ELISA Pro?

I have spent the last two weeks fine-tuning my lab techniques and honing my ELISA skills. The first two human progesterone assays have been abandoned for the time being. We have been working with bovine serum and milk progesterone kits from the United Kingdom. This assay has worked very well, but the assay is not very sensitive and was designed for qualitative results. We are currently verifying parallelism {similarity between serially diluted samples and standard curves} within this assay with several samples from cows in late pregnancy. This looks promising after purchasing an alternate substrate that can be read by a absorbance filter in our possesion. We have also started working with estrone sulfate kits from Australia. This is a sweet little assay which appears very promising. It was specifically designed for pregnancy testing DHIA milk samples. I will be focusing on incresing the sensitivity of the estrone sulfate assay by looking at other assays (human) and possibly building our own estrone sulfate assay by purchasing indivdual components. The Australian kit is designed to confirm pregnancy at 120 days, but our goal is to lower that number.

The above graphs show a quick interpretation of the standard curves from two different human progesterone assays including the negative control bovine samples spiked with equivalent concentrations of progesterone. The Alpha Diagnostic assay appears promising, and we are currently waiting on testing of our negative control serum samples to validate low progesterone levels were present at the time those samples were taken. The Assay Designs kit is a more sensitive assay and has shown interference when bovine samples are used and an inability of the reagents to remain stable in the lab environment. (To view graphs in more detail click on image to increase size)

Introduction to ELISA Procedure

The goal of our lab work this week has been to determine which progesterone assays will work for bovine serum and milk. The two assays we have tried thus far were both designed for human serum. We first produced standard curves with progesterone samples provided in the kit or via serial dilution to determine if the assays were functioning properly. Bovine serum and milk samples were collected from cows enrolled in the G6G Ovsynch program at Nobis Dairy on days where natural progesterone levels were at their lowest concentration. These samples will provide our negative controls. The second day we repeated the standard dilutions and compared them to bovine serum and milk samples which had been spiked with equivalent concentrations of progesterone. This allowed us to look for components in milk or serum samples that may interfere with the reagents of the human progesterone assays. The assays were also run with undiluted, unaltered serum and defatted milk samples from the negative control samples. The assays which will be used for a marketable product need to perform well with unaltered samples of milk. Any extra processing required in an assay drives up production costs and will not allow us to offer a product at an affordable price to producers.

Therefore, I have begun my crash course in ELISAs. Running ELISA's consists of accurately pippetting minute quantities of reagents into small microtiter wells. This sounds fairly simple, especially when well-quipped with sophisticated equipment. I have learned that the degree of accuracy increases with the number of ELISAs the lab tech has run. This is very evident when I try to produce equivalent results when processing duplicate rows of samples compared to the lab techs that make everything look very easy when they dispense their billionth sample.

A standard 96-well ELISA plate. In this plate, bovine serum is being run alongside standards provided for a human serum progesterone assay kit to determine if the components in bovine serum interfere with the reagents of an assay designed for human serum.

This is a portion of the ELISA lab where the experiments for this project are being executed.

Many thanks to the lab techs. Pictured here: Heather Donohue and Beth Lockwood

Bridgette and I collecting blood samples.