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Antigenic Specificity | CD62L (L-Selectin) |
Clone | [CD62L/1588] |
Host Species | Mouse |
Reactive Species | human |
Isotype | IgG1, kappa |
Format | purified |
Size | 0.02 mg (With BSA & Azide at 0.2mg/ml), 0.1 mg (With BSA & Azide at 0.2mg/ml), 0.1 mg (Without BSA & Azide at 1mg/ml) |
Concentration | n/a |
Applications | ELISA (EIA) |
Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
Description | Specificity: Selectins, also designated CD62 antigens, comprise a family of carbohydrate-binding proteins involved in mediating cellular interactions with leukocytes. L-Selectin (also designated LECAM-1 or CD62L) is expressed on the majority of B and naive T cells and on most monocytes, neutrophils and eosinophils. L-Selectin interacts with specific carbohydrates expressed by activated endothelial cells. P-Selectin (also designated GMP-140 or CD62P), expressed on activated platelets and endothelial cells, and E-Selectin (also designated ELMA-1 or CD62E), expressed on endothelial cells, exhibit overlapping ligand specificities. Both recognize sialyl-Le (x) as a ligand and bind to specific carbohydrates on neutrophils and monocytes. |
Immunogen | Immunogen: MAb raised against supernatant from phorbol myristic acid activated human peripheral blood leukocytes. |
Other Names | [A.11; AI528707; CD62 antigen ligand; CD62L; gp90-MEL; IgA nephropathy; susceptibility to; included; L Selectin; L-selectin; LAM1; LECAM1; LEU8; Leukocyte surface antigen Leu-8; Leukocyte-endothelial cell adhesion molecule 1; Lnhr; LSEL; Ly-22; LYAM1; Lymph node homing receptor; Lymphocyte antigen 22; Lymphocyte surface MEL-14 antigen; Pln homing receptor; PLNHR; SELL; TQ1] |
Gene, Accession # | [CD62L], Gene ID: 6402, NCBI: NP_000646.2, UniProt: P14151 |
Catalog # | MBS4381242 |
Price | $190, $340, $340 |
Order / More Info | CD62L (L-Selectin) Antibody from MYBIOSOURCE INC. |
Product Specific References | 1. Lasky, L.A. 1995. Ann. Rev. Biochem. 64: 113-139. 2. Tedder, T.F., et al. 1995. FASEB J. 10: 866-873. |