FRAT1抗体应用：WB 1:500-2000 ELISA 1:5000-20000frequently rearranged in advanced T-cell lymphomas 1(FRAT1) Homo sapiens The protein encoded by this gene belongs to the GSK-3-binding protein family. The protein inhibits GSK-3-mediated phosphorylation of beta-catenin and positively regulates the Wnt signaling pathway. It may function in tumor progression and in lymphomagenesis. [provided by RefSeq, Oct 2008],

FRG2抗体应用：WB 1:500-2000

FRG2C抗体应用：WB 1:500-2000

FRG2C抗体应用：WB 1:500-2000 ELISA 1:5000-20000

FRMD5抗体应用：WB 1:500-2000

FRPD3抗体应用：WB 1:500-2000

FSBP抗体应用：WB 1:500-2000 ELISA 1:5000-20000disease:Defects in RAD54B may be a cause of tumor formation. Homozygous mutations at highly conserved position of RAD54B were observed in human primary lymphoma and colon cancer. These findings suggest that some cancers arise through defects of the RAD54B function.,function:Involved in DNA repair and mitotic recombination. May play an active role in recombination processes in concert with other members of the RAD52 epistasis group.,similarity:Belongs to the SNF2/RAD54 helicase family.,similarity:Contains 1 helicase ATP-binding domain.,similarity:Contains 1 helicase C-terminal domain.,subunit:Interacts with RAD51 through the NH2-terminal domain. Immunoprecipitation experiments show that the interaction is constitutive and not induced by ionizing radiation. The interaction may be indirect.,tissue specificity:Abundantly expressed in testis and spleen. Relatively low levels observed in thymus, prostate, ovary and colon.,

FSD2抗体应用：WB 1:500-2000This gene encodes a protein that belongs to the FN3/SPRY family of proteins. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013],

FSTL5抗体应用：WB 1:500-2000

FTCD抗体应用：WB 1:500-2000 The protein encoded by this gene is a bifunctional enzyme that channels 1-carbon units from formiminoglutamate, a metabolite of the histidine degradation pathway, to the folate pool. Mutations in this gene are associated with glutamate formiminotransferase deficiency. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Dec 2009],