FACS CD14

- Found 986 results

Get tips on using PerCP-Cy™5.5 Rat Anti-Mouse CD4 to perform Flow cytometry Anti-bodies Mouse - CD4

Products BD Biosciences PerCP-Cy™5.5 Rat Anti-Mouse CD4

Get tips on using CD4 Monoclonal Antibody (OKT4 (OKT-4)), FITC, eBioscience™ to perform Flow cytometry Anti-bodies Human - CD4

Products eBioscience CD4 Monoclonal Antibody (OKT4 (OKT-4)), FITC, eBioscience™

Get tips on using CD45 Monoclonal Antibody (30-F11), PE-Cyanine7, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - CD45

Products eBioscience CD45 Monoclonal Antibody (30-F11), PE-Cyanine7, eBioscience™

Get tips on using CD49f (Integrin alpha 6) Monoclonal Antibody (eBioGoH3 (GoH3)), eFluor 450, eBioscience™ to perform Flow cytometry Anti-bodies Human - CD49f/ITGA6

Products eBioscience CD49f (Integrin alpha 6) Monoclonal Antibody (eBioGoH3 (GoH3)), eFluor 450, eBioscience™

Cellular assays Cell Isolation CD4+ T cells

Cellular assays Cell Isolation CD4+ Recent Thymic Emigrant

Cellular assays Cell Isolation Resting CD4+ T Cell

Cellular assays Cell Isolation Memory CD4+ T Cell

Cellular assays Cell Isolation Naive CD4+ T cell

ELISA is the most commonly used method of detecting and quantifying the concentration of an antigen in an unknown sample. During the experiment, If you get a weak signal, then make sure reagents are at room temperature before starting the assay. Try increasing incubation times to ensure maximal antibody binding and amplify the signal. Secondly, if you get values above 0 in the negative control indicates a high background signal. Try to consider reducing your antibody concentration and prevent non-specific binding of antibodies by using affinity-purified antibody and suitable blocking buffers. To avoid high well to well variation, do not stack plates during incubation, no bubbles in the plate and wash wells thoroughly to avoid variation.

Proteins ELISA Human ICAM-1/CD54

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