside with powerful antiviral properties, making it the ideal drug for treating herpes simplex virus and varicella-zoster virus infections. Its mechanism of action is remarkably sophisticated, as it irreversibly inhibits viral DNA polymerase, reducing viral replication and thereby suppressing viral load with utmost efficiency. Synonyms: 1-(α-L-Threofuranosyl)thymine; 1-((2R,3R,4S)-3,4-Dihydroxy-tetrahydro-furan-2-yl)-5-methyl-1H-pyrimidine-2,4-dione. Grade: ≥95%. CAS No. 325683-84-9. Molecular formula: C9H12N2O5. Mole weight: 228.20. | |
| 1-Amino-7-cyclopropylmethyl-7,8-dihydro-8-oxo-9-(b-D-xylofuranosyl)guanine | 1-Amino-7-cyclopropylmethyl-7,8-dihydro-8-oxo-9-(b-D-xylofuranosyl)guanine is a remarkable antiviral medication proficient in managing a range of viral infections caused by herpes simplex virus, varicella-zoster virus, and Epstein-Barr virus. Functioning by thwarting viral DNA polymerase and interrupting viral replication, this product exhibits exceptional proficiency in controlling herpes keratitis and encephalitis, as well as treating viral infections in immunocompromised patients. Its unparalleled potential in augmenting the immune response and suppressing pathological viruses results in its widespread application in medicinal microbiology. Synonyms: 1-Amino-7-cyclopropylmethyl-7,8-dihydro-8-oxo-9-(β-D-xylofuranosyl)guanine; 1,2-diamino-7-(cyclopropylmethyl)-9-((2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-7,9-dihydro-1H-purine-6,8-dione. Grade: ≥95%. CAS No. 2389988-22-9. Molecular formula: C14H20N6O6. Mole weight: 368.35. | |
| 1-Amino-8-benzyloxy-9-(b-D-xylofuranosyl)guanine | 1-Amino-8-benzyloxy-9-(b-D-xylofuranosyl)guanine serves as an antiviral nucleoside analogue drug primarily used to mitigate herpes simplex virus infections. Its mechanism of action involves limiting the activity of viral DNA polymerase, which culminates in the hindrance of viral replication. This therapeutic option remains popular in managing herpes simplex virus infections affecting the immunocompromised and critically ill. Synonyms: 1-Amino-8-benzyloxy-9-(β-D-xylofuranosyl)guanine; 1,2-diamino-9-[(2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-8-phenylmethoxypurin-6-one. Grade: ≥95%. CAS No. 2389988-20-7. Molecular formula: C17H20N6O6. Mole weight: 404.38. | |
| 1-(b-D-Xylofuranosyl)-5-methoxyuracil | 1-(b-D-Xylofuranosyl)-5-methoxyuracil, regarded as a potent and efficacious antiviral drug with its ability to manage and alleviate an array of viral infections such as Herpes simplex virus (HSV), Varicella zoster virus (VZV), and Epstein-Barr virus (EBV), operates to impede and hinder viral DNA polymerase, thwarting the replication of viral DNA and mitigating viral load within human anatomy. Synonyms: 1-(beta-D-Xylofuranosyl)-5-methoxyuracil; 1-((2R,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-methoxypyrimidine-2,4(1H,3H)-dione; 5-Methoxy-1-(β-D-xylofuranosyl)-2,4(1H,3H)-pyrimidinedione. Grade: ≥95%. Molecular formula: C10H14N2O7. Mole weight: 274.23. | |
| 1-beta-D-Arabinofuranosylthymine | 1-beta-D-Arabinofuranosylthymine is a noteworthy nucleoside analog that administers antiviral action when used in the management of herpes simplex and varicella-zoster virus infections. Its mechanism of action involves zoning in on the viral DNA polymerase to halt viral replication. Uses: Antiviral agents. Synonyms: Arabinofuranosyl-5-methyluridine; 1-(β-D-Arabinofuranosyl)-5-methyl-2,4(1H,3H)-pyrimidinedione; 1-(β-D-arabinofuranosyl)-5-methylpyrimidine-2,4(1H,3H)-dione; Spongothymidine; Arabinosylthymine; Thymine arabinoside. Grade: ≥95%. CAS No. 605-23-2. Molecular formula: C10H14N2O6. Mole weight: 258.23. | |
