All GRE Subject Test: Biology Resources
Example Questions
Example Question #451 : Gre Subject Test: Biology
The goal of a PCR reaction is to __________.
produce copies of a targeted DNA region(s)
None of these answers
determine a DNA profile
separate DNA based on fragment size
sequence a DNA template region(s)
produce copies of a targeted DNA region(s)
The purpose of a PCR reaction is to amplify a targeted DNA region into millions of copies. PCR helps to yield several copies of DNA in a few hours allowing analysis. Each PCR cycles approximately doubles the amount of DNA present in the reaction.
Example Question #12 : Dna Analysis
rtPCR quantification method is a technique that __________.
measures the amount of fluorescence produced which is proportional to DNA concentration with each cycle of PCR
determines the melting point of the DNA fragments during each cycle of PCR
determines if the primers used in the PCR reaction are annealing
measures the amount of non-specific amplification products
separates DNA fragments based on their size
measures the amount of fluorescence produced which is proportional to DNA concentration with each cycle of PCR
Real time PCR is a technique that measures the amount of fluorescence that occurs with each cycle of PCR. The amount of fluorescence is directly proportional to the DNA concentration. The assay can also provide info such as the possible presence of inhibitors.
It is important to know how much DNA is present in a sample to optimize downstream processing.
Example Question #2 : Organic Chemistry, Biochemistry, And Metabolism
When would it be appropriate to use extraction in order to separate compounds in a solution?
When the compounds have differing molecular weights, but similar solubilities.
When the compounds have differing conjugated double bond lengths, but similar molecular weights.
When the compounds have similar polarities, but differing solubilities.
When the compounds have similar molecular weights, but differing polarities.
When the compounds have similar polarities, but differing solubilities.
Extraction is a useful separation technique when there is a mixture of compounds in a solution that have similar polarities, but different solubilities. The three-step process of extraction can take advantage of different solubilities by introducing the mixture to different acidic and basic conditions.
Example Question #51 : Lab Techniques
In polymerase chain reaction (PCR), the reaction mixture is heated to approximately 98°C during the first cycling step in the procedure. Which of the following describes the purpose of this step?
Bringing the reaction to the optimal temperature for annealing of the primers to the template
Degradation of non-target sequences within the template
Melting of the DNA template, producing single-stranded DNA to which primers can bind
Activation of Taq polymerase
Solubilizing the dNTPs
Melting of the DNA template, producing single-stranded DNA to which primers can bind
Heating of the reaction to roughly 98°C is required to separate the template DNA strands from one another, thereby producing single strands that can pair to their complementary primer. At this temperature, the hydrogen bonds between base pairs break and the strands separate.
Taq polymerase doesn't require this temperature to be active, non-target sequences are not degraded during PCR, the dNTPs are already soluble, and the optimal annealing temperature for primers is actually much lower than 98°C.
Example Question #2 : Other Lab Techniques
Which technique is best suited to determine if a protein is active and able to bind DNA?
Southern blot
Bradford assay
Northern blot
Western blot
Electrophoretic mobility shift assay (EMSA)
Electrophoretic mobility shift assay (EMSA)
In an EMSA, a radiolabeled sequence of DNA that the protein of interest normally binds is incubated with the protein. This mixutre is then run on a non-denaturing gel. If the protein binds the radiolabeled DNA sequence, radioacitivity will be detected towards the top of the gel; however, if it does not bind, the radiolabeled DNA probe alone will run more quickly towards the bottom of the gel.
Example Question #52 : Lab Techniques
What is the purpose of a electrophoretic mobility supershift assay?
To determine if two proteins interact with one another
To separate proteins by size
To separate proteins by charge
To separate DNA fragments by size
To determine if a certain protein binds a DNA sequence
To determine if a certain protein binds a DNA sequence
The purpose of an electrophoretic mobility supershift assay (EMSA) is to determine if a certain protein binds a DNA sequence. EMSAs determine if a protein is "active", meaning that it is capable of binding its target DNA sequence. In an EMSA, a radiolabelled DNA fragment is incubated with cellular protein lysates, then run on a non-denaturing gel. Any protein-bound DNA fragments will migrate slower than unbound DNA fragments. When performing a supershift, one wants to determine if a specific protein binds a radiolabelled DNA probe by use of an antibody. If the antibody binds the protein-DNA complex, this will migrate even slower than the protein-DNA complex alone.
Example Question #53 : Lab Techniques
Capillary electrophoresis instrumentation involves which of the following components?
Detector
Buffer system
Polymer
All of these
Positive and negative electrodes
All of these
A buffer system is required in a capillary electrophoresis system in order to supply the ions necessary to carry the electric current. Ions become depleted quickly and the buffer system will need to be replenished regularly.
The positive and negative electrodes, in combination with a high voltage power supply create the current. The source of the sample and destination of the sample will have opposite charged electrodes. Migration of the analytes through the polymer filled capillary will depend on the applied electric field and their size.
The detector of a capillary electrophoresis system will vary based on the instrumentation type. It is used to detect the size of the molecules and the speed at which they move through the matrix. Sizing methods and databases are then used for analysis.
Polymer serves as the separation matrix of the system. The viscosity of the polymer in combination with the electroosmotic flow of they system will separate molecules based on their size.
Example Question #54 : Lab Techniques
Compared to slab gel electrophoresis, which is an advantage of capillary electrophoresis?
Data collection can be done in real-time
Less sample consumption
All of these
Automatable sample loading
Reproducibility of matrix viscosity
All of these
Capillary electrophoresis allows for better reproducibility of liquid polymer throughout a capillary compared to slab gels. Much of the time gels are manually poured and uneven gel thickness can occur.
Real time data viewing is possible on a capillary electrophoresis instrument's system computer.
Higher sample consumption is common with slab gels. More sample is required to be loaded in each lane. If retesting is necessary, the sample must be prepared and loaded into a new gel. Very small quantities of sample are consumed in the injection step into the capillary. Samples can be easily retested through reinjection from the original sample vial.
Capillary electrophoresis has the possibility of being a completely automated process, including automated sample loading. This saves analyst time during sample prep, injection, and separation. Gels require manual sample loading and some instruments require gel handling for scanning or photography after the electrophoresis process.
Example Question #55 : Lab Techniques
Which of the following is a method for sample introduction into a capillary electrophoresis system?
Siphoning
All of these
Hydrodynamic injection
Electrokinetic injection
Pressure injection
All of these
All of these methods require the immersion of the capillary end into the sample for introduction into the capillary electrophoresis system.
Example Question #56 : Lab Techniques
Which of the following stains could be used to identify bacteria?
Wright stain
Gram stain
Giemsa stain
Acid fast stain
Eosin stain
Gram stain
Gram staining is used to distinguish different types of bacteria in order to aid in their identification. Since bacteria are generally transparent, they must be stained before viewing under the microscope. Gram-positive microorganisms stain purple and Gram-negative microorganisms stain red or pink.
Acid fast stain is used to identify the causative agent of tuberculosis. White blood cells are differentiated after being stained with Wright's stain. Giemsa is used to stain blood cells and chromosomes. Tissues are stained with eosin.
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