First day done!! Started at 9.30 and finished at 18.00, there
was a lot to take in and it honestly feels like the longest day in history!! I
was introduced to everyone including all of the technicians (those contacts I
know will definitely come in handy soon). Not only did I get an introduction to
the project and a tour around the labs, I actually got to do a few things
myself as well.
I learnt how to use an autoclave and I prepared a few LB
broths and LB agar, ready to be used for liquid and streak plate culturing
respectively. I also made stock solutions of different antibiotics,
ampicillin (AMP) and kanamycin (KAN) (which will be used to select for the
correctly transformed bacteria), and a stock solution of IPTG (which is a
lactose analogue, it will be used to induce expression of my desired proteins).
Each one was filter sterilised near a Bunsen burner and the frozen until we
need it. Using what I had prepared, I made a total of 10 different cultures
from provided glycerol stocks which I incubated overnight.
Today was an introduction and a chance to get used to the
lab whilst preparing some of the things I am going to need over the next few
weeks. It was also an introduction to working on my own, which will prepare me
for what lies ahead.
I also had the chance to meet some of the third year
biochemistry students and listen to their presentations on their dissertations.
This was a huge opportunity as well as giving me the chance to ask questions
about their studies and gain some insight into their research and about the
proteins I will be focusing on over the next few weeks.
Although a bit over my head,I get the gist of it. Very well written. So proud of you. Nan
ReplyDeleteEnjoy, sore feet is worth it, hang in there.
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