HNF1α (Phospho Ser247) rabbit pAb

  • 货号:YP1354
  • 应用:WB
  • 种属:Human;Rat;Mouse;
    • 靶点:
    • HNF1A
    • 简介:
    • >>Maturity onset diabetes of the young
    • 基因名称:
    • HNF1A TCF1
    • 蛋白名称:
    • HNF1α (Ser247)
    • Human Gene Id:
    • 6927
    • Human Swiss Prot No:
    • P20823
    • Mouse Swiss Prot No:
    • P22361
    • 免疫原:
    • Synthesized phosho peptide around human HNF1α (Ser247)
    • 特异性:
    • This antibody detects endogenous levels of Human HNF1α (phospho-Ser247)
    • 组成:
    • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
    • 来源:
    • Polyclonal, Rabbit,IgG
    • 稀释:
    • WB 1:1000-2000
    • 纯化工艺:
    • The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
    • 浓度:
    • 1 mg/ml
    • 储存:
    • -15°C to -25°C/1 year(Do not lower than -25°C)
    • 其他名称:
    • Hepatocyte nuclear factor 1-alpha (HNF-1-alpha) (HNF-1A) (Liver-specific transcription factor LF-B1) (LFB1) (Transcription factor 1) (TCF-1)
    • 实测条带:
    • 69kD
    • 背景:
    • The protein encoded by this gene is a transcription factor required for the expression of several liver-specific genes. The encoded protein functions as a homodimer and binds to the inverted palindrome 5'-GTTAATNATTAAC-3'. Defects in this gene are a cause of maturity onset diabetes of the young type 3 (MODY3) and also can result in the appearance of hepatic adenomas. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015],
    • 功能:
    • disease:Defects in HNF1A are a cause of susceptibility to insulin-dependent diabetes mellitus (IDDM) [MIM:222100].,disease:Defects in HNF1A are the cause of maturity onset diabetes of the young type 3 (MODY3) [MIM:600496]; also symbolized MODY-3. MODY [MIM:606391] is a form of diabetes characterized by an autosomal dominant mode of inheritance, age of onset of 25 years or younger and a primary defect in insulin secretion. The clinical phenotype of MODY3 is characterized by severe insulin secretory defects, and by major hyperglycemia associated with microvascular complications.,disease:Defects in HNF1A may predispose to hepatic adenomas [MIM:142330]. Hepatic adenomas are benign tumors at risk of malignant transformation. Bi-allelic inactivation of HNF1A, whether sporadic or associated with MODY3, may be an early step in the developmant of some hepatocellular carcinomas.,function:Required
    • 细胞定位:
    • Nucleus .
    • 组织表达:
    • Liver.