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Pacific Blue™ anti-mouse FOXP3 Antibody

Pricing & Availability
Clone
MF-14 (See other available formats)
Regulatory Status
RUO
Other Names
Forkhead box protein P3, Scurfin, JM2, IPEX, Zinc finger protein JM2
Isotype
Rat IgG2b, κ
Ave. Rating
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Product Citations
publications
MF-14_PacBlue_FOXP3_Antibody_ICFC_1_042015
C57BL/6 splenocytes were surface stained with CD4 PE and then treated with True-Nuclear™ Transcription Factor Buffer Set. Cells were then stained with FOXP3 (clone MF-14) Pacific Blue™ (top) or rat IgG2b, κ Pacific Blue™ isotype control (bottom).
  • MF-14_PacBlue_FOXP3_Antibody_ICFC_1_042015
    C57BL/6 splenocytes were surface stained with CD4 PE and then treated with True-Nuclear™ Transcription Factor Buffer Set. Cells were then stained with FOXP3 (clone MF-14) Pacific Blue™ (top) or rat IgG2b, κ Pacific Blue™ isotype control (bottom).
  • MF-14_PacBlue_FOXP3_Antibody_ICFC_2_042015
Compare all formats See Pacific Blue™ spectral data
Cat # Size Price Quantity Check Availability Save
126409 25 µg £129
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126410 100 µg £254
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Description

FOXP3 is a 47 kD transcription factor, also known as Forkhead box protein P3, Scurfin, JM2, or IPEX. It is proposed to be a master regulatory gene and more specific marker of T regulatory cells than most cell surface markers (such as CD4 and CD25). Transduced expression of FOXP3 in CD4+/CD25- cells has been shown to induce GITR, CD103, and CTLA4 and impart a T regulatory cell phenotype. FOXP3 is mutated in X-linked autoimmunity-allergic dysregulation syndrome (XLAAD or IPEX) in humans and in "scurfy" mice. Overexpression of FOXP3 has been shown to lead to a hypoactive immune state suggesting that this transcriptional factor is a central regulator of T cell activity.

Product Details
Technical Data Sheet (pdf)

Product Details

Verified Reactivity
Mouse
Antibody Type
Monoclonal
Host Species
Rat
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
Preparation
The antibody was purified by affinity chromatography, and conjugated with Pacific Blue™ under optimal conditions.
Concentration
0.5 mg/ml
Storage & Handling
The antibody solution should be stored undiluted between 2°C and 8°C, and protected from prolonged exposure to light. Do not freeze.
Application

ICFC - Quality tested
Recommended Usage

Each lot of this antibody is quality control tested by intracellular flow cytometry using our True-Nuclear™ Transcription Factor Staining Protocol. The suggested use of this reagent is ≤ 1.0 µg per 106 cells in 100 µl volume. It is highly recommended that the reagent be titrated for optimal performance for each application.

* Pacific Blue™ has a maximum emission of 455 nm when it is excited at 405 nm. Prior to using Pacific Blue™ conjugate for flow cytometric analysis, please verify your flow cytometer's capability of exciting and detecting the fluorochrome.


Alexa Fluor® and Pacific Blue™ are trademarks of Life Technologies Corporation.

View full statement regarding label licenses
Excitation Laser
Violet Laser (405 nm)
Application Notes

NOTE: For flow cytometric staining with this clone, True-Nuclear™ Transcription Factor Buffer Set (Cat. No. 424401) offers improved staining and is highly recommended.

