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Synthgene Structure: 5'-LocusPrimer Nonsense InverseLocusPrimer-3'

ITS Synthgene:

CTTGGTCATTTAGAGGAAGTAATGCCACAGATACGTACCGCTCATAACGCGAACCGAAGCGCAGTAGAAGTACTCCGTATCCTACCTCGGTCGTGGTTTAGGCTATCGACATCTTGCATGGGCTTCCCTAGTGAACTCTTGGGATGTGCATCGATGAAGAACGCAGC

Alignment of primers and synthetic amplicon control molecules (synthgenes): Synthgene_detective.pdf (also on OneDrive).

16S Synthgene:

GTGCCAGCAGCCGCGGTAAGCCACAGATACGTACCGCTCATAACGCGAACCGAAGCGCAGTAGAAGTACTCCGTATCCTACCTCGGTCGTGGTTTAGGCTATCGACATCTTGCATGGGCTTCCCTAGTGAACTCTTGGGATGTATTAGATACCCTAGTAGTCC

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Add 6 ul appropriate 0.25 uM paired primers Molecular IDentifier (MID) Plate:______________

16S Primer Base

  • 515F (5’-GTGYCAGCMGCCGC GGTAA-3’) (Parada et al. 2016)

  •  806R (5’-GGACTACNVGGGTWTCTAAT-3’) (Apprill et al. 2015)

ITS Primer Base

Primer structure

  • 5'-PARTIAL_ILLUMINA_FLOWCELL_SEQbarcodeGTGYCAGCMGCCGCGGTAA-3'

  • 5'-PARTIAL_ILLUMINA_FLOWCELL_SEQbarcodeGGACTACHVGGGTWTCTAAT-3'

  • 5'-PARTIAL_ILLUMINA_FLOWCELL_SEQbarcodeCTTGGTCATTTAGAGGAAGTAA-3'

  • 5'-PARTIAL_ILLUMINA_FLOWCELL_SEQbarcodeGCTGCGTTCTTCATCGATGC-3'

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ul/rxn

Reagent

# of rxns

ul needed

3

5X Kapa HiFi Buffer

60

210

0.45

10M dNTPs

60

31.5

0.3

Kapa HiFi HotStart DNA Pol

60

21

0.5 ul

10 uM F and R FlowCell Primers

60

35

0.75

HPLC H2O

60

52.5

5

Total Volume

60

350

FlowCell Primers

  • AATGATACGGCGACCACCGAGATCTACACTCGTCGGCAGCGTC

  • CAAGCAGAAGACGGCATACGAGATGTCTCGTGGGCTCGG

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Temp C

Cycles

Time

95*

1X

3:00*

98

19X

0:30

55*

19X

0:30

72

19X

0:30

72

1X

5:00

4

1X

0:00

Purify samples using GSAF’s second modified MagBead protocol:

Equilibrate Beads to room Temperature

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Normalize PCR’s via absorbance concentrations. Gregg Randolph What concentration did you normalize to? Or has this not been finalized yet?

Pool normalized PCRs

Check Pool’s molar concentration via qPCR:

Dilute Pool 1:1000

Include NTC and Standards (20 pm, 2 pm, 0.2, 0.02pm, 0.002pm, 0.0002pm)

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