Unit 8: Cell viability by MTT assay - Practice Quiz

BTY555 — Biotechnology Laboratory-I 60 Questions
0 Correct 0 Wrong 60 Left
0/60

1 What does the abbreviation MTT stand for in the MTT assay?

Evaluation of cell viability by MTT assay Easy
A. Mono tetrazolium thymidine triphosphate
B. Methyl thiazol tetrazolium tribromide
C. Methylene tetrazole thiamine bromide
D. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide

2 The MTT assay is primarily used to measure which cellular property?

Evaluation of cell viability by MTT assay Easy
A. Cell viability and metabolic activity
B. Cell surface charge
C. Cell membrane thickness
D. DNA base sequence

3 In the MTT assay, the yellow MTT is converted into a product of what colour?

Evaluation of cell viability by MTT assay Easy
A. Blue
B. Green
C. Colourless
D. Purple

4 The coloured product formed by the reduction of MTT is called:

Evaluation of cell viability by MTT assay Easy
A. Formazan
B. Fluorescein
C. Formamide
D. Formalin

5 Which cellular enzymes are mainly responsible for reducing MTT to formazan?

Evaluation of cell viability by MTT assay Easy
A. Lysosomal lipases
B. Mitochondrial dehydrogenases
C. Nuclear polymerases
D. Cell surface proteases

6 Which cells are able to reduce MTT into formazan?

Evaluation of cell viability by MTT assay Easy
A. Metabolically active (living) cells
B. Only fixed cells
C. Only dead cells
D. Only bacterial spores

7 The MTT assay result is typically measured using which instrument?

Evaluation of cell viability by MTT assay Easy
A. pH meter
B. Autoclave
C. Centrifuge
D. Spectrophotometer / microplate reader

8 Formazan crystals are insoluble in water and must be dissolved using a:

Evaluation of cell viability by MTT assay Easy
A. Solubilizing solvent such as DMSO
B. Physiological saline
C. Distilled water
D. Phosphate buffer only

9 In the MTT assay, higher absorbance (optical density) generally indicates:

Evaluation of cell viability by MTT assay Easy
A. A greater number of viable cells
B. Complete cell death
C. No metabolic activity
D. Fewer viable cells

10 The MTT assay is most commonly performed in which type of labware?

Evaluation of cell viability by MTT assay Easy
A. Test tube rack
B. 96-well microtiter plate
C. Petri dish only
D. Glass beaker

11 The MTT assay is widely used to assess the effect of drugs on cells, a study known as:

Evaluation of cell viability by MTT assay Easy
A. Protein purification
B. Cytotoxicity testing
C. Gram staining
D. Gene sequencing

12 The formazan produced in the MTT assay is best described as:

Evaluation of cell viability by MTT assay Easy
A. A water-soluble gas
B. Water-insoluble crystals
C. A colourless solution
D. A volatile liquid

13 Absorbance of dissolved formazan is commonly measured at a wavelength of about:

Evaluation of cell viability by MTT assay Easy
A. 570 nm
B. 340 nm
C. 260 nm
D. 700 nm

14 The MTT reaction is based on which type of chemical process?

Evaluation of cell viability by MTT assay Easy
A. Polymerization
B. Hydrolysis
C. Reduction
D. Oxidation

15 In a cytotoxicity study, a control well with untreated healthy cells is used to represent:

Evaluation of cell viability by MTT assay Easy
A. 50% cell death
B. 100% cell viability
C. 0% cell viability
D. Complete cell death

16 Percentage cell viability from an MTT assay is usually calculated as:

Evaluation of cell viability by MTT assay Easy
A.
B.
C.
D.

17 A dead or non-viable cell in an MTT assay will:

Evaluation of cell viability by MTT assay Easy
A. Turn MTT green
B. Increase absorbance
C. Produce more formazan
D. Not reduce MTT to formazan

18 The MTT assay is an example of which category of assay?

Evaluation of cell viability by MTT assay Easy
A. Chromatographic assay
B. Colorimetric assay
C. Radioactive assay
D. Electrophoretic assay

19 The stock MTT reagent solution is generally prepared in:

Evaluation of cell viability by MTT assay Easy
A. Concentrated acid
B. Molten agar
C. Absolute ethanol
D. Phosphate buffered saline (PBS)