| 1,N6-Etheno-ara-adenosine | 1,N6-Etheno-ara-adenosine is a synthetic nucleoside analog commonly used in the biomedical industry to study the effects of oxidative damage to DNA. It can also be used to investigate the mechanisms of inhibition and reparation of DNA polymerases, making it valuable in the development of cancer therapies. Synonyms: (2R,3S,4S,5R)-2-(hydroxymethyl)-5-imidazo[2,1-f]purin-3-yloxolane-3,4-diol. Grade: ≥95%. CAS No. 2095417-09-5. Molecular formula: C12H13N5O4. Mole weight: 291.26. | |
| 2-[1-(4,4-Difluorocyclohexyl)-4-piperidinyl]-6-fluoro-2,3-dihydro-3-oxo-1H-isoindole-4-carboxamide | 2-[1-(4,4-Difluorocyclohexyl)-4-piperidinyl]-6-fluoro-2,3-dihydro-3-oxo-1H-isoindole-4-carboxamide is a nuclear protein poly(ADP-ribose) polymerase-1 (PARP-1) inhibitor. PARP-1 is involved with the signaling and repair of DNA and a target in oncology. Group: Biochemicals. Grades: Highly Purified. CAS No. 1262417-51-5. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C20H24F3N3O2, Molecular Weight: 395.42. US Biological Life Sciences. | Worldwide |
| 2,2'-Anhydro-L-uridine | 2,2'-Anhydro-L-uridine is a nucleoside analogue in the realm of biomedicine. It effects an inhibition of select thermophilic DNA polymerases, thereby carving a niche in research focused on antiviral and anticancer drugs. Synonyms: 2,2'-Anhydro-L-uridine; 31501-46-9; (2S,4S,5S,6R)-5-hydroxy-4-(hydroxymethyl)-3,7-dioxa-1,9-diazatricyclo[6.4.0.02,6]dodeca-8,11-dien-10-one; SCHEMBL14208937; DTXSID30446477; (2S,4S,5S,6R)-5-hydroxy-4-(hydroxymethyl)-3,7-dioxa-1,9-diazatricyclo[6.4.0.0,dodeca-8,11-dien-10-one. Grade: 98%. CAS No. 31501-46-9. Molecular formula: C9H10N2O5. Mole weight: 226.19. | |
| 2',3'-Dideoxyadenosine-5'-monothiophosphate | 2',3'-Dideoxyadenosine-5'-monothiophosphate is a vital compound used in the biomedicine industry. Acting as a nucleotide analogue, it inhibits viral reverse transcriptase and DNA polymerase, thus displaying antiviral activity against various retroviruses. Synonyms: 2',3'-Dideoxyadenosine-5'-monothiophosphate; 1266500-93-9; SCHEMBL20028990; SCHEMBL21636992; SCHEMBL22990586. Grade: ≥ 95% (HPLC). CAS No. 1266500-93-9. Molecular formula: C10H14N5O4PS. Mole weight: 331.29. | |
| 2',3'-Dideoxyadenosine-5'-O-(1-Thiotriphosphate) | 2',3'-Dideoxyadenosine-5'-O-(1-Thiotriphosphate) is a biomedically significant reagent used to investigate the intricate mechanisms of DNA synthesis and repair. As a non-hydrolyzable analog of adenosine triphosphate (ATP), it is implicated in inhibiting the activity of reverse transcriptase - a vital aspect of HIV/AIDS treatment. With its remarkable affinity and specificity towards RNA polymerase and other enzymes central to DNA metabolism, this powerful tool is a prized asset for researchers in the biomedical field. Synonyms: Alpha Thiol ddATP; 1-Thio-ddATP. Grade: ≥90% by AX-HPLC. Molecular formula: C10H16N5O10P3S. Mole weight: 491.20. | |
