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D6500

Sigma-Aldrich

2′-Desoxyadenosin-5′-Triphosphat Dinatriumsalz

≥97%

Synonym(e):

dATP

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About This Item

Empirische Formel (Hill-System):
C10H14N5Na2O12P3
CAS-Nummer:
74299-50-6
Molekulargewicht:
535.15
EG-Nummer:
277-809-2
MDL-Nummer:
MFCD00080335
UNSPSC-Code:
41106305
eCl@ss:
32160414
PubChem Substanz-ID:
24894029
NACRES:
NA.51

Biologische Quelle

natural (inorganic)

Assay

≥97%

Form

powder

Lagertemp.

−20°C

SMILES String

[Na+].[Na+].Nc1ncnc2n(cnc12)C3C[C@H](O)[C@@H](COP(O)(=O)OP([O-])(=O)OP(O)([O-])=O)O3

InChI

1S/C10H16N5O12P3.2Na/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(25-7)2-24-29(20,21)27-30(22,23)26-28(17,18)19;;/h3-7,16H,1-2H2,(H,20,21)(H,22,23)(H2,11,12,13)(H2,17,18,19);;/q;2*+1/p-2/t5-,6+,7?;;/m0../s1

InChIKey

JEKDCIBJADJZSK-LNUHRGGJSA-L

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Anwendung

2′-Deoxyadenosine 5′-triphosphate (dATP) is used as a substrate by a variety of polymerases including DNA polymerase(s) and reverse transcriptase(s).
2′-Deoxyadenosine 5′-triphosphate disodium salt has been used:
  • for Smac- X-linked inhibitor of apoptosis protein (Smac-XIAP) binding assay.
  • as a component of polymerase chain reaction (PCR) using AM-toxin primers.
  • to determine the affinity constant (Kd) with the transcription termination factor Rho.
  • to determine the activity of poly ADP-ribose polymerase 1 (PAPR-1 ).

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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Catalytic Cooperativity among Subunits of Escherichia coli Transcription Termination Factor Rho KINETICS AND SUBSTRATE STRUCTURAL REQUIREMENTS
Browne R J, et al.
The Journal of Biological Chemistry, 280(14), 13292-13299 (2005)
Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64
Cheng J, et al.
American Journal of Human Genetics, 89(1), 56-66 (2011)
J E Reardon
Biochemistry, 31(18), 4473-4479 (1992-05-12)
Steady-state and pre-steady-state kinetic constants were determined for reverse transcriptase catalyzed incorporation of nucleotides and nucleotide analogues into defined-sequence DNA primed-RNA templates. 3'-Azido-3'-deoxythymidine 5'-triphosphate (AZTTP) was almost as efficient a substrate (kcat/Km) as dTTP for the enzyme. In contrast, the
Fadia Haddad et al.
Methods in molecular biology (Clifton, N.J.), 630, 261-270 (2010-03-20)
Reverse transcription (RT) is the synthesis of complementary deoxyribonucleic acids (DNA) from single-stranded ribonucleic acid (RNA) templates. This process is catalyzed by the reverse transcriptase enzyme, which is the replicating enzyme of retroviruses. Reverse transcriptase was discovered in 1970, and
Michael Trostler et al.
Biochemistry, 48(21), 4633-4641 (2009-04-08)
We used a series of dATP and dGTP analogues to determine how DNA polymerase I from Bacillus stearothermophilus (BF), a prototypical A family polymerase, uses N-1, N(2), N-3, and N(6) of purine dNTPs to differentiate between right and wrong nucleotide
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