Flowcytometry Secondary Antibody Goat Mouse

Get tips on using TCR beta Monoclonal Antibody (H57-597), FITC, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - TCRbeta

Get tips on using CD137 (4-1BB) Monoclonal Antibody (17B5), APC, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - CD137

Get tips on using CD137 (4-1BB) Monoclonal Antibody (17B5), PE, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - CD137

Get tips on using CD115 (c-fms) Monoclonal Antibody (AFS98), Biotin, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - CD115

Get tips on using CD115 (c-fms) Monoclonal Antibody (AFS98), APC, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - CD115

Get tips on using CD86 (B7-2) Monoclonal Antibody (GL1), APC, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - CD86

Get tips on using CD8a Monoclonal Antibody (53-6.7), eFluor 450, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - CD8a

Get tips on using CD11b Monoclonal Antibody (M1/70), eFluor 450, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - CD11b

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

Flow cytometry is an immunophenotyping technique whereby sing cell suspensions are stained for either cell surface markers or intracellular proteins by fluorescently-labelled antibodies and analyzed with a flow cytometer, where fluorescently-labelled molecules are excited by the laser to emit light at varying wavelengths, which is then detected by the instrument. There are several key criteria which are required to be kept in mind while designing a flow experiment- 1. Antibody titration (optimal dilution of antibodies should be calculated in order to avoid over- or under- saturated signals for proper detection of surface and intracellular markers), 2. Precision (3 or more replicates of the sample should be used per experiment), 3. Specificity (proper isotype controls should be included in the experiment), 4. Day-to-day variability (experiments should be repeated 3 or more times to ensure consistency and avoid variability due to flow cytometer settings), 5. Antibody interaction (Fluorescence minus one or FMO should be used, which is the comparison of signals from panel minus one antibody vs. the full panel), and 6. Antibody stability (fluorescently-labelled antibodies should be stored at 4C).