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TMEM157 Rabbit pAb (bs-14762R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價
產(chǎn)品編號 bs-14762R
英文名稱 TMEM157 Rabbit pAb
中文名稱 TMEM157蛋白抗體
別    名 F174A_HUMAN; FAM174A; HCV NS5A-transactivated protein 6; Hepatitis C virus NS5A-transactivated protein 6; Membrane protein FAM174A; NS5ATP6; RGD1309973; TMEM157; Transmembrane protein 157; UNQ1912/PRO4371.  
研究領(lǐng)域 細胞生物  免疫學(xué)  細菌及病毒  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human,Rabbit,Dog)
產(chǎn)品應(yīng)用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500,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 17 kDa
檢測分子量
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human TMEM157: 81-160/190 <Extracellular>
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 TMEM157 is 190 amino acid protein encoded by a gene mapping to human chromosome 5. With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

Subcellular Location:
Membrane.

Similarity:
Belongs to the FAM174 family.

SWISS:
Q8TBP5

Gene ID:
345757

Database links:

Entrez Gene: 345757 Human

SwissProt: Q8TBP5 Human

Unigene: 729005 Human



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