AdipoGen Life Sciences

anti-FOXP3 (mouse), mAb (MF333F)

CHF 250.00
In stock
AG-20A-0025Y-C05050 µgCHF 250.00
AG-20A-0025Y-C100100 µgCHF 360.00

Replaces Item #AG-20A-0025

More Information
Product Details
Synonyms Forkhead Box Protein P3; Scurfin
Product Type Monoclonal Antibody
Properties
Clone MF333F
Isotype Rat IgG2aκ
Source/Host Purified from concentrated hybridoma tissue culture supernatant.
Immunogen/Antigen Recombinant mouse FOXP3.
Application

ELISA: (direct or indirect: 1:2'000-1:10'000)
Immunocytochemistry
Immunohistochemistry (1:50-1:100, frozen or paraffin sections)
Western blot: (1:2'000-1:5'000 using ECL. Suggested blocking and dilution buffer is TBST with 0.05% Tween 20 and 5% skim milk. Suggested incubation time is 1 hour at rooom temperature).
Optimal conditions should be determined individually for each application.

Crossreactivity Mouse
Specificity

Recognizes mouse FOXP3. Detects a band of ~46-49kDa by Western blot.

Purity ≥95% (SDS-PAGE)
Purity Detail Protein G-affinity purified.
Concentration 1mg/ml
Formulation Liquid. 0.2μm-filtered solution in PBS, pH 7.4. Contains no preservatives.
Isotype Negative Control

Rat IgG2a Isotype Control

Other Product Data

Uniprot: FOXP3 (mouse)

Accession Number Q99JB6
RRID AB_2490107
Shipping and Handling
Shipping BLUE ICE
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice After opening, prepare aliquots and store at -20°C.
Avoid freeze/thaw cycles.
Use/Stability Stable for at least 1 year after receipt when stored at -20°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description

FOXP3 is involved in immune system responses. It functions as the master regulator in the development and function of regulatory T cells. FOX proteins belong to the forkhead/winged-helix family of transcriptional regulators and are presumed to exert control via similar DNA binding interactions during transcription. Defects in FOXP3 are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX); also known as X-linked autoimmunity-immunodeficiency syndrome. IPEX is characterized by neonatal onset insulin-dependent diabetes mellitus, infections, secretory diarrhea, trombocytopenia, anemia and eczema.

Product References
  1. Alternatively activated dendritic cells preferentially secrete IL-10, expand Foxp3+CD4+ T cells, and induce long-term organ allograft survival in combination with CTLA4-Ig: Y.Y. Lan, et al.; J. Immunol. 177, 5868 (2006)
  2. Dendritic cells expressing transgenic galectin-1 delay onset of autoimmune diabetes in mice: M.J. Perone, et al.; J. Immunol. 177, 5278 (2006)
  3. Immunosurveillance of Erbb2 carcinogenesis in transgenic mice is concealed by a dominant regulatory T-cell self-tolerance: E. Ambrosino, et al.; Cancer Res. 66, 7734 (2006)
  4. Regulated compartmentalization of programmed cell death-1 discriminates CD4+CD25+ resting regulatory T cells from activated T cells: G. Raimondi, et al.; J. Immunol. 176, 2808 (2006)
  5. Antimetastatic activity of a preventive cancer vaccine: P. Nanni, et al.; Cancer Res. 67, 11037 (2007)
  6. Rapamycin-conditioned dendritic cells are poor stimulators of allogeneic CD4+ T cells, but enrich for antigen-specific Foxp3+ T regulatory cells and promote organ transplant tolerance: H.R. Turnquist, et al.; J. Immunol. 178, 7018 (2007)
  7. Pretransplant infusion of mesenchymal stem cells prolongs the survival of a semiallogeneic heart transplant through the generation of regulatory T cells: F. Casiraghi, et al.; J. Immunol. 181, 3933 (2008)
  8. Suppression of autoimmune diabetes by soluble galectin-1: M.J. Perone, et al.; J. Immunol. 182, 2641 (2009)
  9. Protective role for TLR4 signaling in atherosclerosis progression as revealed by infection with a common oral pathogen: C. Hayashi, et al.; J. Immunol. 189, 3681 (2012)
  10. Acceleration of diabetes development in CXC chemokine receptor 3 (CXCR3)-deficient NOD mice: Y. Yamada, et al.; Diabetologia 55, 2238 (2012)
  11. Characteristics of CD4 + CD25 + Foxp3 + regulatory T cells in patients with multiple organ dysfunction syndrome: X. Zhang, et al.; Exp. Ther. Med. 11, 1908 (2016)
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