兔抗EVC2多克隆抗体

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.

Applications:

ELISA, WB, IHC

Name of antibody:

EVC2

Immunogen:

Synthetic peptide of human EVC2

Full name:

EvC ciliary complex subunit 2

Synonyms:

LBN; WAD

SwissProt:

Q86UK5

ELISA Recommended dilution:

2000-5000

IHC positive control:

Human cervical cancer and Human colorectal cancer

IHC Recommend dilution:

50-300

WB Predicted band size:

148 kDa

WB Positive control:

Raji and A375 cell lysates

WB Recommended dilution:

500-2000