EVC2 Polyclonal Antibody

• Background :

  This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants.

• Description :

  This is a EVC2 Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.

• Synonyms :

  Ellis van Creveld syndrome 2, LBN, Limbin

• Swiss Prot :

  Q86UK5

• Accession Number :

  NP_667338

• Reactivity :

  Human, Mouse

• Immunogen :

  Synthetic peptide of human EVC2

• Clonality :

  Polyclonal

• Conjugation :

  Unconjugated

• Type :

  Polyclonal Antibody

• Applications :

  WB, IHC, ELISA

• Purification Method :

  Affinity purification

• Assay Type :

  Antibody

• Concentration :

  1.5 mg/mL

• Dilution :

  WB 1:200-1:1000, IHC 1:50-1:200

• Buffer :

  PBS with 0.05% sodium azide and 50% glycerol, PH7.4

• Storage Conditions :

  Store at -20°C. Avoid freeze / thaw cycles.

• Calculated Molecular Weight :

  148 kDa

• Host or Source :

  Rabbit

• Isotype :

  IgG