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英文名稱 Anti-C9orf5
中(zhōng)文名(míng)稱 9號染(rǎn)色體開(kāi)放(fàng)閱(yuè)讀框5抗體(tǐ)
別(bié) 名 C9orf5; TM245_HUMAN; Protein CG-2; Transmembrane protein C9orf5;
詳細(xì)介(jiè)紹：
濃 度 1mg/1ml
規 格(gé) 0.2ml/200μg
抗(kàng)體來源 Rabbit
克隆(lóng)類型 polyclonal
交叉(chā)反(fǎn)應 Human, Dog, Cow, Sheep
產(chǎn)品(pǐn)類(lèi)型(xíng) 一(yī)抗
研(yán)究(jiū)領域(yù) 細胞(bāo)生(shēng)物 免疫學(xué)
蛋(dàn)白分子(zǐ)量(liáng) predicted molecular weight: 101kDa
性(xìng) 狀 Lyophilized or Liquid
免(miǎn) 疫 原 KLH conjugated synthetic peptide derived from human C9orf5
亞 型(xíng) IgG
純(chún)化方(fāng)法(fǎ) affinity purified by Protein A
儲 存(cún) 液(yè) Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
產品(pǐn)應(yīng)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(là)切片(piàn)需做抗原修復(fù)）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
保存(cún)條件(jiàn) 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
相關資(zī)料：
產(chǎn)品介紹(shào) C9orf5 (chromosome 9 open reading frame 5), also known as CG2, is a 911 amino acid multi-pass membrane protein that is widely expressed and exists as four alternatively spliced isoforms. The gene encoding C9orf5 maps to human chromosome 9, which consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Considered 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.
Subcellular Location : Membrane; Multi-pass membrane protein (Potential).
Tissue Specificity : Widely expressed.
Similarity : Belongs to the UPF0118 (TMEM245) family.
Database links : UniProtKB/Swiss-Prot: Q9H330.2
- 上(shàng)一條(tiáo)：9號(hào)染色(sè)體(tǐ)開放閱讀框50抗(kàng)體(tǐ)
- 下一(yī)條(tiáo)：9號(hào)染(rǎn)色體開(kāi)放閱(yuè)讀(dú)框(kuàng)41抗(kàng)體(tǐ)
