產(chǎn)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(biāo)記的銅代謝結(jié)構(gòu)域蛋白9抗體 |
別 名 | COMD9_HUMAN; COMM domain-containing protein 9; COMMD9; HSPC166. |
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(lǐng)域 | 細(xì)胞生物 通道蛋白 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | Mouse, (predicted: Human, Rat, Dog, Pig, Cow, Sheep, ) |
產(chǎn)品應(yīng)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(chǎn)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. |