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PerCP/Cyanine5.5 anti-mouse CD150 (SLAM) Antibody

Pricing & Availability
Clone
TC15-12F12.2 (See other available formats)
Regulatory Status
RUO
Other Names
Signaling Lymphocyte Activation Molecule (SLAM), IPO-3
Isotype
Rat IgG2a, λ
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Product Citations
publications
TC15-12F_PerCPCy55_011508
C57BL/6 mouse splenocytes were stained with CD150 (clone TC15-12F12.2) PerCP/Cyanine5.5 (filled histogram) or rat IgG2a PerCP/Cyanine5.5 isotype control (open histogram).
  • TC15-12F_PerCPCy55_011508
    C57BL/6 mouse splenocytes were stained with CD150 (clone TC15-12F12.2) PerCP/Cyanine5.5 (filled histogram) or rat IgG2a PerCP/Cyanine5.5 isotype control (open histogram).
  • TC15-12F12_PerCPCy5.5_2_102110
    C57BL/6 mouse bone marrow cells were stained with CD150 (clone TC15-12F12.2) PerCP/Cyanine5.5 (filled histogram) or rat IgG2a PerCP/Cyanine5.5 isotype control (open histogram) (gated on lymphoid cell population).
Compare all formats See PerCP/Cyanine5.5 spectral data
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115921 25 µg 95€
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115922 100 µg 259€
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Description

CD150 is a 75-95 kD member of the immunoglobulin superfamily, also known as SLAM (signaling lymphocyte activation molecule) or IPO-3. CD150, a single chain type I transmembrane molecule, is expressed on thymocytes, T cell subsets, B cells, dendritic cells, and endothelial cells. The expression is upregulated upon activation. CD150 expression has been shown to be maintained on Th1 but not Th2 clones. T regulatory cells express a relatively high level of CD150. Antibodies against CD150 have been shown to augment IFN-γ production by Th1 cells, especially when co-stimulated through the TCR. CD150 associates with the src homology 2-domain-containing protein tyrosine phosphatase SHP-2, and this association is thought to be involved in signal transduction. In combination with CD48, CD150 is a useful marker for hematopoietic stem cell studies.

Product Details
Technical Data Sheet (pdf)

Product Details

Verified Reactivity
Mouse
Antibody Type
Monoclonal
Host Species
Rat
Immunogen
Mouse SLAM-human IgG1 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 PerCP/Cyanine5.5 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 ≤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/Cyanine5.5 has a maximum absorption of 482 nm and a maximum emission of 690 nm.

Application Notes

The TC15-12F12.2 antibody has been reported to enhance the production of IFN-? by Th1 cells stimulated through TCR. Additional reported applications (for the relevant formats) include: immunoprecipitaion17, enhancing IFN-? production by Th1 cells when stimulated with CD31, and inhibiting CD3 induced T cell proliferation6. The Ultra-LEAF™ purified antibody (Endotoxin <0.01 EU/µg, Azide-Free, 0.2 µm filtered) is recommended for functional assays (Cat. No. 115949 & 115950).

