ARG63261
anti-EVC2 / Limbin antibody
anti-EVC2 / Limbin antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human
Cell Biology and Cellular Response antibody
Overview
Product Description | Goat Polyclonal antibody recognizes EVC2 / Limbin |
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Tested Reactivity | Hu |
Tested Application | IHC-P, WB |
Specificity | This antibody is expected to recognise isoform 1 (NP_667338.3) and isoform 2 (NP_001159608.1). |
Host | Goat |
Clonality | Polyclonal |
Isotype | IgG |
Target Name | EVC2 / Limbin |
Antigen Species | Human |
Immunogen | C-LNAKKAMRALGMD |
Conjugation | Un-conjugated |
Alternate Names | Ellis-van Creveld syndrome protein 2; WAD; Limbin; EVC2; LBN |
Application Instructions
Application Suggestion |
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Application Note | IHC-P: Antigen Retrieval: Steam tissue section in Citrate buffer (pH 6.0). WB: Recommend incubate at RT for 1h. * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
Form | Liquid |
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Purification | Purified from goat serum by antigen affinity chromatography. |
Buffer | Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA. |
Preservative | 0.02% Sodium azide |
Stabilizer | 0.5% BSA |
Concentration | 0.5 mg/ml |
Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
Database Links | |
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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. [provided by RefSeq, Oct 2009] |
Research Area | Cell Biology and Cellular Response antibody |
Calculated MW | 148 kDa |
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