MOLBIO MIDTERMS Flashcards
Which of the following statement is
FALSE?
-The PCR is usually done in a reaction
volume of 10 – 200 ml in small tubes in a
thermal cycler.
SNPs are detected by Allele-Specific PCR
by
-using Allele-specific primers
Which is INCORRECT about SNPs?
-They usually affect health and
development.
This is added to determine if you have
contaminants on your DNA
Controls
Principle of separation in Capillary zone
electrophoresis
Charge-to-mass ratio
Statements below describes polyacrylamide
gel EXCEPT
Mobility does not depend on DNA
sequence
Extension time is set for () base pairs of
DNA per minute
1000
In array-based CGH, what is the sample
used?
mRNA
In Gel Electrophoresis, how do we make the
DNA migrate through the gel?
We place a positive electrode away from
the wells
This is a type of PRGE in which two fields
are arranged in separated straight angle
FIELD INVERSION GE ELECTRO
After heating and cooling the mixture, which
of the following catalyzes the synthesis of
complementary strands of DNA?
Taq polymerase
Low annealing temperature leads to some
mismatches
True
Pfu polymerase is superior over Taq
polymerase because:
of more accurate amplification
Which is INCORRECT about ASO
hybridization?
The result is analyzed using gel
electrophoresis
When setting up a Sanger sequencing
reaction, each reaction should include
template DNA, deoxyribonucleotides,
dideoxyribonucleotides, buffer, DNA
polymerase, and
Forward OR reverse primer
What would be the effect on the PCR
reaction if any of the following
circumstances arose: 1) there are no primers
in the reaction, 2) enough dNTPs in the
reaction, 3) there is Taq polymerase in the
reaction?
Amplicons will not be produced, false
negative result.
Nonspecific amplification may be a result of
adding:
5.5 mM MgCl2+
The PCR technique was developed by
Mullis
Among those listed below, which is most
common mutation effect that leads to the
development on cancer?
Increase in the activity of a protein.
TRUE for agarose gels
High voltage in a high agarose
concentration can resolve small DNAs
Why do you need to prepare an extra
volume in your Master Mix?
To compensate pipetting errors
What will happen if too much enzyme is
added to the reaction?
Digestion reaction may fail
At what temperature does annealing of
primers to the template takes place?
- 47-60˚C
-10-20˚C below the melting point of primer
-5˚C below the melting point of primer
LAMP PCR requires this range of
temperature:
60-65°C