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ALF_PLT1_2020_END

ALF_PLT2_2020_END

ALF_PLT3_2020_END

ALF_PLT4_2020_END

ALF_PLT5_2020_END

ALF_PLT6_2020_END

ALF_PLT7_2020_END

ALF_PLT8_2020_END

ALF_PLT1_2020_EPI

ALF_PLT2_2020_EPI

ALF_PLT3_2020_EPI

ALF_PLT4_2020_EPI

ALF_PLT5_2020_EPI

ALF_PLT6_2020_EPI

ALF_PLT7_2020_EPI

ALF_PLT8_2020_EPI

MasterMix (make for 16 plates in 50mL conical tube)

ul/rxn

Reagent

# of rxns

ul needed

3

5X Kapa HiFi Buffer

1700

5100

0.45

10M dNTPs

1700

765

0.3

Kapa HiFi HotStart DNA Pol

1700

510

7.25

Ultra Pure H2O

1700

12325

11

Total Volume

1700

18700

...

Temp C

Cycles

Time

95*

1X

3:00*

98

36X

0:30

62

36X

0:30

72

36X

0:30

72

1X

5:00

4

1X

0:00

MagBead Cleanup:

Some plates were cleaned up using the Nimbus platform protocol “AxyPrep MagBead PCR1 No MM”

...

  • Equilibrate Beads to room Temperature

  • Add 24 ul of MagBeads to each well and 15 ul of replicate to same well of replicate

  • Pipette mix up and down 10 times.

  • Incubate at RT for 5 minutes

  • Secure plate on magnet plate; incubate at RT for 5 minutes (until wells are clear)

  • Remove 65 ul from each well; keep tips to left or right depending on the column to avoid bead pellet.

  • Add 100 ul Fresh 80% EtOH to each well. Incubate 30 seconds. Remove 100 ul from each well

  • Add 100 ul Fresh 80% EtOH to each well. Incubate 30 seconds. Remove 100 ul from each well

  • Reaspirate from each well to assure maximum EtOH removal

  • Allow plate to air dry for 7 minutes.

  • Remove sample plate from magnet plate.

  • Add 40 ul TE; pipette mix 10+ times. Incubate 2 minutes at RT.

  • Place sample plate back on magnet for 5 minutes or until all wells are cleared.

  • Transfer 40 ul to labeled transparent plate (Plate name_PCR_MIDs)

qPCR ALF_END_RUN1

  • Make 1:1000 dilutions of column 3 from the PCR plates by adding 1 ul to 999 ul TE in a deep well plate:

...

 

1

2

3

4

5

6

7

8

9

10

11

12

A

ALF_END_PLT1_16S

ALF_END_PLT1_ITS

ALF_END_PLT2_16S

ALF_END_PLT2_ITS

ALF_END_PLT3_16S

ALF_END_PLT3_ITS

ALF_END_PLT4_16S

ALF_END_PLT4_ITS

 

NTC

NTC

NTC

B

ALF_END_PLT1_16S

ALF_END_PLT1_ITS

ALF_END_PLT2_16S

ALF_END_PLT2_ITS

ALF_END_PLT3_16S

ALF_END_PLT3_ITS

ALF_END_PLT4_16S

ALF_END_PLT4_ITS

 

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

ALF_END_PLT1_16S

ALF_END_PLT1_ITS

ALF_END_PLT2_16S

ALF_END_PLT2_ITS

ALF_END_PLT3_16S

ALF_END_PLT3_ITS

ALF_END_PLT4_16S

ALF_END_PLT4_ITS

 

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

ALF_END_PLT1_16S

ALF_END_PLT1_ITS

ALF_END_PLT2_16S

ALF_END_PLT2_ITS

ALF_END_PLT3_16S

ALF_END_PLT3_ITS

ALF_END_PLT4_16S

ALF_END_PLT4_ITS

 

