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EVC2 Rabbit anti-Human, Polyclonal, Invitrogen™

Rabbit Polyclonal Antibody

Manufacturer:  Invitrogen PA550658

Catalog No. PA550658


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Description

Description

The antibody detects endogenous levels of total EVC2 protein.

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.
Specifications

Specifications

EVC2
Polyclonal
Unconjugated
EVC2
Liquid
EVC2
Synthetic peptide corresponding to a region derived from internal residues of human Ellis van Creveld syndrome 2
Antigen affinity chromatography
RUO
Antibody
Polyclonal
Human
Immunohistochemistry (Paraffin), Western Blot
2.6 mg/mL
PBS with 50% glycerol and 0.05% sodium azide; pH 7.3
Q86UK5
LBN
Rabbit
IgG
100 μL
-20°C
Primary
132884
Documents
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