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*Note to educators: you are permitted to share BosterBio's resources and PDFs on your class websites and lab websites. Please make sure to cite or link to the origin.
Keywords: troubleshooting tips, technical, optimization
ELISA is a convenient and simple method to quantitatively or qualitatively detect peptides, proteins, antibodies, and hormones in samples, rendering it as one of the most widely used immunoassays. Despite the many advantages of conducting ELISA, there are some mistakes that could quickly turn your ELISA experiment sour.
Read about the 5 common pitfalls to avoid when performing an ELISA so that you can prevent this situation from happening!
Keywords: ELISA protocol, comparison table, technical tips, ELISA assay format, advantages of sandwich ELISA, indirect, direct, competitive immunoassay
Are you familiar with the multiple methods you could use to perform an ELISA? Among the standard assay formats, it is important to differentiate between the particular strategies that exist specifically for the detection step. An antigen could be captured to the plate by direct adsorption to the surface or through a pre-coated "capture" antibody, as in a sandwich ELISA. However, it is the detection step (direct or indirect detection) that largely determines the sensitivity of an ELISA. Read on to discover which ELISA is for you...
Keywords: ELISA assay optimization tips, checkboard titration principle explanation, ELISA protocol optimize, how to titrate
Optimizing your ELISA immunoassay can be a long and tedious process. Fortunately, using checkboard titration could help you optimize your ELISA assay more quickly, efficiently, and accurately. Here is a how-to-guide for utilizing this method in your next ELISA protocol.
Keywords: ELISA immunoassay, technical tips, troubleshooting, ELISA excess signal, ELISA kit result optimization
Every ELISA kit user comes across the need to troubleshoot their assay at some point. Saturated signals can result from many different possible causes, and this could make troubleshooting complicated. Dr. Booster has come up with a table of recommended solutions for troubleshooting your ELISA assay. If this table does not help your specific experiment, please feel free to contact Boster's technical support at any time. Get better results with Boster!
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Troubleshooting Guides*Note to educators: you are permitted to share BosterBio's resources and PDFs on your class websites and lab websites. Greetings Earthling, Are you familiar with the multiple methods you could use to perform an ELISA? Check our online catalog of comp...
See MoreThe standard curve is prepared through serial dilutions of the standard with known concentrations that should span the standard curve range. To set up a standard curve, ELISA standards should be carefully prepared for accurate sample quantification o...
See MoreOur antibodies are validated using WB, IHC, and flow cytometry against a panel of over 250 tissues and un-transfected cell lines to ensure high affinity and crystal-clear IHC stains. Newsletter Picokine ELISA Kits *Note to educators: you are permi...
See MoreIf you prefer to try a sample kit first, for limited amount of time, we're offering $99 Multiplex ELISA demo kits, limited to one per lab. Troubleshooting guides Traditional ELISA vs. Multiplex ELISA How are traditional ELISA kits and Multiplex ELISA...
See MoreIn order to obtain quantitative ELISA data, constructing the ELISA standard curve is an important and crucial process to estimate the target protein concentrations for your samples. Troubleshooting guides ELISA Data Analysis The ELISA is one of the m...
See MoreOur antibodies are validated using WB, IHC, and flow cytometry against a panel of over 250 tissues and un-transfected cell lines to ensure high affinity and crystal-clear IHC stains. Troubleshooting guides Small Molecule, Hormone, Inflammation ELISA ...
See MoreThe standard curve can help confirm that the quality of the kit and the operation procedures are acceptable for further steps. Our antibodies are validated using WB, IHC, and flow cytometry against a panel of over 250 tissues and un-transfected cell ...
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