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Alexa Fluor® 700 anti-mouse CD45.1 Antibody

Pricing & Availability
Clone
A20 (See other available formats)
Regulatory Status
RUO
Other Names
T200, Ly-5.1, LCA
Isotype
Mouse (A.SW) IgG2a, κ
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Product Citations
publications
A20_Alx700_020608
SJL mouse splenocytes stained with A20 Alexa Fluor® 700
  • A20_Alx700_020608
    SJL mouse splenocytes stained with A20 Alexa Fluor® 700
Compare all formats See Alexa Fluor® 700 spectral data
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110723 25 µg $101
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110724 100 µg $229
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Description

CD45.1 is an alloantigen of CD45, expressed by Ly5.1 bearing mouse strains (e.g., RIII, SJL/J, STS/A, DA). CD45, a member of the protein tyrosine phosphatase (PTP) family, is a 180-240 kD glycoprotein expressed on all hematopoietic cells except mature erythrocytes and platelets. There are multiple isoforms in mice that play key roles in TCR and BCR signal transduction. These isoforms are very specific to the activation and maturation states of the cell as well as specific cell types. The primary ligands for CD45 are galectin-1, CD2, CD3, CD4, TCR, CD22, and Thy-1.

Product Details
Technical data sheet

Product Details

Verified Reactivity
Mouse
Antibody Type
Monoclonal
Host Species
Mouse
Immunogen
SJL mouse thymocytes and splenocytes
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
Preparation
The antibody was purified by affinity chromatography and conjugated with Alexa Fluor® 700 under optimal conditions.
Concentration
0.5 mg/ml
Storage & Handling
The CD45.1 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. The suggested use of this reagent is ≤ 0.25 µg per 106 cells in 100 µl volume. It is highly recommended that the reagent be titrated for optimal performance for each application.

* Alexa Fluor® 700 has a maximum emission of 719 nm when it is excited at 633nm / 635nm. Prior to using Alexa Fluor® 700 conjugate for flow cytometric analysis, please verify your flow cytometer's capability of exciting and detecting the fluorochrome.


Alexa Fluor® and Pacific Blue™ are trademarks of Life Technologies Corporation.

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Excitation Laser
Red Laser (633 nm)
Application Notes

The A20 antibody does not react with leukocytes or mouse cells expressing the CD45.2 alloantigen. Additional reported applications (for relevant formats of this clone) include: immunoprecipitation3, in vitro blocking of B cell responses1,2, immunohistochemical staining of frozen sections: OCT embedded7 and acetone-fixed4-6 (direct immunofluorescence detection with fluorochrome conjugated A20 was used in (5) and (6)).

