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APC anti-mouse CD279 (PD-1) Antibody

Pricing & Availability
Clone
29F.1A12 (See other available formats)
Regulatory Status
RUO
Other Names
PD-1, Programmed Death-1, PDCD1
Isotype
Rat IgG2a, κ
Ave. Rating
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Product Citations
publications
29F.1A12 APC_033010
Con-A and IL-2 stimulated C57BL/6 splenocytes (3 days) stained with 29F.1A12 APC
  • 29F.1A12 APC_033010
    Con-A and IL-2 stimulated C57BL/6 splenocytes (3 days) stained with 29F.1A12 APC
Compare all formats See APC spectral data
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135209 25 µg 91€
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135210 100 µg 237€
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Description

CD279, also known as programmed death-1 (PD-1), is a 50-55 kD glycoprotein belonging to the CD28 family of the Ig superfamily. PD-1 is expressed on activated splenic T and B cells and thymocytes. It is induced on activated myeloid cells as well. PD-1 is involved in lymphocyte clonal selection and peripheral tolerance through binding its ligands, B7-H1 (PD-L1) and B7-DC (PD-L2). It has been reported that PD-1 and PD-L1 interactions are critical to positive selection and play a role in shaping the T cell repertoire. PD-L1 negative costimulation is essential for prolonged survival of intratesticular islet allografts.

Product Details
Technical data sheet

Product Details

Verified Reactivity
Mouse
Antibody Type
Monoclonal
Host Species
Rat
Immunogen
PD-1 cDNA followed by PD-1-Ig fusion protein
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
Preparation
The antibody was purified by affinity chromatography, and conjugated with APC under optimal conditions.
Concentration
0.2 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

FC - Quality tested
Recommended Usage

Each lot of this antibody is quality control tested by immunofluorescent staining with flow cytometric analysis. For flow cytometric staining, the suggested use of this reagent is ≤0.25 µg per million cells in 100 µl volume. It is recommended that the reagent be titrated for optimal performance for each application.

Excitation Laser
Red Laser (633 nm)
Application Notes

Additional reported applications (for the relevant formats) include: immunohistochemical staining of acetone-fixed frozen tissue3, in vivo blocking of PD-1 binding to its ligands2,3, and spatial biology (IBEX)5,6.