20 Which of the following is a key advantage of the MTT assay?

Evaluation of cell viability by MTT assay Easy
A. Cannot be used with cultured cells
B. Gives only qualitative results
C. Requires radioactive isotopes
D. Simple, rapid, and quantitative

21 In the MTT assay, the yellow tetrazolium salt is reduced to formazan primarily by which cellular component?

Evaluation of cell viability by MTT assay Medium
A. Nuclear DNA polymerase enzymes
B. Mitochondrial and cytosolic dehydrogenase (reductase) enzymes
C. Lysosomal hydrolase enzymes
D. Cell membrane transport proteins

22 What is the visible color change that indicates viable cells in the MTT assay?

Evaluation of cell viability by MTT assay Medium
A. Purple solution converts to yellow formazan
B. Colorless solution converts to red precipitate
C. Blue solution converts to green product
D. Yellow solution converts to purple/blue formazan crystals

23 Why must a solubilization agent such as DMSO or acidified isopropanol be added before reading MTT plates?

Evaluation of cell viability by MTT assay Medium
A. To reduce the remaining MTT into formazan
B. To lyse the cells and release DNA
C. To dissolve insoluble formazan crystals into a homogeneous colored solution
D. To neutralize the culture medium pH only

24 At approximately which wavelength is the dissolved formazan product typically measured in the MTT assay?

Evaluation of cell viability by MTT assay Medium
A. 620–650 nm
B. 540–570 nm
C. 260–280 nm
D. 405–410 nm

25 A treated well shows an absorbance of 0.30 while the untreated control shows 0.60. What is the percentage cell viability?

Evaluation of cell viability by MTT assay Medium
A. 50%
B. 30%
C. 60%
D. 90%

26 The value determined from an MTT dose–response curve represents the concentration of a drug that:

Evaluation of cell viability by MTT assay Medium
A. Doubles the cell number
B. Kills 100% of the cells
C. Reduces cell viability by 50% relative to control
D. Produces maximum formazan formation

27 Why does the MTT assay produce a signal that is proportional to viable rather than dead cells?

Evaluation of cell viability by MTT assay Medium
A. MTT binds only to intact nuclear membranes
B. Dead cells absorb more MTT than live cells
C. Only metabolically active cells retain the enzymatic activity needed to reduce MTT
D. Dead cells convert formazan back to MTT

28 Which control is essential to correct for background absorbance from MTT and medium without cells?

Evaluation of cell viability by MTT assay Medium
A. A well with cells but no MTT
B. A well with double the cell concentration
C. A well with only solubilization solvent
D. A blank well containing medium and MTT but no cells

29 A researcher observes unexpectedly high absorbance in all wells including blanks. Which factor is the most likely cause?

Evaluation of cell viability by MTT assay Medium
A. Incomplete removal of medium leaving phenol red or precipitated MTT
B. Reading the plate at 280 nm
C. Excessive DMSO evaporation
D. Too few cells seeded per well

30 Why are cells usually seeded at an optimized density before performing the MTT assay?

Evaluation of cell viability by MTT assay Medium
A. To keep absorbance within the linear range of the assay
B. To eliminate the need for a control
C. To increase phenol red content
D. To ensure cells remain in stationary phase

31 In a cytotoxicity experiment, increasing drug concentration lowers MTT absorbance. This trend indicates that the drug is:

Evaluation of cell viability by MTT assay Medium
A. Promoting cell proliferation
B. Enhancing formazan solubility
C. Reducing the number of metabolically active viable cells
D. Increasing mitochondrial enzyme activity

32 Which statement best explains a key limitation of the MTT assay?

Evaluation of cell viability by MTT assay Medium
A. It requires radioactive labeling of cells
B. It measures metabolic activity, which may not always equal actual cell number
C. It directly counts dead cells by staining
D. It can only be used with bacterial cells

33 Test wells give absorbances of 0.45, 0.55, and 0.50; the control mean is 1.00. What is the mean percentage viability of the test?

