Lab test Flashcards

1
Q

How should liquid from an auto-pipette be drawn?

A

It should be drawn and dispensed slowly.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Why should an auto-pipette be drawn slowly?

A

To ensure the correct volume is drawn & dispensed.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

True/false: Immersion oil should contact the objective lens of a microscope

A

True.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Why should an agar plate be labelled on the base?

A
  • Face down
  • Condensation doesn’t ruin the inoculated plate
  • Scientists can identify who it belongs to without damaging the colony
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Why should a glass spreader dipped in ethanol NOT immediately be used to spread cells?

A

The ethanol will kill or damage the bacterial colony.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Equation: Solve to find C1

A

C1=C2xV2/V1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Equation: Solve to find C2

A

C2=C1xV1/V2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Equation: Solve to find V1

A

V1=C2xV2/C1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Equation: Solve to find V2

A

V2=C1xV1/C2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Equation: Solve to find the diluent

A

Diluent= V2-V1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is Beer’s Law?

A

The linear relationship between absorbance and concentration. It is linear only over a certain range of concentrations.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What if the absorbance reading of an unknown solution is higher than any of the absorbances in the linear range?

A

You cannot assume that Beer’s law is still obeyed so you cannot extrapolate beyond the linear portion of a standard curve.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What happens if Beer’s Law is not obeyed?

A

You must dilute the unknown solution so that its absorbance falls within the linear portion of the curve.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

How do you calculate the amount of protein per assay (P)?

A

Volume x Concentration of the albumin solution.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Explain how to measure the standard curve to find the amount of protein in an unknown solution

A
  • Volume x concentration of solution
  • Put it on the Y axis
  • Rule to the line of best fit
  • Rule down to the X axis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What treatments do you use when Gram staining cells?

A

crystal violet & iodine then a decolourizing agent followed by safranin.

17
Q

What colour do Gram-negative (Gm-) organisms stain?

A

pink or red.

18
Q

What colour do Gram-positive (Gm+) organisms stain?

A

purple or violet

19
Q

What are the cell walls of Gram-negative organisms rich in?

20
Q

What does the decolourizing agent do to the lipid of the cell walls of an organism?

A

Removes the cell wall lipids & decolourizes the cell contents. Safranin then stains them pink or red.

21
Q

What do Gram-positive cells have?

A

a thick peptidoglycan layer.

22
Q

What does the decolourizing agent do to the peptidoglycan layer?

A

the pores shrink and form a barrier, trapping the crystal violet/iodine complex inside the cell.

23
Q

Lag phase

A

Directly after inoculation there’s a period of little to no growth

24
Q

Log phase

A

A period in during which the cell density doubles in some constant time interval

25
Stationary phase
A period of little to no growth
26
What is the 'constant time interval' in the log phase called?
Doubling time
27
Why does the stationary phase occur?
The culture reaches a particular cell density: Environmental conditions - Limited oxygen - Depletion of nutrients - Accumulation of toxic waste products
28
What is the equation to find the dilution factor?
DF=C1/C2
29
How do you find the total dilution factor?
TDF=DF1×DF2×DF3...
30
What is the equation for cell density?
Cell density = cell count / vol. of grid used
31
What is the best standard curve to plot?
Absorbance vs Amount per assay
32
Amount of protein per assay = ?
Concentration of stock protein solution × Volume of stock solution added to assay tube
33
Positive control
Confirms the basic conditions of the experiment can produce a result.
34
What if the positive control shows up negative?
There may be something wrong with the procedure
35
Negative control
The procedure is not showing an unrelated effect. Treated as a background value to be subtracted from the test sample results.
36
What if the negative control shows up positive?
Another variable acted upon the experiment and the data is discarded.
37
Equation for density of original undiluted culture per ml
colony count x TDF / volume plated (ml)
38
Central primary square formula
0.1mm^3 x 1ml/10^3mm^3 = 1 x 10 etc.