Application References

(PubMed link indicates BioLegend citation)
  1. Good-Jacobson KL, et al. 2010. Nat. Immunol. 11:535. (FC) PubMed
  2. Lázár-Molnár E, et al. 2008. Proc. Natl. Acad. Sci. USA 105:2658. (Block)
  3. Liang SC, et al. 2003. Eur. J. Immunol. 33:2706. (FC, IHC, Block)
  4. Tobias J, et al. 2020. Front Immunol. 11:895 (FC, ELISA) PubMed
  5. Radtke AJ, et al. 2020. Proc Natl Acad Sci U S A. 117:33455-65. (SB) PubMed
  6. Radtke AJ, et al. 2022. Nat Protoc. 17:378-401. (SB) PubMed
Product Citations
  1. Wu J et al. 2017. Immunity. 47(6):1114-1128 . PubMed
  2. Saha D et al. 2017. Cancer cell. 32(2):253-267 . PubMed
  3. Campisi L, et al. 2022. Nature. 606:945. PubMed
  4. Chen Q, et al. 2022. Cell Rep. 39:110990. PubMed
  5. Backlund C, et al. 2022. Proc Natl Acad Sci U S A. 119:e2204078119. PubMed
  6. Molina MS, et al. 2022. PLoS One. 17:e0273075. PubMed
  7. Zhu J, et al. 2022. Nat Commun. 13:7466. PubMed
  8. Horkova V, et al. 2023. Nat Immunol. 24:174. PubMed
  9. Xiao J, et al. 2023. J Clin Invest. 133: . PubMed
  10. Ivasko SM, et al. 2023. Front Immunol. 13:1023206. PubMed
  11. Friedman D, et al. 2022. J Immunol. 208:1845. PubMed
  12. Xiao X, et al. 2023. Nat Commun. 14:2859. PubMed
  13. Xie J, et al. 2023. Mol Ther Oncolytics. 29:61. PubMed
  14. Qi Z, et al. 2022. Nat Commun. 13:182. PubMed
  15. Wu Q, et al. 2021. Cancer Commun (Lond). Online ahead of prin. PubMed
  16. Xie A et al. 2017. Endocrinology. 158(10):3140-3151 . PubMed
  17. Zhou J, et al. 2019. Immunity. 50:403. PubMed
  18. Lino AC et al. 2018. Immunity. 49(1):120-133 . PubMed
  19. Wang J, et al. 2019. Front Immunol. 9:3157. PubMed
  20. Liu QZ, et al. 2018. Front Immunol. 1.131944444. PubMed
  21. Waide ML, et al. 2020. Cell Rep. 33:108503. PubMed
  22. Smith T, et al. 2014. J Immunol. 193:3409. PubMed
  23. Almshayakhchi R, et al. 2021. Front Oncol. 11:636977. PubMed
  24. Stokes J, et al. 2020. Oncoimmunology. 9:1758011. PubMed
  25. Wei JL, et al. 2021. J Immunother Cancer. 9: . PubMed
  26. Stewart JM, et al. 2020. ACS Biomater Sci Eng. 6:5941. PubMed
  27. Cha SE, et al. 2021. Oncoimmunology. 10:1899469. PubMed
  28. Len-Letelier RA, et al. 2020. Frontiers in Immunology. 11:583382. PubMed
  29. Lasso P, et al. 2020. Front Immunol. 584959:11. PubMed
  30. Imani J, et al. 2021. JCI Insight. 6:. PubMed
  31. Cheng B, et al. 2022. Cancer Commun (Lond). 42:17. PubMed
  32. Ren Y, et al. 2022. J Immunother Cancer. 10:. PubMed
  33. Pilones KA, et al. 2020. Cancer Immunol Res. 8:1054. PubMed
  34. Habib S, et al. 2018. Infect Immun. 86:e00019. PubMed
  35. LaFleur MW, et al. 2019. Nat Commun. 10:1668. PubMed
  36. Shen M, et al. 2022. Nat Cancer. 3:60. PubMed
  37. Webb ER, et al. 2022. iScience. 25:104995. PubMed
  38. Moon S, et al. 2021. J Exp Med. 218:. PubMed
  39. Koikawa K, et al. 2021. Cell. 184:4753. PubMed
  40. Shiozawa S, et al. 2022. iScience. 25:103537. PubMed
  41. Mandal RK, et al. 2021. Cell Reports. 35(6):109094. PubMed
  42. Gong N, et al. 2020. Nat Nanotechnol. 1.35625. PubMed
  43. Onishi M, et al. 2015. J Immunol. 194:2673. PubMed
  44. Wedekind MF, et al. 2021. iScience. 24(7):102759. PubMed
  45. Zheng Y, et al. 2022. J Immunol. 208:501. PubMed
  46. Molina MS, et al. 2021. Front Immunol. 12:699128. PubMed
  47. Montalban-Arques A, et al. 2021. Cell Host Microbe. :. PubMed
  48. Si J, et al. 2020. Cancer Cell. 38(4):551-566.e11. PubMed
  49. Shimba A et al. 2018. Immunity. 48(2):286-298 . PubMed
  50. Di Pilato M, et al. 2021. Cell. 184(17):4512-4530.e22. PubMed
  51. Wagner AK, et al. 2022. iScience. 25:105137. PubMed
  52. Simoni L, et al. 2020. Cell Rep. 33:108330. PubMed
  53. Charlton J, et al. 2015. PLoS One. 10:119200. PubMed
  54. Li M, et al. 2020. J Immunother Cancer. 8:00. PubMed
  55. Yang FM, et al. 2022. Front Immunol. 13:918241. PubMed
RRID
AB_2159183 (BioLegend Cat. No. 135209)
AB_2159183 (BioLegend Cat. No. 135210)

Antigen Details

Structure
A 50-55 kD glycoprotein belonging to the CD28 family of the Ig superfamily.
Distribution

Induced on splenic T and B lymphocytes, thymocytes, and myeloid cells after stimulation.

