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L-selection Recombinant Rabbit mAb (S-1164-30)

L-selection Recombinant Rabbit mAb (S-1164-30)

Catalog Number: S0B1076 Application: FCM,ICC Reactivity: Human Conjugation: Unconjugated Brand: Starter
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Regular price $100.00 USD
Regular price Sale price $100.00 USD
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Product Details

Product Specification


Host Rabbit
Antigen L-selection
Synonyms CD62 antigen-like family member L; Leukocyte adhesion molecule 1 (LAM-1); Leukocyte surface antigen Leu-8; Leukocyte-endothelial cell adhesion molecule 1 (LECAM1); Lymph node homing receptor; TQ1; gp90-MEL; CD62L; SELL; LNHR, LYAM1
Immunogen Synthetic Peptide
Location Cell membrane
Accession P14151
Clone Number S-1164-30
Antibody Type Recombinant mAb
Isotype IgG
Application FCM, ICC
Reactivity Hu
Positive Sample Jurkat
Predicted Reactivity Pt
Purification Protein A
Concentration 0.1 mg/ml
Conjugation Unconjugated
Physical Appearance Liquid
Storage Buffer

PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300

Stability & Storage

12 months from date of receipt / reconstitution, -20 °C as supplied

Dilution


application dilution species
ICC 1:100 Hu

Background

L-selectin, also known as CD62L, is a type-I transmembrane glycoprotein and cell adhesion molecule that is expressed on most circulating leukocytes. Its function in leukocyte trafficking is highlighted by its role in lymphocyte homing to secondary lymphoid tissues. It mediates the tethering and rolling of lymphocytes on high endothelial venules (HEVs) in peripheral lymph nodes via interactions with glycoproteins expressing sLex epitopes. This process is essential for the proper functioning of the immune system, allowing for the recirculation of lymphocytes and their migration to sites of inflammation. In addition to its role in immune cell trafficking, L-selectin has been implicated in the adhesion of blastocysts to the endometrium during the implantation process in the female reproductive tract. It also plays a role in the recruitment of leukocytes during inflammation and in the homing of lymphocytes.

Picture

FC

Flow cytometric analysis of HeLa (Human cervix adenocarcinoma epithelial cell, Left) / Jurkat (Human T cell leukemia T lymphocyte, Right) labelling L-selection antibody at 1/1000 dilution (0.01 μg) / (Red) compared with a Rabbit monoclonal IgG (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti - Rabbit IgG Alexa Fluor® 488 was used as the secondary antibody.
Negative control: HeLa

Immunocytochemistry

ICC shows positive staining in Jurkat cells (top panel) and negative staining in HeLa cells (below panel). Anti-L-selection antibody was used at 1/100 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 100% ice-cold methanol and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).

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