产品名称
2′-脱氧腺苷5′-三磷酸 钠盐 溶液, 100 mM, pH 7
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
InChI key
YJWCICGGRLOGEH-VWZUFWLJSA-M
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
100 mM
color
colorless
pH
7
foreign activity
DNase, RNase, none detected
shipped in
dry ice
storage temp.
−20°C
Quality Level
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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′-脱氧腺苷5′-三磷酸钠盐水已用于通过末端脱氧核苷酸转移酶dUTP缺口末端标记（TUNEL）技术检测凋亡细胞。还用于促进凋亡蛋白酶活化因子-1(Apaf-1)寡聚化形成名为凋亡体或Apaf-1 procaspase-9凋亡体复合物的七聚体大复合体，并用于研究其基于蛋白降解的分子计时器功能。
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。
Other Notes
T4 DNA连接酶以溶于20 mM Tris-HCl（pH 7.5），50 mM KCl，1 mM DTT和50%（v/v）甘油的溶液形式提供。
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Jager W, et al.
Testing, 8(3), e59536-e59536 (2013)
Srinivas Malladi et al.
The EMBO journal, 28(13), 1916-1925 (2009-06-06)
During stress-induced apoptosis, the initiator caspase-9 is activated by the Apaf-1 apoptosome and must remain bound to retain significant catalytic activity. Nevertheless, in apoptotic cells the vast majority of processed caspase-9 is paradoxically observed outside the complex. We show herein
Paul J Rothwell et al.
The Journal of biological chemistry, 288(19), 13575-13591 (2013-03-26)
Conformational selection plays a key role in the polymerase cycle. Klentaq1 exists in conformational equilibrium between three states (open, closed, and “nucleotide-binding”) whose level of occupancy is determined by the bound substrate. The “nucleotide-binding” state plays a pivotal role in
Christina M Zimanyi et al.
Structure (London, England : 1993), 20(8), 1374-1383 (2012-06-26)
Ribonucleotide reductases (RNRs) provide the precursors for DNA biosynthesis and repair and are successful targets for anticancer drugs such as clofarabine and gemcitabine. Recently, we reported that dATP inhibits E. coli class Ia RNR by driving formation of RNR subunits
Serdal Kirmizialtin et al.
Structure (London, England : 1993), 20(4), 618-627 (2012-04-10)
Nearly every enzyme undergoes a significant change in structure after binding it's substrate. Experimental and theoretical analyses of the role of changes in HIV reverse transcriptase structure in selecting a correct substrate are presented. Atomically detailed simulations using the Milestoning
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