M-cadherin Polyclonal Antibody

    • Catalog No.:YT2677
    • Applications:WB;IHC;IF;ELISA
    • Reactivity:Human;Mouse;Rat
      • Target:
      • M-cadherin
      • Fields:
      • >>Cell adhesion molecules
      • Gene Name:
      • CDH15
      • Protein Name:
      • Cadherin-15
      • Human Gene Id:
      • 1013
      • Human Swiss Prot No:
      • P55291
      • Mouse Swiss Prot No:
      • P33146
      • Immunogen:
      • The antiserum was produced against synthesized peptide derived from human CDH15. AA range:81-130
      • Specificity:
      • M-cadherin Polyclonal Antibody detects endogenous levels of M-cadherin protein.
      • Formulation:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • Source:
      • Polyclonal, Rabbit,IgG
      • Dilution:
      • WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:10000.. IF 1:50-200
      • Purification:
      • The antibody was affinity-purified from rabbit antiserum 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:
      • CDH15;CDH14;CDH3;Cadherin-15;Cadherin-14;Muscle cadherin;M-cadherin
      • Observed Band(KD):
      • 89kD
      • Background:
      • This gene is a member of the cadherin superfamily of genes, encoding calcium-dependent intercellular adhesion glycoproteins. Cadherins consist of an extracellular domain containing 5 cadherin domains, a transmembrane region, and a conserved cytoplasmic domain. Transcripts from this particular cadherin are expressed in myoblasts and upregulated in myotubule-forming cells. The protein is thought to be essential for the control of morphogenetic processes, specifically myogenesis, and may provide a trigger for terminal muscle cell differentiation. [provided by RefSeq, Jul 2008],
      • Function:
      • disease:A chromosomal aberration involving CDH15 and KIRREL3 is found in a patient with severe mental retardation and dysmorphic facial features. Translocation t(11;16)(q24.2;q24).,disease:Defects in CDH15 are the cause of mental retardation autosomal dominant type 3 (MRD3) [MIM:612580]. Mental retardation is characterized by significantly sub-average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period.,function:Cadherins are calcium dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types. M-cadherin is part of the myogenic program and may provide a trigger for terminal muscle differentiation.,similarity:Contains 5 cadherin domains.,tissue specificity:Expressed in the brai
      • Subcellular Location:
      • Cell membrane; Single-pass type I membrane protein.
      • Expression:
      • Expressed in the brain and cerebellum.
      • Products Images
      • Western Blot analysis of various cells using M-cadherin Polyclonal Antibody diluted at 1:500
      • Western blot analysis of lysates from HepG2 and 293 cells, using CDH15 Antibody. The lane on the right is blocked with the synthesized peptide.