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Merck
CN
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文件

14-476-M

Sigma-Aldrich

Cdk7/Cyclin H/MAT1 (CAK complex) Protein, active, 10 µg

Active complex of recombinant full length human Cdk7, containing a C-terminal His6-tag, recombinant full-length human Cyclin H untagged & recombinant full-length human MAT1 containing an N-terminal GST-tag, for use in Kinase Assays.

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别名:
CDKN7, Cell division protein kinase 7, MO15, STK1, Serine/threonine-protein kinase 1
UNSPSC代码:
12352200
eCl@ss:
32160405
NACRES:
NA.41

生物来源

human

质量水平

重组

expressed in baculovirus infected Sf21 cells

形式

liquid

保质期

1 yr

分子量

Mw 37.8 kDa (cyclin H)
Mw 39.9 kDa (cdk7)
Mw 62.8 kDa (MAT1)

制造商/商品名称

Upstate®

技术

activity assay: suitable (kinase)

溶解性

soluble

NCBI登记号

UniProt登记号

储存温度

−70°C

基因信息

human ... CDK7(1022)

一般描述

Research area: APOPTOSIS

Protein Target: CDK7/cyclinH/MAT1 Target Sub-Family: CMGC

Complex of recombinant full length human cdk7, containing a C-terminal His6-tag, recombinant full-length human cyclin H untagged and recombinant full-length human MAT1 containing an N-terminal GST-tag Product Source: All are expressed by baculovirus in Sf21 insect cells

Cdk-activating kinase (CAK) is a trimeric complex composed of cyclin-dependent kinase 7 (Cdk7), cyclin H, and RING finger protein Methionine Adenosyltransferase 1 (MAT1). Cyclin H activates Cdk7, while MAT1 plays a role in influencing the substrate specificity of the complex.

生化/生理作用

The Cdk7/cyclin H/Mat1 (CAK complex) plays a role in both cell cycle regulation and transcription. Within the complex, Cdk7 functions as the Cdk-activating kinase for cell cycle and as a part of the general transcription factor, Transcription Factor II H (TFIIH), for transcription process. Additionally, it also regulates gene expression by phosphorylating transcription factors such as estrogen receptor-α (ER), p53, retinoid receptors, androgen receptor, and estrogen receptor. Elevated expression levels of Cdk7, cyclin H, and MAT1 have been observed in breast cancer patients. Inhibition of cdk7 is associated with the development of colorectal cancer in humans.

包装

Also available in 250μg size, please inquire for pricing and availability.

质量

routinely evaluated by phosphorylation of cdk7 substrate peptide

外形

Ni2+/NTA-agarose

储存及稳定性

1 year at -70°C

其他说明

For Specific Activity data, refer to the Certificate of Analysis for individual lots of this enzyme.

法律信息

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

免责声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Skin Sens. 1

WGK

WGK 2


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Functional analysis of the Cdk7.cyclin H.Mat1 complex in mouse embryonic stem cells and embryos
Shetal A Patel and M Celeste Simon
Journal of Separation Science, 285(20), 15587-15598 (2010)
DK regulators?Cell cycle progression or apoptosis?Scenarios in normal cells and cancerous cells
D'costa M, et al.
Advances in Protein Chemistry and Structural Biology, 135 (2023)
Expression of CDK7, Cyclin H, and MAT1 Is Elevated in Breast Cancer and Is Prognostic in Estrogen Receptor-Positive Breast Cancer
Patel H, et al.
Clinical Cancer Research, 22(23), 5929-5938 (2016)
Eric J Tomko et al.
Journal of molecular biology, 433(14), 166813-166813 (2021-01-17)
The general transcription factor TFIIH contains three ATP-dependent catalytic activities. TFIIH functions in nucleotide excision repair primarily as a DNA helicase and in Pol II transcription initiation as a dsDNA translocase and protein kinase. During initiation, the XPB/Ssl2 subunit of
Tinggui Yin et al.
Molecular cancer therapeutics, 13(6), 1442-1456 (2014-04-02)
DNA-dependent RNA polymerase II (RNAP II) largest subunit RPB1 C-terminal domain (CTD) kinases, including CDK9, are serine/threonine kinases known to regulate transcriptional initiation and elongation by phosphorylating Ser 2, 5, and 7 residues on CTD. Given the reported dysregulation of

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