FA58A Polyclonal Antibody

• Background :

  Family with sequence similarity 58 member A (FAM58A) Homo sapiens Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]

• Gene ID :

  92002

• Swiss Prot :

  Q8N1B3

• Cross Reactivity :

  Human; Mouse; Rat

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  WB; ELISA

• Dilution :

  WB 1:500-2000 ELISA 1:5000-20000

• Buffer :

  Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.

• Molecular Weight :

  27

• Storage Conditions :

  -20°C/1 year

• Protein Weight :

  27