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WBSCR16

Williams-Beuren syndrome chromosome region 16

Sinónimos:
Especie:
ID UniProtKB:
ID del gen:
  • Human(81554) Summary: 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]
  • Mouse(94254) Williams-Beuren syndrome chromosome region 16 homolog (human)
  • Rat(360796) Williams-Beuren syndrome chromosome region 16
  • naked mole-rat(101720236) Williams-Beuren syndrome chromosome region 16
  • Zebrafish(555972) Williams-Beuren syndrome chromosome region 16 homolog (human)
  • cow(513273) Williams-Beuren syndrome chromosomal region 16 protein
  • chicken(417484) Williams-Beuren syndrome chromosome region 16

Custom & Knockdown Gene Products

  • siRNA

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  • shRNA

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  • Custom Gene Products

    We offer a comprehensive portfolio of DNA oligos, RNA oligos and predesigned primers.

Antibodies

Referencia del producto
Descripción
Reactividad de especies
Aplicación
Anti-RCC1L antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
Reactividad de especies
human
Aplicación
immunohistochemistry

esiRNA

Referencia del producto
Descripción
Especie
MISSION® esiRNA, targeting human RCC1L,
Especie
human
MISSION® esiRNA, targeting mouse Wbscr16,
Especie
mouse