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

ALF_END_PLT1_16S

ALF_END_PLT1_ITS

ALF_END_PLT2_16S

ALF_END_PLT2_ITS

ALF_END_PLT3_16S

ALF_END_PLT3_ITS

ALF_END_PLT4_16S

ALF_END_PLT4_ITS

 

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

ALF_END_PLT1_16S

ALF_END_PLT1_ITS

ALF_END_PLT2_16S

ALF_END_PLT2_ITS

ALF_END_PLT3_16S

ALF_END_PLT3_ITS

ALF_END_PLT4_16S

ALF_END_PLT4_ITS

 

2 pM Std

2 pM Std

2 pM Std

G

ALF_END_PLT1_16S

ALF_END_PLT1_ITS

ALF_END_PLT2_16S

ALF_END_PLT2_ITS

ALF_END_PLT3_16S

ALF_END_PLT3_ITS

ALF_END_PLT4_16S

ALF_END_PLT4_ITS

 

20 pM Std

20 pM Std

20 pM Std

H

ALF_END_PLT1_16S

ALF_END_PLT1_ITS

ALF_END_PLT2_16S

ALF_END_PLT2_ITS

ALF_END_PLT3_16S

ALF_END_PLT3_ITS

ALF_END_PLT4_16S

ALF_END_PLT4_ITS

 

 

 

 

Results:

Average results for the following plates (column 3):

...

The full result report can be viewed below:

 MasterMix (make for 16 plates in 50mL conical tube)

ul/rxn

Reagent

# of rxns

ul needed

3

5X Kapa HiFi Buffer

1700

5100

0.45

10M dNTPs

1700

765

0.3

Kapa HiFi HotStart DNA Pol

1700

510

7.25

Ultra Pure H2O

1700

12325

11

Total Volume

1700

18700

...

Temp C

Cycles

Time

95*

1X

3:00*

98

36X

0:30

62

36X

0:30

72

36X

0:30

72

1X

5:00

4

1X

0:00

MagBead Cleanup:

Some plates were cleaned up using the Nimbus platform protocol “AxyPrep MagBead PCR1 No MM”

...

  • Equilibrate Beads to room Temperature

  • Add 24 ul of MagBeads to each well and 15 ul of replicate to same well of replicate

  • Pipette mix up and down 10 times.

  • Incubate at RT for 5 minutes

  • Secure plate on magnet plate; incubate at RT for 5 minutes (until wells are clear)

  • Remove 65 ul from each well; keep tips to left or right depending on the column to avoid bead pellet.

  • Add 100 ul Fresh 80% EtOH to each well. Incubate 30 seconds. Remove 100 ul from each well

  • Add 100 ul Fresh 80% EtOH to each well. Incubate 30 seconds. Remove 100 ul from each well

  • Reaspirate from each well to assure maximum EtOH removal

  • Allow plate to air dry for 7 minutes.

  • Remove sample plate from magnet plate.

  • Add 40 ul TE; pipette mix 10+ times. Incubate 2 minutes at RT.

  • Place sample plate back on magnet for 5 minutes or until all wells are cleared.

  • Transfer 40 ul to labeled transparent plate (Plate name_PCR_MIDs)

qPCR ALF_END_RUN2

  • Make 1:1000 dilutions of column 3 from the PCR plates by adding 1 ul to 999 ul TE in a deep well plate:

...

 

1

2

3

4

5

6

7

8

9

10

11

12

A

ALF_END_PLT5_16S

ALF_END_PLT5_ITS

ALF_END_PLT6_16S

ALF_END_PLT6_ITS

ALF_END_PLT7_16S

ALF_END_PLT7_ITS

ALF_END_PLT8_16S

ALF_END_PLT8_ITS

 

NTC

NTC

NTC

B

ALF_END_PLT5_16S

ALF_END_PLT5_ITS

ALF_END_PLT6_16S

ALF_END_PLT6_ITS

ALF_END_PLT7_16S

ALF_END_PLT7_ITS

ALF_END_PLT8_16S

ALF_END_PLT8_ITS

 

