Immunohistochemistry Collagen VII antibody [LH7.2] Mouse

Get tips on using CD14 Monoclonal Antibody (Sa2-8), FITC, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - CD14

Get tips on using Recombinant Anti-CD204/MSR1 Antibody (FITC), Rabbit Monoclonal to perform Flow cytometry Anti-bodies Mouse - CD204

Get tips on using FOXP3 Monoclonal Antibody (FJK-16s), PE, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - FOXP3

Get tips on using FOXP3 Monoclonal Antibody (FJK-16s), APC, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - FOXP3

Get tips on using CD3e Monoclonal Antibody (145-2C11), Biotin, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - CD3

Get tips on using CD11c Monoclonal Antibody (N418), PE-Cyanine5.5, eBioscience™ to perform Flow cytometry Anti-bodies Mouse - CD11c

Get tips on using CD11b Monoclonal Antibody (M1/70.15), PE-Texas Red to perform Flow cytometry Anti-bodies Mouse - CD11b

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.

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.

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.