Urine microRNA Purification Kit
For research use only and NOT intended for in vitro diagnostics.
Urine microRNA Purification Kit
SKU
29000
Register today to receive an exclusive 15% off* on your first order.
Supporting Data
Kit Specifications
|
|
Volume of Urine Processed
|
0.5 - 1 mL
|
Size of RNA Purified | All sizes, including < 200 nt |
Time to Complete 10 Purifications |
< 30 minutes
|
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.
Component | Cat. 29000 (25 preps) |
---|---|
Lysis Buffer A | 2 x 20 mL |
Wash Solution A | 18 mL |
Elution Solution A | 6 mL |
Mini Spin Columns | 25 |
Collection Tubes | 25 |
Elution Tubes (1.7 mL) | 25 |
Product Insert | 1 |
Documentation
FAQs
Spin Column
We recommend the use of Norgen’s Urine Preservative, which is designed for the preservation of
nucleic acids and proteins in fresh urine samples at ambient temperatures. The components of
the Urine Preservative allow samples to be stored for over 2 years at room temperature with no
detected degradation of urine DNA, RNA or proteins. Norgen’s Urine Preservative is available in
2 convenient formats: in a liquid format in Norgen’s Urine Preservative Single Dose Ampules, as
well as in a dried format in Norgen’s Urine Collection and Preservation Tubes.
A fixed speed centrifuge can be used, however reduced yields may be observed.
This may decrease the binding of the miRNA to the column.
The correct rpm can be calculated using the formula:
RPM= √RCF/(1.118x10-5)(r)
Where RCF = required gravitational acceleration (relative centrifugal force in units of g); r = radius of the rotor in cm; and RPM = the number of revolutions per minute required to achieve the necessary g-force.
RPM= √RCF/(1.118x10-5)(r)
Where RCF = required gravitational acceleration (relative centrifugal force in units of g); r = radius of the rotor in cm; and RPM = the number of revolutions per minute required to achieve the necessary g-force.
All centrifugation steps are performed at room temperature. Centrifugation at 4°C will not adversely affect kit performance.
Yes, you can. All the buffers included in this kit are in a linear relationship to the volume of urine
sample processed. Make sure that you do not deviate from the ratio specified in the product
manual. The minimum recommended urine input is 0.5 mL, and the maximum recommended
input is 1 mL. Please note that the buffers are optimized for an input of 1 mL of urine.
Adding less volume may reduce your miRNA yields. Adding more may not affect the miRNA yields EXCEPT if more Elution solution was added. Eluting miRNA in a higher volume of Elution Solution A will result in diluting your miRNA.
Your miRNA elution will be contaminated with traces of the Wash Solution A. This may dilute the
miRNA yield in the elution. Also, it may interfere with your downstream applications. Re-isolate
the eluted miRNA using the same procedure as you initially isolated the miRNA from urine but
using your elution as your input.
Some urine samples contain very little miRNA. This varies from individual to individual based on numerous factors. In order to increase the yield, the amount of urine 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.
The centrifugation speed may be too low. Check the centrifuge to ensure that it is capable of generating a sufficient centrifugal force that is required to move the liquid phase through the resin. You may also spin an additional two minutes to ensure that the liquid is able to flow completely through the column.
miRNA can be degraded due to following factors:
- RNase contamination
RNases may be introduced during the use of the kit. Ensure proper procedures are followed when working with RNA. Please refer to “Working with RNA” at the beginning of this user guide.
- Procedure not performed quickly enough
In order to maintain the integrity of the RNA, it is important that the procedure be performed quickly.
- The cells are old
Older samples contain prematurely lysed cells which release RNase and can degrade RNA. Fresh urine samples are recommended.
It is recommended that the Urine samples should be centrifuged to prepare cell-free samples before freezing them.
We recommend the following steps to prepare frozen urine for isolation:
We recommend the use of Norgen’s Urine Preservative when collecting urine samples. Norgen’s Urine Preservative is designed for the preservation of nucleic acids and proteins in fresh urine samples at ambient temperatures, therefore no protein precipitation will occur and the purified nucleic acids will be of a higher quality.
We recommend the following steps to prepare frozen urine for isolation:
- Gently warm the sample to room temperature or 37°C for 5 min.
- DO NOT perform a centrifugation step after thawing frozen cell-free Urine samples - this will eliminate the precipitated proteins leading to loss of protein-bound cf-NA or exosomes.
- Proceed with the protocol.
We recommend the use of Norgen’s Urine Preservative when collecting urine samples. Norgen’s Urine Preservative is designed for the preservation of nucleic acids and proteins in fresh urine samples at ambient temperatures, therefore no protein precipitation will occur and the purified nucleic acids will be of a higher quality.