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一(yī)抗
英(yīng)文名(míng)稱 Anti-C10orf62
中文名(míng)稱(chēng) 10號(hào)染色(sè)體開放閱讀框62抗(kàng)體(tǐ)
別(bié) 名(míng) bA548K23.1; Hypothetical protein LOC414157; MERIT40; chromosome 10 open reading frame 62; NBA1; Uncharacterized protein C10orf62; CJ062_HUMAN .
詳(xiáng)細介(jiè)紹：
濃 度 1mg/1ml
規 格 0.2ml/200μg
抗體(tǐ)來(lái)源 Rabbit
克隆類型 polyclonal
交(jiāo)叉(chā)反應(yīng) Human, Mouse, Rat, Pig
產(chǎn)品類型 一抗(kàng)
研究領域(yù) 細胞生物 免疫學
蛋(dàn)白分(fēn)子量 predicted molecular weight: 25kDa
性(xìng) 狀(zhuàng) Lyophilized or Liquid
免 疫 原 KLH conjugated synthetic peptide derived from human C10orf62
亞 型 IgG
純(chún)化方法(fǎ) affinity purified by Protein A
儲 存 液 Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
產(chǎn)品應用 WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=1:20-100 IF=1:50-200
（石蠟切片需做抗(kàng)原(yuán)修復）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
保(bǎo)存條(tiáo)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(xiāng)關(guān)資(zī)料：
產(chǎn)品介(jiè)紹(shào) C10orf62 is a 223 amino acid protein encoded by a gene that maps to human chromosome 10q24.1. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Database links : UniProtKB/Swiss-Prot: Q5T681.1
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