Brilliant Violet 605™ anti-mouse CD69 Antibody

Pricing & Availability
Clone
H1.2F3 (See other available formats)
Regulatory Status
RUO
Other Names
Very Early Activation Antigen (VEA), AIM, EA1, MLR3, gp34/28
Isotype
Armenian Hamster IgG
Ave. Rating
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Product Citations
publications
H1.2F3_BV605_052112
PMA+ionomycin-stimulated (6 hours) C57BL/6 mouse splenocytes were stained with CD69 (clone H1.2F3) Brilliant Violet 605™ (filled histogram).
  • H1.2F3_BV605_052112
    PMA+ionomycin-stimulated (6 hours) C57BL/6 mouse splenocytes were stained with CD69 (clone H1.2F3) Brilliant Violet 605™ (filled histogram).
Compare all formats See Brilliant Violet 605™ spectral data
Cat # Size Price Quantity Check Availability Save
104529 125 µL 172€
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104530 50 µg 210€
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Description

CD69 is a 60 kD type II membrane protein composed of a 27/33 kD disulfide-linked homodimer, also known as Very Early Activation Antigen (VEA), AIM, EA1, MLR3, and gp34/28. It is expressed on a subset of thymocytes and platelets. CD69 is rapidly induced on activated T and B cells, neutrophils, and NK cells. It is a C-type lectin, closely related to the NKR-P1 and Ly-49 NK cell activation molecules. CD69 is involved in the early events of cell activation and thymocyte positive selection.

Product Details
Technical Data Sheet (pdf)

Product Details

Verified Reactivity
Mouse
Antibody Type
Monoclonal
Host Species
Armenian Hamster
Immunogen
Mouse dendritic epidermal T cell line Y245
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 605™ 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 immunofluorescent staining using the µg size, the suggested use of this reagent is ≤0.5 µg per million cells in 100 µl volume. For immunofluorescent 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 605™ excites at 405 nm and emits at 603 nm. The bandpass filter 610/20 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 605™ 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

The H1.2F3 antibody has been reported to augment T cell activation. Additional reported applications (for the relevant formats) include: in vitro T cell and NK cell activation1-3, immunohistochemistry4,5, and immunoprecipitation1.

This antibody has been characterized in the literature as containing a lambda (?) light chain.

Application References
  1. Yokoyama WM, et al. 1988. J. Immunol. 141:369. (IP)
  2. Sobel ES, et al. 1993. J. Immunol. 150:673.
  3. Karlhofer FM, et al. 1991. J. Immunol. 146:3662.
  4. Zhou X, et al. 2005. J. Biol. Chem. 280:31240. (IHC)
  5. Podd BS, et al. 2006. J. Immunol. 176:6532. (IHC)
  6. Lawson BR, et al. 2007. J. Immunol. 178:5366.
  7. Lee JW, et al. 2006. Nature Immunol. 8:181.
  8. Epardaud M, et al. 2008. Cancer Res. 15:2972. PubMed
  9. Jordan JM, et al. 2008. 76:3717. PubMed
  10. Kenna TJ, et al. 2008. Blood 111:2091. PubMed
  11. Ishikawa C, et al. 2013. Biochim Biophys Acta. 167:99. PubMed
Product Citations
  1. Qi X, et al. 2022. FASEB J. 36:e22250. PubMed
  2. Mugarza E, et al. 2022. Sci Adv. 8:eabm8780. PubMed
  3. Scherer S, et al. 2023. Nat Immunol. 24:501. PubMed
  4. Friedman D, et al. 2022. J Immunol. 208:1845. PubMed
  5. Harsha Krovi S, et al. 2020. Nat Commun. 4.790277778. PubMed
  6. Soon MSF, et al. 2020. Nat Immunol. 1.984027778. PubMed
  7. Corria-Osorio J, et al. 2023. Nat Immunol. 24:869. PubMed
  8. Lee K, et al. 2023. JCI Insight. 8:. PubMed
  9. Riffelmacher T, et al. 2023. Nat Cell Biol. 25:877. PubMed
  10. Wang X, et al. 2023. Nat Commun. 14:3440. PubMed
  11. Effern M, et al. 2022. STAR Protoc. 3:101038. PubMed
  12. Hodgins B, et al. 2019. Immun Ageing. 16:27. PubMed
  13. Toomer G, et al. 2022. Viruses. 14:. PubMed
  14. Aldon Y, et al. 2020. J Immunol. 204:903. PubMed
  15. Tan L, et al. 2019. Cell Rep. 27:3657. PubMed
  16. Boothby IC, et al. 2021. Nature. 599:667. PubMed
  17. Misumi I et al. 2019. Cell Rep. 27(2):514-524 . PubMed
  18. Istaces N, et al. 2019. Nat Commun. 10:3306. PubMed
  19. Hossain DMS, et al. 2018. J Clin Invest. 128:644. PubMed
  20. Häselbarth L, et al. 2020. EXCLI J. 19:334. PubMed
  21. Zhang C, et al. 2022. Nat Commun. 13:3468. PubMed
  22. Toubal A, et al. 2020. Nat Commun. 3755:11. PubMed
  23. Kurniawan H, et al. 2020. Cell Metabolism. 31(5):920-936. PubMed
  24. Schuldt N, et al. 2015. PLoS One. 10: 0145762. PubMed
  25. Devi S, et al. 2021. Immunity. 54(6):1219-1230.e7. PubMed
  26. Toshiro Hirai et al. 2019. Immunity. 50(5):1249-1261 . PubMed
  27. Nelson CE et al. 2019. Cell Rep. 28(12):3092-3104 . PubMed
  28. Hoover AR, et al. 2022. Clin Transl Med. 12:e937. PubMed
  29. Highton AJ, et al. 2019. Wellcome Open Res. 4:78. PubMed
  30. Quah B, et al. 2014. J Vis Exp. 88: 51627. PubMed
  31. Hodgson R, et al. 2022. Commun Biol. 5:1216. PubMed
  32. Laczkó D, et al. 2020. Immunity. 53:724. PubMed
RRID
AB_2563062 (BioLegend Cat. No. 104529)
AB_2563062 (BioLegend Cat. No. 104530)

Antigen Details

Structure
C-type lectin, 27/33 kD
Distribution

Activated T cells and B cells, NK cells, granulocytes, thymocytes, platelets

Function
Lymphocyte activation
Cell Type
B cells, Granulocytes, NK cells, Platelets, T cells, Thymocytes, Tregs
Biology Area
Costimulatory Molecules, Immunology, Innate Immunity
Molecular Family
CD Molecules
Antigen References

1. Barclay AN, et al. 1997. The Leukocyte Antigen FactsBook Academic Press.
2. Testi R, et al. 1994. Immunol. Today 15:479.
3. Moretta A, et al. 1991. J. Exp. Med. 174:1393.
4. Yokoyama WM, et al. 1988. J. Immunol. 141:369.

Gene ID
12515 View all products for this Gene ID
UniProt
View information about CD69 on UniProt.org
Go To Top Version: 3    Revision Date: 04/18/2016

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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