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],

Immunogen: Synthesized peptide derived from human protein . at AA range: 30-110

Isotype: Rabbit

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration: 1 mg/ml

Observed band: 27

GeneID: FAM58A

Storage: -20°C/1 year

NOTE: For Research Use Only