WorksheetsIsolation of DNA and RNA, Blotting Techniques
Total questions: 40
Worksheet time: 30mins
The first step in DNA isolation is
Purification
Cell membrane rupture
DNA precipitation
Quantification
EDTA is used in DNA isolation mainly to
Precipitate DNA
Degrade RNA
Chelate metal ions and inhibit DNases
Lyse nucleus
Lysozyme helps in DNA isolation by
Breaking hydrogen bonds
Degrading RNA
Breaking peptidoglycan layer
Denaturing proteins
SDS is used in DNA isolation to
Digest DNA
Remove lipids and denature proteins
Stabilize DNA
Precipitate salts
Which enzyme removes RNA during DNA isolation?
DNase
Protease
RNase
Lysozyme
Phenol-chloroform extraction is used to remove
DNA
RNA
Proteins
Salts
DNA carries which type of charge?
Positive
Neutral
Negative
Variable
Ion-exchange chromatography separates DNA based on
Size
Shape
Charge
The property of DNA that is exploited during agarose gel electrophoresis is
Size
Shape
Charge
Solubility
Ethanol precipitation of DNA requires presence of
Proteins
RNase
Salts like sodium acetate
Detergents
Plant DNA isolation is difficult due to presence of
Nucleus
Cell wall
Ribosomes
Vacuole
mRNA isolation is mainly required for
Genomic library construction
Protein purification
cDNA synthesis
DNA replication
Eukaryotic mRNA contains a special structure called
Cap only
Poly-A tail only
Cap and poly-A tail
Intron
Poly-A tail is present at which end of mRNA?
5′ end
3′ end
Middle
Both ends
Oligo-dT column is used to isolate
rRNA
tRNA
mRNA
DNA
Oligo-dT binds to mRNA due to
Hydrogen bonding
Complementary base pairing
Ionic interaction
Covalent bonding
rRNA and tRNA during oligo-dT chromatography
(a)
In column chromatography, molecules with high affinity for the stationary phase:
Are degraded
Flow through the column
Precipitate
Flow through the column
Low-salt buffer is used to
Bind mRNA
Degrade RNA
Elute mRNA
Stabilize DNA
Guanidinium thiocyanate is used to
Stabilize proteins
Denature RNases
Precipitate DNA
Bind RNA to column
In organic extraction, RNA is found in
Organic phase
Interphase
Upper aqueous phase
Pellet
Chloroform helps in mRNA isolation by
Precipitating RNA
Phase separation
Degrading proteins
Binding mRNA
Blotting technique is used to detect:
Lipids
Carbohydrates
DNA, RNA and proteins
Vitamins
Southern blotting is mainly used to detect:
Proteins
mRNA
DNA fragments
Lipids
Northern blotting is used for the separation of:
DNA
mRNA
Western blotting detects:
DNA
RNA
Protein
Carbohydrates
Southern blotting technique was devised by:
Watson
Crick
Southern
Towbin
The year in which Southern blotting was introduced is:
1969
1975
1979
1985
Western blotting was devised by Towbin in:
1975
1977
1979
1981
Western blotting is based on the principle of:
DNA–DNA hybridization
RNA–DNA hybridization
Antigen–antibody reaction
Enzyme–substrate reaction
The membrane commonly used in blotting techniques is:
Nylon membrane
Agarose gel
Nitrocellulose membrane
Polyacrylamide gel
In Southern blotting, DNA fragments are separated based on:
Shape
Charge
Size
Base composition
Hybridized regions in Southern blotting are detected using:
UV spectrophotometer
X-ray film
Microscope
ELISA reader
Dark bands on X-ray film indicate:
Non-recombinants
Contamination
Recombinants
Degraded DNA
Southern blotting is useful in diagnosing:
Viral infections
Genetic defects
Bacterial infections
All of the above
RFLP mapping is associated with:
Northern blotting
Western blotting
Southern blotting
ELISA
SDS used in Western blotting stands for:
Sodium dodecyl sulphate
Sodium diethyl sulphate
Sulphur dodecyl salt
Sodium dichloride sulphate
Western blotting uses which gel for electrophoresis?
Agarose gel
Polyacrylamide gel
Blocking in Western blotting prevents:
Protein degradation
Gel melting
Non-specific antibody binding
Protein denaturation
Common blocking agents used in Western blotting are:
Glucose and sucrose
BSA or milk powder
Agarose and gelatin
DNA and RNA