Evaluation of cell viability by MTT assay Medium
A. 100%
B. 55%
C. 50%
D. 45%

34 Why is the MTT assay usually performed in the dark or with limited light exposure after adding the reagent?

Evaluation of cell viability by MTT assay Medium
A. Light dissolves formazan crystals
B. Light increases cell proliferation
C. MTT and formazan are light-sensitive and can degrade
D. Light is required for absorbance reading

35 A negative (untreated) control in an MTT assay typically represents:

Evaluation of cell viability by MTT assay Medium
A. The reference point
B. Complete cell death (0% viability)
C. Maximum (100%) viability against which treatments are compared
D. Background absorbance of medium only

36 Which incubation step directly determines the amount of formazan produced in the MTT assay?

Evaluation of cell viability by MTT assay Medium
A. Incubation of the plate in the spectrophotometer
B. Incubation of the plate with solubilizing solvent overnight at 4 °C
C. Incubation of cells with trypsin before seeding
D. Incubation of cells with MTT reagent for a defined period at 37 °C

37 If a test compound is intensely colored and absorbs near 570 nm, what precaution improves MTT assay accuracy?

Evaluation of cell viability by MTT assay Medium
A. Include a compound-only blank to subtract its absorbance
B. Increase the MTT concentration tenfold
C. Skip the solubilization step
D. Read the plate at 260 nm instead

38 Replicate wells are used for each condition in the MTT assay mainly to:

Evaluation of cell viability by MTT assay Medium
A. Ensure cells stay in log phase longer
B. Reduce the amount of MTT reagent needed
C. Increase the total formazan color intensity
D. Improve statistical reliability and account for well-to-well variation

39 Compared with dye-exclusion methods like trypan blue, an advantage of the MTT assay is that it:

Evaluation of cell viability by MTT assay Medium
A. Requires no incubation or reagents
B. Allows high-throughput, automated measurement of many samples
C. Distinguishes apoptosis from necrosis directly
D. Directly visualizes individual dead cells under a microscope

40 During analysis, subtracting the blank absorbance from each well's reading is done in order to:

Evaluation of cell viability by MTT assay Medium
A. Obtain absorbance values due only to cell-derived formazan
B. Remove the need for a solubilizing agent
C. Convert absorbance directly into cell diameter
D. Increase the measured

41 In the MTT assay, the yellow tetrazolium salt is reduced to purple formazan primarily by which cellular process?

Evaluation of cell viability by MTT assay Hard
A. Photochemical reduction driven by assay incubation light
B. NAD(P)H-dependent oxidoreductase activity in metabolically active cells
C. Extracellular oxidation by secreted peroxidases
D. Passive diffusion across the plasma membrane of dead cells

42 A researcher observes that a compound increases MTT signal at low concentrations but the cells show no increase in number under the microscope. What is the most likely explanation?

Evaluation of cell viability by MTT assay Hard
A. The compound bleaches the microplate reader detector
B. The compound directly reduces MTT chemically in solution
C. The compound lyses cells, releasing formazan
D. The compound stimulates mitochondrial dehydrogenase activity per cell without proliferation

43 In an MTT assay, the mean absorbance of untreated control wells is and treated wells is . What is the percent viability of treated cells relative to control?

Evaluation of cell viability by MTT assay Hard
A.
B.
C.
D.

44 Which experimental artifact would most likely cause a falsely LOW MTT absorbance despite high cell viability?

Evaluation of cell viability by MTT assay Hard
A. Reading at nm instead of nm reference
B. Excessive MTT concentration in the wells
C. Incomplete solubilization of formazan crystals before reading
D. Using serum-free medium during incubation

45 Why is a reference wavelength (typically – nm) subtracted from the primary nm reading in MTT assays?

Evaluation of cell viability by MTT assay Hard
A. To correct for background from cell debris, plate imperfections, and turbidity
B. To convert absorbance to formazan molar concentration
C. To account for MTT that was not reduced
D. To normalize for differences in incubation time

46 A test drug is a strong reducing agent (e.g., high ascorbate). What effect will this most likely have on MTT results and how should it be controlled?

Evaluation of cell viability by MTT assay Hard
A. It causes false-high signal via chemical MTT reduction; use cell-free drug + MTT blanks
B. It has no effect because only enzymes reduce MTT; no control needed
C. It quenches formazan color; add extra solubilizer
D. It lowers signal by inhibiting reductases; increase cell number

47 For determining an from an MTT dose-response curve, why is data usually plotted against of concentration rather than linear concentration?

