The Human CD3 FITC/CD16/CD56 PE Cocktail from Assay Genie is a cutting-edge immunology research tool designed to facilitate the analysis of immune cell subsets. This ready-to-use cocktail combines fluorescence-labeled antibodies targeting CD3, CD16, and CD56 antigens, providing a comprehensive solution for flow cytometry experiments.CD3 is a crucial T cell marker, while CD16 and CD56 are commonly found on natural killer cells and subsets of T cells. By simultaneously staining these important cellular markers, researchers can gain valuable insights into the composition and activation status of immune cell populations in human samples.
With high specificity and sensitivity, the Anti-Human CD3 FITC/CD16/CD56 PE Cocktail enables precise identification and characterization of T cells, natural killer cells, and other immune cell subsets. This versatile tool is ideal for studying immune responses in various contexts, including infectious diseases, autoimmune disorders, and cancer immunotherapy research.Trust Assay Genie's innovative antibody cocktail to streamline your immunology research, unlocking new possibilities for understanding human immune cell dynamics and advancing therapeutic interventions.
Product Title:
Anti-Human CD3-FITC/CD16+CD56-PE Cocktail
SKU:
AGEL2709
Size:
20 Tests, 100 Tests, 200 Tests
Clone No:
OKT-3 , 3G8 , 5.1H11 ,
Reactivity:
Human
Application:
FCM
Form:
Liquid
Conjugation:
FITC;PE;
Recommended Use:
For whole blood samples, add 5 μL Anti-Human CD3-FITC/CD16+CD56-PE Cocktail to 100 μL anticoagulant-treated blood sample. Mix and incubate the sample at 4°C in the dark for 30 min. Remove red blood cells with RBC lysis solution following the manufacturer's instruction. Wash the cell with cell staining buffer and discard the supernatant after centrifugation at 300 g for 5 min. Resuspend the cells with 200 μL cell staining buffer and load the sample on flow cytometer for detection. For other samples, 1×106 dissociated single cells are centrifuged at 300 g for 5 min with the supernatant discarded. Resuspend the cells with 100 μL cell staining buffer and add 5 μL Anti-Human CD3-FITC/CD16+CD56-PE Cocktail. Mix and incubate the sample at 4°C in the dark for 30 min. Add cell staining buffer to each tube, centrifuge at 300 g for 5 min and discard the supernatant. Resuspend the cells with 200 μL cell staining buffer and load the sample on flow cytometer for detection.
Spectrum:
Storage Buffer:
Phosphate buffered solution, pH 7.2, containing 0.09% stabilizer and 1% protein protectant.
Stability & Storage:
Keep as concentrated solution. Store at 2~8°C and protected from prolonged exposure to light. Do not freeze. Centrifuge before opening to ensure complete recovery of vial contents. This product is guaranteed up to one year from purchase.
Background:
This product is a FCM antibody cocktail made up of FITC Anti-Human CD3 Antibody [Clone: OKT-3] (Mouse IgG2a, κ), PE Anti-Human CD16 Antibody [Clone: 3G8] (Mouse IgG1, κ) and PE Anti-Human CD56 Antibody [Clone: 5.1H11] (Mouse IgG1, κ).; CD3 is a heterotetrameric protein consisting of a CD3γ, a CDδ and 2 CD3ε. It forms complex with TCR. OKT-3 recognize human CD3ε. Human CD3 is expressed on the surface of T cells and NKT cells.; CD16 is a low affinity receptor for the Fc of IgG. Human CD16 has two isoforms, CD16a and CD16b. CD16a is expressed on NK cells, activated monocytes and macrophages. CD16b is expressed on neutrophils. NK cells exert the function of ADCC by binding Fc of IgG through CD16.; CD56 is also call neural cell adhesion molecule (NCAM), expressed on neurons, glia and skeletal muscle cells. In hematopoietic cells, CD56 is also expressed on NK cells and NKT cells. CD56 can be used to detect NK cells, γ/δ T cells and activated CD8+ cells.;
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