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| Antigenic Specificity | WBSCR17 |
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| Clone | polyclonal |
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| Host Species | Rabbit |
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| Reactive Species | mouse |
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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. 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 | This gene encodes an N-acetylgalactosaminyltransferase, which has 97% sequence identity to the mouse protein. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq]. This WBSCR17 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 411-440 amino acids from the C-terminal region of human WBSCR17. |
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| Immunogen | Human WBSCR17. |
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| Other Names | Putative polypeptide N-acetylgalactosaminyltransferase-like protein 3; Polypeptide GalNAc transferase-like protein 3; GalNAc-T-like protein 3; pp-GaNTase-like protein 3; Protein-UDP acetylgalactosaminyltransferase-like protein 3; polypeptide N-acetylgalactosaminyltransferase-like protein 3; Williams-Beuren syndrome chromosomal region 17 protein; WBSCR17; GALNTL3 |
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| Gene, Accession # | SwissProt: Q6IS24 |
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| Catalog # | abx027246 |
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| Price | |
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| Order / More Info | WBSCR17 Antibody from ABBEXA |
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| Product Specific References | n/a |
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