Final Flashcards

1
Q

Abcissa, dependent variable

A

x-axis

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

Increase working distance by

A

Decreasing mag power of objective lense

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

Log x not log graph

A

semi-log scale

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

Improve resolving power by changing light to

A

violet

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

increase in numerical aperture improves

A

resolution

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

monochromatic light

A

a single wavelength of light

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

standard curve plots

A

absorbance vs. concentration

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

y-axis

A

ordinant axis , independent variables

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

why do we blank

A

to remove the background solution

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

in cell fractionation we used

A

differential centrifugation

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

homogenation

A

disrupts cell boundaries and releases cell contents

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

nuclear fraction

A

pellet 1, contains nuclei intact cells and tissue

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

post-nuclear supernant

A

produces the post-chloroplast supernant

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

chloroplast fraction

A

Pellet 2, contains chloroplast and some organelles

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

post mitochondrial supernant and mitochondrial fraction

A

pellet 3, smallest contains mitochondria, micro bodies and lysosomes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

smaller particles in supernant

A

greater sedimentation coefficient

17
Q

RPM

A

can be used stand alone

18
Q

RCF

A

need rotar size

19
Q

Ph

20
Q

Ph>PI

21
Q

Bromophenyl blue dye

A

tracker dye

22
Q

glycerol

A

weighs down the sample so it will stay in the well

23
Q

anions (-) travel towards

A

anodes (+)

24
Q

Native gel separates based on

A

charge, still have enzymatic activity

25
glyciene
slow runner helps in stacking
26
chloride ion
pushes sample down helps in stacking
27
Non-native separates by
molecular weight
28
Ammonium disulfate
isolates LDH
29
APS
free radicles
30
SDS
constant denaturing to linearize, all will have an overall negative charge. anionic detergent
31
histochemistry
tissue staining
32
4 steps in histotechnique
fixation sectioning staining mounting
33
@low salt
solubility of protein increases, lower H2O solubility
34
@high salt
solubility of protein decreases, higher H2O solubility
35
BME
breaks di-sulfide bonds to linerarize( like chlorine)
36
TEMED
polymerizing agent, works with/activates APS