Milk Bacterial DNA Isolation Kit
For research use only and NOT intended for in vitro diagnostics.
Milk Bacterial DNA Isolation Kit
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Supporting Data
Kit Specifications
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Maximum Milk Input | 1 mL |
Time to Complete 10 Purifications | 1 hour |
DNA Yield* | 500 ng to 8 μg |
Bacteria Species Processed | Gram positive and Gram negative |
Minimum Detection Limit | 10 bacteria in 1 mL of milk |
*The range of the DNA yield will vary depending upon a number of factors including bacterial species and type of milk (fat content and %)
Storage Conditions and Product Stability
All solutions should be kept tightly sealed and stored at room temperature. The Lysozyme should be stored at -20°C upon arrival, and the Resuspension Solution A should be stored at -20°C after addition of the lysozyme. The lyophilized Proteinase K should be stored at -20°C upon arrival and after reconstitution. This kit is stable for 1 year from the date of shipment.
Component | Cat. 21550 (50 preps) |
---|---|
Resuspension Solution A | 6 mL |
Buffer SK | 60 mL |
Wash Solution A | 18 mL |
Elution Buffer B | 15 mL |
Proteinase K | 12 mg |
Lysozyme (powder) | 120 mg |
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:
- The sample is too large.
Ensure that no more than 1 mL of subclinical mastitis milk or no more than 200 µL of clinical mastitis milk is used for the procedure in order to prevent clogging of the column. 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.
- The milk sample is very viscous.
If the sample is very viscous and difficult to pipette, pass the sample through an 18-gauge syringe a few times to reduce the viscosity prior to the first 3 minute spin.
- White, creamy layer was not removed after initial spin.
After the first 3 minute spin, ensure that the white, creamy layer floating on top of the milk sample is removed. This layer should be removed in order to prevent clogging of the column.
Experiencing gelatinous lysate prior to loading onto the column may be due to the following factors:
- White, creamy layer was not removed after initial spin.
After the first 3 minute spin, ensure that the white, creamy layer floating on top of the milk sample is removed. This layer should be removed in order to minimize the thickness of the lysate.
- The sample is too large.
Too many cells are in the lysate preparation. Ensure that no more than 1 mL of milk is used for the procedure. If the milk sample is known to have a high bacterial content or categorized as clinical mastitis, it is recommended no more than 200 µL is used for the input.
The yield of genomic DNA may be lower than expected due to the following:
- The milk sample may not contain any bacterial species.
If the milk sample does not contain any bacteria, then no genomic DNA will be detected.
- Incomplete lysis of cells.
Extend the incubation time of Proteinase K digestion or reduce the amount of milk used for the input. Increase the lysozyme incubation time for Gram-positive strains.
- The DNA elution is incomplete.
Ensure that centrifugation at 14,000 x RPM is performed after the 2,000 x RPM centrifugation cycle, to ensure that all the DNA is eluted.
Sheared genomic DNA may occur due to:
- Improper handling of genomic DNA.
Pipetting steps should be handled as gently as possible. Reduce vortexing times during mixing steps (no more than 10-15 seconds).