Evaluation of cell viability by MTT assay Hard
A. It converts absorbance to percentage automatically
B. It eliminates the effect of chemical interference
C. It removes the need for a control well
D. It linearizes the sigmoidal response, easing accurate midpoint estimation

48 Which condition would most compromise the linear relationship between MTT absorbance and viable cell number?

Evaluation of cell viability by MTT assay Hard
A. Cell density above the linear range causing nutrient/MTT limitation
B. Reading the plate immediately after solubilization
C. Using triplicate wells per condition
D. Including a blank medium control

49 The MTT assay may overestimate cytotoxic potency of a compound that induces cytostasis. Why?

Evaluation of cell viability by MTT assay Hard
A. Arrested cells over-reduce MTT, giving high signal
B. Cytostasis increases membrane permeability to MTT
C. Cytostatic drugs chemically bleach formazan
D. Growth-arrested but viable cells give lower signal, mimicking cell death

50 Phenol red in culture medium can interfere with MTT readings. What is the best mitigation?

Evaluation of cell viability by MTT assay Hard
A. Add more phenol red to saturate the signal
B. Increase MTT incubation time to override phenol red
C. Read only at the reference wavelength
D. Aspirate medium and read formazan dissolved in solubilizer, plus medium blanks

51 In a -well MTT assay, edge wells consistently show deviant absorbance. What is the primary cause?

Evaluation of cell viability by MTT assay Hard
A. Faster formazan solubilization at edges
B. Evaporation and temperature gradients producing the 'edge effect'
C. Higher MTT reduction by plate plastic
D. Light leakage into edge wells during reading

52 Standard curve wells (cell number vs. ) fit where is cell count. A treated well reads . Estimated viable cell number is closest to:

Evaluation of cell viability by MTT assay Hard
A.
B.
C.
D.

53 Why can the MTT assay give misleading results with primary macrophages or highly metabolic quiescent cells?

Evaluation of cell viability by MTT assay Hard
A. They chemically oxidize formazan back to MTT
B. They cannot reduce MTT at all
C. Their high per-cell reductase activity decouples signal from cell number
D. They exclude MTT completely due to thick membranes

54 Which statement best distinguishes MTT from MTS/XTT tetrazolium assays?

Evaluation of cell viability by MTT assay Hard
A. MTT requires no incubation, MTS requires overnight
B. MTT forms insoluble formazan needing solubilization; MTS/XTT form soluble formazan
C. MTT reads at nm, MTS at nm exclusively
D. MTT is reduced only by dead cells, MTS by live cells

55 An MTT incubation time of hours is standard. Extending it to hours would most likely:

Evaluation of cell viability by MTT assay Hard
A. Have no effect since reduction saturates quickly
B. Improve accuracy indefinitely due to more formazan
C. Convert formazan back into soluble MTT
D. Increase background and toxicity, distorting viability estimates

56 In percent-viability calculation, why must the blank (medium + MTT, no cells) absorbance be subtracted from both control and treated wells before ratio calculation?

Evaluation of cell viability by MTT assay Hard
A. To normalize for pipetting volume differences
B. To convert absorbance into cell number directly
C. To account for MTT degradation in cells
D. To remove non-cellular background so the ratio reflects only cell-derived formazan

57 Nanoparticles under test are found to adsorb MTT and formazan. What is the correct interpretive caution?

Evaluation of cell viability by MTT assay Hard
A. Adsorption always increases apparent viability equally in all wells
B. Only the reference wavelength is affected, so no correction is needed
C. Nanoparticle interference control is required; results may be systematically biased
D. Ignore it since particles do not affect optical density

58 Two labs report different values for the same drug on the same cell line using MTT. Which variable most plausibly explains this discrepancy?

Evaluation of cell viability by MTT assay Hard
A. Use of the same nm read wavelength
B. Both subtracting a medium blank
C. Both using DMSO to dissolve formazan
D. Differences in seeding density and exposure duration between labs

59 Why does the MTT assay not distinguish between apoptotic and necrotic cell death?

Evaluation of cell viability by MTT assay Hard
A. It quantifies DNA fragmentation directly
B. It measures only net loss of metabolic reduction, not death mechanism
C. It detects caspase activity specific to apoptosis
D. It stains membrane rupture characteristic of necrosis

60 A high coefficient of variation (CV) among replicate MTT wells is observed. Which corrective action addresses the most common root cause?

Evaluation of cell viability by MTT assay Hard
A. Reduce the number of replicate wells to three
B. Read the plate at a single wavelength only
C. Skip blank subtraction to simplify the data
D. Ensure uniform cell seeding and thorough, consistent formazan solubilization