S-STEM Scholar Dung Le's Blog

That was a successful day at lab. Our group did the good job with cutie gel and nice results.  I joined to do the  gel electrophoresis 1.8 % and ran machine at 85 mA/Rm. I had few pictures for that days:

1. I did the rich media 500 mL agar with the component: + Bacto peptone 5g + Yeast extract 2.5g + Casamino acid 2.5 g + Meat extract 1g beef + Mail extract 2.5 g + Glycerol 1g + MgSO4 x 7H20 0.5g + Tween 80 0.005g + Agar 10g + DI water 500 mL 2. I also did the rich media 500 mL with the component: + Bacto peptone 5g + Yeast extract 2.5g + Casamino acid 2.5 g + Meat extract 1g beef + Mail extract 2.5 g + Glycerol 1g + MgSO4 x 7H20 0.5g + Tween 80 0.005g + Agar 10g 3. I also jointed to make gel electrophoresis 1.8%

This week I did the gram staining for 13 sample of gobi and geo group in 2 days from 2/7/2020 and 2/8/2020. I did washing slides over 5 seconds so it might effect to my results. I have thought I did bad in this week for Gram staining. I will try the best in next time.

Slides were loaded into a BioTek slide in both a coverslip down Optimal exposure settings were determined for each objective using a positive control smear and then applied to all images for both positive and negative controls. Our group used microscope BioTek to do gram staining protocol with sample was CF594 (red color/cell wall) and Dapi (Blue color/ Nuclei) With + DAPI 377/477 1225100 Rev J - Blue + GFP 469/526 1225101 Rev K- green + TEXAS 586/647 125102 Rev J - Red I very like this new technique, and I think it is more exactly than normal gram staining technique I have used before. I hope I will do it few more time in future so I can use to do this new method.

I did the Transformation of E. cloni 10G Chemically Competent cells: 1. Remove Recovery Medium from the freezer and bring to room temperature.  2. Remove E. cloni 10G cells from the -80°C freezer and thaw completely on wet ice (10-15 minutes).  Tube (+) Tube (D) Tube (I) 3. Thaw the tube of pRham™ Vector DNA and microcentrifuge the tube briefly to collect the solution in the bottom of the tube.  4. Add 2 µL (25 ng) of the pRham Vector DNA and 1 to 3 µL (25 to 100 ng) of insert product to the cells. Stir briefly with pipet tip; do not pipet up and down to mix, which can introduce air bubbles and warm the cells.  5. Important: Transfer the mixture of cells and DNA to a pre-chilled disposable polypropylene 15- mL culture tube (17 x 100 mm). Performing the heat shock in the small tube in which the cells are provided will significantly reduce the transformation efficiency.  Summary:  Put 2 µL Prham ™ C-His + 3 µL transformation to tub...