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FOXP1 belongs to subfamily P of the forkhead box (FOX) transcription factor family. Additionally we are shipping FOXP1 Kits (19) and FOXP1 Proteins (14) and many more products for this protein.
Showing 10 out of 175 products:
Human Monoclonal FOXP1 Primary Antibody for CyTOF, FACS - ABIN256072
Fox, Brown, Han, Ashe, Leek, Harris, Banham: Expression of the forkhead transcription factor FOXP1 is associated with estrogen receptor alpha and improved survival in primary human breast carcinomas. in Clinical cancer research : an official journal of the American Association for Cancer Research 2004
Show all 7 references for ABIN256072
Human Polyclonal FOXP1 Primary Antibody for FACS, IHC (p) - ABIN952379
Baró, Espinet, Salido, Colomo, Luño, Florensa, Ferrer, Salar, Campo, Serrano, Solé: FOXP1 status in splenic marginal zone lymphoma: a fluorescence in situ hybridization and immunohistochemistry approach. in Histology and histopathology 2009
Show all 4 references for ABIN952379
Chicken Polyclonal FOXP1 Primary Antibody for IHC, WB - ABIN2779725
Shi, Zhang, Chen, Sulaiman, Feinberg, Ballantyne, Jain, Simon: Integrin engagement regulates monocyte differentiation through the forkhead transcription factor Foxp1. in The Journal of clinical investigation 2004
Show all 4 references for ABIN2779725
Human Monoclonal FOXP1 Primary Antibody for FACS, IHC - ABIN1098120
Chen, Xiao, Zhang, Li, Liu, Zhao, Ma, Luo, Qiu, Huang, Korteweg, Gu: Transcription factors E2A, FOXO1 and FOXP1 regulate recombination activating gene expression in cancer cells. in PLoS ONE 2011
Show all 2 references for ABIN1098120
Human Polyclonal FOXP1 Primary Antibody for WB - ABIN871737
Hamdan, Daoud, Rochefort, Piton, Gauthier, Langlois, Foomani, Dobrzeniecka, Krebs, Joober, Lafrenière, Lacaille, Mottron, Drapeau, Beauchamp, Phillips, Fombonne, Rouleau, Michaud: De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. in American journal of human genetics 2010
Human Monoclonal FOXP1 Primary Antibody for IHC (p) - ABIN1689139
Rouhigharabaei, Finalet Ferreiro, Tousseyn, van der Krogt, Put, Haralambieva, Graux, Maes, Vicente, Vandenberghe, Cools, Wlodarska: Non-IG aberrations of FOXP1 in B-cell malignancies lead to an aberrant expression of N-truncated isoforms of FOXP1. in PLoS ONE 2014
Prominent foxp1 expression is detected in many regions of the developing central nervous system, especially in midbrain-hindbrain boundary, hindbrain, and spinal cord.
FOXP1 has protein-protein interaction with NFAT1 (show NFAT1 Antibodies) on DNA and enhances breast cancer cell migration by repressing NFAT1 (show NFAT1 Antibodies) transcriptional activity.
FOXP1 functions as an oncogene (show RAB1A Antibodies) in promoting cancer stem cell-like characteristics in ovarian cancer cells.
The findings highlight that de novo FOXP1 variants are a cause of sporadic intellectual disability and emphasize the importance of this transcription factor in neurodevelopment.
we provide supportive evidence that genetic variants at FOXP1, BARX1 (show BARX1 Antibodies), and FOXF1 (show FOXF1 Antibodies) confer risk for the development of EAC (show CYLD Antibodies).
Cell-line derived FOXP1 target genes that were highly correlated with FOXP1 expression in primary DLBCL accurately segregated the corresponding clinical subtypes of a large cohort of primary DLBCL isolates
S1PR2 (show S1PR2 Antibodies) is repressed by FOXP1 in activated B-cell and germinal center B-cell DLBCL cell lines with aberrantly high FOXP1 levels; S1PR2 (show S1PR2 Antibodies) expression is further inversely correlated with FOXP1 expression in 3 DLBCL patient cohorts.
FOXP1 represents a novel regulator of genes targeted by the class II MHC (show HLAE Antibodies) transactivator CIITA (show CIITA Antibodies) and CD74 (show CD74 Antibodies).
FOXP1 - novel candidate genes validated in a large case-control sample of schizophrenia.
Studied the expression of FOXP1 in colorectal cancer and its potential associations with outcome in colorectal cancer.
Authors identified forkhead box protein P1 (FOXP1) as a direct target of miR (show MLXIP Antibodies)-504 using microarray analysis and a luciferase assay.
En1 (show EN1 Antibodies)-null cells also fail to express the transcription factor FoxP1, suggesting that FoxP1 lies downstream of En1 (show EN1 Antibodies).
The response of CPLX1 (show CPLX1 Antibodies) and Foxp1 levels to SNCA (show SNCA Antibodies) deficiency supports the notion that these factors are regulated by altered physiological function of alpha-synuclein (show SNCA Antibodies).
These results identify a previously unrecognized role for FOXP1 in the transcriptional control of hepatic glucose homeostasis.
results demonstrate critical roles of Foxp1 in the radial migration and morphogenesis of cortical neurons during development.
a novel role for Foxp1 in controlling HFSC proliferation with cellular dynamic location in response to oxidative stress during hair cycling
Collectively, these findings reveal an important role for the FOXP1, 2, and 4 proteins in governing postnatal alpha cell expansion and function.
Foxp1 mediates programming of limb-innervating motor neurons from mouse and human embryonic stem cells.
Foxp1/2/4 may regulate Runx2 (show RUNX2 Antibodies) during endochondral ossification.
The results unveil a fundamental mechanism of T cell unresponsiveness different from anergy or exhaustion, driven by TGF-beta (show TGFB1 Antibodies) signaling on tumor-associated lymphocytes undergoing Foxp1-dependent transcriptional regulation.
Foxp1 also dampened expression of the costimulatory molecule (show CD276 Antibodies) ICOS (show ICOS Antibodies) and its downstream signaling at early stages of T cell activation
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. Forkhead box P1 protein contains both DNA-binding- and protein-protein binding-domains. This gene may act as a tumor suppressor as it is lost in several tumor types and maps to a chromosomal region (3p14.1) reported to contain a tumor suppressor gene(s). Alternative splicing results in multiple transcript variants encoding different isoforms.
forkhead box P1
, forkhead box protein P1-B
, forkhead box protein P1-like
, forkhead box protein P1
, fork head-related protein like B
, glutamine-rich factor 1
, forkhead-related transcription factor 1