Biotech lab 5 Flashcards

1
Q

After adding ammonium bicarbonate (50mM) to 10 mL of ddH2O, what pH should be observed?

A

8-9

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2
Q

What is in the destaining solution?

A

1 mL of acetonitrile and 1 mL of 50 mM ammonium bicarbonate

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3
Q

What band is taken from the SDS-PAGE gel?

A

the PTEN band, minimize gel amount and use clean scalpel

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4
Q

What is added to the gel band?

A

destain solution

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5
Q

Once the destain solution is added to the gel band, what is done?

A

bench top incubator at 37C for 15 minutes until band becomes clear

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6
Q

How is the gel dehydrated?

A

adding 300uL of acetonitrile

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7
Q

what does acetonitrile do?

A

reduce hydrophobic interactions of CBB and gel

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8
Q

after wash with acetonitrile, where is the gel piece put?

A

speed vacuum for 20 minutes

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9
Q

what protease is used?

A

trypsin

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10
Q

what is in the trypsin digestion buffer?

A

resuspended trypsin, ammonium bicarbonate

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11
Q

how is the sample rehydrated?

A

adding enout trypsin digestion buffer to cover the gel piece

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12
Q

the gel and digestion buffer is incubated where?

A

on ice for 10 mins

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13
Q

how will you know that the trypsin has entered the matrix?

A

gel piece should swell

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14
Q

why is parafilm added after the on ice incubation?

A

to minimize evaporation

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15
Q

where is the gel sample incubated after adding parafilm?

A

bench top shaking incubator for 2 hrs at 37C

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16
Q

if gel isnt covered, what do you add?

A

ammonium bicarbonate

17
Q

How often do you check the gel?

A

every 30 minutes

18
Q

after the incubation, what is added for peptide extraction?

A

vortex and spin down, add formic acid solution and collect supernatant

19
Q

After collecting supernatant what do you do?

A

add 1 ul of sample in maldi pate and add 1 ul of UV absorbing maldi matrix