The MTT assay estimates cell viability by measuring the metabolic activity of living cells.
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2What does MTT stand for?
MTT assay for evaluation of cell viability
Easy
A.Methyl thiazolyl tetrazolium
B.Molecular transfer testing
C.Modified tissue trypsin
D.Membrane transport tracer
Correct Answer: Methyl thiazolyl tetrazolium
Explanation:
MTT is the abbreviation for methyl thiazolyl tetrazolium, a yellow tetrazolium compound.
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3What color is the MTT reagent before it is reduced by viable cells?
MTT assay for evaluation of cell viability
Easy
A.Green
B.Blue
C.Yellow
D.Purple
Correct Answer: Yellow
Explanation:
The MTT reagent is yellow before viable cells reduce it to colored formazan.
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4What colored product is formed during the MTT assay?
MTT assay for evaluation of cell viability
Easy
A.Green chlorophyll
B.Purple formazan
C.Yellow glucose
D.Red hemoglobin
Correct Answer: Purple formazan
Explanation:
Metabolically active cells reduce MTT to purple formazan crystals.
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5Which cells can reduce MTT to formazan?
MTT assay for evaluation of cell viability
Easy
A.Fixed cells only
B.Dead cells only
C.Metabolically active cells
D.Cell-free medium
Correct Answer: Metabolically active cells
Explanation:
Living cells with active metabolism can reduce MTT to formazan.
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6What instrument is commonly used to measure the color produced in an MTT assay?
MTT assay for evaluation of cell viability
Easy
A.Hemocytometer
B.Microplate reader
C.Water bath
D.Centrifuge
Correct Answer: Microplate reader
Explanation:
A microplate reader measures the absorbance of the formazan product.
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7What does higher absorbance generally indicate in an MTT assay?
MTT assay for evaluation of cell viability
Easy
A.Fewer viable cells
B.Less cell metabolism
C.More viable cells
D.More contaminated medium
Correct Answer: More viable cells
Explanation:
Higher absorbance usually reflects more formazan and therefore greater cellular metabolic activity.
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8Why are untreated cells often included in an MTT assay?
MTT assay for evaluation of cell viability
Easy
A.To stop cell growth
B.To stain the plate
C.To provide a control
D.To dissolve formazan
Correct Answer: To provide a control
Explanation:
Untreated cells provide a baseline for comparison with treated cells.
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9What is the purpose of a blank well in an MTT assay?
MTT assay for evaluation of cell viability
Easy
A.To activate the cells
B.To produce more formazan
C.To measure background signal
D.To increase cell number
Correct Answer: To measure background signal
Explanation:
A blank well contains no cells and helps account for background absorbance from the reagents.
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10What happens to MTT in viable cells?
MTT assay for evaluation of cell viability
Easy
A.It is converted to DNA
B.It is reduced to formazan
C.It is changed into glucose
D.It is evaporated from cells
Correct Answer: It is reduced to formazan
Explanation:
Enzymatic activity in viable cells reduces MTT to insoluble formazan.
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11Why is a solvent added after formazan crystals form?
MTT assay for evaluation of cell viability
Easy
A.To increase cell attachment
B.To dissolve the crystals
C.To remove the medium
D.To kill the cells
Correct Answer: To dissolve the crystals
Explanation:
The solvent dissolves formazan crystals so their color can be measured evenly.
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12Which type of plate is commonly used for an MTT assay?
MTT assay for evaluation of cell viability
Easy
A.Microtiter plate
B.Agar plate
C.Microscope slide
D.Petri dish only
Correct Answer: Microtiter plate
Explanation:
MTT assays are commonly performed in multiwell microtiter plates.
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13What is usually removed before adding the solvent to dissolve formazan?
MTT assay for evaluation of cell viability
Easy
A.Cell nucleus
B.Plastic well
C.Culture medium
D.Pipette tip
Correct Answer: Culture medium
Explanation:
The culture medium is commonly removed before the solvent is added to dissolve the formazan crystals.
