SALL4 Polyclonal Antibody

  • 货号:YN2448
  • 应用:WB;ELISA
  • 种属:Human;Mouse
    • 靶点:
    • SALL4
    • 基因名称:
    • SALL4 ZNF797
    • 蛋白名称:
    • Sal-like protein 4 (Zinc finger protein 797) (Zinc finger protein SALL4)
    • Human Swiss Prot No:
    • Q9UJQ4
    • Mouse Swiss Prot No:
    • Q8BX22
    • 免疫原:
    • Synthesized peptide derived from human protein . at AA range: 891-940
    • 特异性:
    • SALL4 Polyclonal Antibody detects endogenous levels of protein.
    • 组成:
    • Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
    • 来源:
    • Polyclonal, Rabbit,IgG
    • 稀释:
    • WB 1:500-2000 ELISA 1:5000-20000
    • 纯化工艺:
    • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
    • 浓度:
    • 1 mg/ml
    • 储存:
    • -15°C to -25°C/1 year(Do not lower than -25°C)
    • 实测条带:
    • 115kD
    • 背景:
    • This gene encodes a zinc finger transcription factor thought to play a role in the development of abducens motor neurons. Defects in this gene are a cause of Duane-radial ray syndrome (DRRS). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015],
    • 功能:
    • disease:Defects in SALL4 are the cause of Duane-radial ray syndrome (DRRS) [MIM:607323]; also known as Okihiro syndrome. DRRS is a disorder characterized by the association of forearm malformations with Duane retraction syndrome.,disease:Defects in SALL4 are the cause of IVIC syndrome [MIM:147750]. IVIC syndrome is an autosomal dominant condition characterized by upper limbs anomalies (radial ray defects, carpal bones fusion), extraocular motor disturbances, congenital bilateral non-progressive mixed hearing loss. Other less consistent malformations include heart involvement, mild thrombocytopenia and leukocytosis (before age 50), shoulder girdle hypoplasia, imperforate anus, kidney malrotation or rectovaginal fistula. The IVIC syndrome is an allelic disorder of Duane-radial ray syndrome (DRRS) with a similar phenotype.,function:Probable transcription factor.,similarity:Belongs to the sa
    • 细胞定位:
    • Cytoplasm. Nucleus.
    • 组织表达:
    • Expressed in testis. Constitutively expressed in acute myeloid leukemia (AML).