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Invitrogen™ EVC2 Polyclonal Antibody

Rabbit Polyclonal Antibody
Brand: Invitrogen™ PA521862
This item is not returnable.
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Description
Recommended positive controls: A431, H1299, HeLa, HepG2. Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
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
| EVC2 | |
| Polyclonal | |
| Unconjugated | |
| EVC2 | |
| Ellis van Creveld syndrome 2; ellis-van Creveld syndrome protein 2; EvC ciliary complex subunit 2; EVC2; LBN; limbin; WAD | |
| Rabbit | |
| Antigen affinity chromatography | |
| RUO | |
| 132884 | |
| Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
| Liquid |
| Western Blot, Immunocytochemistry | |
| 1 mg/mL | |
| 0.1M tris glycine with 10% glycerol and 0.01% thimerosal; pH 7 | |
| Q86UK5 | |
| EVC2 | |
| Synthetic peptide encompassing a sequence within the Intracellular domain of human EVC2. The exact sequence is proprietary. | |
| 100 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
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