| 2',3'-Dideoxyadenosine-5'-Triphosphate | 2',3'-Dideoxyadenosine-5'-Triphosphate is a nucleoside triphosphate analogue commonly used in biomedical research to study polymerases and reverse transcriptases. It can be incorporated into DNA or RNA strands, resulting in chain termination and inhibition of replication. Additionally, 2',3'-Dideoxyadenosine-5'-Triphosphate has potential antiviral properties and has been studied as a treatment for HIV and hepatitis B. Synonyms: ddATP. Grade: ≥95% by AX-HPLC. Molecular formula: C10H16N5O11P3. Mole weight: 475.10. | |
| 2',3'-Dideoxyadenosine-5'-triphosphate lithium salt | 2',3'-Dideoxyadenosine-5'-triphosphate lithium salt, a nucleoside analogue renowned for inhibiting DNA polymerase, has found widespread use in treatments for HIV and research surrounding neurological disorders, whilst also serving as a staple in studying DNA sequencing and a variety of genetic diseases. Synonyms: ddATP. Grade: ≥ 95% (HPLC). CAS No. 93939-70-9. Molecular formula: C10H12N5O11P3·3Li. Mole weight: 498.91. | |
| 2',3'-Dideoxyinosine-5'-Triphosphate | 2',3'-Dideoxyinosine-5'-Triphosphate, a nucleoside analogue predominantly employed for investigating facets of DNA and RNA replication, impeding reverse transcriptases, and regulating DNA polymerases, exhibits immense potential as an efficient therapeutic agent against a host of viral infections, such as HIV. Synonyms: ddITP; Didanosine triphosphate. Grade: ≥90% by AX-HPLC. Molecular formula: C10H15N4O12P3. Mole weight: 476.10. | |
| 2,4-Diaminobenzoic Acid | 2,4-Diaminobenzoic Acid is a reagent used in the optimization of quinazolinones acting as anti-tubercular agents. Also used in the preparation of DNA Polymerase III inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 611-03-0. Pack Sizes: 100mg, 250mg. Molecular Formula: C7H8N2O2, Molecular Weight: 152.15. US Biological Life Sciences. | Worldwide |
| 2,5'-Anhydro-2'-deoxyuridine | 2,5'-Anhydro-2'-deoxyuridine is a specialized biomolecular compound primarily used in the research of viral diseases. Its inhibitory effect on viral RNA or DNA polymerase makes it a vital component in medications fighting Hepatitis B and HIV. Synonyms: (6R,8S,9R)-8-Hydroxy-7,8,9,10-tetrahydro-6,9-epoxypyrimido[2,1-b][1,3]oxazocin-2(6H)-one; 2,5'-Anhydro-1-(2-deoxy-beta-D-erythro-pentofuranosyl)uracil; 6,9-Epoxy-2H,6H-pyrimido[2,1-b][1,3]oxazocin-2-one, 7,8,9,10-tetrahydro-8-hydroxy-, (6R,8S,9R)-. Grade: ≥95%. CAS No. 20701-12-6. Molecular formula: C9H10N2O4. Mole weight: 210.19. | |
| 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'-Amino-2'-deoxy-b-D-arabino-5-methyluridine | 2'-Amino-2'-deoxy-b-D-arabino-5-methyluridine is a nucleoside analog with the ability to inhibit viral reverse transcriptase and DNA polymerase activities. It has been used in the development of antiviral drugs for the treatment of HIV and hepatitis B and C infections. Additionally, it has been studied for its potential use in cancer therapy due to its ability to induce apoptosis in cancer cells. Synonyms: 2,4(1H,3H)-Pyrimidinedione, 1-(2-amino-2-deoxy-β-D-arabinofuranosyl)-5-methyl-; 2'-Amino-2'-deoxy-β-D-arabino-5-methyluridine. Grade: ≥95%. CAS No. 135304-48-2. Molecular formula: C10H15N3O5. Mole weight: 257.24. | |
