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  • 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 7 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)

  • Store in -20 until ready to qPCR

TapeStation

Pool:

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Samples:

Pool, followed by Brock 2, column 2 (sample 5 is the blank)

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Blank:

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qPCR

45 nM

2.2 ul sample plus 97.8 ul RSB to make 1 nM

Sequence Dilution

Dilute to 1 nM:

2.2 ul sample plus 97.8 ul RSB

Add 10% PhiX and dilute to 65 pM:

13 ul sample plus 1.3 ul PhiX plus 185.7 RSB