KDM5C/Jarid1C/SMCX mouse mAb

    • Catalog No.:YM1201
    • Applications:WB;ICC
    • Reactivity:Human
      • Target:
      • KDM5C/Jarid1C/SMCX
      • Gene Name:
      • kdm5c
      • Human Gene Id:
      • 8242
      • Human Swiss Prot No:
      • P41229
      • Mouse Swiss Prot No:
      • P41230
      • Immunogen:
      • Purified recombinant human KDM5C / Jarid1C / SMCX protein fragments expressed in E.coli
      • Specificity:
      • This antibody detects endogenous levels of KDM5C / Jarid1C / SMCX and does not corss-react with related proteins
      • Formulation:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • Source:
      • Monoclonal, Mouse
      • Dilution:
      • wb 1:1000 icc 1:150
      • Purification:
      • The antibody was affinity-purified from mouse ascites by affinity-chromatography using epitope-specific immunogen.
      • Concentration:
      • 1 mg/ml
      • Storage Stability:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • Other Name:
      • DXS1272E;Histone demethylase JARID1C;JARID1C;JmjC domain containing protein SMCX;Jumonji AT rich interactive domain 1C;Jumonji, AT rich interactive domain 1C (RBP2 like);Jumonji/ARID domain-containing protein 1C;KDM5C;KDM5C_HUMAN;Lysine (K) specific demethylase 5C;Lysine-specific demethylase 5C;MRXJ;MRXSCJ;MRXSJ;Protein SmcX;Protein Xe169;rbp2 like protein;Selected cDNA on X;SMCX;Smcx homolog X chromosome;SmcX protein;SmcX protein;Smcy homolog X linked;XE169;Xe169 protein;Xe169 protein.
      • Observed Band(KD):
      • 220kD
      • Background:
      • 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],
      • Function:
      • 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
      • Subcellular Location:
      • Nucleus .
      • Expression:
      • Expressed in all tissues examined. Highest levels found in brain and skeletal muscle.
      • Products Images
      • Western blot detection of KDM5C / Jarid1C / SMCX in Hela and 293 cell lysates using KDM5C / Jarid1C / SMCX mouse mAb (1:1000 diluted).Predicted band size: 176KDa.Observed band size: 220KDa.
      • Immunocytochemistry of HeLa cells using anti-KDM5C / Jarid1C / SMCX mouse mAb diluted 1:150.