| 产品详情 |
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| Antigenic Specificity | WBSCR27 |
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| Clone | polyclonal |
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| Host Species | Rabbit |
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| Reactive Species | human |
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| Isotype | n/a |
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| Format | peptide affinity purified |
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| Size | 80 µl, 400 µl |
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| Concentration | n/a |
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| Applications | WB, IHC. RUO |
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| Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
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| Description | WBSCR27 encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. This WBSCR27 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 5-34 amino acids from the N-terminal region of human WBSCR27. |
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| Immunogen | Human WBSCR27. |
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| Other Names | WBSCR27; Williams-Beuren syndrome chromosomal region 27 protein |
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| Gene, Accession # | WBSCR27, SwissProt: Q8N6F8 |
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| Catalog # | abx025778 |
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| Price | |
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| Order / More Info | WBSCR27 Antibody from ABBEXA |
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| Product Specific References | n/a |
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| 产品资料 |
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