Purified anti-mouse CD62L Antibody

Pricing & Availability
Clone
MEL-14 (See other available formats)
Regulatory Status
RUO
Other Names
L-selectin, LECAM-1, Ly-22, LAM-1, MEL-14
Isotype
Rat IgG2a, κ
Ave. Rating
Submit a Review
Product Citations
publications
1-MEL-14_Purified_090707
C57BL/6 mouse splenocytes stained with purified MEL-14, followed by anti-rat IgG FITC
  • 1-MEL-14_Purified_090707
    C57BL/6 mouse splenocytes stained with purified MEL-14, followed by anti-rat IgG FITC
  • 2-MEL-14_pure_CD62L_Antibody_2_103018
    Fresh, frozen mouse spleen was stained with purified CD62L clone MEL-14 conjugated and detected with a Cy5 CODEX™ oligonucleotide duplex (red). Samples were counterstained with Ly6c Cy3 (green). Data generated at Akoya Biosciences, Inc. using the CODEX™ technology.
Compare all formats
Cat # Size Price Quantity Check Availability Save
104402 500 µg 138 CHF
Check Availability


Need larger quantities of this item?
Request Bulk Quote
Description

CD62L is a 74-95 kD glycoprotein also known as L-selectin, LECAM-1, Ly-22, LAM-1, and MEL-14. It is a member of the selectin family and is expressed on the majority of B and naïve T cells, a subset of memory T cells, monocytes, granulocytes, most thymocytes, and a subset of NK cells. CD62L is important in lymphocyte homing to high endothelial venules (HEV) in peripheral lymph nodes and leukocyte "rolling" on activated endothelium. CD62L also contributes to neutrophil emigration at inflammatory sites. CD62L is rapidly shed from lymphocytes and neutrophils upon cellular activation and the expression levels of CD62L (in conjunction with other markers) have been used to distinguish naïve, effector, and memory T cells. CD62L has been reported to interact with CD34, GlyCAM-1, and MAdCAM-1.

Product Details
Technical Data Sheet (pdf)

Product Details

Verified Reactivity
Mouse
Antibody Type
Monoclonal
Host Species
Rat
Immunogen
C3H/eb mouse B lymphoma 38C-13
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
Preparation
The antibody was purified by affinity chromatography.
Concentration
0.5 mg/ml
Storage & Handling
The antibody solution should be stored undiluted between 2°C and 8°C.
Application

FC - Quality tested
CyTOF®, IHC-F - Verified
IP - Reported in the literature, not verified in house

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 volume. It is recommended that the reagent be titrated for optimal performance for each application.

Application Notes

Additional reported applications (for the relevant formats) include: immunoprecipitation1-3, complement-dependent cytotoxicity4, in vivo and in vitro blocking of adhesion1-3,5, and immunohistochemical staining of acetone-fixed frozen sections and zinc-fixed paraffin-embedded sections6. The Ultra-LEAF™ purified antibody (Endotoxin < 0.01 EU/µg, Azide-Free, 0.2 µm filtered) is recommended for functional assays (Cat. Nos. 104457-104462).

Application References

(PubMed link indicates BioLegend citation)
  1. Gallatin WM, et al. 1983. Nature 304:30. (IP, Block)
  2. Siegelman MH, et al. 1990. Cell 61:611. (IP, Block)
  3. Lewinsohn DM, et al. 1987. J. Immunol. 138:4313. (IP, Block)
  4. Iwabuchi K, et al. 1991. Immunobiology 182:161. (CMCD)
  5. Pizcueta P, et al. 1994. Am. J. Pathol. 145:461.
  6. Reichert RA, et al. 1986. J. Immunol. 136:3535. (IHC, FC)
  7. Olver S, et al. 2006. Cancer Res. 66:571.
  8. Fukushima A, et al. 2006. Invest. Ophthalmol. Vis. Sci. 47:657. PubMed
  9. Benson MJ, et al. 2007. J. Exp. Med. doi:10.1084/jem.20070719. (FC) PubMed
  10. Chappaz S, et al. 2007. Blood doi:10.1182/blood-2007-02-074245. (FC) PubMed
  11. Lee JW, et al. 2006. Nature Immunol. 8:181.
  12. Shigeta A, et al. 2008. Blood 112:4915 (FC) PubMed
  13. de Vries VC, et al. 2009. Am. J. Transplant. 9:2270 PubMed
Product Citations
  1. Kobayashi A, et al. 2021. Front Immunol. 12:650856. PubMed
  2. Cai S, et al. 2020. Sci Rep. 10:14249. PubMed
  3. Moore AR, et al. 2022. Cell Rep. 41:111651. PubMed
  4. Zhang S, et al. 2017. Nature.. 10.1038/nature24283. PubMed
  5. Toubai T, et al. 2017. Blood Adv. 1.095138889. PubMed
  6. Guo R, et al. 2020. Cell Res. 30:21. PubMed
  7. Khan KA, et al. 2020. NPJ Breast Cancer. 6:29. PubMed
  8. Chartrand K, et al. 2018. Front Immunol. 1.642361111. PubMed
  9. Ban YH, et al. 2017. Cell Rep. 2.6375. PubMed
  10. Yang J, et al. 2020. Front Immunol. 10:3048. PubMed
  11. Rieck M, et al. 2017. Eur J Immunol. 47:677. PubMed
  12. Wang W, et al. 2018. Cancer Cell. 34:757. PubMed
  13. Carpenter SM, et al. 2017. PLoS Pathog. 13:e1006704. PubMed
  14. Arimura K, et al. 2017. Mucosal Immunol. 1.08125. PubMed
  15. Muhammad F, et al. 2020. Front Immunol. 975:11. PubMed
  16. Mayer KA, et al. 2021. FASEB J. 35:e21217. PubMed
  17. Delgobo M, et al. 2021. Front Immunol. 12:584538. PubMed
  18. Li W, et al. 2020. J Clin Invest. 130:6718. PubMed
  19. Morabito KM, et al. 2017. Mucosal Immunol. 0.795138889. PubMed
  20. Suzuki Y, et al. 2021. FEBS Open Bio. 11:2619. PubMed
  21. Doorduijn EM, et al. 2018. Front Immunol. 0.416666667. PubMed
  22. Sun H, et al. 2018. J Cell Biol. 217:1453. PubMed
  23. Khan KA, et al. 2020. NPJ Breast Cancer. 6:29. PubMed
  24. Oba T, et al. 2021. J Immunother Cancer. 9:. PubMed
  25. Xie D, et al. 2020. Eur J Immunol. 50:1729. PubMed
  26. Tan Z, et al. 2020. Mol Ther Oncolytics. 16:302. PubMed
  27. Sato Y, et al. 2021. BMC Cancer. 21:1222. PubMed
  28. Liu H, et al. 2020. J Immunol. 205:1207. PubMed
  29. Abboud G, et al. 2018. Front Immunol. 9:1973. PubMed
  30. Hsiao CC, et al. 2021. Cells. 10:. PubMed
  31. Kim SJ, et al. 2017. Nat Immunol. 18:1016. PubMed
  32. Hoves S, et al. 2018. J Exp Med. 215:859. PubMed
  33. Lorsung RM, et al. 2020. Front Bioeng Biotechnol. 0.9375. PubMed
  34. Park GY, et al. 2020. Immune Netw. e43:20. PubMed
  35. Gil-Pulido J, et al. 2017. PLoS One.. 10.1371/journal.pone.0181947. PubMed
  36. Lee JY, et al. 2018. Front Immunol. 0.678472222. PubMed
  37. Liu M, et al. 2018. Diabetologia. 61:2333. PubMed
  38. Kenna T, et al. 2008. Blood. 111:2091. PubMed
  39. Daley D, et al. 2017. Nat Med. 23:556. PubMed
  40. King IL, et al. 2017. Mucosal Immunol. 10:1160. PubMed
  41. Yates K, et al. 2018. Proc Natl Acad Sci U S A. 115:2162. PubMed
  42. Oyarce K, et al. 2018. Front Immunol. 9:112. PubMed
  43. Florek M, et al. 2015. PLoS One. 10: 0145763. PubMed
  44. Tan CL, et al. 2018. Immunohorizons. 0.248611111. PubMed
  45. Karmaus PWF, et al. 2019. Nature. 565:101. PubMed
  46. Flietner E, et al. 2022. Sci Rep. 12:10616. PubMed
  47. Kakaradov B, et al. 2017. Nat Immunol. 18:422. PubMed
  48. Rosenbaum M, et al. 2019. Nat Commun. 2.05. PubMed
  49. Kawabe T, et al. 2017. Sci Immunol. 2:eaam9315. PubMed
  50. Yi J, et al. 2019. Mol Cells. 42:228. PubMed
  51. Benson M, et al. 2007. J Exp Med. 204:1765. PubMed
  52. Stelekati E, et al. 2018. Cell Rep. 2.445833333. PubMed
  53. Cui X, et al. 2017. J Immunol. 199:4066. PubMed
  54. Cané S, et al. 2021. J Immunother Cancer. 9:. PubMed
  55. Jun JC, et al. 2017. PLoS One. 12:e0180688. PubMed
  56. Karuppuchamy T, et al. 2020. Inflamm Bowel Dis. 216:26. PubMed
  57. Olver S, et al. 2005. Cancer Res. 66:571. PubMed
  58. Richards KA, et al. 2018. Front Immunol. 0.829861111. PubMed
  59. Englezou PC, et al. 2018. Mol Ther Nucleic Acids. 12:118. PubMed
  60. Winter C, et al. 2018. Cell Metab. 28:175. PubMed
  61. Zhang J, et al. 2019. Onco Targets Ther. 12:4985. PubMed
  62. Managlia E, et al. 2019. Am J Pathol. 189:604. PubMed
  63. Kästele V, et al. 2021. Mucosal Immunol. 14:717. PubMed
  64. Prabakaran T, et al. 2021. EBioMedicine. 66:103314. PubMed
  65. Sutiwisesak R, et al. 2020. PLoS Pathog. 16:e1009000. PubMed
  66. Fukushima A, et al. 2006. Invest Ophthalmol Vis Sci. 47:657. PubMed
  67. Fritz Y, et al. 2017. J Invest Dermatol. 137:696. PubMed
RRID
AB_313089 (BioLegend Cat. No. 104402)

Antigen Details

Structure
Selectin, 95 kD (neutrophils) or 74 kD (lymphocytes)
Distribution

Subsets of B and T cells, monocytes, granulocytes, subset of NK cells

Function
Lymphocyte homing to HEV, rolling on activated endothelium
Ligand/Receptor
CD34, GlyCAM-1, MAdCAM-1
Cell Type
B cells, Granulocytes, Monocytes, Neutrophils, NK cells, T cells, Tregs
Biology Area
Cell Adhesion, Cell Biology, Costimulatory Molecules, Immunology, Innate Immunity
Molecular Family
Adhesion Molecules, CD Molecules
Antigen References

1. Barclay AN, et al. 1997. The Leukocyte Antigen FactsBook Academic Press.
2. Kishimoto TK, et al. 1990. P. Natl. Acad. Sci. USA 87:2244.
3. Tedder TF, et al. 1995. J. Exp. Med. 181:2259.

Gene ID
20343 View all products for this Gene ID
UniProt
View information about CD62L on UniProt.org
Go To Top Version: 2    Revision Date: 10.30.2018

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.

 

BioLegend, the BioLegend logo, and all other trademarks are property of BioLegend, Inc. or their respective owners, and all rights are reserved.

 

8999 BioLegend Way, San Diego, CA 92121 www.biolegend.com
Toll-Free Phone: 1-877-Bio-Legend (246-5343) Phone: (858) 768-5800 Fax: (877) 455-9587

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.

ProductsHere

Login / Register
Remember me
Forgot your password? Reset password?
Create an Account