Putative Polypeptide N-Acetylgalactosaminyltransferase-Like Protein 3 (WBSCR17) Antibody

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].
Supplier Abbexa Ltd.
Product # abx027246-80UL
Pricing 80 µl USD $326.25
Clonality Polyclonal
Conjugation Unconjugated
Host Rabbit
Tested Applications ELISA, WB
UniProt Primary AC Q6IS24
Dry Ice No
Availability Shipped within 5-10 working days.
Note This product is for research use only.
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