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英文名稱 Anti-C8orf12
中文名(míng)稱 8號染(rǎn)色體開放閱讀(dú)框(kuàng)12抗體
別(bié) 名(míng) Chromosome 8 open reading frame 12; Uncharacterized protein C8orf12; CH012_HUMAN.
詳細介(jiè)紹(shào)：
濃 度(dù) 1mg/1ml
規(guī) 格 0.2ml/200μg
抗(kàng)體來源 Rabbit
克(kè)隆類(lèi)型(xíng) polyclonal
交叉反應 Human
產(chǎn)品類(lèi)型(xíng) 一抗
研究領域(yù) 細胞生物(wù) 免疫學
蛋白分子量 predicted molecular weight: 11kDa
性(xìng) 狀(zhuàng) Lyophilized or Liquid
免 疫(yì) 原 KLH conjugated synthetic peptide derived from human C8orf12
亞 型(xíng) IgG
純化方法 affinity purified by Protein A
儲(chǔ) 存 液(yè) Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
產品應(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(qiē)片需做抗原(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 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.
相關資料(liào)：
產品介(jiè)紹 Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf12 gene product has been provisionally designated C8orf12 pending further characterization.
Database links : UniProtKB/Swiss-Prot: Q96KT0.1
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