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Labster lab report for the biology class
Typology: Lab Reports
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Q U E S T I O N 1 O F 8
To make the DNA molecules move faster through the gel To allow visualization of DNA bands under UV light To change the charge of the DNA molecules To prevent DNA degradation during electrophoresis Q U E S T I O N 2 O F 8
By their electrical charge only By their color after staining By their size as they move through the gel matrix By their temperature sensitivity Q U E S T I O N 3 O F 8
Its positive charge Its negative charge Its neutral charge Its molecular weight Q U E S T I O N 4 O F 8
It provides nutrients for DNA stability It acts as a molecular sieve to separate fragments It neutralizes the charge of DNA molecules It increases the speed of all fragments equally Q U E S T I O N 5 O F 8
Larger fragments with more base pairs Fragments with the strongest negative charge Smaller fragments with fewer base pairs Fragments with the most dye molecules attached Q U E S T I O N 6 O F 8
The concentration of agarose in the gel The electrical field between the electrodes The temperature of the buffer solution The amount of DNA loaded in each well Q U E S T I O N 7 O F 8
To calibrate the electrical current
To provide size reference for DNA fragments To prevent DNA degradation To visualize the direction of migration Q U E S T I O N 8 O F 8
To make the gel run faster To add more bands to the gel To validate experimental results To stain the DNA molecules Amplifier Labster DNA: Gel Photoresis Labster DNA: structure and function Labster Polymerase Chain Reaction Q U E S T I O N 1 O F 8
Breaking down DNA into nucleotides Adding new nucleotides to create a complementary DNA strand Separating double-stranded DNA Connecting RNA primers together
5' to 3' direction only 3' to 5' direction only Both directions simultaneously Random direction DNA polymerase synthesizes new DNA in the 5' to 3' direction only. Explanation: DNA polymerase can only add nucleotides to the 3' end of a growing DNA strand, so the new strand is always built in the 5' to 3' direction. Q U E S T I O N 3 O F 8
Template DNA, primers, nucleotides, and DNA polymerase Template DNA and water only Primers and nucleotides only DNA polymerase and water only The essential components needed for a PCR reaction are: template DNA, primers, nucleotides, and DNA polymerase. Explanation: Template DNA: This is the original DNA molecule that contains the target region to be amplified. Primers: Short DNA sequences that are complementary to the ends of the target region, allowing the DNA polymerase to start building new strands from there. Nucleotides: