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Merck
CN

440736

Sigma-Aldrich

4-硫尿嘧啶

97%

别名:

2-羟基-4-巯基嘧啶

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About This Item

经验公式(希尔记法):
C4H4N2OS
CAS号:
分子量:
128.15
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

表单

powder

mp

295 °C (dec.) (lit.)

溶解性

1 M NaOH: soluble 50 mg/mL

SMILES字符串

Oc1nccc(S)n1

InChI

1S/C4H4N2OS/c7-4-5-2-1-3(8)6-4/h1-2H,(H2,5,6,7,8)

InChI key

OVONXEQGWXGFJD-UHFFFAOYSA-N

应用

4-硫尿嘧啶是在RNA提取过程中,用于胚胎的Schneider培养基中的合适试剂。 它可以用作 Northwestern印迹技术中的试剂。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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Jeanine S Morey et al.
PloS one, 8(6), e66347-e66347 (2013-06-19)
Dinoflagellates possess many physiological processes that appear to be under post-transcriptional control. However, the extent to which their genes are regulated post-transcriptionally remains unresolved. To gain insight into the roles of differential mRNA stability and de novo transcription in dinoflagellates
Michael R Miller et al.
Nature methods, 6(6), 439-441 (2009-05-12)
We found that the combination of spatially restricted uracil phosphoribosyltransferase (UPRT) expression with 4-thiouracil delivery can be used to label and purify cell type-specific RNA from intact complex tissues in Drosophila melanogaster. This method is useful for isolating RNA from
Structure and tautomerism of the neutral and monoanionic forms of 4-thiouracil derivatives.
A Psoda et al.
Journal of the American Chemical Society, 96(22), 6832-6839 (1974-10-30)
Linda Warfield et al.
Molecular cell, 68(1), 118-129 (2017-09-19)
Previous studies suggested that expression of most yeast mRNAs is dominated by either transcription factor TFIID or SAGA. We re-examined the role of TFIID by rapid depletion of S. cerevisiae TFIID subunits and measurement of changes in nascent transcription. We find that
Qing S Wang et al.
RNA (New York, N.Y.), 11(4), 404-411 (2005-02-11)
Isolating the core functional elements of an RNA is normally performed during the characterization of a new RNA in order to simplify further biochemical analysis. The removal of extraneous sequence is challenging and can lead to biases that result from

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