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Prepare two ITS and two 16S PCR plates for the following template plates:

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

  • Add 11 ul to each well of a hard shell, full skirt plate. Seal with bubble strips and store in refrigerator until needed label “ALF PCR”. (If doing manually, one needs 2 ul of template and 2 ul of the primers).

Plates

16S MIDs

ITS MIDs

ALF_PLT1_2020_END

 long16S0A1

 longITS0A1

 long16S0B1

 longITS0B1

ALF_PLT2_2020_END

long16S0C1

 longITS0C1

 long16S0D1

 longITS0D1

ALF_PLT3_2020_END

 long16S0E1

 longITS0E1

 long16S0F1

 longITS0F1

ALF_PLT4_2020_END

long16S0G1

 longITS0G1

 long16S0H1

 longITS0H1

Run on Thermocycler Program GSAF36:

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”

Manually, it was done:

  • 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

 

 

 

 

  • Add 16 ul of Illumina Library Quantification MasterMix to each well:

ul/rxn

Reagent

# of rxns

ul needed

10 ul

KAPA SYBR FAST qPCR MM (2X)

100

1000

2 ul

Primer Premix (10X)

100

200

4 ul

Ultra Pure Water

100

400

16 ul

Total Volume

100

1600

  • Add 4 ul of template, pool, or standards to each well:

 

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):

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:

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

  • Add 11 ul to each well of a hard shell, full skirt plate. Seal with bubble strips and store in refrigerator until needed label “ALF PCR”. (If doing manually, one needs 2 ul of template and 2 ul of the primers).

Plates

16S MIDs

ITS MIDs

ALF_PLT5_2020_END

 long16S0A2

 longITS0A2

 long16S0B2

 longITS0B2

ALF_PLT6_2020_END

 long16S0C2

 longITS0C2

 long16S0D2

 longITS0D2

ALF_PLT7_2020_END

 long16S0E2

 longITS0E2

 long16S0F2

 longITS0F2

ALF_PLT8_2020_END

 long16S0G2

 longITS0G2

 long16S0H2

 longITS0H2

Run on Thermocycler Program GSAF36:

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”

Manually, it was done:

  • 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

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

 

 

04.0002 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

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

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

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

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

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

  • Add 16 ul of Illumina Library Quantification MasterMix to each well:

ul/rxn

Reagent

# of rxns

ul needed

10 ul

KAPA SYBR FAST qPCR MM (2X)

100

1000

2 ul

Primer Premix (10X)

100

200

4 ul

Ultra Pure Water

100

400

16 ul

Total Volume

100

1600

  • Add 4 ul of template, pool, or standards to each well:

 

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):

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:

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

  • Add 11 ul to each well of a hard shell, full skirt plate. Seal with bubble strips and store in refrigerator until needed label “ALF PCR”. (If doing manually, one needs 2 ul of template and 2 ul of the primers).

Plates

16S MIDs

ITS MIDs

ALF_PLT1_2020_EPI

 long16S0A3

 longITS0A3

 long16S0B3

 longITS0B3

ALF_PLT2_2020_EPI

 long16S0C3

 longITS0C3

 long16S0D3

 longITS0D3

ALF_PLT3_2020_EPI

 long16S0E3

 longITS0E3

 long16S0F3

 longITS0F3

ALF_PLT4_2020_EPI

 long16S0G3

 longITS0G3

 long16S0H3

 longITS0H3

Run on Thermocycler Program GSAF36:

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”

Manually, it was done:

  • 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

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

 

 

04.0002 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

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

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

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

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

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

 

 

 

 

  • Add 16 ul of Illumina Library Quantification MasterMix to each well:

ul/rxn

Reagent

# of rxns

ul needed

10 ul

KAPA SYBR FAST qPCR MM (2X)

100

1000

2 ul

Primer Premix (10X)

100

200

4 ul

Ultra Pure Water

100

400

16 ul

Total Volume

100

1600

  • Add 4 ul of template, pool, or standards to each well:

 

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):

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:

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

  • Add 11 ul to each well of a hard shell, full skirt plate. Seal with bubble strips and store in refrigerator until needed label “ALF PCR”. (If doing manually, one needs 2 ul of template and 2 ul of the primers).

Plates

16S MIDs

ITS MIDs

ALF_PLT5_2020_EPI

 long16S0A4

 longITS0A4

 long16S0B4

 longITS0B4

ALF_PLT6_2020_EPI

 long16S0C4

 longITS0C4

 long16S0D4

 longITS0D4

ALF_PLT7_2020_EPI

 long16S0E4

 longITS0E4

 long16S0F4

 longITS0F4

ALF_PLT8_2020_EPI

 long16S0G4

 longITS0G4

 long16S0H4

 longITS0H4

Run on Thermocycler Program GSAF36:

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”

Manually, it was done:

  • 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

 

 

 

 

  • Add 16 ul of Illumina Library Quantification MasterMix to each well:

ul/rxn

Reagent

# of rxns

ul needed

10 ul

KAPA SYBR FAST qPCR MM (2X)

100

1000

2 ul

Primer Premix (10X)

100

200

4 ul

Ultra Pure Water

100

400

16 ul

Total Volume

100

1600

  • Add 4 ul of template, pool, or standards to each well:

 

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):

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:

The full result report can be viewed below:

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