WBSCR16 Proteins
(Williams-Beuren Syndrome Chromosome Region 16 (WBSCR16))
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. [provided by RefSeq, Jul 2008].
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3 results :
custom-made
WBSCR16
Origin: Human
Host: HEK-293 Cells
Recombinant
> 90 % as determined by Bis-Tris PAGE, anti-tag ELISA, Western Blot and analytical SEC (HPLC)
WBSCR16
Origin: Human
Host: Wheat germ
Recombinant
ELISA, WB, AA, AP
1 image
custom-made
WBSCR16
Origin: Human
Host: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
Aliases for WBSCR16 Proteins
RCC1 like (RCC1L) Proteinsreculator of chromosome condensation 1 like (Rcc1l) Proteins
5730496C04Rik Proteins
AU019812 Proteins
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