產(chǎn)品中心
一(yī)抗
9號染(rǎn)色體開(kāi)放(fàng)閱(yuè)讀(dú)框(kuàng)163抗(kàng)體(tǐ)
英(yīng)文(wén)名稱 Anti-C9orf163
中文名稱(chēng) 9號染(rǎn)色體開(kāi)放閱讀框(kuàng)163抗體(tǐ)
別 名 C9orf163; Chromosome 9 open reading frame 163; CI163_HUMAN; FLJ36779; RP11-413M3.11; RP11-413M3.11-001; Uncharacterized protein C9orf163.
詳(xiáng)細介(jiè)紹：
濃 度 1mg/1ml
規 格 0.2ml/200μg
抗體來源(yuán) Rabbit
克隆(lóng)類(lèi)型 polyclonal
交叉(chā)反(fǎn)應 Human
產(chǎn)品(pǐn)類型(xíng) 一抗(kàng)
研(yán)究(jiū)領域 細(xì)胞生物(wù) 免疫學(xué)
蛋白(bái)分(fēn)子量(liáng) predicted molecular weight: 22kDa
性 狀(zhuàng) Lyophilized or Liquid
免 疫 原 KLH conjugated synthetic peptide derived from human C9orf163
亞 型 IgG
純(chún)化方(fāng)法(fǎ) affinity purified by Protein A
儲(chǔ) 存 液(yè) Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
產(chǎn)品應用(yòng) WB=1:100-500 ELISA=1:500-1000 IP=1:20-100 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500
（石(shí)蠟切片需(xū)做抗(kàng)原修(xiū)復）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
保存條件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
相關(guān)資料：
產(chǎn)品介紹 C9orf163 (chromosome 9 open reading frame 163) is a 203 amino acid protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Database links : UniProtKB/Swiss-Prot: Q8N9P6.1
