I ran an ELISA and used two different antibodies in the same plate. I add the standards to first wells but just done the serial dilution for one of the antibodies ! I realized this when I checked my results!So I just have two dilutions :2000ng and 0 . Is there any way to analyse my ELISA or should I run another ELISA? Can I use the standard curve from previous experiments?
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need help! I have forgotten to serial dilute my standard!
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