For this question, measure the distance travelled by dna in each row with a scale that would give you distance in cm. For size of dna in each row, you need to know the size of dna ladder. The size of ladder is always in base pairs. Also smaller dna molecules will travel more distance than latger dna molecules. Wheather the dna is recombinant or plasmid can also be concluded from the size. Also the circular dna will run slowly as compared to linear dna. And also relaxed dna will run slowly as compared to supercoiled dna. Supercoiled dna will run faster than circular dna.
Table 8-3. Interpretation of each lane on the gel. For Lanes 1-8, indicate the size of every DNA ...
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...
How did you EXPECT your uncut lane to look in the gel image? What ACTUALLY happened? What is a plausible explanation if there was any discrepancy? How did the observed BclI and EcoRI digest results compare to the expected results? If they differed, list a potential reason why? BclI was incubated at 50°C, while EcoRI was incubated at 37°C. Why was this necessary? What might you predict to occur if you accidentally switched the temperatures? 3) Using the DNA ladder,...
TTC ach of the DNA fragments on your gel can be determined using another method th The number of base pairs in each of the DNA fragments the size of the known framments from the DNA marker against her method that can be more accurate. This involves graphing ents from the DNA marker against the distance each fough the gel to generate a standard curve. This is most DNA band moved through the gel, to generate a conveniently done on...
3) Image from Biotechnology Explorer Kit, BIO RAD Analysis of DNA Fragments The data you entered for the lambda Hindill digest were the relative positions of DNA bands of known size. Since the exact size and position of these fragments are known, they can be used as standard reference points to estimate the size of unknown fragment bands. A set of fragments of known sizes is called a molecular weight ruler or standards or marker (or sometimes a ladder because...
Question 1. 1 2 3 4 5 6 7 8 Lane Name/Code Ladder 1B | 2B 2 DNA Sample/Treatment DNA ladder Digest Digest Digest Digest Digest Digest 3B 4B 5B Negative Figure 1: 1% Super buffer agarose gel electrophoresis of restriction digest of the plasmid containing the gdhA gene insert. Based on the information above answer the following questions? 1. What ladder size used? 2. What are the two top bands and bottom bands representing? 3. Explain why the observed...
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...
I just need the answers to questions 2 and 3. My DNA ladder is in lane 2 with the yellow arrow pointing to it. Thanks! Part 2: Gel purification and ration Gel Slice and PCR Product Preparation modified from IBSci.com instructions for gel and PCR clean-up system A. Dissolving the Gel Slice 1. Following electrophoresis, excise DNA band from gel and place gel slice in a 1.5ml microcentrifuge tube. 1b. Use an analytical balance to weigh gel slice. Record weight...
b. Make a TABLE 1 with distance migrated (cm or mm) vs size (in bp) of the 1 kb Ladder standard bands. [See Example) Measure distance migrated for each size standard band on gel. (5 pts) DNA Standard Undigested Pstl+Sac!! Pstl+Stul Pstl+Sacll+Stut Pst! BOS S Kilobases Mass (ng) - 10.0 -80 (bp) 3,300 3,000 2.900 2,700 2,500 0 CC 2,700 2,400 2,000 1,800 1,750 1,800 1,600 1,400 1.300 1,250 1,000 850 800 750 700 650 600 550 -0.5 42 500
L= No restriction B=Bam HI E=EcoRI H=Hind III Band 1 27mm 31mm 29mm 29mm Band 2 NA 34mm 41mm 37mm Band 3 NA 41mm 46mm 43mm Band 4 NA 43mm 49mm 52mm Band 5 NA 46mm 57mm 71mm Band 6 NA NA NA 76mm Above is the actual measurements for the distance in mm. Please plug this in with the existing chart located above Gel Electrophoresis lab assignment The following sheets will be used to demonstrate your knowledge of gel...
Skill Check DNA All in Our Genes SU2020) Protected ViewSaved to this PC- Design Draw Layout References Malings Review Help les from the Internet can contain vs. Unless you need to edit it's safe to stay in Protected View farah dowod . Activity 3: Analysis of Forensic Samples Crate Editing This photo is an actual photo of a gel that was run using the samples outlined in this lab From left to right Lane 1: A Hindi DNA digest used...