"WBSCR16" Related Products

Recombinant Human WBSCR16 cell lysate

Cat.No.: WBSCR16-1921HCL
Description: This gene encodes an RCC1-like G-exchanging factor. It is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
Species: Human
Size: 100 ul
Storage Buffer: 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
Applications: Western Blot;
Gene Name: WBSCR16 Williams-Beuren syndrome chromosome region 16 [ Homo sapiens ]
Official Symbol: WBSCR16
Synonyms: WBSCR16; Williams-Beuren syndrome chromosome region 16;
Gene ID: 94293

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