Bio-rad Aurum™ Total RNA 96 Kit Instrukcja Użytkownika Strona 16

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Note: Gradual application of negative pressure is required to prevent
sample spraying and cross-contamination.
The eluted total RNA samples in the sample collection plate can be
used immediately in downstream applications. Alternatively, the sample
collection plate can be sealed with sealing tape and stored at –20°C or
–80°C for later use.
Section 8
Spin Protocol
PleasereadSection5,“BeforeUsingtheAurum™TotalRNA96Kit”before
proceeding.
Except for the first few steps that are specific for the starting sample types
(A,forculturedcelllines;B,forbacteria;andC,foryeast),theremaining
procedures within “All Starting Cell Types” share a common protocol.
Cultured Cell Lines
Follow steps A1–A3, then continue with step 1 of “All Starting Cell Types” on
page 13.
A1. Fornonadherentcellcultures,rinsethecellswithPBSandtransferup
to 1 x 10
6
cells into each well of a 96-well microplate (not provided).
Centrifuge the plate at 300 x g for 5 min then aspirate the supernatant
from each well.
For adherent cell cultures, rinse the wells (each containing up to
1 x 10
6
cells)ofthegrowthvesseloncewithPBSandaspirate.
A2. Add150µloflysissolution(alreadysupplementedwith
1%b-mercaptoethanol) to each well and pipet up and down several times
to lyse cells thoroughly.
A3. Add150µlof70%ethanol(notsupplied)toeachwellandpipetupand
down to mix thoroughly. Make sure that no bilayer is visible and that the
viscosity is substantially reduced.
Bacteria
FollowstepsB1–B3,thencontinuewithstep1of“AllStartingCellTypes”
on page 13. If starting with a grow block of bacterial culture (maximum 1
OD/ml/well),centrifugethegrowblockat1,500xgfor10min.Decantthe
supernatant, and blot the block with paper towels.
B1. Resuspendupto8x10
8
bacterialcellsperwell(1OD/ml/well),adding
100µlof500µg/mllysozymeinTE(10mMTris,1mMEDTA,pH7.5).
Incubate at room temperature for 5 min.
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