Key Product Details

Species Reactivity

Validated:

Human

Cited:

Human

Applications

Validated:

Immunohistochemistry, Adhesion Blockade

Cited:

Immunohistochemistry, Immunohistochemistry-Frozen, Neutralization

Label

Unconjugated

Antibody Source

Monoclonal Mouse IgG1 Clone # 9E1
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Product Specifications

Immunogen

Recombinant human P-Selectin
Extracellular domain

Specificity

This antibody binds to CHO cells transfected with human P-Selectin but not to CHO cells transfected with either human E-Selectin or human L-Selectin.

Clonality

Monoclonal

Host

Mouse

Isotype

IgG1

Endotoxin Level

<0.10 EU per 1 μg of the antibody by the LAL method.

Scientific Data Images for Human P‑Selectin/CD62P Antibody

P-Selectin/CD62P antibody in Human Breast Cancer Tissue by Immunohistochemistry (IHC-P).

P-Selectin/CD62P in Human Breast Cancer Tissue.

P-Selectin/CD62P was detected in immersion fixed paraffin-embedded sections of human breast cancer tissue using 25 µg/mL Human P-Selectin/CD62P Monoclonal Antibody (Catalog # BBA30) overnight at 4 °C. Tissue was stained with the Anti-Mouse HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS002) and counterstained with hematoxylin (blue). View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections.

Detection of P-Selectin/CD62P by Immunohistochemistry

Detection of P-Selectin/CD62P by Immunohistochemistry

SERS-BFNP molecular imaging of atherosclerotic coronary arteries. A single human coronary artery was isolated from the heart of a patient undergoing heart transplantation surgery. The lumen of the artery segment was then injected with a mixture of anti-ICAM-1, anti-VCAM-1, anti-P-selectin, and isotype control BFNP, sutured closed, and incubated at 37 °C/5% CO2 for 12 h. Sutures were then removed and the artery segment was thoroughly washed prior to SERS spectroscopy and subsequent analysis of morphology, expression of adhesion molecules and SERS mapping. (B) Immunofluorescence staining for CD31, and expression of (C) ICAM-1, VCAM-1 and P-selectin are shown in red. Nuclei were counterstained using Hoechst 33342 (blue). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/30613292), licensed under a CC-BY license. Not internally tested by R&D Systems.
Detection of P-Selectin/CD62P by Immunocytochemistry/ Immunofluorescence

Detection of P-Selectin/CD62P by Immunocytochemistry/ Immunofluorescence

Following stimulation, coronary artery endothelial cells (CAEC) express adhesion molecules detectable via immuno-SERS imaging in single and multiplex formats. (A) Fluorescence images of immunohistochemical staining of ICAM-1, VCAM-1 and P-selectin on CAEC in unstimulated and 10 ng/mL TNF-alpha -stimulated conditions. Isotype control, ICAM-1, VCAM-1 and P-selectin staining shown in green; nuclei were counterstained using Hoechst 33342 (blue). (B) CAEC were stimulated with 10 ng/mL TNF-alpha for 24 h, fixed in acetone, and incubated with isotype control, anti-ICAM-1, anti-VCAM-1 or anti-P-selectin BFNP or (C) with all BFNP simultaneously before being subjected to SERS mapping. (D) Representative spectra from anti-ICAM-1 (purple), anti-VCAM-1 (red) and anti-P-selectin (blue) BFNP acquired from the color-matched circles in (C) are shown above their respective reference spectra. Optical images in (B-C) are darkfield images. Scale bars = 20 μm. Results are representative of 3 independent experiments. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/30613292), licensed under a CC-BY license. Not internally tested by R&D Systems.
Detection of P-Selectin/CD62P by Immunocytochemistry/ Immunofluorescence

Detection of P-Selectin/CD62P by Immunocytochemistry/ Immunofluorescence

KD platelets crosstalk with monocytes via forming “adhesion junctions”. A) Flow cytometry analysis showing CD62p expression in platelets from HS (n = 24) and KD patients (n = 24). Unpaired t test. B) Correlation between MPA and CD62p positive platelets in patients with acute KD (n = 24). p value was calculated using correlation analysis. C) Heatmap showing selected ligand–receptor interactions between MPA and subtypes of monocytes. D) Immunostaining of PSGL‐1 (blue), CD14 (green), CD41 (red), and CD62p (gray) in monocytes after coculture with KD platelets for 8 h. Activated CD41+ platelets (red) forming CD62p (gray) and PSGL‐1‐mediated junctions (blue) with CD14+ monocytes (green) are shown (n = 6). Scale bar: 5 µm. E) Immunostaining of CD11b (blue), CD14 (green), CD41 (red), GPIb alpha (gray) in monocytes after coculture with KD platelets for 8 h. Activated CD41+ platelets (red) forming GPIb alpha (gray) and CD11b‐mediated junctions (blue) with CD14+ monocytes (green) are shown (n = 6). Scale bar: 5 µm. F,G) Proximity ligation assay (PLA) showing adhesion junctions of CD62p–PSGL‐1 (F), GPIb alpha –CD11b (G) on monocytes. PLA staining: red; nuclei: blue; wheat germ agglutinin (WGA): green (n = 5). Scale bar: 10 µm. PLT, platelet; HS, healthy subject; KD, Kawasaki disease; MPA, platelet–monocyte aggregate; ITGAM, integrin subunit alpha M (CD11b). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/39665236), licensed under a CC-BY license. Not internally tested by R&D Systems.

Applications for Human P‑Selectin/CD62P Antibody

Application
Recommended Usage

Adhesion Blockade

The adhesion of U937 human histiocytic lymphoma cells (5 x 104 cells/well) to immobilized Recombinant Human P-Selectin/CD62P (Catalog # ADP3, 10 µg/mL, 100 µL/well) was maximally inhibited (80-100%) by 1 µg/mL of the antibody.

Immunohistochemistry

8-25 µg/mL
Sample: Immersion fixed paraffin-embedded sections of human breast cancer tissue

Reviewed Applications

Read 1 review rated 4 using BBA30 in the following applications:

Formulation, Preparation, and Storage

Purification

Protein A or G purified from hybridoma culture supernatant

Reconstitution

Sterile PBS to a final concentration of 0.5 mg/mL.


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Formulation

Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose.

Shipping

The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 6 months, -20 to -70 °C under sterile conditions after reconstitution.

Calculators

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.

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Background: P-Selectin/CD62P

P-Selectin, also known as GMP-140 and PADGEM, is a transmembrane glycoprotein expressed by activated platelets and endothelial cells. P-Selectin binds to PSGL-1 on myeloid cells, neutrophils, monocytes, and lymphocytes. P-Selectin plays a role in the adhesion of leukocytes and neutrophils to the endothelium.

Alternate Names

CD62P, GMP140, GRMP, PADGEM, PSEL, SELP

Entrez Gene IDs

6403 (Human); 20344 (Mouse)

Gene Symbol

SELP

Additional P-Selectin/CD62P Products

Product Documents for Human P‑Selectin/CD62P Antibody

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot or batch number in the search box below.

Note: Certificate of Analysis not available for kit components.

Product Specific Notices for Human P‑Selectin/CD62P Antibody

For research use only

Citations for Human P‑Selectin/CD62P Antibody

Customer Reviews for Human P‑Selectin/CD62P Antibody (1)

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  • Human P-Selectin/CD62P Antibody
    Name: Balaji Mahender
    Application: ELISA
    Sample Tested: EDTA Plasma, Citrate Plasma and Heparin Plasma
    Species: Human
    Verified Customer | Posted 12/20/2017

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Protocols

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