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Merck

SPG21

spastic paraplegia 21 (autosomal recessive, Mast syndrome)

Sinónimos:
ACP33, GL010, MAST
Especie:
ID UniProtKB:
ID del gen:
  • Human(51324) Summary: The protein encoded by this gene was identified by a two-hybrid screen using CD4 as the bait. It binds to the hydrophobic C-terminal amino acids of CD4 which are involved in repression of T cell activation. The interaction with CD4 is mediated by the noncatalytic alpha/beta hydrolase fold domain of this protein. It is thus proposed that this gene product modulates the stimulatory activity of CD4. At least three different transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
  • Mouse(27965) spastic paraplegia 21 homolog (human)
  • Rat(300791) spastic paraplegia 21 homolog (human)
  • domestic cat(101096987) spastic paraplegia 21 (autosomal recessive, Mast syndrome)
  • dog(487599) spastic paraplegia 21 (autosomal recessive, Mast syndrome)
  • Zebrafish(406704) spastic paraplegia 21 (H. sapiens)
  • domestic guinea pig(100713790) spastic paraplegia 21 (autosomal recessive, Mast syndrome)
  • cow(404069) spastic paraplegia 21 (autosomal recessive, Mast syndrome)
  • sheep(101117420) spastic paraplegia 21 (autosomal recessive, Mast syndrome)
  • naked mole-rat(101696663) spastic paraplegia 21 (autosomal recessive, Mast syndrome)
  • chicken(415526) spastic paraplegia 21 (autosomal recessive, Mast syndrome)

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esiRNA

Referencia del producto
Descripción
Especie
MISSION® esiRNA, targeting mouse Spg21,
Especie
mouse
MISSION® esiRNA, targeting human SPG21,
Especie
human