產(chǎn)品編號 | bs-14121R |
英文名稱 | Rabbit Anti-CXorf66 antibody |
中文名稱 | X染色體開放閱讀框66抗體 |
別 名 | Chromosome X open reading frame 66; Hypothetical protein LOC347487; RP11 35F15.2; Uncharacterized protein CXorf66. |
研究領(lǐng)域 | 細(xì)胞生物 免疫學(xué) 發(fā)育生物學(xué) |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | Human |
產(chǎn)品應(yīng)用 | WB=1:500-2000
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
理論分子量 | 38kDa |
細(xì)胞定位 | 細(xì)胞膜 |
性 狀 | Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human CXorf66: 12-120/361 <Extracellular> |
亞 型 | IgG |
純化方法 | affinity purified by Protein A |
緩 沖 液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
保存條件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
注意事項(xiàng) | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
PubMed | PubMed |
產(chǎn)品介紹 |
CXorf66 is a single-pass type I membrane protein that consists of 361 amino acids. The gene encoding CXorf66 maps to human chromosome X. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. Function: The exact function of CXorf66 is not yet known. Subcellular Location: Membrane; Single-pass type I membrane protein SWISS: Q8N9S7 Gene ID: 347487 Database links: Entrez Gene: 347487 Human SwissProt: Q5JRM2 Human |
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