Biotin anti-mouse CD3ε Antibody

Pricing & Availability
Clone
145-2C11 (See other available formats)
Other Names
CD3ε, T3, CD3
Isotype
Armenian Hamster IgG
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Product Citations
publications
145-2C11_Biotin_021606
C57BL/6 mouse splenocytes were stained with biotinylated CD3e (clone 145-2C11) (filled histogram) or Armenian hamster IgG isotype control (open histogram), followed by Sav-PE.
  • 145-2C11_Biotin_021606
    C57BL/6 mouse splenocytes were stained with biotinylated CD3e (clone 145-2C11) (filled histogram) or Armenian hamster IgG isotype control (open histogram), followed by Sav-PE.
Cat # Size Price Quantity Avail. Save
100303 50 µg $35
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100304 500 µg $110
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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

Product Details

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 biotin under optimal conditions. The solution is free of unconjugated biotin.
Concentration
0.5 mg/ml
Storage & Handling
The antibody solution should be stored undiluted between 2°C and 8°C. 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 106 cells in 100 µl. It is recommended that the reagent be titrated for optimal performance for each application.

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. Liao G, et al. 2010. Int Immunol. 1.096527778. PubMed
  2. Ho K, et al. 2014. Cell Death Dis. 5:1518. PubMed
  3. Honda H, et al. 2014. J Leukoc Biol. 96:1087. PubMed
  4. Muro R, et al. 2015. PLoS One. 10:119898. PubMed
  5. Suzuki M, et al. 2015. J Immunol. 195: 1273-1281. PubMed
  6. Matsuzaki Y, et al. 2015. Biomed Rep. 1: 91 - 97. PubMed
  7. Fournier M, Bijl C 2015. Stem Cells Dev. 24: 2413-2422. PubMed
  8. Pearce V, et al. 2015. J Immunol. 195: 3206 - 3217. PubMed
  9. Doisne J, et al. 2015. J Immunol. 195: 3937 - 3945.. PubMed
  10. Lutz J, et al. 2015. Nat Commun. 6: 8575. PubMed
  11. Lim H, et al. 2015. J Immunol. 195: 5432 - 5439. PubMed
  12. Olsson A, et al. 2016. Nature. 10.1038/nature19348. PubMed
  13. Kurkewich J, et al. 2016. PLoS One. 11: 0161468. PubMed
  14. Zysset D, et al. 2016. Nat Commun. 7:13151. PubMed
  15. Bieber K, et al. 2016. Sci Rep. 6:38357. PubMed
  16. Kim O, et al. 2017. Nat Commun. 10.1038/s41467-017-00729-8. PubMed
  17. Bowers E, et al. 2018. Nat Med. 24:95. PubMed
  18. Johnson JL 2018. Immunity. 48:243. PubMed
  19. Smith LK 2018. Immunity. 48:299. PubMed
  20. Tanimura N 2018. Developmental cell. 46:581. PubMed
  21. Giambra V 2018. Cell stem cell. 23:714. PubMed
  22. de Mingo Pulido Á 2018. Cancer cell. 33:60. PubMed
  23. Li Q, et al. 2018. Immunity. 48:258. PubMed
  24. Luo H, et al. 2019. Cell Rep. 26:945. PubMed
  25. Galle-Treger L, et al. 2019. Nat Commun. 10:713. PubMed
  26. Kimball A, et al. 2018. Arterioscler Thromb Vasc Biol. 38:1102. PubMed
  27. Mann M, et al. 2018. Cell Rep. 25:2992. PubMed
  28. Balzano M, et al. 2019. Cell Rep. 26:3257. PubMed
  29. Matsumura T, et al. 2019. Cell Rep. 27:561. PubMed
  30. Goldstein JM, et al. 2019. Cell Rep. 27:1254. PubMed
Publication Library
RRID
AB_312668 (BioLegend Cat. No. 100303)
AB_312669 (BioLegend Cat. No. 100304)

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 CD3e on UniProt.org

Related FAQs

How many biotin molecules are per antibody structure?
We don't routinely measure the number of biotins with our antibody products but the number of biotin molecules range from 3-6 molecules per antibody.
Go To Top Version: 1    Revision Date: 11/30/2012

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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.
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