Skip to main content

Jane Richardson, Necessary Failure

In science, sometimes the only way we can actually reach our destination is with all of the hidden failures along the way that guide us to the end game. I guarantee every scientist will experience their fair amount of failure, but all of it will make you better. In optimization, essentially the entirety of my job, this is especially prevalent. When figuring out the best procedure, you have to go through a lot of failed ones. In addition to the one successful procedure and the one in progress, we now have yet another to optimize. Last week, we started a procedure to extract bacterial DNA from human stool samples. We ran a gel to see if the DNA extraction was successful. Our extraction procedure was utterly unsuccessful. Though it would have been nice to find success on the first try (something I now realize was wishful thinking) it is going to make the end result much more of a success. Without stumbles along the way, we can never get better.

In continuation with our overall project, we have been continuing to prepare slides to look at under the microscope. If we find that the SERT levels are not the reason behind high levels of 5-HTT, we will have to begin optimizing a second IHC procedure for a different protein. I am very excited to optimize the second procedure. So far, we have not decisively concluded our results. We still need to learn how to use the confocal microscope so we can see both contrasts at the same time and exposure. I expect we will begin using the confocal soon. As for the slides, our results have gotten even better. In up-ing the exposure time for 20ms to 40ms, we were able to see the SERT much more clearly and out edits came out much better. I have attached a picture above. One interesting thing we noticed on our last round of slides was the distal colon had much higher levels of SERT than any other portion of the intestine. This was very strange because we usually have the highest levels in the ileum. We will continue to examine this in further slides.

Over the past two weeks, the lab members have truly begun to become my friends. This experience has been incredible and although I am sad to only have two weeks left, I am really looking forward to finishing my project here! Also this week, Ms. Cozine came to Washington, D.C. and had lunch with me and my grad student. I was able to show her the microscope we currently use, which I know get to operate myself. We had a great time and I really appreciate her coming!

Comments

  1. Good luck with your next two weeks! If you have time, read Michelle's blog - she is coming to the same conclusion that you are - it takes lots of trial and error to optimize your results. Hope your tennis matches go well!

    ReplyDelete

Post a Comment

Popular posts from this blog

Evan Bradley, Week 3 at the Missouri Orthopaedic Institute

As mentioned in my previous blog, I have been awaiting ligament, menisci, and cartilage tissue from a canine or human knee joint for (interleukin) IL-1B tissue culture. IL-1B is an inflammatory cytokine that has been proven to increase rates of tissue degeneration and osteoarthritis development in the Thompson Lab. Dr. Stoker wants me to experiment with different types of knee tissues in a co-culture with varying levels of this cytokine to determine its effects on the entire knee joint. This co-culture uses an insert permeable to the media to separate the two tissue samples from physical contact, while allowing them to share the same media. This creates an extremely accurate model for knee tissues in their native environment due to their exposure to the same synovial fluid in the joint. This model would then be treated with the IL-1B and cultured for 21 days. During these 21 days, the media would be collected every three days for biomarker evaluation at the end of the stu...

Kylie Heering, Week 2 at the Goldstein Lab

We started off our week with a congratulatory acai bowl trip to celebrate Preston’s acceptance into a training grant program. Acai bowls in California top Playa Bowls (no question about it). From what I can tell, its a pretty huge honor to be recognized by this grant, but he’s really humble about it. On Monday, Preston and I decided that testing antibodies that have never been tested on prostate epithelial cells before would be a good objective for my first Western blot on my own. We needed to probe for ASCT2, a glutamine transporter, and GLS in order to determine if their corresponding antibodies are functional. Antibodies are crucial for Western blots because they bind to the protein of interest (POI), allowing for us to qualify its expression after imaging. As such, Preston wanted to make sure they worked by probing for ASCT2 and GLS on three different cell lines. Cell lines are commercially purchased human cells that have been immortalized (modified to grow indefinitely) by telome...

Daniel Cheng, In My Own Room

I had no idea that Pennsylvania is this wide. Within the first hour, my train had reached Philly. But to Pittsburgh, it took another seven. Even before I stepped foot into the Search-Based Planning Lab, I was waylaid by some anxious news. The PhD student assigned to be my mentor, Dhruv, texted me that he, Dr. Likhachev, and most of the lab would be out of town for the entire week. So that was that. Fortunately, it was my first week, the week to be spent learning new material, and Dhruv provided me with plenty to digest. I already had ROS (Robot Operating System) installed, so I looked towards the tutorials that ROS provided. I copied commands into my Linux laptop's terminal to run ROS features. I learned the basic structure of ROS: packages, services and clients, publishers and subscribers, messages, nodes, and topics (which nodes communicate messages over). There was one simple yet interesting program I came across in the tutorials called turtlesim, for which using only 2 comm...