MCQ Bank
How are the resultant fragments separated in restriction enzyme mapping?
- A) Polymerase chain reaction
- B) Spectrophotometry
- C) Chromatography
- D) Electrophoresis
What consequence could occur if the RNA pellet is allowed to over-dry during the air-drying step?
- A) No impact on RNA quality
- B) Increased RNA solubility
- C) Decreased RNA solubility
- D) Faster RNA hydration
What distinguishes a stock solution from a working solution in a laboratory setting?
- A) Stock solutions are concentrated solutions of known, accurate concentrations for future dilution, while working solutions are made for actual use in the lab.
- B) Stock solutions are concentrated solutions of unknown concentrations, while working solutions have known and accurate concentrations.
- C)
- D)
How is DNA purity commonly calculated using absorbance readings?
- A) A280/260 ratio
- B) A260/230 ratio
- C) A260/280 ratio
- D) A260/320 ratio
What is the recommended anticoagulant for blood collection in the described DNA extraction protocol?
- A) Ethylenediaminetetraacetic acid (EDTA)
- B) Isopropanol
- C) Sodium chloride (NaCl)
- D) Tris EDTA buffer
What is the primary technique commonly used to determine DNA/RNA yield and purity?
- A) Electrophoresis
- B) Mass spectrometry
- C) Chromatography
- D) Absorbance using Nanodrop
What is the most commonly used concentration of Ethidium bromide stock that is added for DNA quantification in the gel solution?
- A) 10 mg/mL
- B) 15 mg/mL
- C) 1 mg/mL
- D) 5 mg/mL
Which step involves the extraction of proteins from the sample?
- A) DNA Precipitation
- B) Digestion step (Lysis of White blood cells, WBC)
- C) Lysis of Red Blood Cells, RBC
- D) Phase Separation step
DNA concentration is estimated using a spectrophotometer at which of the following UV wavelength?
- A) 280nm
- B) 320nm
- C) 230nm
- D) 260nm
Why is the rate at which a DNA molecule moves through an agarose gel inversely proportional to its size during electrophoresis?
- A) Larger molecules move slower
- B) Smaller molecules move faster
- C) Smaller molecules move slower
- D) Larger molecules move faster
What is the purpose of the "Phase Separation step" in the DNA extraction process?
- A) Extraction of DNA from solution
- B) Precipitation of DNA
- C) Removal of digested protein
- D) Precipitation of DNA
To measure the quantity of RNA, which instrument is commonly used
- A) Nanodrop
- B) Both nanodrop and spectrophotometer
- C) Spectrophotometer
- D) Gel electrophoresis
What is the primary purpose of boiling Agarose in the TAE buffer during gel preparation?
- A) To change colour of agarose gel
- B) To increase gel concentration
- C) To sterilize the gel
- D) To dissolve agarose in the buffer
What does an A260/280 ratio of ~1.8 indicate for DNA?
- A) Low purity
- B) Presence of proteins
- C) Presence of contaminants
- D) High purity
Why is it important not to disturb the RNA pellet during the isopropanol addition step in RNA extraction?
- A) To avoid RNA degradation
- B) To ensure proper mixing
- C) To speed up the process
- D) To prevent contamination
What is the role of 3X Bromophenol blue in the DNA loading process?
- A) To improve gel conductivity
- B) To enhance DNA visibility
- C) To quantify DNA concentration
- D) To act as a loading dye
How are the resultant fragments in restriction mapping separated and their sizes determined in base pairs?
- A) UV-Visible spectroscopy
- B) SDS-PAGE and Western blotting
- C) Agarose gel electrophoresis and comparison with a standard size marker
- D) Northern blotting and comparison with a standard size marker
Why is the correct map crucial in restriction enzyme mapping?
- A) It guarantees the smallest fragments
- B) It predicts the largest fragments
- C) It accounts for all the bands seen on the gel
- D) It ensures the fastest migration rate
To improve the conductivity of the gel During electrophoresis, at what voltage is the process carried out?
- A) 50V
- B) 125V
- C) 75V
- D) 100V
What component is used to create an electric field during agarose gel electrophoresis?
- A) Agarose gel
- B) Ethidium bromide
- C) DNA ladder
- D) Running buffer