Dried Blood Spot (DBS) DNA Isolation Kit
For research use only and NOT intended for in vitro diagnostics.
Norgen's DBS DNA Isolation Kit is a seamless alternative for Norgen's discontinued Blood DNA kit (52100).
Dried Blood Spot (DBS) DNA Isolation Kit
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Supporting Data
Kit Specifications
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Maximum Blood Input
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3 x 3 mm diameter punches
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Average yield* (ng)
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150 ng
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Column Binding Capacity
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> 50 µg
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Time to Complete 10 Purifications
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35 minutes
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* Yield will vary depending on the type of blood 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. The kit contains a ready-to-use Proteinase K, which is dissolved in a specially prepared storage buffer. The buffered Proteinase K is stable for up to 1 year after the date of shipment when stored at room temperature.
Component | Cat. 36000 (50 preps) |
---|---|
Digestion Buffer B | 6 mL |
Lysis Buffer B | 20 mL |
Wash Solution WN | 18 mL |
Wash Solution A | 18 mL |
Elution Buffer B | 15 mL |
Proteinase K | 1.2 mL |
Micro Spin Columns | 50 |
Collection Tubes | 50 |
Elution Tubes | 50 |
Product Insert | 1 |
Documentation
Isolation of DNA from Hair Follicles and Hair Shafts using Norgen’s Dried Blood Spot Genomic DNA Isolation Kit
Total RNA/DNA Purification and Detection from Blood Preserved on a Neoteryx™ Mitra Microsampling Device
FAQs
Spin Column
- Inefficient cell lysis.
Check Proteinase K activity. Also ensure that the correct volume of Lysis Buffer B was added to the blood sample.
- Cell debris may be clogging the column.
When a high cell number is expected in the blood sample, ensure that the optional spin for 2 minutes at 5,000 rpm after the Proteinase K incubation is performed. Take the clean supernatant only for the next binding step.
- The sample is too large.
Too many cells were applied to the column. Ensure that Proteinase K and Lysis Buffer B are proportionally added as the blood volume is increased. Clogging can be alleviated by centrifuging for a longer period of time until the lysate passes through the column.
- DNA was not washed three times with the provided solutions.
Ensure the column was washed one time with Solution WN and two times with Wash Solution A.
- 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.
- High DNA input used in PCR reaction.
For best results, make sure that the final concentration of DNA in the PCR reaction does not exceed 75 ng/μL (1.5 μg DNA per 20 μL PCR reaction)