Brilliant Violet 510™ anti-mouse CD3 Antibody

Pricing & Availability
Clone
17A2 (See other available formats)
Regulatory Status
RUO
Other Names
T cell antigen receptor complex, T3
Isotype
Rat IgG2b, κ
Ave. Rating
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Product Citations
publications
17A2_BV510_CD3_Antibody_FC_082312
C57BL/6 mouse splenocytes were stained with CD3 (clone 17A2) Brilliant Violet 510™.
  • 17A2_BV510_CD3_Antibody_FC_082312
    C57BL/6 mouse splenocytes were stained with CD3 (clone 17A2) Brilliant Violet 510™.
Compare all formats See Brilliant Violet 510™ spectral data
Cat # Size Price Quantity Check Availability Save
100233 125 µL $176
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100234 50 µg $274
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Description

CD3, also known as T3, 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. CD3 is composed of CD3ε, δ, γ and ζ chains. It forms a TCR complex by associating with 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

Verified Reactivity
Mouse
Antibody Type
Monoclonal
Host Species
Rat
Immunogen
γδTCR-positive T-T hybridoma D1
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide and BSA (origin USA).
Preparation
The antibody was purified by affinity chromatography and conjugated with Brilliant Violet 510™ under optimal conditions.
Concentration
µg sizes: 0.2 mg/mL
µL sizes: lot-specific (to obtain lot-specific concentration and expiration, please enter the lot number in our Certificate of Analysis online tool.)
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 using the µg size, the suggested use of this reagent is ≤0.5 µg per million cells in 100 µl volume. For flow cytometric staining using the µl size, the suggested use of this reagent is 5 µl per million cells in 100 µl staining volume or 5 µl per 100 µl of whole blood. It is recommended that the reagent be titrated for optimal performance for each application.

Brilliant Violet 510™ excites at 405 nm and emits at 510 nm. The bandpass filter 510/50 nm is recommended for detection, although filter optimization may be required depending on other fluorophores used. Be sure to verify that your cytometer configuration and software setup are appropriate for detecting this channel. Refer to your instrument manual or manufacturer for support. Brilliant Violet 510™ is a trademark of Sirigen Group Ltd.


Learn more about Brilliant Violet™.

This product is subject to proprietary rights of Sirigen Inc. and is made and sold under license from Sirigen Inc. The purchase of this product conveys to the buyer a non-transferable right to use the purchased product for research purposes only. This product may not be resold or incorporated in any manner into another product for resale. Any use for therapeutics or diagnostics is strictly prohibited. This product is covered by U.S. Patent(s), pending patent applications and foreign equivalents.
Excitation Laser
Violet Laser (405 nm)
Application Notes

Additional reported application (for relevant formats) include: spatial biology (IBEX)1,2.

Application References

(PubMed link indicates BioLegend citation)
  1. Radtke AJ, et al. 2020. Proc Natl Acad Sci U S A. 117:33455-65. (SB) PubMed
  2. Radtke AJ, et al. 2022. Nat Protoc. 17:378-401. (SB) PubMed
Product Citations
  1. Cheng C, et al. 2022. Cell Mol Gastroenterol Hepatol. 15:261. PubMed
  2. Bhaskar A, et al. 2023. iScience. 26:106644. PubMed
  3. Yao RQ, et al. 2023. Mil Med Res. 10:27. PubMed
  4. Su Y, et al. 2022. J Hematol Oncol. 15:99. PubMed
  5. Orvain C, et al. 2022. Arthritis Res Ther. 24:13. PubMed
  6. Liang Y, et al. 2022. Theranostics. 12:7729. PubMed
  7. Yang H, et al. 2023. Cell Death Differ. 30:560. PubMed
  8. Takacs GP, et al. 2023. Front Immunol. 13:993444. PubMed
  9. Zhang B, et al. 2023. Signal Transduct Target Ther. 8:28. PubMed
  10. Reticker-Flynn NE, et al. 2022. Cell. 185:1924. PubMed
  11. Lechuga-Vieco AV, et al. 2020. Sci Adv. 6:eaba5345. PubMed
  12. Platt DJ, et al. 2021. Cell Reports. 35(6):109113. PubMed
  13. Wang L, et al. 2019. Cell Rep. 29:1848. PubMed
  14. Hirata Y et al. 2018. Cell stem cell. 22(3):445-453 . PubMed
  15. Stegelmeier AA, et al. 2022. Biomedicines. 10:. PubMed
  16. Zhang YS, et al. 2018. Cancer Biol Ther. 19:735. PubMed
  17. Feizi N, et al. 2021. Cell Death Dis. 12:1026. PubMed
  18. Menzel L, et al. 2021. Cell Rep. 37:109878. PubMed
  19. Delacher M, et al. 2021. Immunity. 54(4):702-720.e17. PubMed
  20. Reyes RM, et al. 2021. Oncoimmunology. 10:2006529. PubMed
  21. Xiong A, et al. 2022. EBioMedicine. 83:104239. PubMed
  22. Okamoto T, et al. 2020. Cancer Res. 3580:80. PubMed
  23. Qiu F, et al. 2022. J Cancer. 13:2893. PubMed
  24. Ciecko AE, et al. 2019. Cell Rep. 29:3073. PubMed
  25. Kuhn NF, et al. 2020. Nat Commun. 4.74375. PubMed
  26. Bittner–Eddy PD, et al. 2017. Front Immunol. 1.304166667. PubMed
  27. Zhang B, et al. 2021. Nat Biomed Eng. 5:1288. PubMed
  28. Wang F, et al. 2018. Carcinogenesis. 39:889. PubMed
  29. Hu Y, et al. 2022. J Nanobiotechnology. 20:417. PubMed
  30. Mara AB, et al. 2022. NPJ Vaccines. 7:86. PubMed
  31. Sordé L, et al. 2017. Immunity, Inflammation, and Disease. 10.1002/iid3.167. PubMed
  32. Landon J Edgar et al. 2018. Cell chemical biology. 26(1):131-136 . PubMed
  33. Hombrink P, et al. 2016. Nat Immunol. 17:1467-1478. PubMed
  34. Wijewarnasuriya D, et al. 2020. Cancer Immunol Res. 0.841666667. PubMed
  35. Cabrera-Perez J, et al. 2016. J Immunol. 197: 1692 - 1698. PubMed
  36. Cabrera-Perez C, et al. 2015. J Immunol . 194:1609-20. PubMed
  37. Lu YJ, et al. 2021. Cell Rep. 36:109696. PubMed
  38. Fernández-Orth J, et al. 2020. Eur J Immunol. . PubMed
  39. Heil J, et al. 2021. Nat Commun. 12:6963. PubMed
  40. Cerina M, et al. 2017. Brain Behav Immun. 59:103-117. PubMed
  41. Bahmani B, et al. 2021. Nat Commun. 12:1999. PubMed
  42. Hu Y, et al. 2021. J Nanobiotechnology. 19:416. PubMed
  43. Li X, et al. 2021. Front Immunol. 12:779560. PubMed
  44. Yang F, et al. 2021. Nat Commun. 12:3424. PubMed
  45. Ren X, et al. 2021. Cell Death Dis. 12:484. PubMed
RRID
AB_2561387 (BioLegend Cat. No. 100233)
AB_2561387 (BioLegend Cat. No. 100234)