| 2'-Amino-2'-deoxyuridine-5'-triphosphate | 2'-Amino-2'-deoxyuridine-5'-triphosphate, a pivotal constituent employed in the field of molecular biology, assumes the role of a vital substrate for DNA polymerase within the context of PCR amplifications. Such utilization affords the opportunity for the meticulous labeling and integration of modified nucleotides. Advantaged by its indispensability, this product facilitates genetic sequencing, fluorescent labeling, as well as manipulation of genes of utmost significance in the domains of drug discovery and disease diagnostics. Synonyms: 2'Amino-dUTP. Grade: ≥90% by AX-HPLC. CAS No. 61468-90-4. Molecular formula: C9H16N3O14P3. Mole weight: 483.16. | |
| 2-Amino-6,8-dihydroxypurine-13C3 Hydrochloride | Labelled 2-Amino-6,8-dihydroxypurine. 2-Amino-6,8-dihydroxypurine is an 8-oxo-guanine repair pathway coordinated by MUTYH glycosylase and DNA polymerase λ. Synonyms: 2-Amino-7,9-dihydro-1H-purine-6,8-dione-13C3 Hydrochloride; 2-Amino-6,8-purinediol-13C3 Hydrochloride; 8-Hydroxyguanine-13C3 Hydrochloride; 8-Oxo-7,8-dihydroguanine-13C3 Hydrochloride; 8-Oxoguanine-13C3 Hydrochloride; NSC 22720-13C3. Grade: 95% by HPLC; 98.0% atom 13C. Molecular formula: C2[13C]3H6ClN5O2. Mole weight: 206.56. | |
| 2-Amino-6,8-dihydroxypurine-15N5 | 2-Amino-6,8-dihydroxypurine-15N5 is the isotope labelled analog of 2-Amino-6,8-dihydroxypurine (A604921, HCl); an 8-oxo-guanine repair pathway coordinated by MUTYH glycosylase and DNA polymerase &lambda:. Group: Biochemicals. Grades: Highly Purified. CAS No. 1358676-24-0. Pack Sizes: 1mg, 10mg. Molecular Formula: C5H515N5O2, Molecular Weight: 172.09. US Biological Life Sciences. | Worldwide |
| 2-Amino-6-chloro-9-(2'-deoxy-3',5'-di-O-toluoyl-b-D-ribofuranosyl)purine | 2-Amino-6-chloro-9-(2'-deoxy-3',5'-di-O-toluoyl-b-D-ribofuranosyl)purine is an effective antiviral agent utilized to treat chronic hepatitis B and C. Due to its strong ability to halt the replication of the virus through inhibiting viral DNA polymerase activity, it has become a valuable option for treating these diseases. Its potency and low levels of toxicity greatly contribute to its efficacy. Grade: 98%. Molecular formula: C26H24ClN5O5. Mole weight: 521.95. | |
| 2-Amino-6-chloropurine-9-beta-D-(2'-deoxy-2'-fluoro)-arabinoriboside | 2-Amino-6-chloropurine-9-beta-D-(2'-deoxy-2'-fluoro)-arabinoriboside, a robust antiviral agent, exhibits considerable effectiveness in combatting DNA viruses. By suppressing viral replication and diminishing viral load, this nucleoside analogue adeptly obstructs viral DNA polymerase. Remarkably, its exceptional targeting of infected cells while minimizing harm to healthy cells renders it a highly promising candidate for antiviral therapy. Synonyms: 2-Amino-6-chloro-9-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-9H-purine; (2R,3R,4S,5R)-5-(2-amino-6-chloro-9H-purin-9-yl)-4-fluoro-2-(hydroxymethyl)tetrahydrofuran-3-ol; 6-Chloro-9-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-9H-purin-2-amine. Grade: ≥95%. CAS No. 144924-88-9. Molecular formula: C10H11ClFN5O3. Mole weight: 303.68. | |
| 2-Amino-6-chloropurineriboside-5'-Triphosphate | 2-Amino-6-chloropurineriboside-5'-Triphosphate has garnered significant attention as a potent nucleotide analog, penetrating the intricate DNA and RNA polymerases upon interaction. Found commonly in DNA replication and repair mechanisms, its versatility as a molecular tool extends towards illuminating disease patterns mechanized by DNA damage, including the enigmatic realm of viral infections and cancers. Synonyms: 2-Amino-6-Cl-purine-rTP. Grade: ≥90% by AX-HPLC. Molecular formula: C10H15N5O13P3Cl. Mole weight: 541.62. | |
