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Rabbit Anti-GOLGA8H/Gold Conjugated antibody (bs-16258R-Gold)
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說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產品編號 bs-16258R-Gold
英文名稱1 Rabbit Anti-GOLGA8H/Gold Conjugated antibody
中文名稱 膠體金標記的高爾基體自身蛋白8H抗體
別    名 GOLGA6L11; GOG8H_HUMAN; Golgin A8 family, member H; Golgin subfamily A member 8H.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
研究領域 細胞生物  信號轉導  轉運蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, )
產品應用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 71kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human GOLGA8H
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產品介紹 background:
The Golgi complex plays an essential role in the post-translational modification and sorting of proteins transported from the endoplasmic reticulum (ER). The Golgi stack consists of a distinct cis face, or entry face, and a trans face, or exit face, which are connected via the cis, medial and trans Golgi networks. GOLGA8H (putative golgin subfamily A member 8I) is a 632 amino acid protein that belongs to the GOLGA8 family. Localizing to Golgi apparatus, GOLGA8H may play a role in Golgi structure maintenance. The gene encoding GOLGA8H maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.

Subcellular Location:
Golgi Apparatus

Similarity:
Belongs to the GOLGA8 family.

Database links:

Entrez Gene: 728498 Human

SwissProt: P0CJ92 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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