FA58A Polyclonal Antibody
Sizes: 50μL, 100μL
Catalogue Numbers: RA32262-50, RA32262-100
Citations, Manuals and MSDS Available upon request.
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],
Condition: Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
Storage Instructions: -20°C/1 year
Recommended dilutions: WB 1:500-2000 ELISA 1:5000-20000
Applications: WB; ELISA
Species Cross-Reactivity: Human; Mouse; Rat
GeneID (Human): 92002
Protein MW (KDa): 27
SWISS: Q8N1B3
Source: Rabbit
Research Use Only