FA22A抗体应用：WB 1:500-2000

FA22B抗体应用：WB 1:500-2000

FA40B抗体应用：WB 1:500-2000

FA43A抗体应用：WB 1:500-2000

FA53B抗体应用：WB 1:500-2000

FA53C抗体应用：WB 1:500-2000

FA58A抗体应用：WB 1:500-2000 ELISA 1:5000-20000family 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],

FA73B抗体应用：WB 1:500-2000

FA83H抗体应用：WB 1:500-2000 The protein encoded by this gene plays an important role in the structural development and calcification of tooth enamel. Defects in this gene are a cause of amelogenesis imperfecta type 3 (AI3). [provided by RefSeq, Mar 2010],

FA96A抗体应用：WB 1:500-2000