EVC2 antibody [C3], C-term

GeneTex

EVC2 antibody [C3], C-term

9

WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.

ImmunoFluorescence, Western Blot, ImmunoCytoChemistry

Research Use Only

Polyclonal

1 mg/ml

Unconjugated

EVC2

EvC ciliary complex subunit 2

Ellis van Creveld syndrome 2; ellis-van Creveld syndrome protein 2; LBN; limbin; WAD

Rabbit

IgG

Limbin

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. [provided by RefSeq]

Human

-20°C or -80°C,2°C to 8°C

12352203