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- HersheyChase Experiments The graph shown in FIGURE 8.5 is reproduced from an original 1952 publication by Hershey and Chase. Bacteriophage were labeled with radioactive tracers and allowed 10 infect bacteria. The virusbacteria mixtures were then whirled in a blender to dislodge any viral components attached to the exterior of the bacteria. Afterward, radioactivity from the tracers was measured. FIGURE 8.5 Detail of Alfred Hershey and Martha Chases 1952 publication describing their experiments with bacteriophage. Infected bacteria refers to the percentage of bacteria that survived the blender. After 4 minutes in the blender, what percentage of each isotope was extracellular?HersheyChase Experiments The graph shown in FIGURE 8.5 is reproduced from an original 1952 publication by Hershey and Chase. Bacteriophage were labeled with radioactive tracers and allowed 10 infect bacteria. The virusbacteria mixtures were then whirled in a blender to dislodge any viral components attached to the exterior of the bacteria. Afterward, radioactivity from the tracers was measured. FIGURE 8.5 Detail of Alfred Hershey and Martha Chases 1952 publication describing their experiments with bacteriophage. Infected bacteria refers to the percentage of bacteria that survived the blender. The extracellular concentration of which isotope increased the most with blending?HersheyChase Experiments The graph shown in FIGURE 8.5 is reproduced from an original 1952 publication by Hershey and Chase. Bacteriophage were labeled with radioactive tracers and allowed 10 infect bacteria. The virusbacteria mixtures were then whirled in a blender to dislodge any viral components attached to the exterior of the bacteria. Afterward, radioactivity from the tracers was measured. FIGURE 8.5 Detail of Alfred Hershey and Martha Chases 1952 publication describing their experiments with bacteriophage. Infected bacteria refers to the percentage of bacteria that survived the blender. Before blending what percentage of each isotope. 35S and 32P, was extracellular (outside the bacteria)?
- HersheyChase Experiments The graph shown in FIGURE 8.5 is reproduced from an original 1952 publication by Hershey and Chase. Bacteriophage were labeled with radioactive tracers and allowed 10 infect bacteria. The virusbacteria mixtures were then whirled in a blender to dislodge any viral components attached to the exterior of the bacteria. Afterward, radioactivity from the tracers was measured. FIGURE 8.5 Detail of Alfred Hershey and Martha Chases 1952 publication describing their experiments with bacteriophage. Infected bacteria refers to the percentage of bacteria that survived the blender. Do these results imply that viruses inject DNA or protein into bacteria? Why or why not?During proofreading, which of the following enzymes reads the DNA? primase topoisomerase DNA pol helicaseΣ *00 F. C. O Top O Bottom QUESTION 6 The complementary sequence of 5' AATTCGCTTA 3' is (note the polarity 5' and 3 of the DNA and the complementary DNA in the answer) O 5'AATTCGCTTA 3'. O 3'AATTCGCTTA 5'. O5 TAACGCTTAA 3'. O 5'TAAGCGAATT 3'. O 3' TAAGCGAATT 5'. Click Save and Submit to save and submit. Click Save All Answers to save 73°F Rain or O search F12 PrtSc F7 F8 いコ F2 F4 F5 F1 ( & V # 2 7. 4. 5. 3. H B. Alt Ctrl Alt
- Tocts af Recombinant DNA DNA Technology (8 of 8) Teil Me Why NA In Vitro: The Poly Re Why did the discovery and development of restriction enzymes speed up the study of recombinant DNA technology? ChicA Meet - rfc-prp x A G-Unit 5: DNA an X 4 https://docs.goog x y google classroom xP Classes cs.google.com/forms/d/e/1FAlpQLSeyPC6Kmoa0k5JJd1DWGzqqRwaQQobHN0OdqFX_aDbV_6-bKw/formResponse x New Tab D YouTube Маps E Copy of Distance Le. Launch Meeting - . 2020 HORNETS 4N. O StudentVUE 2 Mr. Nussbaum Lan. A Graphing Lines Use the chart to determine the correct amino acid that this DNA would code for - ATA * 1 point GFL E D А Y STOP Alanine U Tyrosine C. STOP Stop V Valine GU Cysteine U Stop G Tryplophan R Arginine G А С U A Leucine S. K Serine A C L UGA Lysine Proline Аsparagine M START H. I R o search 99. Serine ThreonineDNA Replication, Sequencing, and Recombination - PowerPoint Karla Henthorn KH Animations Slide Show Review View Help O Tell me what you want to do A A E. s et Direction- Align Text Shape Fill O Find US abs AV- Aa - ay. A- Stiape Outine- ab Replace- ne Arrange Quick Styles Convert to SmartArt Shape Effects A Se Font Paragraph Drawing 6 5 4 1 3 Ec 2 1 2 3 H4 Kim ACTIVITY Consider the following DNA molecule: ACG GTACACTTA C G A A Henthorn, ic T GCCAT GT GA ATG CT T Rc 1) Draw the 2 strands after they have "unzipped". 2) Follow the rules for pairing and fill in the new strands with the correct nitrogenous bases. Write these new strands in a different color of ink. = Notes Comments 可 DO DELL
- Activity 4. Study the structure of DNA and answer the questions below. Sugar-Phosphate Backbones Nucleotide Key: O Adenine O Thymine I Guanine I Cytosine Hydrogen Bonds Antiparallel DNA Strands DNA Ladder Double Helix Fig. 9.DNA Structure. Retrieved June 19, 2020 from https://ib.bioninja.com.au/standard-level/topic-2-molecular- biology/26-structure-of-dna-and-rna/dna-structure.html 1. What are the common parts of the nucleotide? 2. Name the different kinds of nitrogenous bases found in the DNA molecule. 3. In DNA what is the paring arrangement of the bases?1.00 Oc. Lyse the cells to release the nucleic acid P Flag O d. Break up the DNA question O e. Precipitate the DNA Question 3. The picture below shows the last step of nucleic acid extraction after the centrifugation step, the layer labelled A contains.. Not yet answered Marked out of 1.00 P Flag question Answer: Question In the experiment of amylase extraction from barely seeds, after the second centrifugation- the amylase enzyme will be found inof estion 9 t of uestion THCA ▶ Sou 100- HC This reaction is Entropy is THC San Leafly ATA RNA polymerase SSSSSSSSSS ATTOGOGACATAA ATGACGGATCAGCCOCAAG UACUOCCUAGUC RNA Transcript TACTOCCTAGTCGGCOTTCOOCTTAACCOCTOTATIT (In this picture, RNA is being made by complementary base pairing with DNA.) This reaction is → Entropy is ◆
