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Normalize templates

Use plate reader to quantify templates

Normalize to between 20 ng/ul and 150 ng/ul

2017 alfalfa: Transfer to conical pcr plates. Normalize on nimbus to 100 ng/ul in 30 ul.

Templates:

ALF_PLT5_2017_GBS

ALF_PLT6_2017_GBS

ALF_PLT7_2017_GBS

ALF_PLT8_2017_GBS

ALF_PLT9_2017_GBS

ALF_PLT1_2020_GBS

ALF_PLT2_2020_GBS

ALF_PLT3_2020_GBS

ALF_PLT4_2020_GBS

ALF_PLT5_2020_GBS

ALF_PLT6_2020_GBS

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

Restriction Digestion_GBS_Run3_Part1

(Keep MM and reaction plates on ice)

Add 3 ul Digestion MM to 10 plates using the 8 channel

Reagent

ul/rxn

rxns

ul needed

10x T4 Buffer

1.15

1050

1207.5

5M NaCl

0.12

1050

126

1 mg/ml BSA

0.6

1050

630

H2O

0.73

1050

766.5

MseI (enzyme)

0.12

1050

126

EcoR1 (enzyme)

0.28

1050

294

Total

3

1050

3150

Add 6 ul template to each plate with Benchsmart. Cover and seal each plate, vortex, centrifuge and incubate at 37C for 8 hours. Followed by 65C for 1 hour.

Adaptor Ligation_GBS_Run3_Part1

Spin down plates and add 1.4 ul Ligation MM to each well with 8 channel.

Reagent

ul/rxn

rxns

ul needed

MseI oligo

1

1075

1050

H2O

0.112

1075

117.6

10x T4 Buffer

0.1

1075

105

5M NaCl

0.01

1075

10.5

1 mg/ml BSA

0.05

1075

52.5

T4 DNA ligase

0.1675

1075

175.9

Total

1.4

1075

1511.5

Add 1 ul of EcoR1 Adaptors with 8-channel and Track which template plate gets which MID plate.

Template

EcoR1 MID plate

ALF_PLT5_2017_GBS

GBS Plate7

ALF_PLT6_2017_GBS

GBS Plate 8

ALF_PLT7_2017_GBS

GBS Plate 1

ALF_PLT8_2017_GBS

GBS Plate 2

ALF_PLT9_2017_GBS

GBS Plate 3

ALF_PLT1_2020_GBS

GBS Plate 4

ALF_PLT2_2020_GBS

GBS Plate 5

ALF_PLT3_2020_GBS

GBS Plate 6

ALF_PLT4_2020_GBS

GBS Plate 7

ALF_PLT5_2020_GBS

GBS Plate 8

Label reaction plates with MID plate used.

Cover, vortex, and spin plates. Incubate plates at RT for 2 hours on benchtop.

Add 120 ul of low EDTA TE store at 4C for a month or -20C for longer.

Restriction Digestion_GBS_Run3_Part2

(Keep MM and reaction plates on ice)

Add 3 ul Digestion MM to 9 plates using the 8 channel

Reagent

ul/rxn

rxns

ul needed

10x T4 Buffer

1.15

950

1092.5

5M NaCl

0.12

950

114

1 mg/ml BSA

0.6

950

570

H2O

0.73

950

693.5

MseI (enzyme)

0.12

950

114

EcoR1 (enzyme)

0.28

950

266

Total

3

950

2850

Add 6 ul template to each plate with Benchsmart. Cover and seal each plate, vortex, centrifuge and incubate at 37C for 8 hours. Followed by 65C for 1 hour.

Adaptor Ligation_GBS_Run3_Part2

Spin down plates and add 1.4 ul Ligation MM to each well with 8 channel.

Reagent

ul/rxn

rxns

ul needed

MseI oligo

1

1050

1050

H2O

0.112

1050

117.6

10x T4 Buffer

0.1

1050

105

5M NaCl

0.01

1050

10.5

1 mg/ml BSA

0.05

1050

52.5

T4 DNA ligase

0.1675

1050

175.9

Total

1.4

1050

1470

Add 1 ul of EcoR1 Adaptors with 8-channel and Track which template plate gets which MID plate.

