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英文名稱 Anti-C9orf140
中(zhōng)文(wén)名稱(chēng) 9號染色(sè)體開(kāi)放(fàng)閱讀(dú)框140抗(kàng)體
別(bié) 名 2010317E24Rik; C9orf140; Chromosome 9 open reading frame 140; SAPC2_HUMAN; p42.3; Protein C9orf140; SAPCD2; Suppressor APC domain containing 2; Suppressor APC domain containing protein 2; TS/MDEP; Tumor specificity and mitosis phase-dependent expression protein.
詳(xiáng)細介(jiè)紹(shào)：
濃 度(dù) 1mg/1ml
規(guī) 格 0.2ml/200μg
抗體(tǐ)來(lái)源(yuán) Rabbit
克隆類(lèi)型 polyclonal
交叉(chā)反(fǎn)應 Human, Mouse, Rat, Chicken, Cow, Horse, Rabbit
產(chǎn)品(pǐn)類(lèi)型(xíng) 一抗
研究(jiū)領域(yù) 細胞(bāo)生物(wù) 免(miǎn)疫(yì)學(xué) 腫瘤細胞生(shēng)物標誌物(wù)
蛋白(bái)分子(zǐ)量(liáng) predicted molecular weight: 43kDa
性 狀 Lyophilized or Liquid
免 疫 原 KLH conjugated synthetic peptide derived from human C9orf140
亞 型(xíng) IgG
純(chún)化方法 affinity purified by Protein A
儲(chǔ) 存 液 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)蠟切(qiē)片(piàn)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(bǎo)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(liào)：
產品介紹 C9orf140 (chromosome 9 open reading frame 140), also known as TS/MDEP (tumor specificity and mitosis phase-dependent expression protein) or p42.3, is a 394 amino acid nuclear and cytoplasmic 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.
Subcellular Location : Cytoplasm. Nucleus.
Tissue Specificity : Expressed in 5-month-old fetal tissues, including stomach, intestine, colon, liver, brain, lung, heart, spleen and kidney. Undetectable in non-cancerous adult tissues. Expressed in many primary gastric carcinoma, but almost not in adjacent normal mucosa. Expressed preferentially in M and G1 phases, compared to S and G2 phases.
Database links : UniProtKB/Swiss-Prot: Q86UD0.2
- 上(shàng)一(yī)條(tiáo)：9號染(rǎn)色(sè)體開放(fàng)閱(yuè)讀(dú)框142抗體(tǐ)
- 下(xià)一條：9號染色(sè)體開放閱讀(dú)框139抗體(tǐ)
