购物车
帮助
021-54845833/15800441009
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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. |
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Applications: |
ELISA, WB, IHC |
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Name of antibody: |
EVC2 |
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Immunogen: |
Synthetic peptide of human EVC2 |
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Full name: |
EvC ciliary complex subunit 2 |
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Synonyms: |
LBN; WAD |
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SwissProt: |
Q86UK5 |
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ELISA Recommended dilution: |
2000-5000 |
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IHC positive control: |
Human cervical cancer and Human colorectal cancer |
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IHC Recommend dilution: |
50-300 |
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WB Predicted band size: |
148 kDa |
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WB Positive control: |
Raji and A375 cell lysates |
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WB Recommended dilution: |
500-2000 |
