109909-44-6
Chemical Structure
Deoxycytidine triphosphate trisodium solution (100 mM)
Synonym(s): dCTP trisodium solution (100 mM); 2′-Deoxycytidine-5′-triphosphate trisodium solution (100 mM)
- CAS No.: 109909-44-6
- Formula:C9H13N3Na3O13P3
- Molecular Weight:533.10
IUPAC Name: sodium ((2R,3S,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl hydrogen triphosphate
InChIKey: WBIPTAOOMJEGQO-MILVPLDLSA-K
SMILES: O[C@H]([C@H](O1)COP(OP(OP(O)(O[Na])=O)(O[Na])=O)(O[Na])=O)C[C@@H]1N2C=CC(N)=NC2=O
Biological Activity: Deoxycytidine triphosphate trisodium (dCTP trisodium) solution (100 mM) is a nucleoside triphosphate that can be used for DNA synthesis. Deoxycytidine triphosphate trisodium salt has many applications, such as real-time PCR, cDNA synthesis, and DNA sequencing[1][2][3].
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Deoxycytidine triphosphate trisodium solution (100 mM) | 99.31% | Deoxycytidine triphosphate trisodium (dCTP trisodium) solution (100 mM) is a nucleoside triphosphate that can be used for DNA synthesis. Deoxycytidine triphosphate trisodium salt has many applications, such as real-time PCR, cDNA synthesis, and DNA sequencing. | ||||||||||||||||||||
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Deoxycytidine triphosphate trisodium,100 mM Solution,PCR Grade | 99.0% | Deoxycytidine triphosphate (dCTP; 2′-Deoxycytidine-5′-triphosphate) trisodium,100 mM Solution,PCR Grade is a nucleoside triphosphate that can be used for DNA synthesis. Deoxycytidine triphosphate trisodium,100 mM Solution,PCR Grade has many applications, such as real-time PCR, cDNA synthesis, and DNA sequencing. This product is supplied as an aqueous solution. | ||||||||||||||||||||
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- [1]. A W Harris, et al. Effect of thymidine on the sensitivity of cultured mouse tumor cells to 1-beta-D-arabinofuranosylcytosine. Cancer Res. 1979 Feb;39(2 Pt 1):538-41. [Content Brief]
- [2]. B A Bladergroen, et al. CTP:phosphoethanolamine cytidylyltransferase. Biochim Biophys Acta. 1997 Sep 4;1348(1-2):91-9. [Content Brief]
- [3]. M H Tattersall, et al. Deoxyribonucleoside triphosphates in human cells: changes in disease and following exposure to drugs. Eur J Clin Invest. 1975 Apr;5(2):191-202. [Content Brief]