Here is my response in 200-300 wrods
Please feel free to comment/critique. Thank you so much!
I have faced some of my toughest intellectual challenges while conducting my undergraduate research. When something goes awry in cell and molecular research, no clear-cut solution is available due to the intricate nature of the intracellular processes and interactions. This was the case when I had to optimize the conditions for my co-immunoprecipitation experiment, a procedure used to detect interaction of specific proteins in a cell, due to the repeatedly inconsistent and weak data.
My first logical step was to repeat the experiment with newly made reagents and fresh cells. When the results did not improve, the next plan was scrutinizing every step in the procedure to identify the problem. Because repeating the experiment to test each possible factor could take years, I had to utilize my reasoning skills to select the most promising few. First, I gathered information on the most common errors in co-immunoprecipitation by inquiring other researchers in the lab and investigating published papers and troubleshooting guides. I ran the experiment again paying special attention during the critical steps to see if human error was the cause of the inconsistency. Again, wrong guess. I then decided to evaluate the integrity of each DNA and protein sample but with more efficient and quick tests available. Sequencing each gene and different experiments to test the activity of each protein confirmed the intact functions of each biomaterial. I had hit a wall; it was time to think outside the box.
I began to question the protocols I was given for co-immunoprecipitation. The specific proteins I was studying had their unique characteristics; what if the protocols are not optimal for my proteins? Right away, I began brainstorming possible modifications to the protocols to better accommodate the proteins' biochemical traits and began designing experiments to test my ideas. After two failed trials, I had almost given up when the strong signals on my third set of data caught my eyes. Finally, I had found the key to the solution - a stronger detergent for a better yield in extracting my proteins from the cells.
Please feel free to comment/critique. Thank you so much!
I have faced some of my toughest intellectual challenges while conducting my undergraduate research. When something goes awry in cell and molecular research, no clear-cut solution is available due to the intricate nature of the intracellular processes and interactions. This was the case when I had to optimize the conditions for my co-immunoprecipitation experiment, a procedure used to detect interaction of specific proteins in a cell, due to the repeatedly inconsistent and weak data.
My first logical step was to repeat the experiment with newly made reagents and fresh cells. When the results did not improve, the next plan was scrutinizing every step in the procedure to identify the problem. Because repeating the experiment to test each possible factor could take years, I had to utilize my reasoning skills to select the most promising few. First, I gathered information on the most common errors in co-immunoprecipitation by inquiring other researchers in the lab and investigating published papers and troubleshooting guides. I ran the experiment again paying special attention during the critical steps to see if human error was the cause of the inconsistency. Again, wrong guess. I then decided to evaluate the integrity of each DNA and protein sample but with more efficient and quick tests available. Sequencing each gene and different experiments to test the activity of each protein confirmed the intact functions of each biomaterial. I had hit a wall; it was time to think outside the box.
I began to question the protocols I was given for co-immunoprecipitation. The specific proteins I was studying had their unique characteristics; what if the protocols are not optimal for my proteins? Right away, I began brainstorming possible modifications to the protocols to better accommodate the proteins' biochemical traits and began designing experiments to test my ideas. After two failed trials, I had almost given up when the strong signals on my third set of data caught my eyes. Finally, I had found the key to the solution - a stronger detergent for a better yield in extracting my proteins from the cells.