Application References
  1. Castro AG, et al. 1999. J. Immunol. 163:5860. (FC, Costim, IP)
  2. Forsberg EC, et al. 2005. PLoS Genet. 1:e28. (FC)
  3. Terrazas LI, et al. 2005. Int. J. Parasitol. 35:1349. (FC)
  4. Cannons JL, et al. 2006. J. Exp. Med. 203:1551. (FC)
  5. Umemoto T, et al. 2006. J. Immunol. 177:7733. (FC)
  6. Jordan MA, et al. 2007. J. Immunol. 178:1618. (FC, Block) PubMed
  7. Jung Y, et al. 2007. Blood 110:82. PubMed
  8. Pimanda JE, et al. 2007. Proc. Natl. Acad. Sci. USA 104:840.
  9. Sugiyama T, et al. 2007. Proc. Natl. Acad. Sci. USA 104:175.
  10. Kim I, et al. 2006. Blood 108:737. PubMed
  11. Ema H, et al. 2006. Nat Protoc. 1:2979. PubMed
  12. Fraser ST, et al. 2007. Blood 109:4616. PubMed
  13. Jung Y, et al. 2008. Stem Cells. 26:2042. Pubmed
  14. Song J, et al. 2010. Blood 115:2592. PubMed
  15. Cridland SO, et al. 2009. Blood Cell. Mol. Dis. 43:149. (FC) PubMed
  16. Morita Y, et al. 2010. J. Exp Med. 207:1173. PubMed
  17. Talaei N, et al. 2015. J. Immunol. 195(10):4623. PubMed
Product Citations
  1. Abraham A, et al. 2019. J Clin Invest. 130:2685. PubMed
  2. Bae J, et al. 2019. Nat Commun. 10:3496. PubMed
  3. Ahrends T, et al. 2021. Cell. 184:5715. PubMed
  4. Ramdas B, et al. 2022. Mol Ther. 30:2505. PubMed
  5. Li X, et al. 2022. Cell. 185:1709. PubMed
  6. Gautheron F, et al. 2023. Cell Death Discov. 9:117. PubMed
  7. Schloss MJ, et al. 2022. Nat Immunol. 23:605. PubMed
  8. Davis FM, et al. 2020. J Immunol. 2503:204. PubMed
  9. Zhang B, et al. 2018. Nat Med. 24:450. PubMed
  10. Mitroulis I et al. 2018. Cell. 172(1-2):147-161 . PubMed
  11. Guo B, et al. 2018. Nat Med. 24:360. PubMed
  12. Davis FM, et al. 2019. Arterioscler Thromb Vasc Biol. 39:2353. PubMed
  13. Wu HC, et al. 2021. Cancer Discov. Online ahead of print. PubMed
  14. Simon M, et al. 2019. Cell Metab. 29:871. PubMed
  15. Yoshida K, et al. 2022. Sci Rep. 12:17276. PubMed
  16. McAlpine CS, et al. 2021. Nature. 595:701. PubMed
  17. Ruppert R, et al. 2015. J Exp Med. 212: 1415-1432. PubMed
  18. Kim C, et al. 2019. Cell Rep. 29:2202. PubMed
  19. Georgievski A, et al. 2022. Cell Death Dis. 13:337. PubMed
  20. Elahi S, et al. 2020. Stem Cell Res. 43:101710. PubMed
  21. Frodermann V, et al. 2019. Nat Med. 25:1761. PubMed
  22. Yuzugullu H, et al. 2015. Nat Commun. 6: 8501. PubMed
  23. Sztwiertnia I, et al. 2020. PLoS One. 15:e0233789. PubMed
  24. Agarwal P, et al. 2019. Cell Stem Cell. 24:769. PubMed
  25. Damgaard RB et al. 2016. Cell. 166(5):1215-1230 . PubMed
  26. Morganti C, et al. 2022. EMBO Rep. 23:e54262. PubMed
  27. Xiong X, et al. 2014. Elife. 21:3. PubMed
  28. Heyde A, et al. 2021. Cell. 184(5):1348-1361.e22. PubMed
  29. Agarwal P, et al. 2021. Cell Reports. 36(2):109386. PubMed
  30. Guarnerio J, et al. 2018. Nat Commun. 9:66. PubMed
RRID
AB_2206887 (BioLegend Cat. No. 115921)
AB_2206887 (BioLegend Cat. No. 115922)

Antigen Details

Structure
Ig superfamily, 75-95 kD
Distribution

Thymocytes, T cell subset, B lymphocytes, dendritic cells, endothelial cells

Function
B cell and dendritic cell costimulation
Ligand/Receptor
CD150
Cell Type
B cells, Dendritic cells, Endothelial cells, T cells, Thymocytes, Tregs
Biology Area
Costimulatory Molecules, Immunology, Innate Immunity
Molecular Family
Adhesion Molecules, CD Molecules
Antigen References

1. Cocks BG, et al. 1995. Nature 376:260.
2. Punnonen J, et al. 1997. J. Exp. Med. 185:993.
3. Sidorenko SP, et al. 1993. J. Immunol. 151:4614.

Gene ID
27218 View all products for this Gene ID
UniProt
View information about CD150 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.

 

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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