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10號染色體開放閱讀框132抗體
AK18550
C10orf132
Rabbit
Mouse (predicted: Human,Rat,Chicken,Dog,Pig,Cow,Horse,Sheep)
WB,IHC-P,IHC-F,IF,ELISA
多克隆
貨號 純度 規(guī)格 目錄價 會員價 庫存 數(shù)量 購買
AK18550-50ul 50ul 50ul ¥1380.00 登錄查看
AK18550-100ul 100ul 100ul ¥2380.00 登錄查看
AK18550-200ul 200ul 200ul ¥3480.00 登錄查看
產(chǎn)品詳情

公司產(chǎn)品僅供科研研究實驗,不得用于臨床!

商品詳情:

英文名稱:C10orf132

中文名稱:10號染色體開放閱讀框132抗體

   名;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.

研究領域;細胞生物  免疫學

抗體來源;Rabbit

克隆類型;Polyclonal

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

產(chǎn)品應用;WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 (石蠟切片需做抗原修復)

not yet tested in other applications.

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

理論分子量;18kDa

細胞定位;細胞漿 細胞膜

   狀;Liquid

   度;1mg/ml

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

   型;IgG

純化方法;affinity purified by Protein A

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

保存條件;Shipped at 4℃. Store at -20 °C 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.

產(chǎn)品介紹;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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