DNA is a negatively charged molecule due to the presence phosphate groups in it's backbone and thus it moves towards the positively charged electrode electrode that is the anode, during electrophoresis.
The inclusion of a substance called ethidium bromide in the agarose gel allows the visualization of DNA under UV light. Ethidium bromide interchelates i.e gets trapped in between the double strands of DNA and on exposure to UV exhibits fluorescence. That I it absorbs UV light,gets excited and emits at a higher wavelength in the visible region,which we see as orange bands.
Band C corresponds to the third band from the well in the ladder labe which is 6 Kilobases and band D corresponds to the 6 the band in the ladder which is 3 kilobases. Dbeing smaller than C travelled further in the gel.
During gel electrophoresis, DNA travels towards the positive charge. Including the substance agarose in the gel...
3. The given figure represents the agarose gel electrophoresis results from a restriction digest experiment. Lane 1 is a DNA ladder (values are in kb) and Lane 2 is the DNA sample cut by a restriction enzyme. What is the size of the band C in lane 2? - 1111111 About 1.8 kb Cannot tell based on the information provided 500 bp About 2 kb © Less than 1.5 bp -
While your gel is running, discuss your expected results for each lane on the gel • Remove the gel from the apparatus and image on a UV transilluminator. (Remember to only illuminate the UV light when the shield is in place). 3) Using the DNA ladder, estimate the experimental size of all bands observed in the sample lanes. (3pt) Gel Lane Plasmid Number of bands observed Estimated size (bp) of each band 2 (tube 1) A 3 (tube 2) B...
The picture above represents an agarose gel that was used to analyze plasmid DNA after it was cut with the restriction enzyme HindIll. The plasmid was incubated with Hindill until all of the available Hindlll cut sites were cut by HindIll. After running the sample on the gel, three bands were detected (Note that there are three wells shown at the top of the gel for loading samples, however, only the middle well was loaded with sample). Based on this...
FULL image displayed under of the expected vs actual results of
agarose gel analysis (the top picture is expected and bottom is the
result)
Question: You conclude that the error occurred while preparing
arose gel. What mistake was made? Why does it look like the picture
above and not how you expected?
Gel Question #1: During Lab 7, you and your three teammates performed gel electrophoresis as described in the lab manual. Your team was especially careful while carrying out...
is
a nucleus the sole source of DNA in a eukaryotic cell?
WORKSHEET: EXERCISE 10 NAME: DATE: SECTION Twenty microliters (20 ㎕) of each sample was loaded into your gel. Convert 2OuL to milliliters (mL). I. 2. Describe the charge on the DNA molecule and specify which component of the molecule is responsible for contributing to that charge. Why do some DNA samples travel further in the gel than others? 3. 4. Once electrophoresed, how are the DNA bands visualized?...
I
need the answers for questions 2 and 3. My DNA ladder is in lane 2
marked by the yellow arrow. Thanks!
Here is the only other info I have. Thanks!
Part 2: Gel purification and on Gel Slice and PCR Product Preparin modified from TBSci.com instructions for gaan A. Dissolving the Gel Stie Following electrophores, eral DNA band from grand place glice microcentrifuge tube Ib. Use an analytical balance to weigh pelice Rec die 2. Add 500 balance to...
En (2 points) You isolated your mitochondrial DNA in Part I. In step 6, you discard the supernatant, but keep the pellet. In step 15, you discard the pellet, but keep the supernatant. Explain why the pattern is different between the two steps and the consequence of mixing up these two steps. Procedure Part 1: mt DNA Isolation from your cheek cells. Lysis solution is used to breakdown the cells in this step, you will isolate MEONA from cheek cells....
help with questions 5 to 10 please
PCB 3023L Lab #4 Protocol & Worksheet (30pt) You may work in your lab groups durine class. but all written answers must be completed individually in your own words. 1) Using the plasmid map for orientation 1 and the cDNA map as a guide, complete the plasmid map for orientation #2. (4pt) 612 1318 1 - EcoRi EcoRI Xbal ECORV -Xbal- 1662 +Bell EcoRI EcoRV Not FP -- Xhol X 2015 PRSP +...