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10号染色体开放阅读框132抗体

PK18780
Rabbit Anti-C10orf132 antibody,C10orf133; Chromosome 10 open reading frame 132; GOLGA7B; Golgi autoantigen golgin subfamily a 7B; golgin subfamily A member 7B; MGC131701; Uncharacterized protein C10orf132; GOG7B_HUMAN.
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货号 纯度 规格 目录价 会员价 库存 数量 购买
PK18780-50ul 50ul ¥1380.00 登录查看
PK18780-100ul 100ul ¥2380.00 登录查看
PK18780-200ul 200ul ¥3480.00 登录查看

公司产品仅供科研研究实验,不得用于临床!


商品详情:


英文名称:C10orf132
中文名称:10号染色体开放阅读框132抗体
   :C10orf133; Chromosome 10 open reading frame 132; GOLGA7B; Golgi autoantigen golgin subfamily a 7B; golgin subfamily A member 7B; MGC131701; Uncharacterized protein C10orf132; GOG7B_HUMAN.

研究领域:细胞生物  免疫学

抗体来源:Rabbit

克隆类型:Polyclonal

交叉反应:Mouse,  (predicted: Human, Rat, Chicken, Dog, Pig, Cow, Horse, Sheep, )

产品应用:WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 (石蜡切片需做抗原修复)

not yet tested in other applications.

optimal dilutions/concentrations should be determined by the end user.

理论分子量:18kDa

细胞定位:细胞浆 细胞膜

   :Liquid

   :1mg/ml

:KLH conjugated synthetic peptide derived from human C10orf132/GOLGA7B: 61-167/167

   :IgG

纯化方法:affinity purified by Protein A

:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

保存条件:Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

注意事项:This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
10号染色体开放阅读框132抗体产品介绍:GOLGA7B , also known as C10orf132 or C10orf133, is a 167 amino acid lipid anchor protein belonging to the Erf4 family. Localizing to Golgi apparatus membrane, GOLGA7B may be involved in the transport of proteins from Golgi to cell surface. The gene encoding GOLGA7B maps to human chromosome 10q24.2 and mouse chromosome 19 C3. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome and Wolman’s syndrome.

Function:

May be involved in protein transport from Golgi to cell surface (By similarity).

 

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