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Key Documents

U2383

Sigma-Aldrich

Ubiquitin Carrier Protein H3/CDC34 human

≥95% (SDS-PAGE), recombinant, expressed in E. coli overproducing strain

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About This Item

MDL號碼:
分類程式碼代碼:
12352202
NACRES:
NA.56

生物源

human

品質等級

重組細胞

expressed in E. coli overproducing strain

化驗

≥95% (SDS-PAGE)

形狀

solution

分子量

~32 kDa

UniProt登錄號

應用

cell analysis

運輸包裝

dry ice

儲存溫度

−70°C

基因資訊

生化/生理作用

Cdc34 is an essential gene for viability in yeast. Cdc34 mediates the transition from G1 to S-phase of the cell cycle by degrading the S-phase cyclin/CDK inhibitor, SIC1 in yeast and p27(KIP1) in human. Cdc34 is also known to interact with the Skp1/Cdc53/F-box (SCF) ubiquitin ligase subunits Cul1 to degrade the NF-κB inhibitor IκBα in a phosphorylation-dependent manner.
Infected cell protein 0 of herpes simplex virus 1 was shown to bind UbcH3 and induce its degradation by promoting its polyubiquination. This resulted in increased expression of an UbcH3-target gene cyclin D1 and aided in further viral infection.

外觀

Solution in 50 mM HEPES, 200 mM NaCl, 1 mM TCEP (pH 7.5), and 10% glycerol.

其他說明

Manufactured for Sigma by Boston Biochem. Inc.

儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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Ryan Hagglund et al.
Proceedings of the National Academy of Sciences of the United States of America, 99(2), 631-636 (2002-01-24)
Infected cell protein 0 (ICP0) of herpes simplex virus 1, a multifunctional ring finger protein, enhances the expression of genes introduced into cells by infection or transfection, interacts with numerous cellular and viral proteins, and is associated with the degradation
Evangelia Koutelou et al.
The Journal of biological chemistry, 283(7), 3846-3853 (2007-12-14)
Notch signaling constitutes an evolutionarily conserved mechanism that mediates cell-cell interactions in various developmental processes. Numerous regulatory proteins interact with the Notch receptor and its ligands and control signaling at multiple levels. Ubiquitination and endocytosis followed by endosomal sorting of

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