Flow cytometric analysis of Human CD107a expression in Jurkat cells. Cells from Jurkat (Human T cell leukemia T lymphocyte) was fixed with 4% paraformaldehyde and permeabilized with 90% methanol and then stained with either FITC Mouse IgG1, κ Isotype Control (Black line histogram) or SDT FITC Mouse Anti-Human CD107a antibody (Red line histogram) at 1.25 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.
Product Details
Product Details
Product Specification
Host | Mouse |
Antigen | CD107a |
Synonyms | Lysosome-associated membrane glycoprotein 1; LAMP-1; Lysosome-associated membrane protein 1 Curated; CD107 antigen-like family member A; LAMP1 |
Location | Cell membrane |
Accession | P11279 |
Clone Number | S-3027 |
Antibody Type | Mouse mAb |
Isotype | IgG1,k |
Application | ICFCM |
Reactivity | Hu |
Positive Sample | Jurkat |
Purification | Protein G |
Concentration | 0.2 mg/ml |
Conjugation | FITC |
Physical Appearance | Liquid |
Storage Buffer | PBS, 1% BSA, 0.3% Proclin 300 |
Stability & Storage | 12 months from date of receipt / reconstitution, 2 to 8 °C as supplied |
Dilution
application | dilution | species |
ICFCM | 1.25μl per million cells in 100μl volume | Hu |
Background
CD107a, also termed lysosome-associated membrane protein-1 (LAMP-1), is a heavily glycosylated type-I transmembrane glycoprotein encoded by the LAMP1 gene, constituting ~50 % of all proteins in the lysosomal membrane where its dense carbohydrate coat protects against self-digestion, while in immune cells it functions as a universally accepted surrogate marker of cytotoxic degranulation because, upon NK- or CD8⁺ T-cell activation, the lytic granules fuse with the plasma membrane and transiently expose CD107a on the cell surface, enabling flow-cytometric quantification of perforin/granzyme release; beyond immunology, CD107a shuttles between lysosomes, endosomes and the plasma membrane, provides carbohydrate ligands for selectins to facilitate leukocyte adhesion, and its overexpression on tumor cells correlates with enhanced metastatic potential .
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