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Rabbit Anti-SEC63  antibody (bs-19620R)  
~~~促銷代碼KT202411~~~
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產(chǎn)品編號 bs-19620R
英文名稱 Rabbit Anti-SEC63  antibody
中文名稱 轉(zhuǎn)運蛋白SEC63抗體
別    名 ERdj2; PRO2507; SEC 63; SEC63L; Translocation protein SEC63 homolog.  
研究領域 細胞生物  信號轉(zhuǎn)導  轉(zhuǎn)運蛋白  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Pig,Chicken,Horse)
產(chǎn)品應用 ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 88kDa
細胞定位 細胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SEC63: 351-250/760 <Cytoplasmic>
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 The Sec61 complex is the central component of the protein translocation apparatus of the endoplasmic reticulum (ER) membrane. The protein encoded by this gene and SEC62 protein are found to be associated with ribosome-free SEC61 complex. It is speculated that Sec61-Sec62-Sec63 may perform post-translational protein translocation into the ER. The Sec61-Sec62-Sec63 complex might also perform the backward transport of ER proteins that are subject to the ubiquitin-proteasome-dependent degradation pathway. The encoded protein is an integral membrane protein located in the rough ER. [provided by RefSeq, Jul 2008]

Function:
SEC63 and SEC62 proteins are found to be associated with the ribosome-free SEC61 complex, which is the central component of the protein translocation apparatus of the endoplasmic reticulum (ER) membrane. It is speculated that Sec61-Sec62-Sec63 may perform post-translational protein translocation into the ER. The Sec61-Sec62-Sec63 complex might also perform the backward transport of ER proteins that are subject to the ubiquitin-proteasome-dependent degradation pathway. Mutations in SEC63 cause autosomal dominant polycystic liver disease.

Subcellular Location:
Endoplasmic reticulum membrane; Multi pass membrane protein.

DISEASE:
The disease is caused by mutations affecting the gene represented in this entry. Disease description:A hepatobiliary disease characterized by overgrowth of biliary epithelium and supportive connective tissue, resulting in multiple liver cysts.

SWISS:
Q9UGP8

Gene ID:
11231

Database links:

Entrez Gene: 11231 Human

Entrez Gene: 140740 Mouse

Entrez Gene: 309858 Rat

Omim: 608648 Human

SwissProt: Q9UGP8 Human

SwissProt: Q8VHE0 Mouse

Unigene: 26904 Human



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