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

ALF_END_PLT5_16S

ALF_END_PLT5_ITS

ALF_END_PLT6_16S

ALF_END_PLT6_ITS

ALF_END_PLT7_16S

ALF_END_PLT7_ITS

ALF_END_PLT8_16S

ALF_END_PLT8_ITS

 

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

ALF_END_PLT5_16S

ALF_END_PLT5_ITS

ALF_END_PLT6_16S

ALF_END_PLT6_ITS

ALF_END_PLT7_16S

ALF_END_PLT7_ITS

ALF_END_PLT8_16S

ALF_END_PLT8_ITS

 

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

ALF_END_PLT5_16S

ALF_END_PLT5_ITS

ALF_END_PLT6_16S

ALF_END_PLT6_ITS

ALF_END_PLT7_16S

ALF_END_PLT7_ITS

ALF_END_PLT8_16S

ALF_END_PLT8_ITS

 

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

ALF_END_PLT5_16S

ALF_END_PLT5_ITS

ALF_END_PLT6_16S

ALF_END_PLT6_ITS

ALF_END_PLT7_16S

ALF_END_PLT7_ITS

ALF_END_PLT8_16S

ALF_END_PLT8_ITS

 

2 pM Std

2 pM Std

2 pM Std

G

ALF_END_PLT5_16S

ALF_END_PLT5_ITS

ALF_END_PLT6_16S

ALF_END_PLT6_ITS

ALF_END_PLT7_16S

ALF_END_PLT7_ITS

ALF_END_PLT8_16S

ALF_END_PLT8_ITS

 

20 pM Std

20 pM Std

20 pM Std

H

ALF_END_PLT5_16S

ALF_END_PLT5_ITS

ALF_END_PLT6_16S

ALF_END_PLT6_ITS

ALF_END_PLT7_16S

ALF_END_PLT7_ITS

ALF_END_PLT8_16S

ALF_END_PLT8_ITS

 

 

 

 

Results:

Average results for the following plates (column 3):

...

The full result report can be viewed below:

MasterMix (make for 16 plates in 50mL conical tube)

ul/rxn

Reagent

# of rxns

ul needed

3

5X Kapa HiFi Buffer

1700

5100

0.45

10M dNTPs

1700

765

0.3

Kapa HiFi HotStart DNA Pol

1700

510

7.25

Ultra Pure H2O

1700

12325

11

Total Volume

1700

18700

...

Temp C

Cycles

Time

95*

1X

3:00*

98

36X

0:30

62

36X

0:30

72

36X

0:30

72

1X

5:00

4

1X

0:00

MagBead Cleanup:

Some plates were cleaned up using the Nimbus platform protocol “AxyPrep MagBead PCR1 No MM”

...

  • Equilibrate Beads to room Temperature

  • Add 24 ul of MagBeads to each well and 15 ul of replicate to same well of replicate

  • Pipette mix up and down 10 times.

  • Incubate at RT for 5 minutes

  • Secure plate on magnet plate; incubate at RT for 5 minutes (until wells are clear)

  • Remove 65 ul from each well; keep tips to left or right depending on the column to avoid bead pellet.

  • Add 100 ul Fresh 80% EtOH to each well. Incubate 30 seconds. Remove 100 ul from each well

  • Add 100 ul Fresh 80% EtOH to each well. Incubate 30 seconds. Remove 100 ul from each well

  • Reaspirate from each well to assure maximum EtOH removal

  • Allow plate to air dry for 7 minutes.

  • Remove sample plate from magnet plate.

  • Add 40 ul TE; pipette mix 10+ times. Incubate 2 minutes at RT.

  • Place sample plate back on magnet for 5 minutes or until all wells are cleared.

  • Transfer 40 ul to labeled transparent plate (Plate name_PCR_MIDs)

qPCR ALF_EPI_RUN1

  • Make 1:1000 dilutions of column 3 from the PCR plates by adding 1 ul to 999 ul TE in a deep well plate:

...

 

1

2

3

4

5

6

7

8

9

10

11

12

A

ALF_EPI_PLT1_16S

ALF_EPI_PLT1_ITS

ALF_EPI_PLT2_16S

ALF_EPI_PLT2_ITS

ALF_EPI_PLT3_16S

ALF_EPI_PLT3_ITS

ALF_EPI_PLT4_16S

ALF_EPI_PLT4_ITS

 

NTC

NTC

NTC

B

ALF_EPI_PLT1_16S

ALF_EPI_PLT1_ITS

ALF_EPI_PLT2_16S

ALF_EPI_PLT2_ITS

ALF_EPI_PLT3_16S

ALF_EPI_PLT3_ITS

ALF_EPI_PLT4_16S

ALF_EPI_PLT4_ITS

 

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

ALF_EPI_PLT1_16S

ALF_EPI_PLT1_ITS

ALF_EPI_PLT2_16S

ALF_EPI_PLT2_ITS

ALF_EPI_PLT3_16S

ALF_EPI_PLT3_ITS

ALF_EPI_PLT4_16S

ALF_EPI_PLT4_ITS

 

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

ALF_EPI_PLT1_16S

ALF_EPI_PLT1_ITS

ALF_EPI_PLT2_16S

ALF_EPI_PLT2_ITS

ALF_EPI_PLT3_16S

ALF_EPI_PLT3_ITS

ALF_EPI_PLT4_16S

ALF_EPI_PLT4_ITS

 

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

ALF_EPI_PLT1_16S

ALF_EPI_PLT1_ITS

ALF_EPI_PLT2_16S

ALF_EPI_PLT2_ITS

ALF_EPI_PLT3_16S

ALF_EPI_PLT3_ITS

ALF_EPI_PLT4_16S

ALF_EPI_PLT4_ITS

 

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

ALF_EPI_PLT1_16S

ALF_EPI_PLT1_ITS

ALF_EPI_PLT2_16S

ALF_EPI_PLT2_ITS

ALF_EPI_PLT3_16S

ALF_EPI_PLT3_ITS

ALF_EPI_PLT4_16S

ALF_EPI_PLT4_ITS

 

2 pM Std

2 pM Std

2 pM Std

G

ALF_EPI_PLT1_16S

ALF_EPI_PLT1_ITS

ALF_EPI_PLT2_16S

ALF_EPI_PLT2_ITS

ALF_EPI_PLT3_16S

ALF_EPI_PLT3_ITS

ALF_EPI_PLT4_16S

ALF_EPI_PLT4_ITS

 

20 pM Std

20 pM Std

20 pM Std

H

ALF_EPI_PLT1_16S

ALF_EPI_PLT1_ITS

ALF_EPI_PLT2_16S

ALF_EPI_PLT2_ITS

ALF_EPI_PLT3_16S

ALF_EPI_PLT3_ITS

ALF_EPI_PLT4_16S

ALF_EPI_PLT4_ITS

 

 

 

 

Results:

Average results for the following plates (column 3):

...

The full result report can be viewed below:

MasterMix (make for 16 plates in 50mL conical tube)

ul/rxn

Reagent

# of rxns

ul needed

3

5X Kapa HiFi Buffer

1700

5100

0.45

10M dNTPs

1700

765

0.3

Kapa HiFi HotStart DNA Pol

1700

510

7.25

Ultra Pure H2O

1700

12325

11

Total Volume

1700

18700

...

Temp C

Cycles

Time

95*

1X

3:00*

98

36X

0:30

62

36X

0:30

72

36X

0:30

72

1X

5:00

4

1X

0:00

MagBead Cleanup:

Some plates were cleaned up using the Nimbus platform protocol “AxyPrep MagBead PCR1 No MM”

...

  • Equilibrate Beads to room Temperature

  • Add 24 ul of MagBeads to each well and 15 ul of replicate to same well of replicate

  • Pipette mix up and down 10 times.