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14A decrease in MTT absorbance after treatment most likely suggests what?
MTT assay for evaluation of cell viability
Easy
A.Higher formazan formation
B.Increased cell number
C.Greater metabolic activity
D.Reduced cell viability
Correct Answer: Reduced cell viability
Explanation:
Lower absorbance generally indicates less metabolic activity and fewer viable cells.
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15What is a major limitation of the MTT assay?
MTT assay for evaluation of cell viability
Easy
A.It directly counts every cell
B.It identifies all cell types
C.It measures metabolism indirectly
D.It measures cell shape exactly
Correct Answer: It measures metabolism indirectly
Explanation:
The assay estimates viability from metabolic activity rather than directly counting living cells.
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16What does a cell viability percentage compare?
MTT assay for evaluation of cell viability
Easy
A.Nuclei with cytoplasm
B.Proteins with carbohydrates
C.Medium with solvent
D.Treated cells with control cells
Correct Answer: Treated cells with control cells
Explanation:
Cell viability is commonly expressed by comparing treated-cell absorbance with control-cell absorbance.
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17Why are replicate wells used in an MTT assay?
MTT assay for evaluation of cell viability
Easy
A.To prevent cell metabolism
B.To improve result reliability
C.To change the assay color
D.To remove the control group
Correct Answer: To improve result reliability
Explanation:
Replicates help reduce the effect of random variation and improve confidence in the results.
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18Which result usually indicates greater cell viability?
MTT assay for evaluation of cell viability
Easy
A.Lower formazan absorbance
B.Higher formazan absorbance
C.No color in treated wells
D.No difference from the blank
Correct Answer: Higher formazan absorbance
Explanation:
Greater formazan absorbance generally indicates more metabolically active viable cells.
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19What is the main role of cellular enzymes in the MTT assay?
MTT assay for evaluation of cell viability
Easy
A.They remove the plate
B.They reduce MTT
C.They dissolve the microplate
D.They produce culture medium
Correct Answer: They reduce MTT
Explanation:
Cellular enzymes involved in metabolism reduce MTT to the colored formazan product.
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20What should be kept consistent between control and treated wells?
MTT assay for evaluation of cell viability
Easy
A.Cell number and assay conditions
B.Only the plate position
C.Only the well color
D.Only the label font
Correct Answer: Cell number and assay conditions
Explanation:
Consistent cell numbers and assay conditions allow a fair comparison between control and treated wells.
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21What cellular property is primarily measured by the MTT assay?
MTT assay for evaluation of cell viability
Medium
A.Metabolic reduction capacity of viable cells
B.Concentration of extracellular proteins
C.Number of nuclei released after lysis
D.Total amount of cellular DNA
Correct Answer: Metabolic reduction capacity of viable cells
Explanation:
Viable cells reduce yellow MTT to purple formazan through metabolically active reducing systems. The measured signal therefore reflects metabolic activity, which is commonly used as an indicator of viability.
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22Why does the MTT reagent change from yellow to purple during the assay?
MTT assay for evaluation of cell viability
Medium
A.The plate reader changes the reagent color
B.The medium becomes acidic during incubation
C.Cell membranes absorb the yellow reagent
D.Formazan crystals are produced by reduction
Correct Answer: Formazan crystals are produced by reduction
Explanation:
Metabolically active cells reduce MTT to insoluble purple formazan crystals. The intensity of the purple color is then measured spectrophotometrically.
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23A treatment produces an absorbance of 0.42, while untreated cells produce 0.70 after blank subtraction. What is the approximate percentage viability?
MTT assay for evaluation of cell viability
Medium
A.60%
B.40%
C.70%
D.168%
Correct Answer: 60%
Explanation:
Relative viability is calculated as .
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24What is the main purpose of wells containing medium and MTT but no cells?
MTT assay for evaluation of cell viability
Medium
A.To increase the treatment concentration
B.To measure maximum cell proliferation
C.To measure background absorbance
D.To provide additional viable cells
Correct Answer: To measure background absorbance
Explanation:
Cell-free blank wells account for absorbance from the medium, MTT, and plate. Their signal is subtracted from sample readings when appropriate.
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25Why is a solvent such as DMSO added after MTT incubation?
MTT assay for evaluation of cell viability
Medium
A.To neutralize the untreated control
B.To dissolve insoluble formazan crystals
C.To convert MTT into a fluorescent product
D.To stimulate additional cell division
Correct Answer: To dissolve insoluble formazan crystals
Explanation:
Formazan accumulates as an insoluble product. DMSO or another validated solvent dissolves the crystals, producing a uniform solution for absorbance measurement.
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26Which wavelength is commonly used to measure dissolved formazan in an MTT assay?
MTT assay for evaluation of cell viability
Medium
A.Around 450 nm
B.Around 570 nm
C.Around 700 nm
D.Around 280 nm
Correct Answer: Around 570 nm
Explanation:
Dissolved MTT formazan is commonly measured near 570 nm, although the exact wavelength can depend on the protocol and plate reader.
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27A compound is strongly colored at the MTT measurement wavelength. What is the most appropriate control?
MTT assay for evaluation of cell viability
Medium
A.Cells exposed to a second test compound
B.Compound-containing wells without cells
C.Untreated wells with extra cells
D.Medium-only wells without compound
Correct Answer: Compound-containing wells without cells
Explanation:
Cell-free wells containing the compound can reveal direct optical interference. This background can then be distinguished from absorbance caused by cellular formazan.
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28If cell density is increased beyond the linear range of the assay, what result is most likely?
MTT assay for evaluation of cell viability
Medium
A.The blank absorbance automatically becomes zero
B.Formazan production becomes completely independent of cells
C.Absorbance becomes poorly proportional to cell number
D.All wells produce exactly the same absorbance
Correct Answer: Absorbance becomes poorly proportional to cell number
Explanation:
MTT assays require a validated linear range. At excessive cell densities, nutrients, reagent availability, or optical limits can cause signal saturation and reduce proportionality.
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29Why are untreated control wells included in an MTT experiment?
MTT assay for evaluation of cell viability
Medium
A.To establish the reference viability
B.To prevent all treatment effects
C.To dissolve formazan before reading
D.To eliminate the need for blanks
Correct Answer: To establish the reference viability
Explanation:
Untreated controls represent normal cellular activity under the assay conditions. Treatment results are commonly expressed relative to this reference.
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30A positive cytotoxicity control is included mainly to confirm that:
MTT assay for evaluation of cell viability
Medium
A.The solvent increases metabolic activity
B.The plate contains equal cell numbers
C.The treatment has no effect on cells
D.The assay can detect reduced viability
Correct Answer: The assay can detect reduced viability
Explanation:
A positive cytotoxicity control should produce a known decrease in MTT signal, demonstrating that the assay is capable of detecting loss of viability.
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31Why should the MTT incubation time be kept consistent between experimental wells?
C.Formazan production depends on incubation duration
D.The solvent evaporates only from control wells
Correct Answer: Formazan production depends on incubation duration
Explanation:
Longer exposure to MTT generally allows more formazan to form. Unequal incubation times can therefore introduce differences unrelated to the treatment.
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32What is a likely consequence of incomplete dissolution of formazan crystals?
MTT assay for evaluation of cell viability
Medium
A.A direct measurement of cell number
B.Complete removal of treatment interference
C.Guaranteed linearity across all samples
D.Increased measurement variability
Correct Answer: Increased measurement variability
Explanation:
Undissolved crystals can settle unevenly or scatter light, causing inconsistent absorbance readings and reducing assay precision.
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33A treatment lowers MTT absorbance but does not reduce cell number. Which interpretation is most appropriate?
MTT assay for evaluation of cell viability
Medium
A.The treatment definitely caused complete cell death
B.The MTT assay directly measured DNA content
C.The treatment may suppress cellular metabolism
D.The treatment must have increased cell attachment
Correct Answer: The treatment may suppress cellular metabolism
Explanation:
MTT primarily reflects metabolic reducing activity rather than cell number alone. A treatment can lower metabolism without causing immediate loss of cells.
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34Why should treatment solvent concentration be identical in control and treatment wells?
MTT assay for evaluation of cell viability
Medium
A.The solvent prevents formazan formation
B.The solvent itself may affect cell viability
C.The solvent determines the MTT wavelength
D.The solvent replaces the need for replication
Correct Answer: The solvent itself may affect cell viability
Explanation:
Solvents such as DMSO can alter cell function at sufficient concentrations. Matching solvent levels ensures that observed effects are more likely due to the test compound.
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35What is the best reason for using technical replicate wells in an MTT assay?
MTT assay for evaluation of cell viability
Medium
A.To replace the untreated control group
B.To convert absorbance into fluorescence
C.To guarantee that treatment is effective
D.To estimate variability from repeated measurements
Correct Answer: To estimate variability from repeated measurements
Explanation:
Technical replicates help assess pipetting and well-to-well variation. They improve confidence in the average signal but do not replace independent biological replicates.
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36A compound causes a concentration-dependent decrease in relative MTT viability. What does this pattern generally suggest?
MTT assay for evaluation of cell viability
Medium
A.The absorbance values were all identical
B.The cells cannot reduce MTT
C.The compound may have a dose-dependent effect
D.The assay contains no untreated controls
Correct Answer: The compound may have a dose-dependent effect
Explanation:
A consistent decline in viability as concentration increases is compatible with a dose-dependent reduction in metabolic activity, although additional controls may be needed to confirm cytotoxicity.
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37Why should edge wells sometimes be avoided or filled with sterile buffer in an MTT plate?
MTT assay for evaluation of cell viability
Medium
A.Edge wells may experience greater evaporation
B.Edge wells cannot contain viable cells
C.Edge wells prevent MTT reduction
D.Edge wells always produce fluorescent signals
Correct Answer: Edge wells may experience greater evaporation
Explanation:
Evaporation at the plate edges can change solute concentrations and affect cell growth. Using buffer or avoiding edge wells can reduce these edge effects.
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38Which calculation is most suitable for reporting treatment effects relative to an untreated control after blank correction?
MTT assay for evaluation of cell viability
Medium
A.
B.
C.
D.
Correct Answer:
Explanation:
After subtracting the appropriate blank, relative viability is commonly calculated as .
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39What is the main advantage of measuring absorbance at a wavelength near the formazan maximum?
MTT assay for evaluation of cell viability
Medium
A.It changes formazan into a soluble reagent
B.It improves sensitivity of formazan detection
C.It prevents cells from attaching to plastic
D.It eliminates the need for untreated controls
Correct Answer: It improves sensitivity of formazan detection
Explanation:
Measuring near the absorbance maximum of formazan generally gives a stronger signal relative to background, improving detection of differences among samples.
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40A sample has a blank-corrected absorbance higher than the untreated control. Which conclusion is most justified?
MTT assay for evaluation of cell viability
Medium
A.The sample cannot contain assay interference
B.The sample has greater metabolic signal than control
C.The sample definitely contains more living cells
Correct Answer: The sample has greater metabolic signal than control
Explanation:
A higher MTT signal indicates greater metabolic reducing activity under the assay conditions. It does not necessarily prove a proportional increase in cell number or exclude compound interference.
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41A compound reduces MTT absorbance by 40% after 24 hours, but microscopic inspection shows unchanged cell number and morphology. Which conclusion is most justified?
MTT assay for evaluation of cell viability
Hard
A.The compound increased cell proliferation but blocked crystal dissolution
B.The compound may have impaired cellular metabolic reduction of MTT
C.The compound caused apoptosis without affecting cellular metabolism
D.The compound definitely caused 40% cell death
Correct Answer: The compound may have impaired cellular metabolic reduction of MTT
Explanation:
MTT absorbance reflects cellular reducing activity as well as cell number. An unchanged cell population with lower signal suggests altered metabolism or direct assay interference rather than confirmed cell death.
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42A 96-well MTT experiment produces high absorbance in untreated wells but also substantial absorbance in wells containing medium, MTT, and drug without cells. What is the most appropriate response?
MTT assay for evaluation of cell viability
Hard
A.Subtract the untreated-cell control from every experimental well
B.Increase the MTT concentration to overcome the drug signal
C.Interpret the drug wells as highly viable cell cultures
D.Treat the drug-containing blank signal as nonspecific background
Correct Answer: Treat the drug-containing blank signal as nonspecific background
Explanation:
Cell-free wells containing the drug identify chemical or optical interference. Their signal should be measured and subtracted from matching drug-treated wells before estimating viability.
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43Untreated wells have an average corrected absorbance of , while treated wells have . The corresponding cell-free treated blanks have absorbance . Assuming the untreated blank is negligible, what is the estimated viability?
MTT assay for evaluation of cell viability
Hard
A.
B.
C.
D.
Correct Answer: $30\%
Explanation:
Correct the treated signal first: . Relative viability is .
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44A researcher uses a single untreated well as the denominator for all treatment groups, although untreated replicate wells vary substantially. Which analysis is most defensible?
MTT assay for evaluation of cell viability
Hard
A.Normalize each treated well to the mean untreated replicate signal
B.Use the untreated well closest to each treated measurement
C.Normalize each treated well to the highest untreated replicate signal
D.Average all treatment values before subtracting one untreated value
Correct Answer: Normalize each treated well to the mean untreated replicate signal
Explanation:
The mean of valid untreated biological or technical replicates provides a more stable reference than one arbitrarily selected well. Replicate variability should also be reported.
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45In a dose-response experiment, absorbance increases with dose at low concentrations and then declines at higher concentrations. Which interpretation is most scientifically appropriate?
MTT assay for evaluation of cell viability
Hard
A.The compound may stimulate metabolism at low dose and inhibit it at high dose
B.The cells must have been accidentally omitted from the high-dose wells
C.The assay must be invalid because viability cannot exceed baseline
D.The MTT reagent becomes more concentrated when the drug concentration rises
Correct Answer: The compound may stimulate metabolism at low dose and inhibit it at high dose
Explanation:
A biphasic response can reflect hormesis, metabolic stimulation, or other biological effects. It should be confirmed with controls and an independent viability or cell-number method.
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46Why is it problematic to compare MTT absorbance values obtained from two cell lines without first establishing comparable calibration ranges?
MTT assay for evaluation of cell viability
Hard
A.Different cell lines always require different wavelengths
B.Cell lines cannot be compared using replicate measurements
C.Different cell lines can differ in MTT reduction per cell
D.MTT crystals form only in transformed cell lines
Correct Answer: Different cell lines can differ in MTT reduction per cell
Explanation:
MTT signal per cell depends on metabolic state, mitochondrial activity, cell size, and other properties. Equal absorbance does not necessarily represent equal cell number across cell lines.
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47The standard curve relating cell number to MTT absorbance is linear from to cells but plateaus above cells. How should samples above the linear range be handled?
MTT assay for evaluation of cell viability
Hard
A.Calculate viability using the plateau absorbance directly
B.Extend the linear regression through all observed concentrations
C.Dilute or reseed samples so measurements fall within the linear range
D.Multiply plateau values by the nominal cell number
Correct Answer: Dilute or reseed samples so measurements fall within the linear range
Explanation:
Quantitative interpretation requires measurements within the validated linear range. Saturated signals cannot reliably distinguish differences in cell number or metabolic activity.
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48A hydrophobic test compound precipitates after MTT addition and increases turbidity at the measurement wavelength. Which control is most important for identifying this artifact?
MTT assay for evaluation of cell viability
Hard
A.Cells with MTT but without the test compound
B.Cells with the solvent but without MTT
C.Medium with MTT and the test compound but without cells
D.Untreated cells measured at a different wavelength
Correct Answer: Medium with MTT and the test compound but without cells
Explanation:
A cell-free compound-plus-MTT control reveals absorbance or turbidity caused by precipitation, color, or chemical reduction rather than formazan produced by cells.
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49After adding the solubilization solution, a plate contains visible purple crystals and large well-to-well variation despite careful pipetting. Which procedural change is most likely to improve measurement reliability?
MTT assay for evaluation of cell viability
Hard
A.Ensure complete crystal dissolution with standardized mixing
B.Use untreated wells as substitutes for missing blank wells
C.Reduce the incubation time for the MTT reaction to zero
D.Read the plate immediately before adding solubilization solution
Correct Answer: Ensure complete crystal dissolution with standardized mixing
Explanation:
Undissolved formazan causes heterogeneous light scattering and sampling error. Consistent solubilization and mixing are essential before measuring absorbance.
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50A treatment causes cells to detach from the plate. The investigator washes the wells before adding MTT and reports the remaining signal as viability. What bias is most likely?
MTT assay for evaluation of cell viability
Hard
A.Viability may be underestimated because MTT becomes more concentrated
B.Viability may reverse because washing converts formazan to MTT
C.Viability may be overestimated because detached dead cells were removed
D.Viability is unaffected because detached cells cannot reduce MTT
Correct Answer: Viability may be overestimated because detached dead cells were removed
Explanation:
Removing detached cells before measurement can remove dead or injured cells from the assay population, leaving only adherent survivors and artificially increasing apparent viability.
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51A solvent used for the test compound reduces cell viability by 15% at its working concentration. Which design best isolates the compound effect?
MTT assay for evaluation of cell viability
Hard
A.Increase the compound concentration to overcome solvent toxicity
B.Use a vehicle-matched control at the same solvent concentration
C.Compare the compound group with untreated cells only
D.Omit solvent controls because all groups receive MTT
Correct Answer: Use a vehicle-matched control at the same solvent concentration
Explanation:
The vehicle control establishes the baseline effect of the solvent. Compound-treated wells should be compared with that matched control, not necessarily with solvent-free cells.
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52A compound is strongly colored at the MTT measurement wavelength but does not react with MTT. Which result could occur if cell-free compound blanks are omitted?
MTT assay for evaluation of cell viability
Hard
A.The compound color would be removed during cell lysis
B.Apparent viability could only be falsely reduced
C.Apparent viability could be falsely elevated
D.Apparent viability must be exactly unchanged
Correct Answer: Apparent viability could be falsely elevated
Explanation:
Compound absorbance adds to the formazan signal. Without subtracting the cell-free compound blank, the calculated viability may be higher than the true cellular signal.
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53A treatment reduces absorbance but increases the amount of total cellular protein per surviving cell. Why might MTT results disagree with a cell-counting assay?
MTT assay for evaluation of cell viability
Hard
A.Cell counting measures absorbance rather than survival
B.MTT measures metabolic reduction, not cell number alone
C.MTT results are independent of cellular metabolic state
D.Protein content prevents MTT from entering every well
Correct Answer: MTT measures metabolic reduction, not cell number alone
Explanation:
Changes in metabolism per cell can alter MTT reduction without proportional changes in cell number. Orthogonal assays are needed when treatment changes cell physiology.
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54In a 96-well plate, wells at the perimeter show systematically lower absorbance than interior wells in every treatment group. What is the most likely experimental concern?
