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Rabbit Anti-COMMD9/Gold Conjugated antibody (bs-8180R-Gold)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產品編號 bs-8180R-Gold
英文名稱1 Rabbit Anti-COMMD9/Gold Conjugated antibody
中文名稱 膠體金標記的銅代謝結構域蛋白9抗體
別    名 COMD9_HUMAN; COMM domain-containing protein 9; COMMD9; HSPC166.  
規格價格 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  通道蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse,  (predicted: Human, Rat, Dog, Pig, Cow, Sheep, )
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 22kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human COMMD9
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:
COMMD9 (COMM domain containing 9) is a 198 amino acid ubiquitously expressed protein that contains one COMM domain and may be involved in signaling events throughout the cell. The gene encoding COMMD9 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.

Tissue Specificity:
Ubiquitous.

Similarity:
Contains 1 COMM domain.

Database links:

Entrez Gene: 29099 Human

Omim: 612299 Human

SwissProt: Q9P000 Human

Unigene: 279836 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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