Anti-FAM135B/FITC Conjugated抗体
产品名称: Anti-FAM135B/FITC Conjugated抗体
英文名称: Anti-FAM135B/FITC
产品编号: YB--9063R-FITC
产品价格: null
产品产地: 中国/美国
品牌商标: Ybscience
更新时间: 2023-08-17T10:24:20
使用范围: 科研使用
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Anti-FAM135B/FITC Conjugated抗体
产品编号 | YB-9063R-FITC |
英文名称 | Anti-FAM135B/FITC |
中文名称 | FITC标记的FAM135B蛋白抗体 |
别 名 | C8ORFK32; F135B_HUMAN; fam135b; Family with sequence similarity 135 member B; Hypothetical protein LOC51059; MGC126009; MGC126010; MGC33221; Protein FAM135B. |
规格价格 | 100ul/2980元 购买 大包装/询价 |
说 明 书 | 100ul |
研究领域 | 肿瘤 细胞生物 免疫学 |
抗体来源 | Rabbit |
克隆类型 | Polyclonal |
交叉反应 | Human, Mouse, Rat, |
产品应用 | IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
分 子 量 | 156kDa |
性 状 | Lyophilized or Liquid |
浓 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human FAM135B |
亚 型 | IgG |
纯化方法 | affinity purified by Protein A |
储 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
保存条件 | 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. |
产品介绍 | background: 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 FAM135B gene product has been provisionally designated FAM135B pending further characterization. Similarity: Belongs to the FAM135 family. Database links: Entrez Gene: 51059 Human SwissProt: Q49AJ0 Human Unigene: 126024 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |