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Purified anti-human CD162 Antibody

Pricing & Availability
Clone
KPL-1 (See other available formats)
Regulatory Status
RUO
Other Names
PSGL-1, p-selectin glycoprotein ligand-1
Isotype
Mouse IgG1, κ
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Product Citations
publications
KPL-1_Pure_082808.jpg
Human peripheral blood lymphocytes stained with purified KPL-1, followed by anti-mouse IgG FITC
  • KPL-1_Pure_082808.jpg
    Human peripheral blood lymphocytes stained with purified KPL-1, followed by anti-mouse IgG FITC
  • KPL-1_PURE_CD162_Antibody_IHC_Validated_092617
    Human paraffin-embedded tonsil tissue slices were prepared with a standard protocol of deparaffinization and rehydration. Antigen retrieval was done with Tris-Buffered Saline 1X (1.0M, pH7.4) at 95°C for 40 minutes. Tissue was washed with PBS/0.05% Tween 20 twice for five minutes and blocked with 5% FBS and 0.2% gelatin for 30 minutes. Then, the tissue was stained with 10 µg/ml of Purified anti-CD162 (Clone KPL-1) overnight at 4°C. On the next day, tissue was washed twice with PBS and stained with Alexa Fluor® 594 goat anti-mouse IgG antibody (Clone POLY4053, red) for an hour at room temperature. Nuclei were counter-stained with DAPI (blue). The image was scanned with a 10X objective and stitched with MetaMorph® software.
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328802 100 µg 96€
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Description

CD162, also known as p-selectin glycoprotein ligand-1 (PSGL-1), is a 120 - 220 kD, mucin-like type I transmembrane glycoprotein. CD162 binds to CD62P (P-Selectin), CD62E (E-Selectin) and CD62L (L-Selectin). The interactions between P-selectin and P-selectin glycoprotein ligand-1 (PSGL-1) mediate the earliest "rolling" of leukocytes on the lumenal surface of activated endothelium, and the interaction between leukocytes and activated platelets or other leukocytes found at sites of inflammation. CD162 is expressed on neutrophils, monocytes, and most lymphocytes including NK and T cells but PSGL-1 stains B cells at significantly lower levels than other cell types.

Product Details
Technical Data Sheet (pdf)

Product Details

Verified Reactivity
Human, Cynomolgus, Rhesus
Reported Reactivity
African Green, Baboon
Antibody Type
Monoclonal
Host Species
Mouse
Immunogen
PSGL-1 transfected murine 300.19 pre B-cell line
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
IHC-P - Verified
IHC-F, IP, WB - 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 ≤ 0.5 µg per million cells in 100 µL volume. For immunohistochemical staining on formalin-fixed paraffin-embedded tissue sections, the suggested use of this reagent is 5.0 - 10 µg/mL. It is recommended that the reagent be titrated for optimal performance for each application.

Application Notes

Clone KPL-1 is reported to recognize the tyrosine sulfation consensus motif of PSGL-11. Additional reported applications (for the relevant formats) include: Western Blot1, immunoprecipitation2, immunohistochemical staining of acetone-fixed frozen tissue sections and formalin-fixed paraffin embedded tissue sections1, blocks the recognition of PSGL-1 with P- and L-selectin1.

Application References
  1. Snapp KR, et al. 1998. Blood 91:154.
  2. Snapp KR, et al. 1998. J. Cell Biol. 142:263.
  3. Yoshino N, et al. 2000. Exp. Anim. (Tokyo) 49:97. (FC)
  4. Miyamura K, et al. 2011. J. Gen. Virol. 92:287. PubMed
  5. Cheng Q, et al. 2012. Lupus. 21:632. PubMed.
Product Citations
  1. Weigert A, et al. 2022. Nat Commun. 13:6078. PubMed
  2. Cheng Q, et al. 2012. Lupus. 1.313888889. PubMed
  3. Pereira JL, et al. 2021. Transl Oncol. 14:101125. PubMed
  4. Perdomo J, et al. 2019. Nat Commun. 10:1322. PubMed
  5. Belmonte B, et al. 2021. Cancers (Basel). 13:. PubMed
  6. Miyamura K, et al. 2011. J Gen Virol. 92:287. PubMed
  7. Aleisa FA, et al. 2020. J Biol Chem. 295:3719. PubMed
  8. Donnelly C, et al. 2018. Sci Rep. 0.625. PubMed
RRID
AB_961085 (BioLegend Cat. No. 328802)

Antigen Details

Distribution

Neutrophils, monocytes, and most lymphocytes

Function
Mediates the earliest "rolling" of leukocytes on the lumenal surface of activated endothelium, and the interaction between leukocytes and activated platelets or other leukocytes found at sites of inflammation.
Ligand/Receptor
CD62P (P-Selectin), CD62E (E-Selectin) and CD62L (L-Selectin)
Cell Type
Lymphocytes, Monocytes, Neutrophils
Biology Area
Cell Adhesion, Immunology
Molecular Family
Adhesion Molecules, CD Molecules
Antigen References

1. Snapp KR, et al. 1998. Blood 91:154.

Gene ID
6404 View all products for this Gene ID
Specificity (DOES NOT SHOW ON TDS):
CD162
Specificity Alt (DOES NOT SHOW ON TDS):
CD162
App Abbreviation (DOES NOT SHOW ON TDS):
FC,IHC-P,IHC-F,IP,WB
UniProt
View information about CD162 on UniProt.org

Related FAQs

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Go To Top Version: 2    Revision Date: 04.22.2015

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.
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