重组人Cdk5蛋白(ab56282)
Key features and details
- Expression system: Escherichia coli
- Purity: > 90% SDS-PAGE
- Tags: GST tag N-Terminus
- Suitable for: SDS-PAGE
描述
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产品名称
重组人Cdk5蛋白
参阅全部 CDK5 蛋白酶 -
纯度
> 90 % SDS-PAGE. -
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
Human -
预测分子量
58 kDa -
标签
GST tag N-Terminus
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相关产品
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Related Products
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sELISA pair antibody
技术指标
Our Abpromise guarantee covers the use of ab56282 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 on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.
pH: 7.50
Constituents: 0.0038% EGTA, 0.00174% PMSF, 0.00385% DTT, 0.79% Tris HCl, 0.00292% EDTA, 25% Glycerol (glycerin, glycerine), 0.87% Sodium chloride
常规信息
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别名
- Cdk 5
- Cdk5
- CDK5_HUMAN
see all -
功能
Probably involved in the control of the cell cycle. Interacts with D1 and D3-type G1 cyclins. Can phosphorylate histone H1, tau, MAP2 and NF-H and NF-M. Also interacts with p35 which activates the kinase. -
序列相似性
Belongs to the protein kinase superfamily. CMGC Ser/Thr protein kinase family. CDC2/CDKX subfamily.
Contains 1 protein kinase domain. -
细胞定位
Cytoplasm. Cell projection > lamellipodium. Cell projection > growth cone. In axonal growth cone with extension to the peripheral lamellipodia. - Information by UniProt
图片
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SDS-PAGE analysis of ab56282 with molecular weight markers. Approximate molecular weight 58 kDa.
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Standard Curve for Cdk5 (Analyte: Cdk5 protein (Tagged) (ab56282)); dilution range 1pg/ml to 1µg/ml using Capture Antibody Mouse monoclonal [2G2] to Cdk5 (ab28441) at 5µg/ml and Detector Antibody Rabbit polyclonal to Cdk5 (ab21249) at 0.5µg/ml.
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)
ab56282 尚未被引用在任何文献中。