6751 bp3652 bp2827 bp1568 bp1118 bp825 bp630 bp(-)M CS1 CS2 12 3 4(+)LaneTube1MarkersCS 1CS 2123459526374DNA Standard MarkerDNA from crime scene cut with Enzyme 1DNA from crime scene cut with Enzyme 2DNA from Suspect 1 cut with Enzyme 1DNA from Suspect 1 cut with Enzyme 2DNA from Suspect 2 cut with Enzyme 1DNA from Suspect 2 cut with Enzyme 2Using the image here, select all bands (based on approximate sizes) that were presentin Suspect #1 cut with Enzyme 2.600700150030003700

1. Understanding the lanes:Lane 1 (Marker): This lane contains DNA fragments of known sizes…

Answered: 6751 bp 3652 bp 2827 bp 1568 bp 1118 bp…

Human Anatomy & Physiology (11th Edition)

11th Edition

ISBN:9780134580999

Author:Elaine N. Marieb, Katja N. Hoehn

Publisher:Elaine N. Marieb, Katja N. Hoehn

Chapter1: The Human Body: An Orientation

Section: Chapter Questions

Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...

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Similar questions

What is the sequence of the sample DNA submitted for sequencing given the gel electrophoresis profile from the Sanger sequencing method?
BamHI KpnI SpeI XhoI PatI HindIII 400 500 200 300 700 NotI 75 2580 ECORI Frog DNA BamHI 575 KpnI HindIII 625 2150 HindIII 700 PstI clal 750 РКАВОО 2700bp 915 1900 SpeI AluI 1050 1525 BamHI ori You wish to make a recombinant DNA molecule that will contain one piece of pKABOO vector DNA and one piece of frog DNA so that you can clone a segment of frog DNA. You want cells containing your recombinant plasmid to be amp' and tet and you want to use enzymes that cut within the insertional marker gene. (Note that tet means that there is no functional tet gene in the plasmid.) Be sure that your plasmid has the ability to replicate autonomously in a bacterial cell. You do not have to include the entire frog DNA given below in your recombinant plasmid. Restriction enzymes would be used to clone segment of frog DNA The size of the recombinant plasmid is bp. The recombinant plasmid when transformed into E. coli confers resistance to which of the following antibiotics: Oampicillin only Otetracycline…
Please do question number 2 only
please help
Write the number of each variation for the remaining STR loci to create a DNA profile of this person: STR Locus Variation number(s) D3S1358 14, 15 THO1 D21S11 D18S51 Penta E
How is the DNA used for catching crime suspects. Describe the procedure and cite particular example where it helped solve a case or absolved an innocent person from any wrongdoing
Lane 1 Lane 2 Lane 3 Sample2: PBR3222 Base Pairs DNA Mass (ng/Sul) Sample1: TUC19 2888 4.000 3,000 2,500 2,000 DNA 34 ladder 1,500 92 1,000 23 750 30 -500 45 250 1% TAE agarose gel Resuits of DNA gel electrophoresis (after editing brightnessm DNA ladder that we used as marker in Lane no 1 Lane 1 Lane 2 Lane 3 Base Pairs DNA Mass (ng/5ul) Sample2: PBR3222 1988° Sample1: TUC19 4,000 3.000 2.500 -2.000 1,500 34 20 DNA 1,000 92 ladder 23 750 30 500 45 250 1% TAE agarose gel Resuits of DNA gel| electrophoresis (before editing brightness) DNA ladder that we used as marker in Lane no ! Determine whether sample 1 and sample 2 are plasmid OR genomic DNA, justify your answer
can you please discuss and interupt these plasmid DNA maps.
1/V (uM x min-1)-1 1. To the right is a Lineweaver-Burk plot for an enzyme that can cleave both DNA (D) and RNA (R). 2200 2000 1800 a. What is the KM when cleaving DNA? I 1/V R 1600 • 1/V D b. What is the KM when cleaving RNA? 1400 1200 C. What is the Vmax when cleaving DNA? Z 1000 800 d. What is the Vmax when cleaving RNA? 600 e. On the graph, draw an appropriate line for a 400 noncompetitive inhibitor for cleaving DNA. Label clearly. f. On the graph, draw an appropriate line for an uncompetitive inhibitor for cleaving RNA. Label clearly. 200 8 10 11 1/S (µM)-1
What allows the peaks to be different colors?
A ssDNA solution is diluted by taking 3uL of a stock solution, which is made up to 60uL withwater. From this stock, 10uL is taken and diluted to 100uL with water. The solution is then madeup to 3mL. The A260 was 0.012. Calculate the concentration of DNA in the original stock inug/mL
Use the gel to answer the following questions. You will be constructing a map of the plasmid, pDiddy. What is the largest fragment size that the BamHI/NcoI double digest produces? 2.250 kb 2.500 kb 2kb 750 b

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