MTT assay for evaluation of cell viability
Hard
A.A wavelength shift restricted to interior wells
B.Selective MTT reduction by cells located near the plate center
C.Complete failure of the negative control in perimeter wells
D.A positional edge effect caused by evaporation or temperature variation
Correct Answer: A positional edge effect caused by evaporation or temperature variation
Explanation:
Perimeter wells are more susceptible to evaporation and environmental gradients. Randomization, plate-layout controls, humidification, or exclusion of edge wells can reduce this bias.
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55A cytotoxic treatment produces an MTT viability of , but a membrane-integrity assay gives viable cells. Which explanation best accounts for the discrepancy?
MTT assay for evaluation of cell viability
Hard
A.MTT cannot detect any change in cellular metabolism
B.Both assays must be averaged to obtain the true viability
C.The treatment may increase MTT reduction in damaged cells
D.The membrane assay always overestimates viability by definition
Correct Answer: The treatment may increase MTT reduction in damaged cells
Explanation:
Damaged or stressed cells can retain or alter reducing activity, producing a relatively high MTT signal despite loss of membrane integrity. The assays measure related but nonidentical endpoints.
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56A positive-kill control gives nearly the same absorbance as the medium blank. What does this primarily indicate about the assay?
MTT assay for evaluation of cell viability
Hard
A.The untreated control should be replaced by the positive control
B.The positive control successfully defines a low-signal reference
C.The positive control proves that all treated cells are viable
D.The MTT incubation must have produced excessive formazan
Correct Answer: The positive control successfully defines a low-signal reference
Explanation:
A strong killing control should approach the background signal, demonstrating that the assay can detect a substantial loss of metabolic activity.
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57A plate reader reports absorbance values above the validated upper limit for several untreated wells. Which action is most appropriate before interpreting treatment effects?
MTT assay for evaluation of cell viability
Hard
A.Repeat using fewer cells or a shorter MTT incubation
B.Convert all saturated values to viability
C.Accept the values because higher absorbance confirms healthier cells
D.Subtract the untreated values from all treatment values
Correct Answer: Repeat using fewer cells or a shorter MTT incubation
Explanation:
Signals above the validated range may be nonlinear or saturated. Adjusting cell density or reaction time can bring measurements into a quantitative range.
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58A treatment is tested in six wells on one plate, and the experiment is repeated on three separate days. Which description correctly distinguishes the replicates?
MTT assay for evaluation of cell viability
Hard
A.The three days are repeated measurements of one technical replicate
B.The six wells are biological replicates and the days are technical replicates
C.The six wells are technical replicates and the days provide independent experimental replicates
D.All eighteen wells are independent biological replicates
Correct Answer: The six wells are technical replicates and the days provide independent experimental replicates
Explanation:
Wells within one run generally share the same preparation and are technical replicates. Independent runs on separate days capture experimental variation and support biological inference.
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59A compound is reported to have an MTT half-maximal inhibitory concentration of . Which statement is the most cautious interpretation?
MTT assay for evaluation of cell viability
Hard
A.It permanently eliminates half the cells at every exposure time
B.It has the same half-maximal effect in all cell types
C.It kills exactly half the cells at
D.It reduces the measured MTT signal to half the fitted control response
Correct Answer: It reduces the measured MTT signal to half the fitted control response
Explanation:
An MTT-derived describes the concentration associated with half of the assay response under specified conditions. It does not automatically equal direct cell killing or generalize across systems.
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60A researcher subtracts the average medium blank from every well but ignores that the test compound has a different blank absorbance. What is the principal analytical error?
MTT assay for evaluation of cell viability
Hard
A.The MTT reaction is converted into a protein assay
B.The treatment-specific optical contribution remains in the corrected signal
C.The blank subtraction reverses the dose-response relationship
D.The untreated control becomes independent of cell number
Correct Answer: The treatment-specific optical contribution remains in the corrected signal
Explanation:
Background should be matched to the relevant treatment whenever compounds contribute absorbance, scattering, or chemical reduction. A universal medium blank may not remove treatment-specific interference.
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