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94 °C for 4 min, followed by 34 cycles of 30 s at 94 °C, 40 s at 55 °C (or 58 °C) and 1 min at 72 °C, with a final step of 10 min at 72 °C.

Dilute and Array Primers

Primers arrived 100uM in 50 ul

Add 575 to get primers to 8 uM with Integra Pipette using Pipette/Mix setting

Add 87.5 ul to new Primer plates

Use Nimbus to array first four plates using FULLITS_Primer_Prep_Adjustable

PCR MasterMix

ul/rxn

Reagent

# of rxns

ul needed

3

5X Kapa HiFi Buffer

384

1320

0.45

10M dNTPs

384

198

0.3

7.5

Kapa HiFi HotStart DNA

Pol

2X

384

120

132

900

7

4.

25

5

HPLC H2O

384

120

3190

540

11

12

Total Volume

384

4840

1440

  • Add 11 ul to each well of a hard shell, full skirt plate. Add 2 1 uL of 0.5 uM primers and 2uL of template to each well.

  • Primers:

...

Run fullITS plates on thermocycler program fullITS:

Step

Temp C

Cycles

Time

Denature

95

1X

10:00

Denature

94

35X

0:30

Annealing** (Row C)

55

35X

0:40

Extension/Elongation

72

35X

1:00

Final Extension

72

1X

10:00

Hold

4

1X

0:00

Run 16S plates on Thermocycler Program GSAF35:

Temp C

Cycles

Time

95*

1X

3:00*

98

35X

0:30

62

35X

0:30

72

35X

0:30

72

1X

5:00

4

1X

0:00

Pool duplicates together.

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  • Pool 2 ul of the TRNL and 16S samples separately. Make 1:1000 dilutions of each pool and run in triplicate.

  • Make 1:1000 dilutions of columns 1,6, and 12 for each plate using 999 of TE and 1uL of sample into a deep well plate.

 

1

2

3

4

5

6

7

8

9

10

11

12

A

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

 

NTC

NTC

NTC

B

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

 

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

 

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

 

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

 

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

 

2 pM Std

2 pM Std

2 pM Std

G

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

 

20 pM Std

20 pM Std

20 pM Std

H

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

 

 

 

 

  • 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)

110

1100

2 ul

Primer Premix (10X)

110

220

4 ul

Ultra Pure Water

110

440

16 ul

Total Volume

110

1760

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

 

1

2

3

4

5

6

7

8

9

10

11

12

A

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

TRNL1_1_16S_Pool

 

NTC

NTC

NTC

B

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

TRNL1_1_16S_Pool

 

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

TRNL1_1_16S_Pool

 

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

TRNL1_1_T_Pool

 

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

TRNL1_1_T_Pool

 

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

TRNL1_1_T_Pool

 

2 pM Std

2 pM Std

2 pM Std

G

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

 

20 pM Std

20 pM Std

20 pM Std

H

TRNL1_1_16S_Col1

TRNL1_1_16S_Col6

TRNL1_1_16S_Col12

TRNL1_1_T_Col1

TRNL1_1_T_Col6

TRNL1_1_T_Col12

 

 

 

 

Results:

The TRNL pool via standard size estimation returned a mean of ? nM. This should be adjusted for the difference between the standards' fragment sizes and the expected product size (452 vs 220). 9.41x(452/220) = 19.33 nM

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