重组小鼠S100 beta蛋白(ab222956)
Key features and details
- Expression system: Escherichia coli
- Purity: > 95% SDS-PAGE
- Suitable for: SDS-PAGE
描述
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产品名称
重组小鼠S100 beta蛋白
参阅全部 S100 beta 蛋白酶 -
纯度
> 95 % SDS-PAGE.
ab222956 was purified using conventional chromatography techniques. -
表达系统
Escherichia coli -
Accession
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蛋白长度
Full length protein -
无动物成分
No -
性质
Recombinant -
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种属
Mouse -
序列
MSELEKAMVALIDVFHQYSGREGDKHKLKKSELKELINNELSHFLEEIKE QEVVDKVMETLDEDGDGECDFQEFMAFVAMVTTACHEFFEHE -
预测分子量
11 kDa -
氨基酸
1 to 92 -
额外的序列信息
NP_033141.
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技术指标
Our Abpromise guarantee covers the use of ab222956 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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应用
SDS-PAGE
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形式
Liquid -
Concentration information loading...
制备和贮存
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稳定性和存储
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
pH: 7.40
Constituents: 10% Glycerol (glycerin, glycerine), PBS
常规信息
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别名
- NEF
- Protein S100 B
- Protein S100-B
see all -
功能
Weakly binds calcium but binds zinc very tightly-distinct binding sites with different affinities exist for both ions on each monomer. Physiological concentrations of potassium ion antagonize the binding of both divalent cations, especially affecting high-affinity calcium-binding sites. Binds to and initiates the activation of STK38 by releasing autoinhibitory intramolecular interactions within the kinase. Interaction with AGER after myocardial infarction may play a role in myocyte apoptosis by activating ERK1/2 and p53/TP53 signaling. -
组织特异性
Although predominant among the water-soluble brain proteins, S100 is also found in a variety of other tissues. -
序列相似性
Belongs to the S-101 family.
Contains 2 EF-hand domains. -
细胞定位
Cytoplasm. Nucleus. - Information by UniProt
实验方案
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
数据表及文件
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SDS download
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Datasheet download
文献 (0)
ab222956 尚未被引用在任何文献中。