Fungi/Yeast Genomic DNA Isolation Kits
For research use only and NOT intended for in vitro diagnostics.
Fungi/Yeast Genomic DNA Isolation Kits
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Supporting Data
Kit Specifications
|
|
Column Binding Capacity |
50 ÎŒg
|
Maximum Column Loading Volume |
650 ÎŒL
|
Maximum Amount of Starting Material: Fungi (wet weight) Yeast or Bacteria Culture |
50 mg 0.5mL - 1mL |
Average Yield* Pichia sp. (yeast) Botrytis cinerea âFusarium sp. Aspergillis niger Mucor racemosus Cladosporium cladosporioides Penicillium sp. Rhizopus oryzae Alternaria tenuissima |
25 ÎŒg 32 ÎŒg 42 ÎŒg 26 ÎŒg 15 ÎŒg 12 ÎŒg 40 ÎŒg 7 ÎŒg 30 ÎŒg |
Time to Complete 10 purifications |
30 minutes
|
* Yield will vary depending on the type of sample processed
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. 27300 (50 preps) | Cat. 27350 (192 preps) |
---|---|---|
Lysis Buffer L | 30 mL | 2 x 60 mL |
Resuspension Solution A | 20 mL | 60 mL |
Solution BX | 28 mL | 2 x 28 mL |
Wash Solution A | 18 mL | 2 x 38 mL |
Elution Buffer B | 15 mL | 30 mL |
Bead Tubes | 50 | 200 |
Spin Columns | 50 | - |
Collection Tubes | 50 | - |
96-Well Plate | - | 2 |
96-Well Collection Plate | - | 2 |
Adhesive Tape | - | 4 |
Elution Tubes (1.7 mL) | 50 | - |
96-Well Elution Plate | - | 2 |
Product Insert | 1 | 1 |
Documentation
FAQs
Spin Column, High Throughput
Clogged columns/wells may occur due to the sample being too large:
- Too many cells were applied to the column.
Ensure that the amount of cells used is less than 1 x 108 viable yeast cells or 50 mg (wet weight) of fungal culture. 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.
Turbidity in elution may be due to the sample being too large:
- Depending on fungi species, sometimes turbidity can be observed in the elution. This may inhibit downstream applications. Reduce the amount of cells used, and perform a third wash during the Wash step.
If the DNA does not perform well in downstream applications, it may be due to one or more of the following:
- The sample is too large.
Too many cells were applied to the column. Ensure that the amount of cells used is less than 1 x 108 viable yeast/bacterial cells or 50 mg (wet weight) of fungal culture.
- 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 columns/wells were 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 the 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.