别名:LBN; WAD应用:WB,IHC
反应种属:Human, Mouse
规格:50μl/100μl
| Description |
|---|
| 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. |
| Specification | |
|---|---|
| Aliases | LBN; WAD |
| Swissprot | Q86UK5 |
| WB Predicted band size | 148 kDa |
| Host/Isotype | Rabbit IgG |
| Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
| Species Reactivity | Human, Mouse |
| Immunogen | Synthetic peptide of human EVC2 |
| Formulation | pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
| Application | |
|---|---|
| WB | 1/500-1/2000 |
| IHC | 1/50-1/300 |
| ELISA | 1/2000-1/5000 |
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Gel: 6%SDS-PAGE, Lysate: 40 μg, Lane 1-2: Raji and A375 cell lysates, Primary antibody: P11749(EVC2 Antibody) at dilution 1/500, Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution, Exposure time: 30 seconds |
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The image is immunohistochemistry of paraffin-embedded Human cervical cancer tissue using P11749(EVC2 Antibody) at dilution 1/75. (Original magnification: ×200) |
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The image is immunohistochemistry of paraffin-embedded Human colorectal cancer tissue using P11749(EVC2 Antibody) at dilution 1/75. (Original magnification: ×200) |
本公司的所有产品仅用于科学研究或者工业应用等非医疗目的,不可用于人类或动物的临床诊断或治疗,非药用,非食用。
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本公司的所有产品仅用于科学研究或者工业应用等非医疗目的,不可用于人类或动物的临床诊断或治疗,非药用,非食用。
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