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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
for future use below -18°C
- 保质期:
See instructions
- 英文名:
Ubiquitin G76A
- 库存:
常规产品有备货
- 供应商:
上海经科化学科技有限公司
- CAS号:
无
- 规格:
5ug/20ug/1mg
| 规格: | 5ug | 产品价格: | ¥1080.0 |
|---|---|---|---|
| 规格: | 20ug | 产品价格: | ¥2415.0 |
| 规格: | 1mg | 产品价格: | ¥47334.0 |

CATALOGUE NUMBER
PRO-280
SYNONYMS
INTRODUCTION
Ubiquitination occurs through sequential steps catalyzed by activating (E1), conjugating (E2), and ligase (E3) enzymes. The final step results in the formation of an isopeptide bond between Ub’s C-terminal glycine residue (G76) and a lysine residue of the target protein, although N-terminal ubiquitination is also known.
Outcomes of this modification include destabilization of the conjugated protein, altered protein trafficking and functional modulation.
After targeting the protein for specific localizations, ubiquitin is released from the substrate by deubiquitinating enzymes.
A mutant ubiquitin, having a Gly to Ala substitution at the C-terminus (G76A ubiquitin) supported several downstream reactions of the proteolytic pathway but inhibits the deubiquitination process.
As consequence, the Ub derivative becomes irreversibly conjugated to protein, shifting the equilibrium between the bound and unbound form in the direction of conjugation, at the expense of the free form.
DESCRIPTION
Ubiquitin G76A is expressed in E.coliand purified by ion-exchange chromatography.
SOURCE
PHYSICAL APPEARANCE
FORMULATION
STABILITY
Please prevent freeze-thaw cycles.
PURITY
SAFETY DATA SHEET
SDS
USAGE
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文献和实验Recombinant human ubiquitin featuring a Gly76 to Ala76 mutation that, by inhibiting the ubiquitin hydrolases, prevents the removal of ubiquitin from protein ubiquitin conjugates.
Ubiquitin G76A is expressed in E.coliand purified by ion-exchange chromatography.
Figure 1.10.3 Page from the Human Gene Mutation Database (HGMD) showing entries for the phenylalanine hydroxylase ( PAH ) gene by mutation type and phenotype.
Selection of a Platform for Mutation Detection
here is on applications involving human disease, many of these platforms can be easily adapted to the study of other organisms. Curr. Protoc. Hum. Genet. 56:7.15.1?7.15.30. © 2008 by John Wiley & Sons, Inc. Keywords: mutation detection; mutation
Discovery Genetics: The History and Future of Spontaneous Mutation Research
, D. 2001. The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes. Dev. Biol. 237:345‐353.
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