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Rabbit Anti-FOXP1 Recombinant Antibody (CBXF-0872) (CBMAB-F1401-CQ)

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Summary

Host Animal
Rabbit
Specificity
Human, Mouse, Rat, Monkey
Clone
CBXF-0872
Antibody Isotype
IgG
Application
FC

Basic Information

Specificity
Human, Mouse, Rat, Monkey
Antibody Isotype
IgG
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
Forkhead Box P1
Introduction
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.
Entrez Gene ID
Human27086
Mouse108655
Rat297480
Monkey694726
UniProt ID
HumanQ9H334
MouseP58462
RatQ498D1
MonkeyA0A2K5X1C6
Alternative Names
Forkhead Box P1; Fork Head-Related Protein Like B; Mac-1-Regulated Forkhead; Glutamine-Rich Factor 1; MFH; PAX5/FOXP1 Fusion Protein;
Function
Transcriptional repressor (PubMed:18347093, PubMed:26647308).

Can act with CTBP1 to synergistically repress transcription but CTPBP1 is not essential (By similarity).

Plays an important role in the specification and differentiation of lung epithelium. Acts cooperatively with FOXP4 to regulate lung secretory epithelial cell fate and regeneration by restricting the goblet cell lineage program; the function may involve regulation of AGR2. Essential transcriptional regulator of B-cell development. Involved in regulation of cardiac muscle cell proliferation. Involved in the columnar organization of spinal motor neurons. Promotes the formation of the lateral motor neuron column (LMC) and the preganglionic motor column (PGC) and is required for respective appropriate motor axon projections. The segment-appropriate generation of spinal chord motor columns requires cooperation with other Hox proteins. Can regulate PITX3 promoter activity; may promote midbrain identity in embryonic stem cell-derived dopamine neurons by regulating PITX3. Negatively regulates the differentiation of T follicular helper cells T(FH)s. Involved in maintenance of hair follicle stem cell quiescence; the function probably involves regulation of FGF18 (By similarity).

Represses transcription of various pro-apoptotic genes and cooperates with NF-kappa B-signaling in promoting B-cell expansion by inhibition of caspase-dependent apoptosis (PubMed:25267198).

Binds to CSF1R promoter elements and is involved in regulation of monocyte differentiation and macrophage functions; repression of CSF1R in monocytes seems to involve NCOR2 as corepressor (PubMed:15286807, PubMed:18799727, PubMed:18347093).

Involved in endothelial cell proliferation, tube formation and migration indicative for a role in angiogenesis; the role in neovascularization seems to implicate suppression of SEMA5B (PubMed:24023716).

Can negatively regulate androgen receptor signaling (PubMed:18640093).

Acts as a transcriptional activator of the FBXL7 promoter; this activity is regulated by AURKA (PubMed:28218735).
Isoform 8:
Involved in transcriptional regulation in embryonic stem cells (ESCs). Stimulates expression of transcription factors that are required for pluripotency and decreases expression of differentiation-associated genes. Has distinct DNA-binding specifities as compared to the canonical form and preferentially binds DNA with the sequence 5'-CGATACAA-3' (or closely related sequences) (PubMed:21924763).

