別 名 Fanconi Anemia Complementation Group F; FACF; FAF; Fanconi anemia group F protein; MGC126856; Protein FACF; FANCF_HUMAN.
研究領(lǐng)域 免疫學(xué) 細(xì)胞凋亡 抗體來(lái)源 Rabbit 克隆類型 Polyclonal 交叉反應(yīng) Human, Mouse, Rat, Cow, 產(chǎn)品應(yīng)用 IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. 分 子 量 42kDa 性 狀 Lyophilized or Liquid 濃 度 1mg/ml 免 疫 原 KLH conjugated synthetic peptide derived from human FANCF
亞 型 IgG 純化方法 affinity purified by Protein A 儲(chǔ) 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. 保存條件 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.
Anti-FANCF/FITC,FITC標(biāo)記的范可尼貧血相關(guān)蛋白F抗體產(chǎn)品介紹:The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group F.