Antigen Details

Structure
Ig superfamily, CD3/TCR, 20 kD
Distribution

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

Function
Antigen recognition, TCR signal transduction, T cell activation
Ligand/Receptor
Peptide antigen/MHC-complex
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
12502 View all products for this Gene ID
Specificity (DOES NOT SHOW ON TDS):
CD3
Specificity Alt (DOES NOT SHOW ON TDS):
CD3
App Abbreviation (DOES NOT SHOW ON TDS):
FC
UniProt
View information about CD3 on UniProt.org

Other Formats

View All CD3 Reagents Request Custom Conjugation
Description Clone Applications
FITC anti-mouse CD3 17A2 FC
PE anti-mouse CD3 17A2 FC
Purified anti-mouse CD3 17A2 FC,IHC-F,IP,ICC
Alexa Fluor® 647 anti-mouse CD3 17A2 FC,IHC-F,3D IHC,SB
Alexa Fluor® 488 anti-mouse CD3 17A2 FC,IHC-F,3D IHC
Pacific Blue™ anti-mouse CD3 17A2 FC
Alexa Fluor® 700 anti-mouse CD3 17A2 FC
PerCP/Cyanine5.5 anti-mouse CD3 17A2 FC
PE/Cyanine7 anti-mouse CD3 17A2 FC
APC/Cyanine7 anti-mouse CD3 17A2 FC
Brilliant Violet 421™ anti-mouse CD3 17A2 FC,ICC
Brilliant Violet 570™ anti-mouse CD3 17A2 FC
Brilliant Violet 650™ anti-mouse CD3 17A2 FC
Brilliant Violet 785™ anti-mouse CD3 17A2 FC
Brilliant Violet 510™ anti-mouse CD3 17A2 FC
APC anti-mouse CD3 17A2 FC
Ultra-LEAF™ Purified anti-mouse CD3 17A2 FC,IHC-F,IP,ICC
Brilliant Violet 605™ anti-mouse CD3 17A2 FC
Alexa Fluor® 594 anti-mouse CD3 17A2 IHC-F,FC,3D IHC,SB
Brilliant Violet 711™ anti-mouse CD3 17A2 FC
Biotin anti-mouse CD3 17A2 FC,IHC-F
PE/Dazzle™ 594 anti-mouse CD3 17A2 FC
APC/Fire™ 750 anti-mouse CD3 17A2 FC
Brilliant Violet 750™ anti-mouse CD3 17A2 FC
TotalSeq™-A0182 anti-mouse CD3 17A2 PG
TotalSeq™-B0182 anti-mouse CD3 17A2 PG
Spark Blue™ 550 anti-mouse CD3 17A2 FC
Spark NIR™ 685 anti-mouse CD3 17A2 FC
TotalSeq™-C0182 anti-mouse CD3 17A2 PG
APC/Fire™ 810 anti-mouse CD3 17A2 FC
PE/Fire™ 640 anti-mouse CD3 17A2 FC
Spark YG™ 570 anti-mouse CD3 17A2 IHC-F
PE/Fire™ 700 anti-mouse CD3 17A2 FC
PE/Cyanine5 anti-mouse CD3 17A2 FC
Spark Blue™ 574 anti-mouse CD3 Antibody 17A2 FC
Spark Violet™ 423 anti-mouse CD3 17A2 FC
PE/Fire™ 810 anti-mouse CD3 17A2 FC
Spark Red™ 718 anti-mouse CD3 17A2 FC
Spark UV™ 387 anti-mouse CD3 17A2 FC
Go To Top Version: 1    Revision Date: 11/30/2012

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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