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5號染(rǎn)色體(tǐ)開(kāi)放(fàng)閱讀(dú)框(kuàng)48抗(kàng)體
英(yīng)文(wén)名稱 Anti-C5orf48
中(zhōng)文名稱(chēng) 5號(hào)染(rǎn)色體(tǐ)開放閱讀框48抗體
別 名(míng) C5orf48; CE048_HUMAN; Chromosome 5 open reading frame 48; Uncharacterized protein C5orf48.
詳細(xì)介(jiè)紹(shào)：
濃 度 1mg/1ml
規(guī) 格 0.2ml/200μg
抗(kàng)體(tǐ)來源 Rabbit
克(kè)隆(lóng)類型 polyclonal
交叉(chā)反(fǎn)應 Human, Mouse, Rat, Dog, Cow, Horse, Rabbit
產品(pǐn)類型(xíng) 一(yī)抗
研(yán)究領(lǐng)域(yù) 細(xì)胞生物 免疫(yì)學
蛋白(bái)分(fēn)子(zǐ)量 predicted molecular weight: 15kDa
性 狀(zhuàng) Lyophilized or Liquid
免 疫(yì) 原(yuán) KLH conjugated synthetic peptide derived from human C5orf48
亞(yà) 型 IgG
純化(huà)方法 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(yīng)用 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
（石蠟切(qiē)片需做(zuò)抗(kàng)原修復）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
保(bǎo)存條件(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(xiāng)關(guān)資(zī)料(liào)：
產品介紹 C5orf48 (chromosome 5 open reading frame 48), also known as FLJ27505, MGC163367 or MGC163369, is a 134 amino acid protein. Encoded by a gene that maps to human chromosome 5q23.2, C5orf48 is linked to Autosomal dominant leukodystrophy (ADLD). Chromosome 5 makes up approximately 6% of the human genome and contains 181 million base pairs, which encode 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is caused by insertions or deletions within the TCOF1 gene and is also associated with chromosome 5. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
Database links : UniProtKB/Swiss-Prot: Q6ZNM6.1
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