SmcX Monoclonal Antibody

    • 货号:YM1096
    • 应用:WB;IF
    • 种属:Human;Mouse;Rat;Bovine;Dog
      • 靶点:
      • SmcX
      • 基因名称:
      • KDM5C
      • 蛋白名称:
      • Lysine-specific demethylase 5C
      • Human Gene Id:
      • 8242
      • Human Swiss Prot No:
      • P41229
      • Mouse Swiss Prot No:
      • P41230
      • 免疫原:
      • Purified recombinant human SmcX (C-terminus) protein fragments expressed in E.coli.
      • 特异性:
      • SmcX Monoclonal Antibody detects endogenous levels of SmcX protein.
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Monoclonal, Mouse
      • 稀释:
      • WB 1:1000 - 1:2000. IF 1:100 - 1:500. Not yet tested in other applications.
      • 纯化工艺:
      • Affinity purification
      • 浓度:
      • 1 mg/ml
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 其他名称:
      • KDM5C;DXS1272E;JARID1C;SMCX;XE169;Lysine-specific demethylase 5C;Histone demethylase JARID1C;Jumonji/ARID domain-containing protein 1C;Protein SmcX;Protein Xe169
      • 分子量:
      • 176kD
      • 背景:
      • This gene is a member of the SMCY homolog family and encodes a protein with one ARID domain, one JmjC domain, one JmjN domain and two PHD-type zinc fingers. The DNA-binding motifs suggest this protein is involved in the regulation of transcription and chromatin remodeling. Mutations in this gene have been associated with X-linked mental retardation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009],
      • 功能:
      • cofactor:Alpha-ketoglutarate.,cofactor:Fe(2+).,disease:Defects in KDM5C are a cause of X-linked mental retardation (XLMR) [MIM:300534]. Mental retardation is usually defined as cognitive impairment with an IQ less than 70. Etiologically, mental retardation is a very heterogeneous condition that involves environmental, stochastic and/or genetic factors.,domain:Both the JmjC domain and the JmjN domain are required for enzymatic activity.,domain:The first PHD-type zinc finger domain recognizes and binds H3-K9Me3.,function:Histone demethylase that specifically demethylates 'Lys-4' of histone H3, thereby playing a central role in histone code. Does not demethylate histone H3 'Lys-9', H3 'Lys-27', H3 'Lys-36', H3 'Lys-79' or H4 'Lys-20'. Demethylates trimethylated and dimethylated but not monomethylated H3 'Lys-4'. Participates in transcriptional repression of neuronal genes by recruiting hist
      • 细胞定位:
      • Nucleus .
      • 组织表达:
      • Expressed in all tissues examined. Highest levels found in brain and skeletal muscle.
      • 产品图片
      • Western Blot analysis using SmcX Monoclonal Antibody against HeLa, 293 cell lysate.
      • Immunofluorescence analysis of HeLa cells using SmcX Monoclonal Antibody.