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Full name | EVC2 rabbit polyclonal antibody |
Alternative names | 50 μl/100 μl |
Reactivity | rabbit polyclonal |
Applications | WB, IHC |
Host | Rabbit |
Clone type | rabbit polyclonal |
Target 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. |
Swissprot No | Q86UK5 |
Gene Accession | NP_001159608 |
WB Predicted band size | Immunohistochemical analysis of paraffin-embedded Human colorectal cancer tissue or EVC2 antigen-treated (Neutralization experiment) using P102738(EVC2 Antibody) at dilution 1/75 |
WB Positive control | P102738-WB-1-P |
WB Recommended dilution | 148 kDa |
IHC predicted cell location | Predicted cell location: Cytoplasm and Cell membrane |
IHC positive control | Positive control: Human cervical cancer |
IHC Recommed dilution | Recommended dilution: 50-300 |
-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
P102738-WB-1-P
Immunohistochemical analysis of paraffin-embedded Human cervical cancer tissue or EVC2 antigen-treated (Neutralization experiment) using P102738(EVC2 Antibody) at dilution 1/75
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