Application References

(PubMed link indicates BioLegend citation)
  1. Yakura H, et al. 1983. J. Exp. Med. 157:1077. (Block)
  2. Yakura H, et al. 1986. J. Immunol. 136:2729. (Block)
  3. Shen FW, et al. 1986. Immunogenetics 24:146. (IP)
  4. Suzuki K, et al. 2000. Immunity 13:691. (IHC-F)
  5. Werner N, et al. 2002. Arterioscler. Thromb. Vasc. Biol. 22:1567. (IHC-F)
  6. Lessner SM, et al. 2002. Am. J. Pathol. 160:2145. (FC, IHC-F)
  7. Chen CC, et al. 2005. P. Natl. Acad. Sci. USA 102:11408 (IHC-F)
  8. Pascal V, et al. 2007. J. Immunol. 179:1751. (FC)
  9. Mende I, et al. 2006. Blood 107:1383. (IHC-F, FC)
  10. Phan TG, et al. 2007. Nature Immunol. 8:992. (FC)
  11. Wither DR, et al. 2009. J. Immunol. 183:5079. PubMed
  12. Pascal V, et al.2007. J. Immunol. 179:1751. PubMed
  13. Lee SW, et al. 2009. J. Immunol. 182:6753. PubMed
  14. Takada K, et al. 2009. J. Exp Med. 206:2253. PubMed
  15. Beamer CA, et al. 2007. Am. J. Respir. Cell. Mol. Biol. 37:729. (FC) PubMed
  16. Li LX, et al. 2010. J. Immunol. 184:1728. PubMed
  17. Hosoi A, et al. 2008. Cancer Res. 68:3941. (FC) PubMed
  18. Kenna TJ, et al. 2008. Blood 111:2091. PubMed
  19. Kohlmeier JE, et al. 2008. Immunity. 29:101. (FC) PubMed
Product Citations
  1. Grigsby SM, et al. 2021. Cancers (Basel). 13:. PubMed
  2. Behr FM, et al. 2021. Eur J Immunol. 51:151. PubMed
  3. Horkova V, et al. 2023. Nat Immunol. 24:174. PubMed
  4. Scherer S, et al. 2023. Nat Immunol. 24:501. PubMed
  5. Lucca L, et al. 2014. J Immunol. 193:3267. PubMed
  6. Koyama M, et al. 2015. J Exp Med. 212: 1303 - 1321. PubMed
  7. Soon MSF, et al. 2020. Nat Immunol. 1.984027778. PubMed
  8. Charpentier JC, et al. 2020. Nat Commun. 11:180. PubMed
  9. Withers D, et al. 2009. J Immunol. 183:5079. PubMed
  10. van Elsas MJ, et al. 2023. J Immunother Cancer. 11:. PubMed
  11. Roco JA et al. 2019. Immunity. 51(2):337-350 . PubMed
  12. Baldwin SL, et al. 2021. PLoS One. 16:e0247990. PubMed
  13. Park JH, et al. 2022. STAR Protoc. 3:101607. PubMed
  14. Garidou L, et al. 2012. J Virol. 86:7060. PubMed
  15. Turner JS et al. 2018. Cell reports. 25(6):1395-1403 . PubMed
  16. Delás MJ, et al. 2019. Cell Rep. 27:719. PubMed
  17. Castellanos CA, et al. 2021. Sci Immunol. 6:eabh0707. PubMed
  18. Huang W, et al. 2014. J Immunol. 193:2267. PubMed
  19. Semmrich M, et al. 2011. Mucosal Immunol. 0.3125. PubMed
  20. Chen J et al. 2018. Cell reports. 25(12):3393-3404 . PubMed
  21. Bowers E, et al. 2018. Nat Med. 24:95. PubMed
  22. Paprckova D, et al. 2022. Front Immunol. 13:1009198. PubMed
  23. Hayatsu N et al. 2017. Immunity. 47(2):268-283 . PubMed
  24. Nakamura‐Ishizu A et al. 2018. Cell reports. 25(7):1772-1785 . PubMed
  25. Rengarajan S, et al. 2020. Cell Rep Med. :1. PubMed
  26. Zenke S, et al. 2020. Immunity. 52(2):313-327. PubMed
  27. Kleppe M et al. 2018. Cancer cell. 33(1):29-43 . PubMed
  28. Ng SS, et al. 2020. Nat Immunol. 21:1205. PubMed
  29. Baasch S, et al. 2021. Cell. . PubMed
  30. Dietmar Herndler‐Brandstetter et al. 2018. Immunity. 48(4):716-729 . PubMed
  31. Chen Z et al. 2019. Immunity. 51(5):840-855 . PubMed
  32. Tondini E, et al. 2022. NPJ Vaccines. 7:64. PubMed
  33. Li C, et al. 2021. Cell Metabolism. 33(8):1610-1623.e5. PubMed
  34. Zhang J, et al. 2021. Nature. 590:457. PubMed
  35. Yabas M, et al. 2016. PLoS One. 11: 0146774. PubMed
  36. Kobayashi H, et al. 2020. Cell Reports. 28(1):145-158.e9.. PubMed
  37. Zeis P, et al. 2020. Immunity. 53:775. PubMed
  38. Li C, et al. 2018. Cell. 174:285. PubMed
  39. Yabas M, et al. 2011. PLoS One. 6:e26440. PubMed
  40. Chen Z, et al. 2021. Cell. 184(5):1262-1280.e22. PubMed
  41. Huang W, et al. 2014. J Leukoc Biol. 96:55. PubMed
  42. Rodríguez L, et al. 2021. Biomolecules. 11: . PubMed
  43. Chao JL, et al. 2021. Cell Rep Med. 2:100399. PubMed
  44. Li J, et al. 2021. Cell Rep. 37:110124. PubMed
  45. Sabouri Z, et al. 2016. Nat Commun. 7:13381. PubMed
  46. Senatus L, et al. 2020. JCI Insight. 5:00. PubMed
  47. Hoyer FF, et al. 2020. Immunity. 51(5):899-914.e7.. PubMed
  48. Swarnalekha N, et al. 2021. Sci Immunol. 6:. PubMed
  49. Säwen P et al. 2018. eLife. 7 pii: e41258. PubMed
  50. Eftychi C et al. 2019. Immunity. 51(2):367-380 . PubMed
  51. Kerdidani D, et al. 2022. J Exp Med. 219:. PubMed
  52. Schuran FA, et al. 2020. Cell Mol Gastroenterol Hepatol. . PubMed
  53. Severe N et al. 2019. Cell Stem Cell. 25(4):570-583 . PubMed
RRID
AB_493732 (BioLegend Cat. No. 110723)
AB_493732 (BioLegend Cat. No. 110724)

Antigen Details

Structure
Protein tyrosine phosphatase (PTP) family, 180-240 kD
Distribution

All hematopoietic cells except mature erythrocytes and platelets of the CD45.1 strain of mice

Function
Phosphatase, T and B cell activation
Ligand/Receptor
Galectin-1, CD2, CD3, CD4
Biology Area
Cell Biology, Immunology, Inhibitory Molecules, Neuroscience, Neuroscience Cell Markers
Molecular Family
CD Molecules
Antigen References

1. Barclay A, et al. 1997. The Leukocyte Antigen FactsBook Academic Press.
2. Trowbridge IS, et al. 1993. Annu. Rev. Immunol. 12:85.
3. Kishihara K, et al. 1993. Cell 74:143.
4. Pulido R, et al. 1988. J. Immunol. 140:3851.

Gene ID
19264 View all products for this Gene ID
UniProt
View information about CD45.1 on UniProt.org
Go To Top Version: 2    Revision Date: 06/27/2014

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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