Pipetting
Dilutions & Concentrations
Gel Electrophoresis
Spectrophotometry
PCR & Molecular Biology
100

What pipette would you use to measure 11 µL?

P20

100

If you dilute 1 mL into 9 mL, what is the dilution factor?

1:10


100

What is the primary purpose of gel electrophoresis?

Separates DNA by size


100

DNA is measured at what wavelength?

260 nm


100

What happens to PCR if there are no primers?

Reaction won’t start

200

What pipette would you use for 675 µL?

P1000

200

After 3 1:10 dilutions, what is the final dilution factor?

1:1000

200

What factor primarily determines the rate of DNA migration?

Size of DNA fragments


200

Proteins are measured at what wavelength?

280 nm


200

What does Taq polymerase do in PCR?

Builds new DNA strands (heat-stable DNA polymerase)

300

What color tip is used for 75 µL?

Yellow Tip

300

A 1000 µg/mL stock is diluted 10^-2. What’s the new concentration?

10 µg/mL


300

What does DNA dye do?

Binds with DNA to visualize bands


300

Bacterial cell density is measured at what wavelength?

600 nm


300

Why is Taq polymerase better than regular DNA polymerase for PCR?

Taq can survive high heat during PCR cycles, unlike regular DNA polymerase, which denatures


400

What’s the first step in calibrating a micropipette if it gives inconsistent results?

Tare balance with water and weigh

400

If you do 4 serial dilutions of 1:10, what’s the total dilution factor?

1:10,000

400

What does loading dye do?

Adds color/weight to track sample in wells


400

Why do we use a standard curve in spectrophotometry?

To compare unknowns to known concentrations

400

Give one example of how a change in genotype can alter phenotype.

Mutation → altered protein → changed trait (e.g., colony morphology)

500

Why is calibration important in micropipetting?

Ensures accuracy and reproducibility in experiments


500

Why do scientists use serial dilutions instead of one large dilution?

More accurate and manageable steps


500

Agarose vs. Agar — which one is used for DNA gels, and which for bacterial growth?

Agarose = DNA electrophoresis, Agar = bacterial colonies

500

What feature shows a “good” standard curve?

Straight, linear line with best fit


500

What are three essential components (ingredients) needed for PCR, besides the DNA template?

Primers, nucleotides (dNTPs), and Taq polymerase