Team:BYU Provo/Notebook/SmallPhage/Springexp/Period1/Exp/Team:BYU Provo/5.5 Amplification from a plaque test

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===5.5 Amplification from a plaque test===
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| colspan="3" | <font color="#333399" size="5" font face="Calibri"> '''Small Phage May - June Notebook: Experiments'''</font>
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: <u> '''Small Phage''' </u> </font>
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: [[Team:BYU Provo/Notebook/SmallPhage/Winterexp|March-April]]
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: [[Team:BYU Provo/Notebook/SmallPhage/Springexp|May-June]]
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: [[Team:BYU Provo/Notebook/SmallPhage/Summerexp|July-August]]
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: [[Team:BYU Provo/Notebook/SmallPhage/Fallexp|September-October]]
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<font size="5"> '''5.5 Amplification from a plaque test''' </font>
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'''I) Purpose'''
'''I) Purpose'''
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'''III) Reagants Used'''
'''III) Reagants Used'''
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: E. Coli BL21 overnight from 5.4; ×6 plate from [[5.3 T7 phage selection method test]]; LB from 4.3
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: E. Coli BL21 overnight from 5.4; ×6 plate from [[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period1/Exp/Team:BYU_Provo/5.3 Phage Amplification/Purification|5.3 T7 phage selection method test]]; LB from 4.3
'''IV) Actual Procedure'''
'''IV) Actual Procedure'''
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1. Amplifying phage from a single plaque (5.5)
1. Amplifying phage from a single plaque (5.5)
: To a test tube, add 1mL of E coli BL21 overnight (5.4) and 4mL of LB
: To a test tube, add 1mL of E coli BL21 overnight (5.4) and 4mL of LB
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: Stab one of the plaques on a ×6 plate from the [[5.3 T7 phage selection method test]] with a 1mL pipet tip, puncturing the agar. The plaque in question is labeled with a circle.
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: Stab one of the plaques on a ×6 plate from the [[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period1/Exp/Team:BYU_Provo/5.3 Phage Amplification/Purification|5.3 T7 phage selection method test]] with a 1mL pipet tip, puncturing the agar. The plaque in question is labeled with a circle.
: The pipet tip is then dipped into the overnight/LB solution. The solution is then pipetted up and down several times to maximize the amount of phage that gets into the solution.
: The pipet tip is then dipped into the overnight/LB solution. The solution is then pipetted up and down several times to maximize the amount of phage that gets into the solution.
: The solution was then incubated for approximately 24 hours (5.5 noon - 5.6 2:00pm )
: The solution was then incubated for approximately 24 hours (5.5 noon - 5.6 2:00pm )
2. Spot test to test amplification results (5.6)
2. Spot test to test amplification results (5.6)
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: Phage liquid culture was purified and spot test was performed using procedures similar to those in [[5.3 T7 phage amplification/purification]]. Stock created was labeled '''5.4'''
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: Phage liquid culture was purified and spot test was performed using procedures similar to those in [[Team:BYU_Provo/Notebook/SmallPhage/Springexp/Period1/Exp/Team:BYU_Provo/5.3 Phage Amplification/Purification|5.3 T7 phage amplification/purification]]. Stock created was labeled 5.4
: Spot test plates were incubated overnight (5.6 4:00pm - 5.7 12:00pm )
: Spot test plates were incubated overnight (5.6 4:00pm - 5.7 12:00pm )
'''V) Results (5.7)'''
'''V) Results (5.7)'''
: Our method of amplification from a single plaque was successful. Phage plaque was observed up to -7
: Our method of amplification from a single plaque was successful. Phage plaque was observed up to -7
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: [[File:5.4 stock spot test.JPG|600px|left]]
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Latest revision as of 13:34, 9 September 2013


Small Phage May - June Notebook: Experiments



Small Phage
March-April
May-June
July-August
September-October

5.5 Amplification from a plaque test



I) Purpose

Test the procedure for creating phage liquid culture from a single plaque on a plate

II) Expected Outcome

In spot test, we should see plaques until the phage dilution series became too diluted.

III) Reagants Used

E. Coli BL21 overnight from 5.4; ×6 plate from 5.3 T7 phage selection method test; LB from 4.3

IV) Actual Procedure

1. Amplifying phage from a single plaque (5.5)

To a test tube, add 1mL of E coli BL21 overnight (5.4) and 4mL of LB
Stab one of the plaques on a ×6 plate from the 5.3 T7 phage selection method test with a 1mL pipet tip, puncturing the agar. The plaque in question is labeled with a circle.
The pipet tip is then dipped into the overnight/LB solution. The solution is then pipetted up and down several times to maximize the amount of phage that gets into the solution.
The solution was then incubated for approximately 24 hours (5.5 noon - 5.6 2:00pm )

2. Spot test to test amplification results (5.6)

Phage liquid culture was purified and spot test was performed using procedures similar to those in 5.3 T7 phage amplification/purification. Stock created was labeled 5.4
Spot test plates were incubated overnight (5.6 4:00pm - 5.7 12:00pm )

V) Results (5.7)

Our method of amplification from a single plaque was successful. Phage plaque was observed up to -7
5.4 stock spot test.JPG