Template

EcoR1 MID plate

ALF_PLT6_2020_GBS

GBS Plate 1

ALF_PLT1_2020_END

GBS Plate 2

ALF_PLT2_2020_END

GBS Plate 3

ALF_PLT3_2020_END

GBS Plate 4

ALF_PLT4_2020_END

GBS Plate 5

ALF_PLT5_2020_END

GBS Plate 6

ALF_PLT6_2020_END

GBS Plate 7

ALF_PLT7_2020_END

GBS Plate 8

ALF_PLT8_2020_END

GBS Plate 1

Label reaction plates with MID plate used.

Cover, vortex, and spin plates. Incubate plates at RT for 2 hours on benchtop.

Add 120 ul of low EDTA TE store at 4C for a month or -20C for longer.

PCR Amplification_GBS_Run3

Create working pools. For pools 3A, 3C, 3E, 3G, 3I pool ligated plates matching well to well. For pool 3B, 3D, 3F, 3H, 3J pool ligated plates with even plates flipped upside down (H12 in A1). Mix together 20 ul from each well of each plate for pooled plate using the Benchsmart. After pooling all samples, vortex and spin down plates then use 4 ul from the pooled plates for PCR templates. We are doing duplicate PCR.

Pool

Plate1

Plate2

Plate3

Plate4

3A

ALF_PLT5_2017_GBS

ALF_PLT6_2017_GBS

ALF_PLT7_2017_GBS

ALF_PLT8_2017_GBS

Pool

Plate1

Plate2

Plate3

Plate4

3B

ALF_PLT5_2017_GBS

ALF_PLT6_2017_GBS

(FLIPPED)

ALF_PLT7_2017_GBS

ALF_PLT8_2017_GBS

(FLIPPED)

Pool

Plate1

Plate2

Plate3

Plate4

3C

ALF_PLT9_2017_GBS

ALF_PLT1_2020_GBS

ALF_PLT2_2020_GBS

ALF_PLT3_2020_GBS

Pool

Plate1

Plate2

Plate3

Plate4

3D

ALF_PLT9_2017_GBS

ALF_PLT1_2020_GBS

(FLIPPED)

ALF_PLT2_2020_GBS

ALF_PLT3_2020_GBS

(FLIPPED)

Pool

Plate1

Plate2

Plate3

Plate4

3E

ALF_PLT4_2020_GBS

ALF_PLT5_2020_GBS

ALF_PLT6_2020_GBS

ALF_PLT1_2020_END

Pool

Plate1

Plate2

Plate3

Plate4

3F

ALF_PLT4_2020_GBS

ALF_PLT5_2020_GBS

(FLIPPED)

ALF_PLT6_2020_GBS

ALF_PLT1_2020_END

(FLIPPED)

Pool

Plate1

Plate2

Plate3

Plate4

3G

ALF_PLT2_2020_END

ALF_PLT3_2020_END

ALF_PLT4_2020_END

ALF_PLT5_2020_END

Pool

Plate1

Plate2

Plate3

Plate4

3H

ALF_PLT2_2020_END

ALF_PLT3_2020_END

(FLIPPED)

ALF_PLT4_2020_END

ALF_PLT5_2020_END

(FLIPPED)

Pool

Plate1

Plate2

Plate3

3I

ALF_PLT6_2020_END

ALF_PLT7_2020_END

ALF_PLT8_2020_END

Pool

Plate1

Plate2

Plate3

3J

ALF_PLT6_2020_END

ALF_PLT7_2020_END

(FLIPPED)

ALF_PLT8_2020_END

PCR1_3A-3D:

Reagent

ul/rxn

rxns

ul needed

H2O

9.52

450

4284

5x iProof buffer

4

450

1800

10 mM dNTPs

0.4

450

180

50 mM MgCl2

0.4

450

180

5 uM Illumina Primers

1.33

450

598.5

iProof TAQ

0.2

450

90

DMSO

0.15

450

67.5

total

16

450

7200

Add 16 ul of PCR1 MM to each well of four new hard shell PCR plates.

Add 4uL of template from pooled plates.

