Olive Oil DNA Isolation Kit
For research use only and NOT intended for in vitro diagnostics.
Olive Oil DNA Isolation Kit
Register today to receive an exclusive 15% off* on your first order.
Supporting Data
Kit Specifications
|
|
Maximum Column Binding Capacity
|
10 µg
|
Maximum Column Loading Volumes
|
650 µL
|
Time to Complete 10 Purifications |
25 minutes
|
Storage Conditions and Product Stability
All solutions should be kept tightly sealed and stored at room temperature. This kit is stable for 1 year after the date of shipment.
Component | Cat. 61700 (50 preps) |
---|---|
Lysis Buffer L | 60 mL |
Binding Buffer B | 40 mL |
Wash Solution A | 38 mL |
Elution Buffer B | 8 mL |
Homogenization Tubes | 50 |
Spin Columns | 50 |
Collection Tubes | 50 |
Elution Tubes (1.7 mL) | 50 |
Product Insert | 1 |
Documentation
FAQs
Spin Column
Clogged columns may occur due to improper oil removal. Too much oil was carried over to the lysate. Repeat Step 1d and 1e to minimize the oil carry over. Clogging can be alleviated by increasing the g-force and/or centrifuging for a longer period of time until the lysate passes through the column.
If the DNA does not perform well in downstream applications, it may be due to one or more of the following:
- Low DNA yield.
Depending on the oil extraction process, DNA can be damaged or lost. Increase the input volume up to 1 mL, as well as the other buffers and solutions proportionally.
- Ethanol carryover.
Ensure that the dry spin under the Column Wash procedure is performed in order to remove traces of ethanol prior to elution. Ethanol is known to interfere with many downstream applications.
- The column was not washed twice with the provided Wash Solution A.
Traces of salt from the binding step may remain in the sample if the column is not washed twice with Wash Solution A. Salt may interfere with downstream applications, and thus must be washed from the column.
- PCR reaction conditions need to be optimized.
Take steps to optimize the PCR conditions being used, including varying the amount of template (20 ng to 50 ng for 20 µL of PCR reaction), changing the source of Taq polymerase, adding BSA (final concentration is 0.1 µg/µL), looking into the primer design, and adjusting the annealing conditions.
The yield varies a lot with the variety and processing status of the olive oil.