Pacific Blue™ anti-mouse F4/80 Antibody

Pricing & Availability
Clone
BM8 (See other available formats)
Regulatory Status
RUO
Other Names
EMR1, Ly71
Isotype
Rat IgG2a, κ
Ave. Rating
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Product Citations
publications
BM8_Blue_021808
Thioglycollate elicited Balb/c peritoneal macrophage cells stained with Pacific Blue™ BM8
  • BM8_Blue_021808
    Thioglycollate elicited Balb/c peritoneal macrophage cells stained with Pacific Blue™ BM8
Compare all formats See Pacific Blue™ spectral data
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123123 25 µg 111€
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123124 100 µg 243€
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Description

F4/80, also known as EMR1 or Ly71, is a 160 kD glycoprotein of the epidermal growth factor (EGF)-transmembrane 7 (TM7) family. F4/80 has been widely used as a murine macrophage marker. It is expressed on a majority of tissue macrophages, including macrophages in the lung, gut, peritoneal cavity, thymus, and red pulp of the spleen, Kupffer cells, Langerhans cells, microglia, and certain dendritic cells. It is not expressed on macrophages located in the T cell areas of the spleen, lymph node, or Peyer's patch. The biological ligand of F4/80 has not been identified, but it has been reported that F4/80 is required for the induction of CD8+ T cells-mediated peripheral tolerance.

Product Details
Technical Data Sheet (pdf)

Product Details

Verified Reactivity
Mouse
Antibody Type
Monoclonal
Host Species
Rat
Immunogen
Murine macrophages
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
Preparation
The antibody was purified by affinity chromatography, and conjugated with Pacific Blue™ under optimal conditions.
Concentration
0.5 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 ≤ 0.25 µg per 106 cells in 100 µl. It is recommended that the reagent be titrated for optimal performance for each application.

* Pacific Blue™ has a maximum emission of 455 nm when it is excited at 405 nm. Prior to using Pacific Blue™ 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.

View full statement regarding label licenses
Excitation Laser
Violet Laser (405 nm)
Application Notes

Additional reported applications (for the relevant formats) include: immunohistochemical staining of acetone-fixed frozen sections1,2 and formalin-fixed paraffin-embedded sections6,7, Western blotting, and spatial biology (IBEX)12,13.

Application References
  1. Schaller E, et al. 2002. Mol. Cell. Biol. 22:8035. (IHC)
  2. Stevceva L, et al. 2001. BMC Clin Pathol. 1:3. (IHC)
  3. Kobayashi M, et al.2008. J. Leukoc. Biol. 83:1354. PubMed
  4. Poeckel D, et al. 2009. J. Biol Chem. 284:21077. PubMed
  5. Glass AM, et al. 2013. J. Immunol. 190:4830. PubMed
  6. Koehm S, et al. 2007. J. Allergy Clin. Immunol. 120:570. (IHC)
  7. Rankin AL, et al. 2010. J. Immunol. 184:1526. (IHC)
  8. Sasi SP, et al. 2014. J Biol Chem. 289:14178. PubMed
  9. Thakus VS, et al. 2014. Toxicol Lett. 230:322. PubMed
  10. Watson NB, et al. 2015. J Immunol. 194:2796. PubMed
  11. Hirakawa H, et al. 2015. PLoS One. 10:119360. PubMed
  12. Radtke AJ, et al. 2020. Proc Natl Acad Sci U S A. 117:33455-65. (SB) PubMed
  13. Radtke AJ, et al. 2022. Nat Protoc. 17:378-401. (SB) PubMed
Product Citations
  1. Bucher K, et al. 2015. J Leukoc Biol. 2015;98: 365-372. PubMed
  2. Shah D, et al. 2021. Oncoimmunology. 10:1939601. PubMed
  3. Gerlach BD, et al. 2021. Cell Metab. 33:2445. PubMed
  4. Xin B, et al. 2022. Hepatology. 76:630. PubMed
  5. Zhou Y, et al. 2022. Br J Pharmacol. 179:1978. PubMed
  6. Du Y, et al. 2022. FASEB J. 36:e22248. PubMed
  7. Shi C, et al. 2023. Nat Nanotechnol. 18:86. PubMed
  8. Schneider C, et al. 2018. Cell. 174:271. PubMed
  9. Kwon O, et al. 2016. Stem Cell Res. 16: 682-691. PubMed
  10. Chen WS, et al. 2021. Cell Rep. 37:109974. PubMed
  11. Jard T, et al. 2020. Cell Stem Cell. 27(4):646-662.e7. PubMed
  12. Ganeshan K et al. 2019. Cell. 177(2):399-413 . PubMed
  13. Murphy M, et al. 2017. Eur J Immunol. 47:880. PubMed
  14. Tanaka Y, et al. 2015. PLoS One. 10: 0138621. PubMed
  15. Jtte BB, et al. 2021. iScience. 24(8):102833. PubMed
  16. Yang Y, et al. 2021. Nat Commun. 12:525. PubMed
  17. Dichtl S, et al. 2021. Sci Adv. 7: . PubMed
  18. Marangoni F, et al. 2021. Cell. . PubMed
  19. Philip N, et al. 2016. PLoS Pathog. 12:e1005910. PubMed
  20. Ni P, et al. 2014. J Immunol . 193:1778. PubMed
  21. Billi AC, et al. 2019. JCI Insight. 4:8. PubMed
  22. Syed A, et al. 2015. Infect Immun . 83: 3428-3437. PubMed
  23. Izquierdo-Useros N, et al. 2014. J Immunol . 192:4852-4858. PubMed
  24. Zhang B, et al. 2016. Mol Cell. 63: 976-89. PubMed
  25. Jassinskaja M, et al. 2021. Cell Reports. 34(12):108894. PubMed
  26. Haase C, et al. 2022. Nat Methods. 19:1622. PubMed
  27. Saravia J, et al. 2015. PLoS Pathog. 11: e1005217. PubMed
  28. Goncalves R, et al. 2011. J Exp Med. 208:1253. PubMed
  29. Leonard JD et al. 2017. Immunity. 47(1):107-117 . PubMed
  30. Liu D et al. 2019. Immunity. 51(1):64-76 . PubMed
  31. Schadt L, et al. 2020. Cell Reports. 29(5):1236-1248.e7.. PubMed
  32. Krishnamurthy B, et al. 2015. Diabetes. 64: 3229-3238. PubMed
  33. Okamura T, et al. 2021. Front Immunol. 12:669629. PubMed
  34. Dar HH, et al. 2022. JCI Insight. 7:. PubMed
  35. Ringel AE, et al. 2020. Cell. 183(7):1848-1866.e26. PubMed
  36. Cohen H, et al. 2015. J Immunol. 195: 3828 - 3837. PubMed
  37. Stolt C, et al. 2016. J Immunol. 197: 834 - 846. PubMed
  38. Boukelmoune N, et al. 2021. Brain Behav Immun. 93:43. PubMed
  39. Zhang X, et al. 2020. Endocr Relat Cancer. 27:469. PubMed
  40. Challa TD, et al. 2020. Cell Reports. 30(10):3424-3433. PubMed
  41. Kälin S et al. 2017. Cell metabolism. 26(3):475-492 . PubMed
  42. Georgoudaki A, et al. 2016. Cell Rep. 15: 2000-2011. PubMed
  43. Nagatake T, et al. 2018. J Allergy Clin Immunol. 142:470. PubMed
  44. Draijer C, et al. 2018. Sci Rep. 8:5105. PubMed
  45. Jones M, et al. 2010. J Immunol. 185:3583. PubMed
  46. Jiang L, et al. 2020. Cell. 183(5):1219-1233.e18. PubMed
  47. O'Leary CE, et al. 2021. Curr Protoc. 1:e77. PubMed
  48. Flores AM, et al. 2020. Nat Nanotechnol. 0.731944444. PubMed
  49. Clemente–Casares X, et al. 2017. Immunity. 47:974. PubMed
  50. Huang WC, et al. 2020. Adv Mater. 32:e2005637. PubMed
  51. Chao JL, et al. 2021. Cell Rep Med. 2:100399. PubMed
  52. Jee JJ, et al. 2022. Nat Commun. 13:18. PubMed
  53. Stack G, et al. 2015. PLoS Pathog. 11:1004641. PubMed
  54. Serr I, et al. 2016. Nat Commun. 7:10991. PubMed
  55. Huanga J, et al. 2013. J Immunol Methods. 387:254. PubMed
  56. Fotakis P, et al. 2019. Arterioscler Thromb Vasc Biol. 39:e253. PubMed
RRID
AB_893475 (BioLegend Cat. No. 123123)
AB_893475 (BioLegend Cat. No. 123124)

Antigen Details

Structure
EGF-TM7 family member, 160 kD glycoprotein
Distribution

Majority of tissue macrophages including peritoneal macrophages, macrophages in lung, gut, thymus and red pulp of spleen, Kupffer cells, Langerhans cells, bone marrow stromal cells, and a subset of dendritic cells

Function
Induction of immunological tolerance
Cell Type
Dendritic cells, Langerhans cells, Macrophages, Tregs
Biology Area
Cell Biology, Immunology, Innate Immunity, Neuroinflammation, Neuroscience
Antigen References

1. Austy JM and Gordon S. 1981. Eur. J. Immunol. 11:805.
2. Hume DA, et al. 1983. J. Exp. Med. 158:1522.
3. Ruedl C, et al. 1996. Eur. J. Immunol. 26:1801.
4. McKnight AJ, et al. 1996. J. Biol. Chem. 271:486.
5. Lin HH, et al. 2005. J. Exp. Med. 201:1615.

Gene ID
13733 View all products for this Gene ID
Specificity (DOES NOT SHOW ON TDS):
F4/80
Specificity Alt (DOES NOT SHOW ON TDS):
F4/80
App Abbreviation (DOES NOT SHOW ON TDS):
FC
UniProt
View information about F4/80 on UniProt.org

Other Formats

View All F4/80 Reagents Request Custom Conjugation
Description Clone Applications
Brilliant Violet 605™ anti-mouse F4/80 BM8 FC
Purified anti-mouse F4/80 BM8 FC,IHC,WB
Biotin anti-mouse F4/80 BM8 FC,IHC
FITC anti-mouse F4/80 BM8 FC
PE anti-mouse F4/80 BM8 FC
PE/Cyanine5 anti-mouse F4/80 BM8 FC
PE/Cyanine7 anti-mouse F4/80 BM8 FC
APC anti-mouse F4/80 BM8 FC
APC/Cyanine7 anti-mouse F4/80 BM8 FC
Alexa Fluor® 488 anti-mouse F4/80 BM8 FC,IHC-F,3D IHC
Alexa Fluor® 647 anti-mouse F4/80 BM8 FC,IHC-F,3D IHC
Pacific Blue™ anti-mouse F4/80 BM8 FC
PerCP anti-mouse F4/80 BM8 FC
PerCP/Cyanine5.5 anti-mouse F4/80 BM8 FC
Alexa Fluor® 700 anti-mouse F4/80 BM8 FC
Brilliant Violet 421™ anti-mouse F4/80 BM8 FC,IHC-F,SB
Brilliant Violet 510™ anti-mouse F4/80 BM8 FC
Alexa Fluor® 594 anti-mouse F4/80 BM8 IHC-F
Brilliant Violet 785™ anti-mouse F4/80 BM8 FC
Purified anti-mouse F4/80 (Maxpar® Ready) BM8 FC,CyTOF®
PE/Dazzle™ 594 anti-mouse F4/80 BM8 FC
Brilliant Violet 650™ anti-mouse F4/80 BM8 FC
Brilliant Violet 711™ anti-mouse F4/80 BM8 FC
APC/Fire™ 750 anti-mouse F4/80 BM8 FC
TotalSeq™-A0114 anti-mouse F4/80 BM8 PG
TotalSeq™-B0114 anti-mouse F4/80 BM8 PG
TotalSeq™-C0114 anti-mouse F4/80 BM8 PG
Spark YG™ 570 anti-mouse F4/80 BM8 IHC-F
KIRAVIA Blue 520™ anti-mouse F4/80 BM8 FC
Ultra-LEAF™ Purified anti-mouse F4/80 BM8 FC,IHC,WB
APC/Fire™ 810 anti-mouse F4/80 BM8 FC
Spark NIR™ 685 anti-mouse F4/80 BM8 FC
Spark Blue™ 550 anti-mouse F4/80 BM8 FC
Brilliant Violet 570™ anti-mouse F4/80 BM8 FC
Brilliant Violet 750™ anti-mouse F4/80 BM8 FC
PE/Fire™ 810 anti-mouse F4/80 BM8 FC
Spark Red™ 718 anti-mouse F4/80 (Flexi-Fluor™) BM8 FC
Spark Blue™ 574 anti-mouse F4/80 (Flexi-Fluor™) BM8 FC
Go To Top Version: 2    Revision Date: 10.25.2013

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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