  • Incubate at RT for 5 minutes

  • Secure plate on magnet plate; incubate at RT for 5 minutes (until wells are clear)

  • Remove 65 ul from each well; keep tips to left or right depending on the column to avoid bead pellet.

  • Add 100 ul Fresh 80% EtOH to each well. Incubate 30 seconds. Remove 100 ul from each well

  • Add 100 ul Fresh 80% EtOH to each well. Incubate 30 seconds. Remove 100 ul from each well

  • Reaspirate from each well to assure maximum EtOH removal

  • Allow plate to air dry for 7 minutes.

  • Remove sample plate from magnet plate.

  • Add 40 ul TE; pipette mix 10+ times. Incubate 2 minutes at RT.

  • Place sample plate back on magnet for 5 minutes or until all wells are cleared.

  • Transfer 40 ul to labeled transparent plate (Plate name_PCR_MIDs)

qPCR ALF_EPI_RUN2

  • Make 1:1000 dilutions of column 3 from the PCR plates by adding 1 ul to 999 ul TE in a deep well plate:

...

 

1

2

3

4

5

6

7

8

9

10

11

12

A

ALF_EPI_PLT5_16S

ALF_EPI_PLT5_ITS

ALF_EPI_PLT6_16S

ALF_EPI_PLT6_ITS

ALF_EPI_PLT7_16S

ALF_EPI_PLT7_ITS

ALF_EPI_PLT8_16S

ALF_EPI_PLT8_ITS

 

NTC

NTC

NTC

B

ALF_EPI_PLT5_16S

ALF_EPI_PLT5_ITS

ALF_EPI_PLT6_16S

ALF_EPI_PLT6_ITS

ALF_EPI_PLT7_16S

ALF_EPI_PLT7_ITS

ALF_EPI_PLT8_16S

ALF_EPI_PLT8_ITS

 

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

ALF_EPI_PLT5_16S

ALF_EPI_PLT5_ITS

ALF_EPI_PLT6_16S

ALF_EPI_PLT6_ITS

ALF_EPI_PLT7_16S

ALF_EPI_PLT7_ITS

ALF_EPI_PLT8_16S

ALF_EPI_PLT8_ITS

 

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

ALF_EPI_PLT5_16S

ALF_EPI_PLT5_ITS

ALF_EPI_PLT6_16S

ALF_EPI_PLT6_ITS

ALF_EPI_PLT7_16S

ALF_EPI_PLT7_ITS

ALF_EPI_PLT8_16S

ALF_EPI_PLT8_ITS

 

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

ALF_EPI_PLT5_16S

ALF_EPI_PLT5_ITS

ALF_EPI_PLT6_16S

ALF_EPI_PLT6_ITS

ALF_EPI_PLT7_16S

ALF_EPI_PLT7_ITS

ALF_EPI_PLT8_16S

ALF_EPI_PLT8_ITS

 

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

ALF_EPI_PLT5_16S

ALF_EPI_PLT5_ITS

ALF_EPI_PLT6_16S

ALF_EPI_PLT6_ITS

ALF_EPI_PLT7_16S

ALF_EPI_PLT7_ITS

ALF_EPI_PLT8_16S

ALF_EPI_PLT8_ITS

 

2 pM Std

2 pM Std

2 pM Std

G

ALF_EPI_PLT5_16S

ALF_EPI_PLT5_ITS

ALF_EPI_PLT6_16S

ALF_EPI_PLT6_ITS

ALF_EPI_PLT7_16S

ALF_EPI_PLT7_ITS

ALF_EPI_PLT8_16S

ALF_EPI_PLT8_ITS

 

20 pM Std

20 pM Std

20 pM Std

H

ALF_EPI_PLT5_16S

ALF_EPI_PLT5_ITS

ALF_EPI_PLT6_16S

ALF_EPI_PLT6_ITS

ALF_EPI_PLT7_16S

ALF_EPI_PLT7_ITS

ALF_EPI_PLT8_16S

ALF_EPI_PLT8_ITS

 

 

 

 

Results:

Average results for the following plates (column 3):

...