1EAST

1EAST

128 samples from Isaaac Eastlund for 16S amplicon

Added TE blank to all wells of column 5 except F5 and G5 that got mock community

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

ul/rxn

Reagent

# of rxns

ul needed

ul/rxn

Reagent

# of rxns

ul needed

3

5X Kapa HiFi Buffer

600

1800

0.45

10M dNTPs

600

270

0.3

Kapa HiFi HotStart DNA Pol

600

180

7.25

HPLC H2O

600

4350

11

Total Volume

600

6600

  • Add 9 ul to each well of a hard shell, full skirt plate. Seal with bubble strips and store in refrigerator until needed label. (If doing manually, one needs 2 ul of template and 2 ul of the primers).

Plate

16S Primer

16S Primer

Plate

16S Primer

16S Primer

1EAST1

long16S0G11

long16S0H11

1EAST2

long16S0C12

 

Run on Thermocycler Program GSAF36:

Temp C

Cycles

Time

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:

Plates were cleaned up utilizing the BenchSmart 96 channel pipette:

  • 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 4 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)

  • Normalize to 5 ng/ul

  • Store in -20 until ready to qPCR

Tapestation

2 samples, 1 Mock Community positive control, and one NTC were checked for amplification for both loci. They matched expectations.

qPCR and dilution