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PerCP anti-mouse CD3ε Antibody

Pricing & Availability
Clone
145-2C11 (See other available formats)
Regulatory Status
RUO
Other Names
CD3ε, T3, CD3
Isotype
Armenian Hamster IgG
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Product Citations
publications
145-2C11_PerCP_011508
C57BL/6 mouse splenocytes were stained with CD3e (clone 145-2C11) PerCP (filled histogram) or Armenian hamster IgG PerCP isotype control (open histogram).
  • 145-2C11_PerCP_011508
    C57BL/6 mouse splenocytes were stained with CD3e (clone 145-2C11) PerCP (filled histogram) or Armenian hamster IgG PerCP isotype control (open histogram).
Compare all formats See PerCP spectral data
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100325 25 µg £61
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100326 100 µg £180
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Description

CD3ε is a 20 kD transmembrane protein, also known as CD3 or T3. It is a member of the Ig superfamily and primarily expressed on T cells, NK-T cells, and at different levels on thymocytes during T cell differentiation. CD3ε forms a TCR complex by associating with the CD3δ, γ and ζ chains, as well as the TCR α/β or γ/δ chains. CD3 plays a critical role in TCR signal transduction, T cell activation, and antigen recognition by binding the peptide/MHC antigen complex.

Product Details
Technical Data Sheet (pdf)

Product Details

Verified Reactivity
Mouse
Antibody Type
Monoclonal
Host Species
Armenian Hamster
Immunogen
H-2Kb-specific mouse cytotoxic T lymphocyte clone BM10-37
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
Preparation
The antibody was purified by affinity chromatography, and conjugated with PerCP under optimal conditions.
Concentration
0.2 mg/ml
Storage & Handling
The CD3ε 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 ≤1.0 µg per million cells in 100 µl volume. It is recommended that the reagent be titrated for optimal performance for each application.

* PerCP has a maximum absorption of 482 nm and a maximum emission of 675 nm.

Excitation Laser
Blue Laser (488 nm)
Application Notes

Clone 145-2C11 is useful for in vitro blocking of target-specific CTL-mediated cell lysis1, as well as T cell activation assays, inducing proliferation and cytokine production1,2,7,12,16. It also induces apoptosis in immature thymocytes32,  and in vivo T cell depletion8-10. Additional reported applications (for relevant formats of this clone) include: immunoprecipitation1, immunohistochemical staining14,15 of acetone-fixed frozen sections and zinc-fixed paraffin-embedded sections, Western blotting4, complement-mediated cytotoxicity6, in vitro and in vivo stimulation of T cells1,2,7,12,16, immunofluorescent staining5, and in vivo T cell depletion8-10. The 145-2C11 antibody has been reported to block the binding of 17A2 antibody to CD3 epsilon-specific T cells11. Clone 145-2C11 is not recommended for formalin-fixed paraffin embedded sections. The LEAF™ purified antibody (Endotoxin <0.1 EU/µg, Azide-Free, 0.2 µm filtered) is recommended for functional assays (Cat. No. 100314). For in vivo studies or highly sensitive assays, we recommend Ultra-LEAF™ purified antibody (Cat. No. 100340) with a lower endotoxin limit than standard LEAF™ purified antibodies (Endotoxin <0.01 EU/µg).

Application References

(PubMed link indicates BioLegend citation)
  1. Leo O, et al. 1987. P. Natl. Acad. Sci. USA 84:1374. (IP, Activ, Block)
  2. Kruisbeek AM, et al. 1991. In Current Protocols in Immunology. 3.12.1. (Activ)
  3. Duke RC, et al. 1995. Current Protocols in Immunology. 3.17.1.
  4. Salvadori S, et al. 1994. J. Immunol. 153:5176. (WB)
  5. Payer E, et al. 1991. J. Immunol. 146:2536. (IF)
  6. Jacobs H, et al. 1994. Eur. J. Immunol. 24:934. (CMCD)
  7. Vossen ACTM, et al. 1995. Eur. J. Immunol. 25:1492. (Activ)
  8. Henrickson M, et al. 1995. Transplantation 60:828. (Deplete)
  9. Kinnaert P, et al. 1996. Transpl. Int. 9:386. (Deplete)
  10. Han WR, et al. 1999. Transpl. Immunol. 7:207. (Deplete)
  11. Miescher GC, et al. 1989. Immunol. Lett. 23:113. (Block)
  12. Terrazas LI, et al. 2005. Intl. J. Parasitology. 35:1349. (Activ)
  13. Ko SY, et al. 2005. J. Immunol. 175:3309.
  14. Podd BS, et al. 2006. J. Immunol. 176:6532. (IHC-F)
  15. Tilley SL, et al. 2007. J. Immunol. 178:3208. (IHC-F)
  16. Wang W, et al. 2007. J. Immunol. 178:4885. (Activ)
  17. Xiao S, et al. 2007. J. Exp. Med. 204:1691.
  18. Chappaz S, et al. 2007. Blood doi:10.1182/blood-2007-02-074245. (FC) PubMed.
  19. Curtsinger JM, et al.2005. J. Immunol. 175:4392. PubMed
  20. Guo Y, et al. 2008. Blood 112:480. PubMed
  21. Kenna TJ, et al. 2008. Blood 111:2091.
  22. Perchonock CE, et al. 2007. J. Immunol. 179:1768. PubMed
  23. Perchonock GE, et al. 2006. Mol. Cell. Biol. 26:6005. PubMed
  24. Kanaya T, et al. 2008. Am. J. Physiol. Gastrointest. Liver Physiol. 295:G273. PubMed
  25. de Koning BA, et al. 2006. Int. Immunol. 18:941. PubMed
  26. Schulteis RD, et al. 2008. Blood 295:G273. PubMed
  27. Qi Q, et al. 2009. Blood 114:564. PubMed
  28. Helmersson S, et al. 2013. Am J Pathol. 9440:123. Pubmed
  29. Wu S, et al. 2014. Clin Vaccine Immunol. 21:156. PubMed
  30. Yan J, et al. 2014. Vaccine. 32:2833. PubMed
  31. Guiterrez DA, et al. 2014. Diaebetes. 63:3827. PubMed
  32. Shi YF, et al. 1991. J Immunol. 146:3340. (Apop)
Product Citations
  1. Cha JH et al. 2018. Molecular cell. 71(4):606-620 . PubMed
  2. Xu X, et al. 2020. Chin Med. 15:33. PubMed
  3. Könnecke I, et al. 2014. Bone. 64c:155. PubMed
  4. Cabrera-Mora M, et al. 2016. J Immunol. 197: 2748 - 2761. PubMed
  5. Li P, et al. 2020. J Cell Mol Med. 24:10151. PubMed
  6. Bettke JA, et al. 2022. Infect Immun. 90:e0007022. PubMed
  7. Zhang H, et al. 2022. Eur J Immunol. 52:978. PubMed
  8. Ajay AK, et al. 2022. Cell Rep. 38:110473. PubMed
  9. Li X, et al. 2023. J Clin Invest. 133:. PubMed
  10. Chen F, et al. 2023. Acta Biomater. 164:387. PubMed
  11. Ferrere G, et al. 2021. JCI Insight. 6:. PubMed
  12. Koh CH, et al. 2020. Cancer Immunol Res. 8:698. PubMed
  13. AbuEid M, et al. 2021. iScience. 24(6):102653. PubMed
  14. Iwamoto H et al. 2018. Cell metabolism. 28(1):104-117 . PubMed
  15. Lino AC et al. 2018. Immunity. 49(1):120-133 . PubMed
  16. Xia S, et al. 2014. J Leukoc Biol. 95:733. PubMed
  17. Fasbender F, et al. 2017. Front Immunol. 0.88125. PubMed
  18. Oyarce C, et al. 2018. Front Immunol. 8:1794. PubMed
  19. Neumann AM et al. 2017. PloS one. 12(11):e0187330 . PubMed
  20. Xie X, et al. 2010. Proc Natl Acad Sci U S A. 107:8754. PubMed
  21. Markov SD, et al. 2021. Mol Cancer Ther. 20:2457. PubMed
  22. Mitchell JE, et al. 2021. Cell Reports. 35(2):108966. PubMed
  23. Wang LT, et al. 2021. STAR Protocols. 2(1):100337. PubMed
  24. Hsu JM, et al. 2018. Nat Commun. 9:1908. PubMed
  25. Ma YS, et al. 2021. Mol Ther Oncolytics. 484:20. PubMed
  26. Cha H, et al. 2010. J Immunol. 184:6799. PubMed
  27. Ito C, et al. 2015. PLoS One. 10: e0140808. PubMed
  28. Pérez-Girón J, et al. 2015. J Vis Exp. 100: 52803. PubMed
  29. Chang J, et al. 2010. PLoS One. 5:e12925. PubMed
  30. Liu S, et al. 2020. Cell Host & Microbe. 26(6):779-794.e8.. PubMed
  31. Aguilera M, et al. 2021. Int J Mol Sci. 22:. PubMed
  32. Daneshmandi S, et al. 2021. Elife. 10:. PubMed
  33. Schreiber K, et al. 2020. Cancer Immunol Res. 8:192. PubMed
  34. Murdock BJ, et al. 2021. JCI Insight. 6:. PubMed
  35. Wang LT, et al. 2020. Cell Rep. 32:108188. PubMed
  36. Daneshmandi S, et al. 2021. Cell Reports. 34(10):108831. PubMed
  37. Li Z, et al. 2020. Front Cell Dev Biol. 8:572689. PubMed
  38. Terp MG, et al. 2021. Mol Oncol. 15:3299. PubMed
  39. Li X, et al. 2017. Front Immunol. 8:1186. PubMed
  40. Hering L, et al. 2020. Front Immunol. 1.747222222. PubMed
  41. Nakao R, et al. 2022. NPJ Vaccines. 7:153. PubMed
  42. Arima Y et al. 2017. eLife. 6 pii: e25517. PubMed
  43. Stack G, et al. 2015. PLoS Pathog. 11:1004641. PubMed
  44. Tian T, et al. 2020. Cancer Immunol Res. 660:8. PubMed
RRID
AB_893317 (BioLegend Cat. No. 100325)
AB_893317 (BioLegend Cat. No. 100326)

Antigen Details

Structure
Ig superfamily, forms CD3/TCR complex with CD3δ, γ and ζ subunits and TCR (α/β and γ/δ), 20 kD
Distribution

Thymocytes (differentiation dependent), mature T cells, NK-T cells

Function
TCR signal transduction, T cell activation, antigen recognition
Ligand/Receptor
Peptide antigen/MHC-complex
Cell Type
NKT cells, T cells, Thymocytes, Tregs
Biology Area
Immunology
Molecular Family
CD Molecules, TCRs
Antigen References

1. Barclay A, et al. 1997. The Leukocyte Antigen FactsBook Academic Press.
2. Davis MM. 1990. Annu. Rev. Biochem. 59:475.
3. Weiss A, et al. 1994. Cell 76:263.

Gene ID
12501 View all products for this Gene ID
UniProt
View information about CD3epsilon on UniProt.org

Related FAQs

How stable is PerCP/Cyanine5.5 tandem as compared to PerCP alone?

PerCP/Cyanine5.5 is quite photostable and also better than PerCP alone in withstanding fixation.

Go To Top Version: 1    Revision Date: 11/30/2012

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

 

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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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