Seal, Vortex, Spin down, and then run on Thermocycler program: GBS1:

Temp C

Cycles

Time

95*

1X

3:00

98

30X

0:30

60

30X

0:30

72

30X

0:40

72

1X

10:00

4*

1X*

0:00*

*pause step

Extra PCR

Add 2.125 ul of the MM directly to the previous PCR

Reagent

ul/rxn

rxns

ul needed

5x Iproof buffer

0.425

460

195.5

10 mM dNTPs

0.4

460

184

Primers

1.33

460

611.8

Total

2.155

460

991.3

Then continue with the last four unlisted steps for GBS1 from above:

Temp C

Cycles

Time

98

1X

3:00

60

1X

2:00

72

1X

10:00

4

1X

0:00

Comparisons_GBS_Run3_3A-3D

qPCR

  • 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

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

 

NTC

NTC

NTC

B

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

 

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

 

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

 

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

 

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

 

2 pM Std

2 pM Std

2 pM Std

G

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

 

20 pM Std

20 pM Std

20 pM Std

H

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

 

 

 

 

  • Combine 5uL from each well of GBS_Run3_3A into a pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • Combine 5uL from each well of GBS_Run3_3B into a pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • Combine 5uL from each well of GBS_Run3_3C into a pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • Combine 5uL from each well of GBS_Run3_3D into a pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • After 1:1000 pools have been made for each PCR plate, combine 3A and 3B undiluted pools together into one tube and label GBS_Run3AB_Pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • After 1:1000 pools have been made for each PCR plate, combine 3C and 3D undiluted pools together into one tube and label GBS_Run3CD_Pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • 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

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

GBS_Run3_3A Pool

NTC

NTC

NTC

B

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

GBS_Run3_3B Pool

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

GBS_Run3_3C Pool

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

GBS_Run3_3D

Pool

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

GBS_Run3_3AB

Pool

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

GBS_Run3_3CD

Pool

2 pM Std

2 pM Std

2 pM Std

G

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

20 pM Std

20 pM Std

20 pM Std

H

GBS_Run3_3A_Col1

GBS_Run3_3A_Col6

GBS_Run3_3B_Col1

GBS_Run3_3B_Col6

GBS_Run3_3C_Col1

GBS_Run3_3C_Col6

GBS_Run3_3D_Col1

GBS_Run3_3D_Col6

 

 

 

Results:

Average quantities observed for all products:

GBS_Run3_3A_Col1: 216.38 nanomoles

GBS_Run3_3A_Col6: 256.31 nanomoles

GBS_Run3_3B_Col1: 222.92 nanomoles

GBS_Run3_3B_Col6: 223.83 nanomoles

GBS_Run3_3C_Col1: 225.86 nanomoles

GBS_Run3_3C_Col6: 227.98 nanomoles

GBS_Run3_3D_Col1: 210.1 nanomoles

GBS_Run3_3D_Col6: 252.31 nanomoles

GBS_Run3_3A Pool: 258.54 nanomoles

GBS_Run3_3B Pool: 246.36 nanomoles

GBS_Run3_3C Pool: 244.65 nanomoles

GBS_Run3_3D Pool: 202.94 nanomoles

GBS_Run3_3AB Pool: 248.88 nanomoles

GBS_Run3_3CD Pool: 207.51 nanomoles

The full result report can be viewed below:

Bioanalyzer

BioAnalyzer Chip Set up:

Well 1: GBS_Run3_3A Pool

Well 2: GBS_Run3_3B Pool

Well 3: GBS_Run3_3C Pool

Well 4: GBS_Run3_3D Pool

Well 5: GBS_Run3_3AB Pool

Well 6: GBS_Run3_3CD Pool

Well 7: GBS_Run3_3A C1

Well 8: GBS_Run3_3A G9

Well 9: GBS_Run3_3B C1

Well 10: GBS_Run3_3B G9

Well 11: GBS_Run3_3C D5

Well 12: GBS_Run3_3D D5

Gel:

Electropherogram:

EPG 3A, 3B, 3C, 3D Pools:

EPG 3AB-3CD Pools:

EPG 3A & 3B Well Comparison:

EPG 3C & 3D Well Comparison:

PCR1_3E-3H:

Reagent

ul/rxn

rxns

ul needed

H2O

9.52

450

4284

5x iProof buffer

4

450

1800

10 mM dNTPs

0.4

450

180

50 mM MgCl2

0.4

450

180

5 uM Illumina Primers

1.33

450

598.5

iProof TAQ

0.2

450

90

DMSO

0.15

450

67.5

total

16

450

7200

Add 16 ul of PCR1 MM to each well of four new hard shell PCR plates.

