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抗Human FOXP1 抗体:
抗Mouse (Murine) FOXP1 抗体:
抗Rat (Rattus) FOXP1 抗体:
Human Monoclonal FOXP1 Primary Antibody for IHC (f), IHC (fro) - ABIN2689508
Brown, Ashe, Leich, Burek, Barrans, Fenton, Jack, Pulford, Rosenwald, Banham: Potentially oncogenic B-cell activation-induced smaller isoforms of FOXP1 are highly expressed in the activated B cell-like subtype of DLBCL. in Blood 2008
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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
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Cow (Bovine) 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
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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
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Mouse (Murine) Monoclonal FOXP1 Primary Antibody for ChIP, EMSA - ABIN2668950
Wang, Lin, Li, Tucker: Multiple domains define the expression and regulatory properties of Foxp1 forkhead transcriptional repressors. in The Journal of biological chemistry 2003
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Human Monoclonal FOXP1 Primary Antibody for ELISA, WB - ABIN565325
Brown, Kagaya, Banham: Characterization of human FOXP1 isoform 2, using monoclonal antibody 4E3-G11, and intron retention as a tissue-specific mechanism generating a novel FOXP1 isoform. in Histopathology 2008
Human Monoclonal FOXP1 Primary Antibody for IHC (fro), IHC (p) - ABIN2473693
Pink, Seidel, Ziegelitz, Correns, Knappe: [TSH base values in thyroid gland functional diagnosis with an improved radioimmunoassay technic]. in Radiobiologia, radiotherapia 1980
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Human Monoclonal FOXP1 Primary Antibody for FACS - ABIN4897665
Gringhuis, Kaptein, Wevers, van der Vlist, Klaver, van Die, Vriend, de Jong, Geijtenbeek: Fucose-based PAMPs prime dendritic cells for follicular T helper cell polarization via DC-SIGN-dependent IL-27 production. in Nature communications 2015
Prominent foxp1 expression is detected in many regions of the developing central nervous system, especially in midbrain-hindbrain boundary, hindbrain, and spinal cord.
MiR (显示 MLXIP 抗体)-92a may act as a tumor inducer in OSCC by suppressing FOXP1 expression.
the varients of FOXP1 and FOXF1 (显示 FOXF1 抗体) genes are functionally associated with oesophageal adenocarcinoma in Chinese population.
Results show that FOXP1 acts as the functional protein of SNHG12. Its expression is regulated by SNHG12 and miR (显示 MLXIP 抗体)-101-3p in glioma cells.
Having a SNP in the FOXP1 gene in the absence of Reflux symptoms had an odds ratio of developing Barrett's esophagus of 1.5.
FOXP1 expression is epigenetically regulated by PRMT5 (显示 PRMT5 抗体).
we have identified a novel de novo missense variant in FOXP1 that is identical to the most well-studied etiological variant in FOXP2 (显示 FOXP2 抗体). Functional characterization revealed clear similarities between these equivalent mutations in terms of their impact on protein function.
FOXP1-related intellectual disability syndrome (ID) is a recognisable entity with wide clinical spectrum and frequent systemic involvement; more ID and neuromotor delay, sensorineural hearing loss and feeding difficulties are more common in patients with interstitial 3p deletions versus patients with monogenic FOXP1 defects; Mutations result in impaired transcriptional repression and/or reduced protein stability
Prognostic value of decreased FOXP1 protein expression in various tumors, is reported.
Blimp1 (显示 PRDM1 抗体), Foxp1 and pStat3 are expressed in extranodal diffuse large B-cell lymphomas
Two rare novel FOXP1 variants associated with a phenotype similar to Mental Retardation with Language Impairment and with or without Autistic Features (MIM (显示 MTSS1 抗体) 613670).
we have shown that the Foxp1 pathway is involved in regulating the migration kinetics of activated CD4 (显示 CD4 抗体)+ T cells toward B cell follicles, indicating that Foxp1 is involved in Tfh cell differentiation from the beginning of a CD4 (显示 CD4 抗体)+ T cell response.
These results identify Foxp1 as a physiological regulator of mature B cell survival mediated in part via the control of Bcl-xl (显示 BCL2L1 抗体) expression and imply that this pathway might contribute to the pathogenic function of aberrant Foxp1 expression in lymphoma.
FOXP1-knockdown in utero reduces NSC differentiation and migration during corticogenesis. FOXP1 represses expression of Notch (显示 NOTCH1 抗体) pathway genes.
Foxp1 has a putative HuR (显示 ELAVL1 抗体) binding sites in the 3' UTR (显示 UTS2R 抗体). HuR (显示 ELAVL1 抗体) suppresses Foxp1 translation during early neocortical neurogenesis (E13). In HuR (显示 ELAVL1 抗体) knockout mice, decreased Foxp1 mRNA was paralleled by increased Foxp1 protein at E13. Phosphorylation sites on HuR (显示 ELAVL1 抗体) act in post-transcriptional regulation of Foxp1.
Study identified the roles of Foxo1 as a positive regulator and Foxp1 as a negative regulator of TH9 cell differentiation and antitumor activity.
deletion of Foxp1 in the developing forebrain leads to impairments in neonatal vocalizations as well as neocortical cytoarchitectonic alterations via neuronal positioning and migration
Foxp1 conditional knock-out (Foxp1(cKO)) mice with loss of Foxp1 in the neocortex and hippocampus display autism and intellectual-disability-relevant behaviors
These results indicate that FOXP1 attenuates MSC (显示 MSC 抗体) senescence by orchestrating their cell-fate switch while maintaining their replicative capacity in a dose- and age-dependent manner.
Although the mutant huntingtin (显示 HTT 抗体) gene is expressed widely, neurons of the striatum and cortex are selectively affected in Huntington's disease (HD). Our results suggest that this selectivity is attributable to the reduced expression of Foxp1, a protein expressed selectively in striatal and cortical neurons that plays a neuroprotective role in these cells.
studies suggest that Foxp1 enforces naive CD8 (显示 CD8A 抗体)(+) T cell quiescence by simultaneously repressing key pathways in both cellular metabolism and cell cycle progression
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