EVC2 polyclonal, anti-human, mouse

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.

Synonyms: LBN, WAD

Cellular Location: Cytoplasm Cell membrane

Immunogen:
A synthetic peptide of human EVC2

Gene Symbol: EVC2

Gene ID: 132884

Swiss prot: Q86UK5

Calculated MW: 148 kDa

Recommended dilution:
WB 1:500-2000, IHC 1:50-300,

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.