| 2-Aminopurine-2'-deoxyriboside-Triphosphate | 2-Aminopurine-2'-deoxyriboside-Triphosphate is a crucial component in biomedical research for studying genetic mutations and diseases. It is commonly used as a substrate for DNA polymerases and DNA sequencing techniques. This nucleotide analogue assists in detecting and characterizing mutations, including those related to cancer and genetic disorders, providing valuable insights for drug development and personalized medicine. Synonyms: 2-Aminopurine-drTP; 9-(2-Deoxy-5-O-(hydroxy((hydroxy(phospho nooxy)phosphinyl)oxy)phophinyl)-beta-D-erythro-pentofuranosyl)-9H-purin-2-amine; 1-(2-Amino-9H-purine-9-yl)-1,2-dideoxy-beta-D-erythro-pentofuranose 5-triphosphoric acid; (((2R,3S,5R)-5-(2-amino-9H-purin-9-yl)-3-hydroxytetrahydrofuran-2-yl)methyl)triphosphoric acid. Grade: ≥90% by AX-HPLC. CAS No. 26666-45-5. Molecular formula: C10H16N5O12P3. Mole weight: 491.10. | |
| 2'-Azido-2'-deoxyadenosine-5'-triphosphate lithium salt | 2'-Azido-2'-deoxyadenosine-5'-triphosphate lithium salt, an indispensable compound within the biomedical sector, finds application in a myriad of areas. Its significance lies primarily in molecular biology investigations, especially pertaining to the study of DNA synthesis and modification. Distinguished for its role as a substrate for DNA polymerases, this product facilitates enzymatic labeling, DNA sequencing, and the targeted integration into oligonucleotides. Synonyms: 2'-Azido-dATP. Grade: 98%. Molecular formula: C10H15N8O12P3. Mole weight: 532.19 (free acid). | |
| 2'-Azido-2'-deoxycytidine-5'-Triphosphate | 2'-Azido-2'-deoxycytidine-5'-Triphosphate is derived from 2'-Azido-2'-deoxycytidine, which is a key component in nucleic acid research and drug discovery. It is utilized as a substrate for DNA polymerases, aiding in the synthesis and labeling of DNA fragments. Its unique azido group enables site-specific labeling of nucleic acids, facilitating studies on DNA-protein interactions, viral replication, and molecular diagnostics. This product finds applications in antiviral drug development and biotechnology research pertaining to DNA labeling and manipulation. Synonyms: 2'-Azido-dCTP; 2'-Deoxy-2'-azidocytidine triphosphate. Grade: ≥90% by AX-HPLC. CAS No. 62192-83-0. Molecular formula: C9H15N6O13P3. Mole weight: 508.17. | |
| 2'-Azido-dGTP | 2'-Azido-dGTP, a nucleoside analogue utilized for analyzing DNA replication and repair in biomedical investigation, has manifold applications. Its functions span from detection of DNA synthesis, to DNA polymerase inhibition, and even the exploration of viral replication phenomena. Synonyms: 2'-Azido-2'-deoxyguanosine-5'-Triphosphate. Grade: ≥90% by AX-HPLC. Molecular formula: C10H15N8O13P3. Mole weight: 548.19. | |
| 2'-Azido-N4-benzoyl-2',3'-dideoxy-5'-O-DMT-cytidine | 2'-Azido-N4-benzoyl-2',3'-dideoxy-5'-O-DMT-cytidine is an exceedingly potent antiviral compound, emerging as an exalted tool in research against dread viral afflictions. Most notably efficacious against pernicious RNA-dependent DNA polymerase-dependent viruses encompassing indomitable HIV and formidable hepatitis B, this compound ventures to ensnare and subvert the bustling viral reverse transcriptase, thus impeding the pernicious replication and dissemination of viral entities within the corporeal domain. CAS No. 170236-33-6. Molecular formula: C37H34N6O6. Mole weight: 658.70. | |
