MCQ practice Flashcards
If bacterial chromosome is digested by endonucleases in four sites giving rise to DNA fragments of which two are equal in length – How many bands would you see after agarose gel electrophoresis?
(A) 3
(B) 4
(C) 5
(D) Only one fragment
(E) None of the above
3- Because two of them are at the same length
Which of the following statements is NOT true about agarose gel electrophoresis?
(A) Electrophoresis in agarose is a common way to separate DNA molecules according to size.
(B) Ethidium bromide is used to detect DNA.
(C) DNA migrates towards the cathode.
(D) Small DNA fragments migrate faster than larger ones.
(E) None of the above
C) DNA migrates towards the cathode
-In electrophoresis the DNA or the sample will always move towards the Anode which is the positive side (Goes from negative to positive)
In PCR, if the oligonucleotides used were slightly shorter and more variable than the intended primers sequences?
A) PCR would not commence.
(B) PCR would stop after the first cycle.
(C) PCR would commence but a single short PCR product will be generated.
(D) A mixture of non-specific PCR products will be released.
(E) None of the above.
D) A mixture of non-specific PCR products will be released- Because it is not long enough
Coomassie blue is used to stain …………………. in …………………….
(A) Gram positive bacteria in Gram staining.
(B) DNA fragments in SDS-PAGE.
(C) Proteins in agarose gel electrophoresis.
(D) DNA fragments in agarose gel electrophoresis.
(E) Proteins in sodium dodecyl sulphate–polyacrylamide gel electrophoresis
(E) Proteins in sodium dodecyl sulphate–polyacrylamide gel electrophoresis - That’s what Coomaasie brilliant blue staining is used for.
A 53-year-old man has been feeling unwell and suffering general aches and pains, loss of appetite,diarrhoea and yellowish skin and eyes. Serum sample is collected for detection and quantificationof the DNA of hepatitis B virus (HBV) and the RNA of hepatitis C virus (HCV). Which technique you will use for detection and quantification of HBV and HCV?
(A) RT qPCR and RTPCR respectively.
(B) RT qPCR for both viruses.
(C) RTPCR and RT qPCR respectively.
(D) Reverse transcription polymerase chain reaction for both viruses.
(E) None of the above
(C) RTPCR and RT qPCR respectively.- (RT)-PCR assay is used for the detection, identification and quantification of hepatitis B virus (HBV), hepatitis C virus (HCV) and (HIV-1) in plasma or serum
You are carrying out western blot for detection of hemagglutinin and neuraminidaseproteins of influenza A virus. The most commonly used gel in western blotting is:
(A) Agarose.
(B) Polyacrylamide.
(C) Both (A) and (B) are correct.
(D) Semisolid gel.(E) None of the above
(B) Polyacrylamide that is what is used for the SDS-PAGE
In Gram staining, ……………. is used to fix the primary stain to bacterial cell wall while……………. is used as a secondary stain which stains Gram ……………… bacteria……………..
(A) Gram’s iodine, carbol fuchusin, positive, purple
(B) Ethanol, carbol fuchsin, negative, red
(C) Ethanol, safranin, negative, red
(D) Gram’s iodine, safranin, negative, red
(E) None of the above is correct
(D) Gram’s iodine, safranin, negative, red
In agarose gel electrophoresis, for effective separation of …………… you will use 2% (w/v) of agarose in the gel while you use 0.8% (w/v) of agarose in the gel for the effective separation of……………
(A) Bacterial chromosome, specific bacterial gene.(B) Bacterial genome, specific bacterial gene.
(C) Specific bacterial gene, bacterial genome.
(D) Bacterial plasmid, specific bacterial gene.
(E) Larger size DNA fragments, smaller size DNA fragment
(C) Specific bacterial gene, bacterial genome.
Which of these statements is FALSE about western blotting?
(A) Western blotting is more sensitive than Coomassie staining
(B) All of the above are true about western blotting
(C) Western blotting does not require a Coomassie staining step.
(D) Western blotting always requires an antibody.
(E) In western blotting the protein of interest acts as an antigen
(B) All of the above are true about western blotting
In agarose gel electrophoresis, DNA will migrate towards …..?
(A) Negative electrode or cathode.
(B) Positive electrode or cathode.
(C) None of the above.
(D) Positive electrode or anode.
(E) Negative electrode or anode.
(D) Positive electrode or anode.
The purpose of using bromophenol blue in the sample buffer in SDS-PAGE is to…..?
(A) Adjust the pH of the sample
(B) lonze the sample.
(C) Use it as a standard control
(D) Both C and Dare correct
(E) Monitor the electrophoretic run.
(E) Monitor the electrophoretic run.
In SDS-PAGE, sodium dodecyl sulphate is used as ….?
(A) A cationic exchanger.
(B None of the above.
(C) A cationic detergent.
D) An anionic detergent.
(E) An anionic exchanger.
D) An anionic detergent. -Its positive
Which of the following is TRUE for the SDS-PAGE?
(A) It cannot be used to separate proteins bound by cysteine bonds.
B) The main ingredient in the gel is agarose.
(C) It cannot be used to separate proteins that have an initial positive charge.
(D) It requires a protein-denaturing gel and buffer system.
(E) The samples can be visualised with ethidium bromide.
(D) It requires a protein-denaturing gel and buffer system.
Gram staining distinguishes bacteria into Gram positive and Gram negative, based on their ………………
And…… bacteria retain crystal violet after the use of solvent?
(A) Cell wall, Gram positive.
B) Peptidoglycan, Gram negative.
(C Cell wall, acid fast.
D) LPS, Gram negative.
(E) Cell wall, Gram variable
(A) Cell wall, Gram positive.
……. iS used for separation of proteins while ……….. is used for nucleic acid separation?
(A) Polyacrylamide, agarose.
(B) Agar, polyacrylamite.
C) None of the above.
(D) Agarose, polyacrylamide.
(E) Polyacrylamide, agar.
(A) Polyacrylamide, agarose.