Chemistry test 2012 #4 assesses knowledge of biochemical processes like oxidative phosphorylation and enzyme kinetics. Key skills tested include understanding of NADH functions, ATP production, and enzyme inhibition. Essential for learners in advanced chemistry courses.
Cause your sample to renature
Cause your sample to run off the edge of the gel
Affect blocking stage
Decrease the amount of separation between bands
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Intracrine
Paracrine
Autocrine
Endocrine
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NAD+
NAD
NADH
NADH2
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Globular proteins
Affect rate of reactions
Have a quaternary structure
Activity dependant on pH
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Cut a strand of DNA at specific locations.
Cut both strands of DNA to yield a set of double stranded DNA with single stranded sticky ends.
Cut both strands of DNA to yield two fragments of single stranded DNA.
Cut RNA strands at specific locations
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+ 10.6
- 4
- 7.3
+ 3.3
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Southern blotting
Northern blotting
Western blotting
Eastern blotting
Hybridization
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A
B
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On nucleoproteins
On cytoplasmic recptors
On plasma membrane
Circulating carrier proteins
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Increase the electrical charge of your sample
Mark the locations of known molecular weights
Determine if samples were loaded evenly across wells
Denature your sample
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The nitrocellulose membrane must be on the positive electrode side of the gel
The nitrocellulose membrane must be on the negative elect role side of the gel
The sample will always transfer to the nitrocellulose membrane regardless of orientation
All molecular width bands will always transfer to the nitrocellulose membrane
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Are synthetic
Produce ADP
Produce NAD
Produce ATP
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All three statements are true
Two of these statements are true
Two of these statements are false
One of these statements are true
None of these statements are true
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Nitrocellulose is soaked in blocking solution which contains DNA, RNA or protein
None required since probe binds only to target molecule
Electrophoresis of target molecule prior to application of probe
Antibody attached to probe identifies target molecule
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NAD yields 3 ATP via oxidative phosphorylation pathway
FAD yields 2 ATP via oxidative phosphorylation pathway
NADH yields 3 ATP via oxidative phosphorylation pathway
FADH yields 2 ATP via oxidative phosphorylation pathway
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N4 where N is the number of cycles
N2/2 where N is the number of cycles
P2 + 2PQ + Q2=1 Where P and Q are the number of primers
2n where n is the number of cycles
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DNA polymerase
Taq RNA polymerase
RNA polymerase
Taq DNA polymerase
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Anneal, extend and denature
Denature, anneal and extend
Extend, anneal and denature
Extend, denature and anneal
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Allow for greater separation of lower molecular weight bands
Allow for greater separation of higher molecular weight bands
Cause all bands to migrate faster, reducing your run time
Cause all bands to migrate slower, increasing your run time
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A
B
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In the 5' to 3' direction
In the 3' to 5' direction
In both directions
Only at the methylated end of DNA strands
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Synthetic and degradative pathways are distinct and separate pathways
Each pathway has one or more rate-limiting reactions
The rate-limiting reactions in a metabolic pathway are catalyzed by allosteric enzymes
The reaction curve displaying the kinetics of allosteric enzymes are hyperbolic
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Southern blotting
PCR
Northern blotting
Western blotting
Eastern blotting
Transferring unimportant material that doesn't matter
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Mosaicisms
Chimeras
Amplicons
Restriction fragment length polymorphisms
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Single stranded DNA probe that binds between two primers which is labeled with fluorophore
DOuble stranded DNA probe that binds between the two primers which is labelled with a fluorescent quencher
Single stranded DNA probe that binds between the two primers which is labeled with a fluorophore and a fluorescent quencher
DOuble stranded DNA probe that binds between the two primers which is labeled with a fluorescent quencher and a fluorophore
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Competitive inhibition
Enzyme modulation
Non-competitive inhibition
Enzyme activity
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Amine
Steroid
Protein/polypeptide
Glucocoritco steroid
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Are bound with a high affinity to a carrier protein in the circulation
Remain free in the circulation
Are conjugated to glucuronides
Are bound with low affinity to albumin
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An oligonucleotide with repeating sequence of A-A-A at the 5' end
A molecule of 5,000 base pairs with a high number of A-T base pairs
An oligonucleotide with repeating sequences of C-G-C codons
A DNA polymer of 100,000 base pairs
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Thryroxine
Calcitonin
TSH
Triiodothyronine
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The RNA must be denatured to form single strands for annealing to primers
RNA shoulds never be used in a PCR reaction because thermostable enzymes cannot synthesize strands to anneal it
A reverse transcription procedure must be performs to form cDNA
RNA must first be treated with RNases to remove interfering substances from the target
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Fatty acid cycle
Citric acid cycle
Catabolic
Anabolic
Only b and c
Only a and d
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Template DNA, an oligonucleotide primer, nucleosides in excess
Template DNA, two oligonucleotide primer, nucleosides in excess, Taq polymerase
Template DNA, two oligonucleotide primer, nucleotides in excess, Taq polymerase
Template DNA, Two oligonucleotide primers in excess, nucleosides in excess, Taq polymerase
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Increase the electrical charge of your sample
Mark the locations of known molecular weights
Determine if samples were loaded evenly across the wells
Denature your sample
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3' GGUU 5' and 5' CUUAG 3'
3' GGGTT 5' and 5' CTTAG 3'
5' GGGTT 3' and 3' CTTAG 5'
3' GGGTT 5' and 3' CTTAG 5'
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Cross the plasma membrane and bind to cytoplasmic receptors
Cross plasma membrane and bind to nuclear receptors initiating or altering the expression of a gene
Bind to the receptors located on the plasma membrane and initiate a secondary messenger
Active transport across the plasma membrane and attach to cytoplasmic protein receptors
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To the left decreasing Km
To the right decreasing Km
To the left increasing Km
To the right increasing Km
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Gel electrophoresis, blocking, transfer to solid support, preparing the probe, hybridization, washing and detection of probe.
Gel electrophoresis, transfer to solid support, washing, blocking, preparing the probe, hybridization and detection fo probe.
Gel electrophoresis, transfer to solid support, blocking, preparing the probe, blocking, hybridization, washing, detection of probe.
Gel electrophoresis, transfer to solid support, blocking, preparing the probe, hybridization, washing, detection of probe.
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Increase FT4, decreased TSH
Decreased TSH, increased FT4
Increased FT4, increased TSH
Increased TSH, decreased FT4
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The virus must be inserted into hman DNA by viral integrate prior to PCR
Substituted deoxyuridine triphosphate in place of deoxythymidine triphosphate in the master mix
Add heat-stable reverse transcriptase enzymes to the master mix
Substitute ribonucleotide triphosphates for deoxyribonucleotide triphosphates in the master mix
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