| 2'-Bromo-dATP | 2-Bromo-dATP is a nucleotide analog featuring structural modification, finding extensive use within biomedical research. Its application predominantly occurs as a substrate for DNA polymerases in diverse DNA sequencing techniques and assays. Notably, owing to its unique properties, 2-Bromo-dATP exhibits the ability to impede DNA synthesis, rendering it highly valuable in the exploration of replication and repair mechanisms. Synonyms: (2'Br-dATP); 2'-Bromo-2'-deoxyadenosine-5'-triphosphate, Sodium salt. Grade: ≥ 95% by HPLC. CAS No. 107245-23-8. Molecular formula: C10H15N5O12P3Br (free acid). Mole weight: 570.08 (free acid). | |
| 2'-C-b-Methyl-4-deoxyuridine | 2'-C-b-Methyl-4-deoxyuridine is an immensely robust antiviral nucleoside analogue extensively employed in the biomedical industry, manifests as an incredible solution for the research of viral infections due to herpes simplex virus types 1 and 2, varicella-zoster virus, and Epstein-Barr virus. Through its selective targeting of viral polymerases, this extraordinary compound remarkably obstructs viral DNA replication. Synonyms: 1-(2-b-C-Methyl-b-D-ribofuranosyl)-2-(1H)-pyrimidinone; 1-((2R,3R,4R,5R)-3,4-Dihydroxy-5-(hydroxymethyl)-3-methyltetrahydrofuran-2-yl)pyrimidin-2(1H)-one; 2'-β-C-Methyl-4-deoxyuridine. Grade: ≥95%. CAS No. 1106032-88-5. Molecular formula: C10H14N2O5. Mole weight: 242.23. | |
| 2'-Chloro-2'-deoxyuridine 5'-triphosphate | 2'-Chloro-2'-deoxyuridine 5'-triphosphate is an imperative entity in the realm of biomedicine, often employed as a substrate for DNA polymerases across diverse molecular biology contexts. This compound facilitates the synthesis of altered DNA, thereby enabling meticulous investigations into DNA replication, mutagenesis, and gene expression. Furthermore, its integration into DNA serves as a valuable instrument for scrutinizing drug resistance and mechanisms pertaining to DNA repair. Synonyms: 2'-Chloro-2'-DUTP; 5-Chloro-dUTP; 1-[2-Chloro-2-deoxy-5-O-(hydroxy{[hydroxy(phosphonooxy)phosphoryl]oxy}phosphoryl)pentofuranosyl]-4-hydroxypyrimidin-2(1H)-one. CAS No. 61468-91-5. Molecular formula: C9H14ClN2O14P3. Mole weight: 502.59. | |
| 2-Deoxy-2,2-difluoroadenosine 5'-triphosphate, tetra-lithium salt | 2-Deoxy-2,2-difluoroadenosine 5'-triphosphate, tetra-lithium salt is an exceedingly potent nucleotide analog, finding extensive application in the field of biomedicine. Notably, it stands as an invaluable substrate for DNA polymerases, crucial enzymes responsible for catalyzing DNA synthesis. Affording itself to incorporation into DNA during replication, its presence effectively hampers the progress of further DNA synthesis. Grade: ≥ 95%. | |
| 2-Deoxy-2-chloroadenosine 5'-triphosphate, tetra-lithium salt | 2-Deoxy-2-chloroadenosine 5'-triphosphate, tetra-lithium salt is an important reagent in biomedicine. It acts as a substrate for DNA polymerases and DNA ligases enabling site-directed mutagenesis and labeling of nucleotides. It has also been utilized in synthetic biology as a building block for the development of biosensors and molecular switches. Additionally, its application has been studied in the treatment of various neurological disorders and cancers. Grade: ≥ 95%. | |
