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New Control Samples:

Start Reaction Plate Setup:

  • Add Ultrapure H2O to the reaction plates in the following pattern:

NOTE: Water in the master mix has been adjusted to a lower amount. The plate set up below will replace the water usually added to the master mix while also showing if a decrease in water and an increase in template will increase PCR yields.

 

1

2

3

4

A

6ul

4ul

 

B

6ul

4ul

 

C

6ul

4ul

 

D

6ul

4ul

 

E

6ul

4ul

 

F

6ul

4ul

 

G

6ul

4ul

 

H

6ul

4ul

 

MasterMix

ul/rxn

Reagent

# of rxns

ul needed

3

5X Kapa HiFi Buffer

24

120

0.45

10M dNTPs

24

18

0.3

Kapa HiFi HotStart DNA Pol

24

12

0.25

HPLC H2O

24

10

1

ISD

24

40

5

Total Volume

24

200

  • Add 5 ul to each well of a hard shell, full skirt plate.

  • Add 10 ng/ul Mock Community to the plate in the following pattern:

 

1

2

3

4

A

2ul

4ul

8ul

 

B

2ul

4ul

8ul

 

C

2ul

4ul

8ul

 

D

2ul

4ul

8ul

 

E

2ul

4ul

8ul

 

F

2ul

4ul

8ul

 

G

2ul

4ul

8ul

 

H

2ul

4ul

8ul

 

  • Add 2 ul 1-step primers (from columns 7-9):

  • Seal with bubble seals. Vortex briefly. Spin down.

  • 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 (Do not reuse any tips):

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:

  • Make 3 separate 1:1000 dilutions 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

RA6

RA14

RA22

LL1A_J

WG3A_S

LY2A_S

MCA_2

MCA_4

MCA_8

NTC

NTC

NTC

B

RA7

RA15

RA23

LL1B_J

WG3B_S

LY2B_S

MCB_2

MCB_4

MCB_8

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

RA8

RA16

RA24

LL2A_J

WG4A_S

LY3B_S

MCC_2

MCC_4

MCC_8

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

RA9

RA17

RA25

LL2B_J

WG4B_S

LY1A_S

MCD_2

MCD_4

MCD_8

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

RA10

RA18

RA26

LL4A_J

WG2A_S

LY1B_S

MCA_2_clean

MCA_4_clean

MCA_8_clean

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

RA11

RA19

RA27

LL4B_J

WG2B_S

LY4A_S

MCB_2_clean

MCB_4_clean

MCB_8_clean

2 pM Std

2 pM Std

2 pM Std

G

RA12

RA20

RA28

LL3A_J

WG1A_S

LY4B_S

MCC_2_clean

MCC_4_clean

MCC_8_clean

H

RA13

RA21

RA29

LL3B_J

WG1B_S

BLANK

MCD_2_clean

MCD_4_clean

MCD_8_clean

 

 

 

Plate

5LVD5

5LVD5

5LVD5

5DG5

5DG5

5DG5

Controls

Controls

Controls

Column

1

2

3

4

5

6

  • Add 16 ul of Illumina Library Quantification MasterMix to each well of 4 plates:

ul/rxn

Reagent

# of rxns

ul needed

10 ul

KAPA SYBR FAST qPCR MM (2X)

80

800

2 ul

Primer Premix (10X)

80

160

4 ul

Ultra Pure Water

80

320

16 ul

Total Volume

80

1280

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

 

1

2

3

4

5

6

7

8

9

10

11

12

A

RA6

RA14

RA22

RA6

RA14

RA22

RA6

RA14

RA22

NTC

NTC

NTC

B

RA7

RA15

RA23

RA7

RA15

RA23

RA7

RA15

RA23

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

RA8

RA16

RA24

RA8

RA16

RA24

RA8

RA16

RA24

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

RA9

RA17

RA25

RA9

RA17

RA25

RA9

RA17

RA25

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

RA10

RA18

RA26

RA10

RA18

RA26

RA10

RA18

RA26

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

RA11

RA19

RA27

RA11

RA19

RA27

RA11

RA19

RA27

2 pM Std

2 pM Std

2 pM Std

G

RA12

RA20

RA28

RA12

RA20

RA28

RA12

RA20

RA28

20 pM Std

20 pM Std

20 pM Std

H

RA13

RA21

RA29

RA13

RA21

RA29

RA13

RA21

RA29

 

