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经验公式(希尔记法):
C10H13N5Na3O13P3
化学文摘社编号:
分子量:
573.13
NACRES:
NA.52
PubChem Substance ID:
UNSPSC Code:
41106305
EC Number:
300-026-5
MDL number:
产品名称
2′-脱氧鸟苷5′-三磷酸 三钠盐, 100 mM (pH 7)
InChI key
IWGGLKOTEOCWQP-BIHLCPNHSA-K
InChI
1S/C10H16N5O13P3.3Na/c11-10-13-8-7(9(17)14-10)12-3-15(8)6-1-4(16)5(26-6)2-25-30(21,22)28-31(23,24)27-29(18,19)20;;;/h3-6,16H,1-2H2,(H,21,22)(H,23,24)(H2,18,19,20)(H3,11,13,14,17);;;/q;3*+1/p-3/t4-,5+,6+;;;/m0.../s1
SMILES string
[Na+].[Na+].[Na+].NC1=Nc2c(ncn2[C@H]3C[C@H](O)[C@@H](COP([O-])(=O)OP([O-])(=O)OP(O)([O-])=O)O3)C(=O)N1
assay
≥99%
form
liquid
concentration
100 mM (pH 7)
color
colorless
foreign activity
DNase, RNase, none detected
shipped in
dry ice
storage temp.
−20°C
Quality Level
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Application
2′-脱氧鸟苷5′-三磷酸三钠盐可用于DNA测序、PCR和其他基于DNA聚合酶的DNA合成和修复技术。
2′-Deoxyguanosine 5′-triphosphate trisodium salt solution has been used:
- in a reverse transcription-polymerase chain reaction (RT-PCR) for DNA amplification.
- as a component of the PCR mix for in situ reverse transcription-polymerase chain reaction (RT-PCR) amplification of mRNA from prokaryotic and eukaryotic ribosomes
- to study the mutations in the HBB gene via amplification refractory mutation system (ARMS)-PCR
General description
2′-脱氧鸟苷5′-三磷酸(dGTP)的结构为鸟嘌呤碱基连接脱氧核糖,糖的5′-羟基位再连接三个磷酸残基链。可用于通过DNA聚合酶合成DNA。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Alex von Kriegsheim et al.
Methods in molecular biology (Clifton, N.J.), 484, 177-192 (2008-07-02)
Signaling pathways transduce extracellular stimuli from the membrane to the nucleus. Constitutive and thus inappropriate stimulation of these kinase cascades is associated with and observed in a majority of tumors. The transduction of signals in these pathways is achieved through
Functional Protein Microarrays in Drug Discovery (2008)
Analysis of beta globin gene mutations in Diyarbakir
Tekecs S, et al.
Turkish Journal of Biology (2021)
Marco Gatti et al.
Cell reports, 32(5), 107985-107985 (2020-08-07)
PARP inhibitors (PARPi) cause synthetic lethality in BRCA-deficient tumors. Whether specific vulnerabilities to PARPi exist beyond BRCA mutations and related defects in homology-directed repair (HDR) is not well understood. Here, we identify the ubiquitin E3 ligase TRIP12 as negative regulator
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