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  1. Make sample spreadsheet and plate test samples by adding 30uL of sample to the corresponding well.

  2. Quantify samples on Synergy HTX.

  3. Normalize samples to 10ng/uL.

  4. Choose 4 plant and 4 stool to run PCR test.

  5. Make 1 step PCR MMX and plate in the template format below (Replace P1, P2, …. and S1, S2… with actual sample names):

PCR MasterMix

ul/rxn

Reagent

# of rxns

ul needed

3

5X Kapa HiFi Buffer

80

240

0.45

10M dNTPs

80

36

0.3

Kapa HiFi HotStart DNA Pol

80

24

7.25

HPLC H2O

80

580

11

Total Volume

80

880

...

 

1

2

3

4

5

6

7

8

9

10

11

12

A

P2_A

P7_A

P9_A

P14_A

GM2_A

SB4_A

SB1_A

AT16_A

 

NTC

NTC

NTC

B

P2_B

P7_B

P9_B

P14_B

GM2_B

SB4_B

SB1_B

AT16_B

 

0.0002 pM Std

0.0002 pM Std

0.0002 pM Std

C

P2_C

P7_C

P9_C

P14_C

GM2_C

SB4_C

SB1_C

AT16_C

 

0.002 pM Std

0.002 pM Std

0.002 pM Std

D

P2_D

P7_D

P9_D

P14_D

GM2_D

SB4_D

SB1_D

AT16_D

 

0.02 pM Std

0.02 pM Std

0.02 pM Std

E

P2_E

P7_E

P9_E

P14_E

GM2_E

SB4_E

SB1_E

AT16_E

 

0.2 pM Std

0.2 pM Std

0.2 pM Std

F

P2_F

P7_F

P9_F

P14_F

GM2_F

SB4_F

SB1_F

AT16_F

 

2 pM Std

2 pM Std

2 pM Std

G

P2_G

P7_G

P9_G

P14_G

GM2_G

SB4_G

SB1_G

AT16_G

 

20 pM Std

20 pM Std

20 pM Std

H

P2_H

P7_H

P9_H

P14_H

GM2_H

SB4_H

SB1_H

AT16_H

 

 

 

 

Results:

Results Straight Off ABI 7500

Average results