GCFC1抗体应用：WB 1:500-2000 ELISA 1:5000-20000

GCC1抗体应用：WB 1:500-2000 ELISA 1:5000-20000

GKN2抗体应用：WB 1:500-2000 ELISA 1:5000-20000

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

FOXC2抗体应用：WB 1:500-2000 ELISA 1:5000-20000forkhead box C2(FOXC2) Homo sapiens This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined; however, it may play a role in the development of mesenchymal tissues. [provided by RefSeq, Jul 2008],

FOXF1抗体应用：WB 1:500-2000 ELISA 1:5000-20000forkhead box F1(FOXF1) Homo sapiens This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it may play a role in the regulation of pulmonary genes as well as embryonic development. [provided by RefSeq, Jul 2008],

FOXG1抗体应用：WB 1:500-2000 This locus encodes a member of the forked-head transcription factor family. The encoded protein, which functions as a repressor, may play a role in brain development. Mutations at this locus have been associated with Rett syndrome. [provided by RefSeq, Feb 2012],

FOXM1抗体应用：WB 1:500-2000 ELISA 1:5000-20000forkhead box M1(FOXM1) Homo sapiens The protein encoded by this gene is a transcriptional activator involved in cell proliferation. The encoded protein is phosphorylated in M phase and regulates the expression of several cell cycle genes, such as cyclin B1 and cyclin D1. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011],

FOXN1抗体应用：WB 1:500-2000 ELISA 1:5000-20000forkhead box N1(FOXN1) Homo sapiens Mutations in the winged-helix transcription factor gene at the nude locus in mice and rats produce the pleiotropic phenotype of hairlessness and athymia, resulting in a severely compromised immune system. This gene is orthologous to the mouse and rat genes and encodes a similar DNA-binding transcription factor that is thought to regulate keratin gene expression. A mutation in this gene has been correlated with T-cell immunodeficiency, the skin disorder congenital alopecia, and nail dystrophy. Alternative splicing in the 5' UTR of this gene has been observed. [provided by RefSeq, Jul 2008],

FOXP4抗体应用：WB 1:500-2000 This gene belongs to subfamily P of the forkhead box (FOX) transcription factor family. Forkhead box transcription factors play important roles in the regulation of tissue- and cell type-specific gene transcription during both development and adulthood. Many members of the forkhead box gene family, including members of subfamily P, have roles in mammalian oncogenesis. This gene may play a role in the development of tumors of the kidney and larynx. Alternative splicing of this gene produces multiple transcript variants, some encoding different isoforms. [provided by RefSeq, Jul 2008],