| 2'-Deoxy-2'-fluoro-2,6-Diaminopurineriboside | 2'-Deoxy-2'-fluoro-2,6-Diaminopurineriboside is a remarkable nucleoside analog renowned in the realm of biomedicine. Purposefully designed for combating herpesviruses, this invaluable compound holds the key to curtailing the notorious herpes simplex virus (HSV) infections. Its unrivaled efficacy lies in its intricate interference with viral DNA replication, effectively repressing viral DNA polymerase and triumphing over the viral onslaught. Grade: ≥ 99%. | |
| 2'-Deoxy-2'-fluorocytidine-5'-triphosphate trilithium salt | 2'-Deoxy-2'-fluorocytidine-5'-triphosphate lithium salt is an indispensable compound in the field of biomedicine, finding extensive application in the research and development of antiviral agents to combat problematic viral infections such as HIV and hepatitis C. Offering exceptional efficacy, this product acts as a highly proficient substrate for DNA polymerases, thereby impeding viral replication through the disruption of nucleotide integration into the viral DNA structure. Synonyms: 2'-F-dCTP lithium salt; 2'-Fluoro-2'-deoxycytidine-5'-triphosphate, lithium salt; 2'-F-dCTP trilithium salt; Lithium ((2R,3R,4R,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-4-fluoro-3-hydroxytetrahydrofuran-2-yl)methyl hydrogen triphosphate; 2'-Deoxy-2'-fluorocytidine 5'-(tetrahydrogen triphosphate) trilithium salt; 2'-Deoxy-2'-fluorocytidine triphosphate trilithium salt; 2'-Fluoro CTP trilithium salt; 2'-Fluoro-2'-deoxy-CTP trilithium salt; 2'-Fluoro-dCTP trilithium salt. Grade: 95%. Molecular formula: C9H12FLi3N3O13P3. Mole weight: 502.94. | |
| 2'-Deoxy-2'-fluoroguanosine-5'-triphosphate lithium salt | 2'-Deoxy-2'-fluoroguanosine-5'-triphosphate lithium salt, an indispensable constituent in biomedicine, plays a vital and intricate role in the synthesis of nucleic acids. As an essential nucleotide analog, this compound facilitates the in-depth investigation of intricate DNA sequencing, replication, and transcription phenomena. Moreover, its integration in the development of antiviral pharmaceuticals specifically targeting viral DNA polymerases and reverse transcriptases contributes substantially to the realm of therapeutic interventions against a vast array of viral infections. Grade: 95%. Molecular formula: C10H11FN5O13P3Li4. Mole weight: 548.90. | |
| 2'-Deoxy-2'-fluoroguanosine 5'-triphosphate trilithium salt | 2'-Deoxy-2'-fluoroguanosine 5'-Triphosphate is a crucial component in current biomedical research, utilized for the study of DNA synthesis and polymerase chain reactions (PCR). This modified nucleoside triphosphate acting as an effective substrate analog for DNA polymerases and assists in investigating nucleic acid structures and functions. It is extensively utilized in drug discovery studies targeting viral infections, such as HIV and hepatitis C, aiding in the development of potential antiviral therapies. Synonyms: 2'-F-dGTP lithium salt; 2'-Deoxy-2'-fluoroguanosine-5'-triphosphate lithium salt; 2'-F-dGTP trilithium salt; Lithium ((2R,3R,4R,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-4-fluoro-3-hydroxytetrahydrofuran-2-yl)methyl hydrogen triphosphate; 2'-F-dGTP trilithium salt; 2'-Deoxy-2'-fluoroguanosine 5'-(tetrahydrogen triphosphate) trilithium salt; 2'-Fluoro GTP trilithium salt; 2'-Fluoro-2'-deoxy-GTP trilithium salt; 2'-Fluoro-2'-deoxyguanosine-5'-triphosphate lithium salt. Grade: ≥95%. Molecular formula: C10H12FLi3N5O13P3. Mole weight: 542.97. | |