Add 4uL of template from pooled plates.

Seal, Vortex, Spin down, and then run on Thermocycler program: GBS1:

Temp C

Cycles

Time

95*

1X

3:00

98

30X

0:30

60

30X

0:30

72

30X

0:40

72

1X

10:00

4*

1X*

0:00*

*pause step

Extra PCR

Add 2.125 ul of the MM directly to the previous PCR

Reagent

ul/rxn

rxns

ul needed

5x Iproof buffer

0.425

460

195.5

10 mM dNTPs

0.4

460

184

Primers

1.33

460

611.8

Total

2.155

460

991.3

Then continue with the last four unlisted steps for GBS1 from above:

Temp C

Cycles

Time

98

1X

3:00

60

1X

2:00

72

1X

10:00

4

1X

0:00

Comparisons_GBS_Run3_3E-3H

qPCR

  • 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

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

 

NTC

NTC

NTC

B

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

 

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

 

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

 

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

 

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

 

2 pM Std

2 pM Std

2 pM Std

G

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

 

20 pM Std

20 pM Std

20 pM Std

H

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

 

 

 

 

  • Combine 5uL from each well of GBS_Run3_3E into a pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • Combine 5uL from each well of GBS_Run3_3F into a pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • Combine 5uL from each well of GBS_Run3_3G into a pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • Combine 5uL from each well of GBS_Run3_3H into a pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • After 1:1000 pools have been made for each PCR plate, combine 3E and 3F undiluted pools together into one tube and label GBS_Run3EF_Pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • After 1:1000 pools have been made for each PCR plate, combine 3G and 3H undiluted pools together into one tube and label GBS_Run3GH_Pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • 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

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

GBS_Run3_3E

Pool

NTC

NTC

NTC

B

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

GBS_Run3_3F

Pool

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

GBS_Run3_3G Pool

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

GBS_Run3_3H

Pool

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

GBS_Run3_3EF

Pool

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

GBS_Run3_3GH

Pool

2 pM Std

2 pM Std

2 pM Std

G

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

20 pM Std

20 pM Std

20 pM Std

H

GBS_Run3_3E_Col1

GBS_Run3_3E_Col6

GBS_Run3_3F_Col1

GBS_Run3_3F_Col6

GBS_Run3_3G_Col1

GBS_Run3_3G_Col6

GBS_Run3_3H_Col1

GBS_Run3_3H_Col6

 

 

 

Results:

Average quantities observed for all products:

GBS_Run3_3E_Col1: 117.35 nanomoles

GBS_Run3_3E_Col6: 166.34 nanomoles

GBS_Run3_3F_Col1: 116.57 nanomoles

GBS_Run3_3F_Col6: 121.27 nanomoles

GBS_Run3_3G_Col1: 131.49 nanomoles

GBS_Run3_3G_Col6: 141.38 nanomoles

GBS_Run3_3H_Col1: 128.91 nanomoles

GBS_Run3_3H_Col6: 125.3 nanomoles

GBS_Run3_3E Pool: 155.11 nanomoles

GBS_Run3_3F Pool: 128.89 nanomoles

GBS_Run3_3G Pool: 135.65 nanomoles

GBS_Run3_3H Pool: 137.78 nanomoles

GBS_Run3_3EF Pool: 120.23 nanomoles

GBS_Run3_3GH Pool: 128.13 nanomoles

The full result report can be viewed below:

Bioanalyzer

BioAnalyzer Chip Set up:

Well 1: GBS_Run3_3E Pool

Well 2: GBS_Run3_3F Pool

Well 3: GBS_Run3_3G Pool

Well 4: GBS_Run3_3H Pool

Well 5: GBS_Run3_3EF Pool

Well 6: GBS_Run3_3GH Pool

Well 7: GBS_Run3_3E C1

Well 8: GBS_Run3_3E G9

Well 9: GBS_Run3_3F C1

Well 10: GBS_Run3_3F G9

Well 11: GBS_Run3_3G D5

Well 12: GBS_Run3_3H D5

PCR1_3I-3J:

Reagent

ul/rxn

rxns

ul needed

H2O

9.52

250

2380

5x iProof buffer

4

250

1000

10 mM dNTPs

0.4

250

100

50 mM MgCl2

0.4

250

100

5 uM Illumina Primers

1.33

250

332.5

iProof TAQ

0.2

250

50

DMSO

0.15

250

37.5

total

16

250

4000

Add 16 ul of PCR1 MM to each well of two new hard shell PCR plates.

