Plasma/Serum cfc-DNA/cfc-RNA Advanced Fractionation Kit
For research use only and NOT intended for in vitro diagnostics.
Plasma/Serum cfc-DNA/cfc-RNA Advanced Fractionation Kit
SKU
68300
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Supporting Data
Kit Specifications
|
|
Minimum Plasma/Serum Input
|
1 mL |
Maximum Plasma/Serum Input
|
6 mL
|
Size of cfc-RNA Purified
|
All sizes, including miRNA and small RNA (< 200 nt)
|
Optimal size of purified cfc-DNA
|
146 - 180 bp
|
Elution Volume |
25-50 µL
|
Time to Complete 10 Purifications |
45 minutes
|
Average Yields* | Variable depending on specimen |
*Please check page 5 in the product manual for the Plasma/Serum Average Yields and the Common RNA Quantification Methods.
Storage Conditions and Product Stability
All solutions should be kept tightly sealed and stored at room temperature. This kit is stable for 2 years 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 2 years after the date of shipment when stored at room temperature.
Component | Cat. 68300 (50 preps) |
---|---|
Binding Buffer A | 20 mL |
Proteinase K | 6.5 mL |
Slurry E | 12.5 mL |
Lysis Buffer A | 130 mL |
Wash Solution A | 2 x 38 mL |
Elution Buffer C | 2 x 8 mL |
Elution Buffer F | 1 x 6 mL 1 x 15 mL |
Elution Solution A | 6 mL |
Micro Spin Columns | 100 |
Mini Filter Spin Columns | 50 |
Collection Tubes | 150 |
Elution Tubes (1.7 mL) | 150 |
Product Insert | 1 |
Documentation
FAQs
Spin Column
A fixed speed centrifuge can be used, however reduced yields may be observed.
All centrifugation steps are performed at room temperature. Centrifugation at 4°C will not
adversely affect kit performance.
Adding more or less than the specified volumes may reduce both the quality and the quantity of the
purified RNA. Eluting your Nucleic Acid in high volumes will increase the yield but will lower the
concentration. Eluting in small volumes will increase the concentration but will lower the overall yield.
Your purified Nucleic Acid will be contaminated with the Wash Solution A. This may reduce the quality of your purified Nucleic Acid and will interfere with your downstream applications.
Yes, but it is recommended that the 2nd elution be in a smaller volume (50% of 1st Elution). It is also recommended to perform the 2nd elution into a separate elution tube to avoid diluting the 1st elution.
Varying the incubation time will result in a reduction in your Nucleic Acid yields.
Plasma/Serum samples contain very little cfc-Nucleic Acid. This varies from individual to individual. In order to increase the yield, the amount of Plasma/Serum input could be increased.
If a different Elution solution was used other than the one provided in the kit, the buffer should be checked for any components that may interfere with the application. Common components that are known to interfere are high salts (including EDTA), detergents and other denaturants. Check the compatibility of your Elution Buffer with the intended use.