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

FABP5抗体应用：WB 1:500-2000 ELISA 1:5000-20000fatty acid binding protein 5(FABP5) Homo sapiens This gene encodes the fatty acid binding protein found in epidermal cells, and was first identified as being upregulated in psoriasis tissue. Fatty acid binding proteins are a family of small, highly conserved, cytoplasmic proteins that bind long-chain fatty acids and other hydrophobic ligands. FABPs may play roles in fatty acid uptake, transport, and metabolism. Polymorphisms in this gene are associated with type 2 diabetes. The human genome contains many pseudogenes similar to this locus.[provided by RefSeq, Feb 2011],

FABP6抗体应用：WB 1:500-2000 ELISA 1:5000-20000fatty acid binding protein 6(FABP6) Homo sapiens This gene encodes the ileal fatty acid binding protein. Fatty acid binding proteins are a family of small, highly conserved, cytoplasmic proteins that bind long-chain fatty acids and other hydrophobic ligands. FABP6 and FABP1 (the liver fatty acid binding protein) are also able to bind bile acids. It is thought that FABPs roles include fatty acid uptake, transport, and metabolism. Transcript variants generated by alternate transcription promoters and/or alternate splicing have been found for this gene. [provided by RefSeq, Jul 2008],

FACE2抗体应用：WB 1:500-2000 ELISA 1:5000-20000Ras converting CAAX endopeptidase 1(RCE1) Homo sapiens This gene encodes an integral membrane protein which is classified as a member of the metalloproteinase family. This enzyme is thought to function in the maintenance and processing of CAAX-type prenylated proteins. [provided by RefSeq, Jul 2008],

FAF2抗体应用：WB 1:500-2000 The protein encoded by this gene is highly expressed in peripheral blood of patients with atopic dermatitis (AD), compared to normal individuals. It may play a role in regulating the resistance to apoptosis that is observed in T cells and eosinophils of AD patients. [provided by RefSeq, Jul 2008],

FAH2B抗体应用：WB 1:500-2000

FAIM1抗体应用：WB 1:500-2000 ELISA 1:5000-20000Fas apoptotic inhibitory molecule(FAIM) Homo sapiens The protein encoded by this gene protects against death receptor-triggered apoptosis and regulates B-cell signaling and differentiation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011],