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PE/Cyanine7 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_PECyanine7_CD279_Antibody_1_061324
Con-A and IL-2 stimulated (3 days) C57BL/6 mouse splenocytes were stained with anti-mouse CD3ε FITC (clone 145-2C11) and anti-mouse CD279 (PD-1) (clone 29F.1A12) PE/Cyanine7 (left) or rat IgG2a, κ PE/Cyanine7 isotype control (right).
  • 29F-1A12_PECyanine7_CD279_Antibody_1_061324
    Con-A and IL-2 stimulated (3 days) C57BL/6 mouse splenocytes were stained with anti-mouse CD3ε FITC (clone 145-2C11) and anti-mouse CD279 (PD-1) (clone 29F.1A12) PE/Cyanine7 (left) or rat IgG2a, κ PE/Cyanine7 isotype control (right).
Compare all formats See PE/Cyanine7 spectral data
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135215 25 µg 104€
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135216 100 µg 278€
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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 (pdf)

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 PE/Cyanine7 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
Blue Laser (488 nm)
Green Laser (532 nm)/Yellow-Green Laser (561 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. Zimmerman SM, et al. 2022. Oncogene. 41:4983. PubMed
  2. Lao L, et al. 2023. Cancer Immunol Res. 11:320. PubMed
  3. Read KA, et al. 2023. Nat Commun. 14:1652. PubMed
  4. Pankhurst TE, et al. 2023. Cell Rep. 42:112310. PubMed
  5. Zhang YN, et al. 2023. Nat Commun. 14:1985. PubMed
  6. Sandu I, et al. 2020. Nat Commun. 11:4454. PubMed
  7. Liu J, et al. 2021. Front Immunol. 12:747730. PubMed
  8. Campisi L, et al. 2022. Nature. 606:945. PubMed
  9. Dölz M, et al. 2022. iScience. 25:105372. PubMed
  10. Edwards SC, et al. 2023. J Exp Med. 220: . PubMed
  11. Yeh CH, et al. 2022. Immunity. 55:272. PubMed
  12. Logan K Smith et al. 2018. Immunity. 48(2):299-312 . PubMed
  13. Aggen DH, et al. 2020. Clin Cancer Res. . PubMed
  14. Wang L, et al. 2019. Cell Rep. 29:1848. PubMed
  15. Wei H, et al. 2021. Malar J. 20:89. PubMed
  16. Zhang J, et al. 2021. MedComm (Beijing). 2:256. PubMed
  17. Liang S, et al. 2022. Acta Pharm Sin B. 12:2494. PubMed
  18. Mogilenko DA, et al. 2020. Immunity. 54(1):99-115.e12. PubMed
  19. Shi B, et al. 2018. J Immunol. 200:586. PubMed
  20. Delacher M, et al. 2021. Immunity. 54(4):702-720.e17. PubMed
  21. Browning LM, et al. 2020. Cell Rep. 33:108219. PubMed
  22. Choi H et al. 2019. Cell Rep. 27(3):806-819 . PubMed
  23. Wiede F, et al. 2021. Cancer Discov. Online ahead of print. PubMed
  24. Wu J, et al. 2020. Sci Adv. 6:eaba3458. PubMed
  25. Saumyaa, et al. 2016. J Immunol. 196: 3677 - 3685. PubMed
  26. Cassidy BR, et al. 2020. J Neuroinflammation. 17:259. PubMed
  27. Kelsey E Sivick et al. 2018. Cell reports. 25(11):3074-3085 . PubMed
  28. Saumyaa S, et al. 2013. Infect Immun . 81:3426. PubMed
  29. Grzelak A, et al. 2018. Int J Mol Sci. 19:. PubMed
  30. Yue X, et al. 2019. Nat Commun. 10:2011. PubMed
  31. Srivastava S, et al. 2019. Cancer Cell. 35:489. PubMed
  32. Cervera–Carrascon V, et al. 2020. Oncoimmunology. 9:1761229. PubMed
  33. Kennedy EM, et al. 2022. Nat Commun. 13:5907. PubMed
  34. Watanabe M, et al. 2020. Nat Commun. 4.808333333. PubMed
  35. Mirando AC, et al. 2020. Oncoimmunology. 9:1760685. PubMed
  36. Ullrich L, et al. 2021. Front Immunol. 12:729607. PubMed
  37. Moore MJ et al. 2018. eLife. 7 pii: e33057. PubMed
  38. Blanchard L, et al. 2022. STAR Protoc. 3:101444. PubMed
  39. Lou Y, et al. 2021. Int J Mol Sci. 22:. PubMed
  40. Moguche AO et al. 2017. Cell host & microbe. 21(6):695-706 . PubMed
  41. Sandu I, et al. 2020. Cell Reports. 32(8):108078. PubMed
  42. Dong X, et al. 2022. Front Immunol. 13:896472. PubMed
  43. Stephens WZ, et al. 2021. Cell Rep. 37:109916. PubMed
  44. Zhang YN, et al. 2021. Sci Adv. 7:eabj3107. PubMed
  45. Zeis P, et al. 2020. Immunity. 53:775. PubMed
  46. Burton B, et al. 2014. Nat Commun. 5:4741. PubMed
  47. Yermanos A, et al. 2020. Front Immunol. 1.143055556. PubMed
  48. Skadow M, et al. 2019. J Immunol. 203:370. PubMed
  49. Raju S, et al. 2020. Cell Reports. 29(9):2556-2564.e3.. PubMed
  50. Hu J, et al. 2022. J Immunother Cancer. 10:. PubMed
  51. Baumann D, et al. 2020. Nat Commun. 1.969444444. PubMed
  52. Tian D, et al. 2019. Nat Commun. 10:4246. PubMed
  53. Xu W, et al. 2021. Immunity. 54(3):526-541.e7. PubMed
  54. Sheriff L, et al. 2022. STAR Protoc. 11:. PubMed
  55. Srivastava S, et al. 2020. Cancer Cell. 39(2):193-208.e10. PubMed
  56. Guo Y, et al. 2021. Nat Immunol. 22:746. PubMed
  57. NB M, et al. 2017. J Immunol. 198:1142-1155. PubMed
  58. Liang Z, et al. 2022. iScience. 25:105233. PubMed
  59. Trindade BC, et al. 2021. Immunity. 54:2273. PubMed
  60. Liu Y, et al. 2021. Nat Commun. 12:6831. PubMed
RRID
AB_10689635 (BioLegend Cat. No. 135215)
AB_10689635 (BioLegend Cat. No. 135216)

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
UniProt
View information about CD279 on UniProt.org

Related FAQs

There are no FAQs for this product.

Other Formats

View All PD-1 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: 3    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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