小鼠NAD依赖性蛋白脱乙酰酶sirtuin-1(SIRT1)
ELISA试剂盒Mouse NAD-dependent deacetylase sirtuin-1(Sirt1)ELISA Kit- ￥2500 - 3600
- CUSABIO
- 0.156 ng/mL-10 ng/mL
- 0.039 ng/mL
- CN
- CSB-E16187m
- 2026年01月19日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
200
- 供应商：
武汉华美生物工程有限公司
- 检测范围：
0.156 ng/mL-10 ng/mL
- 检测方法：
Sandwich
- 应用：
ELISA
- 适应物种：
Mus musculus (Mouse)
- 标记物：
Non-conjugated
- 灵敏度：
0.039 ng/mL
- 规格：
96T/48T
| 规格： | 96T | 产品价格： | ￥3600.0 |
|---|---|---|---|
| 规格： | 48T | 产品价格： | ￥2500.0 |
产品类型：
ELISA Kit英文名称：
Mouse NAD-dependent deacetylase sirtuin-1(Sirt1)ELISA Kit中文名称：
小鼠NAD依赖性蛋白脱乙酰酶sirtuin-1(SIRT1)酶联免疫试剂盒货号：
CSB-E16187m别名：
Sirt1 ELISA Kit; Sir2l1 ELISA Kit; NAD-dependent protein deacetylase sirtuin-1 ELISA Kit; EC 2.3.1.286 ELISA Kit; NAD-dependent protein deacylase sirtuin-1 ELISA Kit; EC 2.3.1.- ELISA Kit; Regulatory protein SIR2 homolog 1 ELISA Kit; SIR2-like protein 1 ELISA Kit; SIR2alpha ELISA Kit; Sir2 ELISA Kit; mSIR2a) [Cleaved into: SirtT1 75 kDa fragment ELISA Kit; 75SirT1)] ELISA Kit缩写：
SIRT1Uniprot No.：
Q923E4种属：
Mus musculus (Mouse)样本类型：
serum, plasma, tissue homogenates检测范围：
0.156 ng/mL-10 ng/mL灵敏度：
0.039 ng/mL反应时间：
1-5h样本体积：
50-100ul检测波长：
450 nm研究领域：
Epigenetics and Nuclear Signaling测定原理：
quantitative测定方法：
Sandwich货期：
3-5 working days靶点名称：
sirtuin (silent mating type information regulation 2 homolog) 1 (S. cerevisiae)请点击“在线询价”找客服索取产品说明书及引用文献目录，产品实时更新参数、价格信息、更多文献信息可以查看cusabio官网
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文献和实验Sirtuins are a class of enzymes with important functions in regulation aging, metabolism, and genome stability. They were originally known as nicotinamide adenine dinucleotide (NAD)-dependent protein lysine deacetylases. However, recently
Circadian Measurements of Sirtuin Biology
series of interlocking transcriptional/translational feedback loops that oscillate with a periodicity of ~24 h. Recent evidence has implicated NAD+ biosynthesis and the sirtuin family of NAD+ -dependent protein deacetylases as part of a novel feedback
In Vivo Measurement of the Acetylation State of Sirtuin Substrates as a Proxy for Sirtuin Activity
acetylation status of select sirtuin substrates in vivo remains an important tool for evaluating changes in sirtuin activity. Here, we describe how to perform the analysis of the acetylation status of key SIRT1 and SIRT3 targets in rodent tissues and cultured
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