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Merck
CN

D6920

2′-脱氧腺苷5′-三磷酸 钠盐 溶液

10 mM

别名:

dATP

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关于此项目

NACRES:
NA.52
UNSPSC Code:
41106305
EC Number:
217-662-3
Assay:
≥99%
Form:
liquid
Storage temp.:
−20°C

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产品名称

2′-脱氧腺苷5′-三磷酸 钠盐 溶液, 10 mM

InChI key

YJWCICGGRLOGEH-VWZUFWLJSA-M

InChI

1S/C10H16N5O12P3.Na/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;+1/p-1/t5-,6+,7+;/m0./s1

SMILES string

[Na+].Nc1ncnc2n(cnc12)[C@H]3C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)([O-])=O)O3

assay

≥99%

form

liquid

concentration

10 mM

color

colorless

foreign activity

DNase, RNase, NICKase, none detected

shipped in

dry ice

storage temp.

−20°C

Quality Level

200

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相关类别

Application

2′-脱氧腺苷5′-三磷酸盐钠盐可用于DNA合成反应，如PCR、DNA测序和分子克隆技术。
2′-Deoxyadenosine 5′-triphosphate sodium salt solution has been used as a component of the dNTP mix for labelling of ribosomal 18s rDNA probe and telomeric (TTAGG)n probe.

General description

2′-脱氧腺苷5′-三磷酸（dATP）由脱氧核糖上的一个碱基和糖上与一个由三个磷酸残基组成的链相结合的糖上的5′-羟基组成。细胞利用dATP通过DNA聚合酶合成DNA。

存储类别

11 - Combustible Solids

wgk

WGK 3

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000444050
0000444050
0000406310
0000406310
0000394150

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Critical reviews in biochemistry and molecular biology, 47(1), 50-63 (2011-11-05)
Ribonucleotide reductase (RNR) is the only source for de novo production of the four deoxyribonucleoside triphosphate (dNTP) building blocks needed for DNA synthesis and repair. It is crucial that these dNTP pools are carefully balanced, since mutation rates increase when
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We herein describe the synthesis of fluorescent 5-(5,6-dimethoxybenzothiazol-2-yl)-2'-deoxyuridine 5'-triphosphate (d(bt)UTP) and primer extension reactions using d(bt)UTP. We also carried out primer extension reactions using the (bt)U template. B family DNA polymerases, such as KOD, Deep Vent (exo-), and 9°N(m) DNA
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实验方案

Amplification of DNA Using Jumpstart™ REDTaq® DNA Polymerase (D8187)

Protocol using antibody mediated hot start polymerase with a red dye for easy gel loading. Method has short activation period (<1min), and results in higher yields and more specificity over standard PCR methods.

使用Jumpstart™Taq DNA聚合酶(D9307)扩增DNA

使用抗体介导热启动聚合酶的实验方案。一种具有短活化阶段的方法（<1min), and results in higher yields and more specificity over standard PCR methods.

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