 

 

 

1

2

3

4

5

6

7

8

9

10

11

12

A

LL1A_J

WG3A_S

LY2A_S

LL1A_J

WG3A_S

LY2A_S

LL1A_J

WG3A_S

LY2A_S

NTC

NTC

NTC

B

LL1B_J

WG3B_S

LY2B_S

LL1B_J

WG3B_S

LY2B_S

LL1B_J

WG3B_S

LY2B_S

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

LL2A_J

WG4A_S

LY3B_S

LL2A_J

WG4A_S

LY3B_S

LL2A_J

WG4A_S

LY3B_S

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

LL2B_J

WG4B_S

LY1A_S

LL2B_J

WG4B_S

LY1A_S

LL2B_J

WG4B_S

LY1A_S

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

LL4A_J

WG2A_S

LY1B_S

LL4A_J

WG2A_S

LY1B_S

LL4A_J

WG2A_S

LY1B_S

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

LL4B_J

WG2B_S

LY4A_S

LL4B_J

WG2B_S

LY4A_S

LL4B_J

WG2B_S

LY4A_S

2 pM Std

2 pM Std

2 pM Std

G

LL3A_J

WG1A_S

LY4B_S

LL3A_J

WG1A_S

LY4B_S

LL3A_J

WG1A_S

LY4B_S

20 pM Std

20 pM Std

20 pM Std

H

LL3B_J

WG1B_S

BLANK

LL3B_J

WG1B_S

BLANK

LL3B_J

WG1B_S

BLANK

 

 

 

 

1

2

3

4

5

6

7

8

9

10

11

12

A

MCA_2

MCA_4

MCA_8

MCA_2

MCA_4

MCA_8

MCA_2

MCA_4

MCA_8

NTC

NTC

NTC

B

MCB_2

MCB_4

MCB_8

MCB_2

MCB_4

MCB_8

MCB_2

MCB_4

MCB_8

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

MCC_2

MCC_4

MCC_8

MCC_2

MCC_4

MCC_8

MCC_2

MCC_4

MCC_8

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

MCD_2

MCD_4

MCD_8

MCD_2

MCD_4

MCD_8

MCD_2

MCD_4

MCD_8

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

MCA_2_clean

MCA_4_clean

MCA_8_clean

MCA_2_clean

MCA_4_clean

MCA_8_clean

MCA_2_clean

MCA_4_clean

MCA_8_clean

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

MCB_2_clean

MCB_4_clean

MCB_8_clean

MCB_2_clean

MCB_4_clean

MCB_8_clean

MCB_2_clean

MCB_4_clean

MCB_8_clean

2 pM Std

2 pM Std

2 pM Std

G

MCC_2_clean

MCC_4_clean

MCC_8_clean

MCC_2_clean

MCC_4_clean

MCC_8_clean

MCC_2_clean

MCC_4_clean

MCC_8_clean

20 pM Std

20 pM Std

20 pM Std

H

MCD_2_clean

MCD_4_clean

MCD_8_clean

MCD_2_clean

MCD_4_clean

MCD_8_clean

MCD_2_clean

MCD_4_clean

MCD_8_clean

 

 

 

Controls

Controls

Controls

Controls

Controls

Controls

Controls

Controls

Controls

Results:

5LVD5 Results:

5DG5 Results:

MC_MagBead Results:

Pooling and Sequencing:

Pool 2 ul from all original product plates. Make 3 1:1000 dilutions of pool and qPCR as usual. Dilute pool to 1nM. Dilute to loading concentration with 20% PhiX.

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