Human FoxP1 Antibody Summary
Leu231-Gly420
Accession # Q9H334
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of Human FoxP1 by Western Blot. Western blot shows lysates of Daudi human Burkitt's lymphoma cell line. Gels were loaded with 30 µg of whole cell lysate (WCL), 20 µg of cytoplasmic (Cyto), and 10 µg of nuclear extracts (Nuc). PVDF membrane was probed with 1 µg/mL Goat Anti-Human FoxP1 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF4534) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (Catalog # HAF017). A specific band for FoxP1 was detected at approximately 82 - 90 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: FoxP1
Forkhead Box P1 (FOXP1) is a member of the FOX family of transcription factors. FoxP1 has been implicated in cardiac, lung, and lymphocyte development. FoxP1 knock out mice die at embryonic day 14.5 due to heart valve and outflow tract abnormalities. FoxP1 contains both a DNA binding domain as well as protein-protein interaction domains. FoxP1 can homo or heterodimeize with FoxP2 and FoxP4, with dimerization necessary for DNA binding. FoxP1 shows both oncogenic and tumor suppressive characteristics. Overexpression in lymphomas leads to poor prognosis, whereas, loss of FoxP1 in breast cancer also implicates a poor prognosis.
Product Datasheets
Citations for Human FoxP1 Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Citations: Showing 1 - 7
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Single-cell transcriptomic analysis reveals diversity within mammalian spinal motor neurons
Authors: ES Liau, S Jin, YC Chen, WS Liu, M Calon, S Nedelec, Q Nie, JA Chen
Oncogene, 2023-01-03;14(1):46.
Species: Mouse
Sample Types: Embryos
Applications: IHC -
Onecut-dependent Nkx6.2 transcription factor expression is required for proper formation and activity of spinal locomotor circuits
Authors: M Toch, A Harris, O Schakman, E Kondratska, JL Boulland, N Dauguet, S Debrulle, C Baudouin, M Hidalgo-Fi, A Gow, JC Glover, F Tissir, F Clotman
Sci Rep, 2020-01-22;10(1):996.
Species: Mouse
Sample Types: Whole Cells
Applications: Flow Cytometry -
The Onecut Transcription Factors Regulate Differentiation and Distribution of Dorsal Interneurons during Spinal Cord Development
Authors: KU Kabayiza, G Masgutova, A Harris, V Rucchin, B Jacob, F Clotman
Front Mol Neurosci, 2017-05-26;10(0):157.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC -
The role of Sema3-Npn-1 signaling during diaphragm innervation and muscle development
J Cell Sci, 2016-07-27;0(0):.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC-Fr -
Fasciculation and Guidance of Spinal Motor Axons in the Absence of FGFR2 Signaling.
Authors: Huettl RE, Haehl T, Huber AB
PLoS ONE, 2012-07-17;7(7):e41095.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC-Fr -
Npn-1 contributes to axon-axon interactions that differentially control sensory and motor innervation of the limb.
Authors: Huettl RE, Soellner H, Bianchi E, Novitch BG, Huber AB
PLoS Biol., 2011-02-22;9(2):e1001020.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC -
Dynamic expression of the Onecut transcription factors HNF-6, OC-2 and OC-3 during spinal motor neuron development.
Neuroscience, 2009-10-02;165(1):116-29.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC-Fr
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