Promotes ESC self-renewal and pluripotency (By similarity).
Biological Process
Cellular response to DNA damage stimulus Source: ARUK-UCL
Endothelial cell activation Source: UniProtKB
Macrophage activation Source: UniProtKB
Monocyte activation Source: UniProtKB
Negative regulation of androgen receptor signaling pathway Source: UniProtKB
Negative regulation of B cell apoptotic process Source: UniProtKB
Negative regulation of gene expression Source: ARUK-UCL
Negative regulation of transcription, DNA-templated Source: UniProtKB
Negative regulation of transcription by RNA polymerase II Source: GO_Central
Osteoclast development Source: UniProtKB
Osteoclast differentiation Source: UniProtKB
Positive regulation of B cell receptor signaling pathway Source: ARUK-UCL
Positive regulation of endothelial cell migration Source: UniProtKB
Positive regulation of interleukin-21 production Source: UniProtKB
Positive regulation of smooth muscle cell proliferation Source: UniProtKB
Regulation of chemokine (C-X-C motif) ligand 2 production Source: UniProtKB
Regulation of defense response to bacterium Source: UniProtKB
Regulation of endothelial tube morphogenesis Source: UniProtKB
Regulation of gene expression Source: UniProtKB
Regulation of inflammatory response Source: UniProtKB
Regulation of interleukin-12 production Source: UniProtKB
Regulation of interleukin-1 beta production Source: UniProtKB
Regulation of macrophage colony-stimulating factor production Source: UniProtKB
Regulation of monocyte differentiation Source: UniProtKB
Regulation of transcription by RNA polymerase II Source: GO_Central
Regulation of tumor necrosis factor production Source: UniProtKB
Response to lipopolysaccharide Source: UniProtKB
T follicular helper cell differentiation Source: UniProtKB
Cellular Location
Nucleus. Not found in the nucleolus.
Involvement in disease
A chromosomal aberration involving FOXP1 is found in acute lymphoblastic leukemia. Translocation t(9;3)(p13;p14.1) with PAX5.
Mental retardation with language impairment and autistic features (MRLIAF):
A developmental disorder characterized by mild to moderate mental retardation, language impairment, and autistic features. Patients show global delay, delayed walking, severely delayed speech development, and behavioral abnormalities, including irritability, hyperactivity, aggression, and stereotypical rigid behaviors.
More Infomation

Li, H., Han, X., Yang, S., Wang, Y., Dong, Y., & Tang, T. (2021). FOXP1 drives osteosarcoma development by repressing P21 and RB transcription downstream of P53. Oncogene, 40(15), 2785-2802.

Lozano, R., Gbekie, C., Siper, P. M., Srivastava, S., Saland, J. M., Sethuram, S., ... & Kolevzon, A. (2021). FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring. Journal of Neurodevelopmental Disorders, 13(1), 1-18.

Braden, R. O., Amor, D. J., Fisher, S. E., Mei, C., Myers, C. T., Mefford, H., ... & Morgan, A. T. (2021). Severe speech impairment is a distinguishing feature of FOXP1‐related disorder. Developmental Medicine & Child Neurology, 63(12), 1417-1426.

Hu, Z., Cai, M., Zhang, Y., Tao, L., & Guo, R. (2020). miR-29c-3p inhibits autophagy and cisplatin resistance in ovarian cancer by regulating FOXP1/ATG14 pathway. Cell Cycle, 19(2), 193-206.

Wang, S., Zhang, Y., Cai, Q., Ma, M., Jin, L. Y., Weng, M., ... & Quan, Z. (2019). Circular RNA FOXP1 promotes tumor progression and Warburg effect in gallbladder cancer by regulating PKLR expression. Molecular cancer, 18(1), 1-15.

Cherubini, A., Barilani, M., Rossi, R. L., Jalal, M. M. K., Rusconi, F., Buono, G., ... & Lazzari, L. (2019). FOXP1 circular RNA sustains mesenchymal stem cell identity via microRNA inhibition. Nucleic Acids Research, 47(10), 5325-5340.

Zhuang, T., Liu, J., Chen, X., Zhang, L., Pi, J., Sun, H., ... & Zhang, Y. (2019). Endothelial Foxp1 suppresses atherosclerosis via modulation of Nlrp3 inflammasome activation. Circulation research, 125(6), 590-605.

Ren, J., Han, L., Tang, J., Liu, Y., Deng, X., Liu, Q., ... & Wang, H. (2019). Foxp1 is critical for the maintenance of regulatory T-cell homeostasis and suppressive function. PLoS Biology, 17(5), e3000270.

Sheng, H., Li, X., & Xu, Y. (2019). Knockdown of FOXP1 promotes the development of lung adenocarcinoma. Cancer biology & therapy, 20(4), 537-545.

Konopacki, C., Pritykin, Y., Rubtsov, Y., Leslie, C. S., & Rudensky, A. Y. (2019). Transcription factor Foxp1 regulates Foxp3 chromatin binding and coordinates regulatory T cell function. Nature immunology, 20(2), 232-242.

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For research use only. Not intended for any clinical use.

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