Application References

(PubMed link indicates BioLegend citation)
  1. Ono M, et al. 2007. Nature 446:685.
  2. Hori S, et al. 2003. Science 299:1057.
  3. Fontenot JD, et al. 2003 Nature Immunol 4:330.
  4. Fallarino F, et al. 2009. J. Immunol. 183:6033. PubMed
  5. Barber A, et al. 2009 J. Immunol. 183:6939. PubMed
  6. Nakashima H, et al. 2010. J. Immunol. 184:4637. PubMed
Product Citations
  1. Marchelletta RR, et al. 2021. J Clin Invest. 131:. PubMed
  2. Xiong T, et al. 2022. Cancer Sci. 113:1955. PubMed
  3. Chen Q, et al. 2022. Cell Rep. 39:110990. PubMed
  4. Zhang B, et al. 2023. Signal Transduct Target Ther. 8:28. PubMed
  5. van Elsas MJ, et al. 2023. J Immunother Cancer. 11:. PubMed
  6. Zhuang WR, et al. 2023. Nat Commun. 14:1675. PubMed
  7. Zhu C, et al. 2018. Sci Rep. 5.113194444. PubMed
  8. Shears RK, et al. 2020. J Allergy Clin Immunol. 145:1272. PubMed
  9. Hering L, et al. 2021. Int J Mol Sci. 22:. PubMed
  10. Zhang B, et al. 2021. Nat Biomed Eng. 5:1288. PubMed
  11. Pierini A, et al. 2015. J Immunol. 195: 347 - 355. PubMed
  12. Kaur A, et al. 2019. Cancer Discov. 9:64. PubMed
  13. Studniberg SI, et al. 2022. Mol Syst Biol. 18:e10824. PubMed
  14. Pandey S, et al. 2014. J Immunol. 193:3632. PubMed
  15. Echevarría-Vargas IM, et al. 2018. EMBO Mol Med. 10:e8446. PubMed
  16. Chen RJ, et al. 2022. iScience. 25:105595. PubMed
  17. Ouyang S, et al. 2019. J Immunol. 202:1441. PubMed
  18. Qi J, et al. 2021. Nat Commun. 12:4755. PubMed
  19. Tsai HI, et al. 2021. EMBO Mol Med. 13:e12834. PubMed
  20. Zhang C, et al. 2021. J Immunother Cancer. 9:. PubMed
  21. Jeon Y, et al. 2015. PLoS One. 10: e0139845. PubMed
  22. Hering L, et al. 2020. Front Immunol. 1.747222222. PubMed
  23. Sadtler K, et al. 2017. Tissue Eng Part A. 23:1044. PubMed
  24. Chow AK, et al. 2021. Cellular and Molecular Gastroenterology and Hepatology. :. PubMed
  25. Stienne C, et al. 2022. Cell Rep. 38:110553. PubMed
RRID
AB_2105047 (BioLegend Cat. No. 126409)
AB_2105047 (BioLegend Cat. No. 126410)

Antigen Details

Structure
50-55 kd protein. Forkhead/winged-helix transcription factor family, contains zinc finger and forkhead domains.
Distribution

Nuclear; expressed in Treg cells.

Function
Master regulatory gene in Treg cell development, crucial for immune homeostasis.
Interaction
Interacts with DNA
Cell Type
Tregs
Biology Area
Immunology
Molecular Family
Nuclear Markers
Antigen References

1. Ono M, et al. 2007. Nature 446:685.
2. Hori S, et al. 2003. Science 299:1057.
3. Fontenot JD, et al. 2003 Nature Immunol 4:330.

Regulation
Present at high level in T reg cells. Induced by T cell activation.
Gene ID
20371 View all products for this Gene ID
UniProt
View information about FOXP3 on UniProt.org

Related FAQs

Can I stain whole blood with anti-FOXP3 using your Foxp3 staining kit?

It is not recommended. It is best to use PBMCs for this testing.

Can FOXP3 be costained with cytokines?

The larger holes created by the nuclear permeabilization required for FOXP3 may allow cytokines to leak out of the cell, making it harder to detect lowly-expressed cytokines. You may have to use a control where the cells are only permeabilized through the cell membrane.

Go To Top Version: 3    Revision Date: 04/21/2015

For Research Use Only. Not for diagnostic or therapeutic use.

 

This product is supplied subject to the terms and conditions, including the limited license, located at www.biolegend.com/terms) ("Terms") and may be used only as provided in the Terms. Without limiting the foregoing, BioLegend products may not be used for any Commercial Purpose as defined in the Terms, resold in any form, used in manufacturing, or reverse engineered, sequenced, or otherwise studied or used to learn its design or composition without express written approval of BioLegend. Regardless of the information given in this document, user is solely responsible for determining any license requirements necessary for user’s intended use and assumes all risk and liability arising from use of the product. BioLegend is not responsible for patent infringement or any other risks or liabilities whatsoever resulting from the use of its products.

 

BioLegend, the BioLegend logo, and all other trademarks are property of BioLegend, Inc. or their respective owners, and all rights are reserved.

 

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This data display is provided for general comparisons between formats.
Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors.
If you need assistance with selecting the best format contact our expert technical support team.

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