Function
Involved in lymphocyte clonal selection and peripheral tolerance, prolonged survival of allografts.
Ligand/Receptor
B7-H1 (PD-L1) and B7-DC (PD-L2)
Cell Type
B cells, T cells
Biology Area
Cancer Biomarkers, Immunology, Inhibitory Molecules
Molecular Family
CD Molecules, Immune Checkpoint Receptors
Antigen References

1. Nishimura H, et al. 2001. Science 291:319
2. Agata Y, et al. 1996. Int. Immunol. 8:765
3. Liang SC, et al. 2003. Eur. J. Immunol. 33:2706
4. Barber DL, et al. 2006. Nature 439:682
5. Keir ME, et al. 2005. J. Immunol. 175:7372
6. Koehn BH. et al. 2008. J Immunol. 181:5313

Gene ID
18566 View all products for this Gene ID
Specificity (DOES NOT SHOW ON TDS):
CD279
Specificity Alt (DOES NOT SHOW ON TDS):
CD279
App Abbreviation (DOES NOT SHOW ON TDS):
FC
UniProt
View information about CD279 on UniProt.org

Related FAQs

There are no FAQs for this product.

Other Formats

View All CD279 Reagents Request Custom Conjugation
Description Clone Applications
PE anti-mouse CD279 (PD-1) 29F.1A12 FC
Purified anti-mouse CD279 (PD-1) 29F.1A12 FC,IHC-F,Block,ELISA
PerCP/Cyanine5.5 anti-mouse CD279 (PD-1) 29F.1A12 FC
APC anti-mouse CD279 (PD-1) 29F.1A12 FC
Biotin anti-mouse CD279 (PD-1) 29F.1A12 FC
FITC anti-mouse CD279 (PD-1) 29F.1A12 FC
PE/Cyanine7 anti-mouse CD279 (PD-1) 29F.1A12 FC
Brilliant Violet 421™ anti-mouse CD279 (PD-1) 29F.1A12 FC,SB
Brilliant Violet 605™ anti-mouse CD279 (PD-1) 29F.1A12 FC
APC/Cyanine7 anti-mouse CD279 (PD-1) 29F.1A12 FC
Brilliant Violet 785™ anti-mouse CD279 (PD-1) 29F.1A12 FC
PE/Dazzle™ 594 anti-mouse CD279 (PD-1) 29F.1A12 FC
Alexa Fluor® 647 anti-mouse CD279 (PD-1) 29F.1A12 FC
Brilliant Violet 711™ anti-mouse CD279 (PD-1) 29F.1A12 FC
GoInVivo™ Purified anti-mouse CD279 (PD-1) 29F.1A12 FC
APC/Fire™ 750 anti-mouse CD279 (PD-1) 29F.1A12 FC
Brilliant Violet 510™ anti-mouse CD279 (PD-1) 29F.1A12 FC
Ultra-LEAF™ Purified anti-mouse CD279 (PD-1) 29F.1A12 FC,IHC-F,Block
APC/Fire™ 810 anti-mouse CD279 (PD-1) Antibody 29F.1A12 FC
PE/Fire™ 810 anti-mouse CD279 (PD-1) Antibody 29F.1A12 FC
PE/Cyanine5 anti-mouse CD279 (PD-1) 29F.1A12 FC
PE/Fire™ 640 anti-mouse CD279 (PD-1) 29F.1A12 FC
Spark Red™ 718 anti-mouse CD279 (PD-1) 29F.1A12 FC
PerCP/Fire™ 806 anti-mouse CD279 (PD-1) 29F.1A12 FC
Brilliant Violet 750™ anti-mouse CD279 (PD-1) 29F.1A12 FC
PerCP/Fire™ 780 anti-mouse CD279 (PD-1) 29F.1A12 FC
PE/Fire™ 700 anti-mouse CD279 (PD-1) 29F.1A12 FC
Brilliant Violet 650™ anti-mouse CD279 (PD-1) 29F.1A12 FC
Spark Blue™ 574 anti-mouse CD279 (PD-1) (Flexi-Fluor™) 29F.1A12 FC
Spark PLUS B550™ anti-mouse CD279 (PD-1) 29F.1A12 FC
Go To Top Version: 2    Revision Date: 09.11.2014

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.

 

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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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