| 2-Deoxy-2-fluoroisoguanosine | 2-Deoxy-2-fluoroisoguanosine is a formidable antiviral compound, exhibiting its efficacy in research of combating viral infections instigated by DNA viruses, such as herpesviruses. By impeding viral replication via selective inhibition of viral DNA polymerase, this compound effectively diminishes viral load. It is renowned for its nucleoside analog properties. Grade: ≥ 98%. | |
| 2'-Deoxy-2'-fluoronucleoside-5'-triphosphates Kit | 2'-Deoxy-2'-fluoronucleoside-5'-triphosphates Kit: This kit contains 2'-deoxy-2'-fluoronucleoside-5'-triphosphates for research purposes. These modified nucleotides are used in molecular biology for site-directed mutagenesis, DNA sequencing, and labeling. They can also be used as antiviral drugs due to their ability to inhibit viral DNA polymerase. | |
| 2'-Deoxy-2'-fluorouridine-5'-triphosphate sodium salt | 2'-Deoxy-2'-fluorouridine-5'-triphosphate sodium salt is a vital component in the biomedicine field. It is commonly used in molecular biology research and drug development. This compound serves as a substrate for reverse transcriptases and DNA polymerases, playing a crucial role in the synthesis of various modified nucleic acids. It is particularly utilized in the study of RNA function and structure and the development of antiviral drugs targeting RNA viruses. Synonyms: 2'F-dUTP.Na. Grade: 95%. Molecular formula: C9H14FN2O14P3·Na. Mole weight: 509.12 (free acid). | |
| 2'-Deoxy-5-hydroxymethyluridine-5'-triphosphate triethylammonium salt | 2'-Deoxy-5-hydroxymethyluridine-5'-triphosphate triethylammonium salt is an indispensable recompound employed in biomedical research across diverse applications, functioning as a fundamental constituent for the enzymatic synthesis of altered DNA molecules. It simultaneously serving as a DNA polymerase substrate enabling PCR amplification. This product assuming a pivotal role in comprehending and manipulating DNA's intricate structure and functionality, thereby expediting investigations concerning genetic disorders, mutagenesis, and the advancement of therapeutic pharmaceuticals. Synonyms: Hydroxymethyldeoxyuridine triphosphate. Grade: ≥ 90%. Molecular formula: C10H13N2O15P3·4C6H16N. Mole weight: 902.93. | |
| 2'-Deoxy-5-methyl-isocytidine triphosphate | 2'-Deoxy-5-methyl-isocytidine triphosphate, a paramount substance in the realm of biomedical research, serves as an indispensable component for synthesizing intricate DNA and RNA molecules. Its significance lies in its role as a substrate for DNA polymerases, thereby assuming a pivotal position in an array of molecular biology methodologies encompassing PCR, DNA sequencing, and mutagenesis investigations. Synonyms: 4(1H)-Pyrimidinone, 2-amino-1-[2-deoxy-5-O-[hydroxy[[hydroxy(phosphonooxy)phosphinyl]oxy]phosphinyl]-β-D-erythro-pentofuranosyl]-5-methyl-; 2-Amino-1-[2-deoxy-5-O-[hydroxy[[hydroxy(phosphonooxy)phosphinyl]oxy]phosphinyl]-β-D-erythro-pentofuranosyl]-5-methyl-4(1H)-pyrimidinone; ((2R,3S,5R)-5-(2-amino-5-methyl-4-oxopyrimidin-1(4H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl tetrahydrogen triphosphate; 2'-Deoxy-5-methylisocytidine 5'-triphosphoric acid. CAS No. 139157-80-5. Molecular formula: C10H18N3O13P3. Mole weight: 481.18. | |
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