Add 4uL of template from pooled plates.

Seal, Vortex, Spin down, and then run on Thermocycler program: GBS1:

Temp C

Cycles

Time

95*

1X

3:00

98

30X

0:30

60

30X

0:30

72

30X

0:40

72

1X

10:00

4*

1X*

0:00*

*pause step

Extra PCR

Add 2.125 ul of the MM directly to the previous PCR

Reagent

ul/rxn

rxns

ul needed

5x Iproof buffer

0.425

260

110.5

10 mM dNTPs

0.4

260

104

Primers

1.33

260

345.8

Total

2.155

260

560.3

Then continue with the last four unlisted steps for GBS1 from above:

Temp C

Cycles

Time

98

1X

3:00

60

1X

2:00

72

1X

10:00

4

1X

0:00

Comparisons_GBS_Run3_3I-3J

qPCR

  • 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

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

 

NTC

NTC

NTC

B

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

 

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

 

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

 

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

 

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

 

2 pM Std

2 pM Std

2 pM Std

G

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

 

20 pM Std

20 pM Std

20 pM Std

H

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

 

  • Combine 5uL from each well of GBS_Run3_3I into a pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • Combine 5uL from each well of GBS_Run3_3J into a pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • After 1:1000 pools have been made for each PCR plate, combine 3I and 3J undiluted pools together into one tube and label GBS_Run3IJ_Pool. Make a 1:1000 dilution of this pool to run on qPCR.

  • 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)

90

900

2 ul

Primer Premix (10X)

90

180

4 ul

Ultra Pure Water

90

360

16 ul

Total Volume

90

1440

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

 

1

2

3

4

5

6

7

8

9

10

11

12

A

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

GBS_Run3_3I

Pool

NTC

NTC

NTC

B

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

GBS_Run3_3I

Pool

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

GBS_Run3_3J

Pool

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

GBS_Run3_3J

Pool

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

GBS_Run3_3IJ

Pool

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

GBS_Run3_3IJ

Pool

2 pM Std

2 pM Std

2 pM Std

G

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

20 pM Std

20 pM Std

20 pM Std

H

GBS_Run3_3I_Col1

GBS_Run3_3I_Col6

GBS_Run3_3I_Col12

GBS_Run3_3J_Col1

GBS_Run3_3J_Col6

GBS_Run3_3J_Col12

 

 

 

Results:

Average quantities observed for all products:

GBS_Run3_3I_Col1: 142.1

GBS_Run3_3I_Col6: 173.9

GBS_Run3_3I_Col12: 192.35

GBS_Run3_3J_Col1: 173.05

GBS_Run3_3J_Col6: 236.9

GBS_Run3_3J_Col12: 182.26

GBS_Run3_3I Pool: 241.93

GBS_Run3_3J Pool: 229.64

GBS_Run3_3IJ Pool: 230.58

The full result report can be viewed below:

Bioanalyzer

BioAnalyzer Chip Set up:

Well 1: GBS_Run3_3I Pool

Well 2: GBS_Run3_3J Pool

Well 3: GBS_Run3_3IJ Pool

Well 4: GBS_Run3_3I C1

Well 5: GBS_Run3_3I G4

Well 6: GBS_Run3_3I 7A

Well 7: GBS_Run3_3I 10E

Well 8: GBS_Run3_3I 12D

Well 9: GBS_Run3_3J B2

Well 10: GBS_Run3_3J H5

Well 11: GBS_Run3_3J C6

Well 12: GBS_Run3_3J A9

Gel:

EPG 3I-3J:

EPG 3I-3J Pools:

EPG 3I Wells:

EPG 3J Wells:

  • No labels