Name: Urine microRNA Purification Kit
Brand: Norgen Biotek Corp.
SKU: 29000
Price: 279.000000 USD
Availability: InStock

Features and Benefits

Isolate high quality total RNA (including small RNA and microRNA) and all sizes of circulating and exosomal RNA, including microRNA from urine and cerebrospinal fluid (CSF) samples
Small urine and CSF input ranging from as low as 0.5 mL to 1 mL
No phenol extractions
Very sensitive and linear down to a few cells without the need for carrier RNA
Bind and elute all RNA irrespective of size or GC content, without bias
Rapid and convenient spin column protocol
Purification is based on spin column chromatography that uses Norgen’s proprietary resin separation matrix

Norgen’s Urine microRNA Purification Kit provides a rapid method for the isolation and purification of small RNA molecules (All sizes, including < 200 nt) from urine samples. These small RNAs include regulatory RNA molecules such as microRNA (miRNA) as well as tRNA and 5S rRNA. Small RNA molecules are often studied due to their ability to regulate gene expression. Typically miRNAs are 20-25 nucleotides long and regulate gene expression by binding to mRNA molecules and affecting their stability or translation. Several recent studies have shown that miRNA regulates cell growth and apoptosis. Furthermore, clinical and experimental analyses suggested that miRNAs may function as a novel class of oncogenes or tumor suppressor genes. MicroRNA expression profiles of different tumor types, relative to their normal tissues, have recently been shown to provide phenotypic signatures for particular cancer types. Unique patterns of aberrant miRNA expression may serve as molecular biomarkers for tumor diagnosis, prognosis of disease-specific outcomes, and prediction of therapeutic responses.

Details

Supporting Data

Figure 1. Isolation and Detection of microRNA from Urine Samples. Norgen's Urine microRNA Purification Kit was used to isolate microRNA from 8 different 1.5 mL urine samples. The purified microRNA was then used as the template in an RT-qPCR reaction to detect the human miR-21 gene. Five microlitres of the isolated RNA were used as the template in the RT step, and 5 µL from the RT step was used in the qPCR reaction. As it can be seen, the qPCR was able to successfully detect and amplify the miR-21 gene in all cases, indicating the high quality of the isolated urine microRNA. The black line in the graph above corresponds to the No Template Control.

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

RELATED BLOGS

FAQs

Spin Column

If I am not going to process my samples immediately, how should I store my samples?

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.

What if a variable speed centrifuge is not available?

A fixed speed centrifuge can be used, however reduced yields may be observed.

What will happen if my centrifugation speed varied from the recommended speed?

This may decrease the binding of the miRNA to the column.

My centrifuge speeds are defined in rpm and not in g-force. How can I convert g-force to rpm?

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.

At what temperature should I centrifuge my samples?

All centrifugation steps are performed at room temperature. Centrifugation at 4°C will not adversely affect kit performance.

Can I process a different urine volume?

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.

What if I added more or less of the specified reagents’ volume?

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.

What if I forgot to do a dry spin after my third wash?

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.

Why did my samples show very low miRNA yields?

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.

Why does my miRNA not perform well in downstream applications?

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.

What if the solutions did not flow through the column?

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.

Why is the miRNA degraded?

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.

Can I use frozen Urine samples for isolating miRNA?

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:

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.

Citations

Title	A universal lateral flow assay for microRNA visual detection in urine samples
Citation	Talanta 2023.
Authors	Eleni Lamprou, Markos Sotiriou, Panagiota M. Kalligosyfri, Despina P. Kalogianni, Theodore K. Christopoulos

Title	Combination of Urinary MiR-501 and MiR-335 With Current Clinical Diagnostic Parameters as Potential Predictive Factors of Prostate Biopsy Outcome
Citation	Cancer Genomics Proteomics 2023.
Authors	JAROSLAV JURACEK, MARIE MADRZYK, KAROLINA TRACHTOVA, MICHAELA RUCKOVA, JULIA BOHOSOVA, DOMINIK A. BARTH, MARTIN PICHLER, MICHAL STANIK and ONDREJ SLABY

Title	Decrease in the Ratio proBDNF/BDNF in the Urine of Aging Female Patients with OAB
Citation	Metabolites 2023.
Authors	Claudia Covarrubias, Phillipe G Cammisotto, Samer Shamout and Lysanne Campeau

Title	Micro RNA in Semen/Urine from Non-Obstructive Azoospermia Patients as Biomarkers to Predict the Presence of Testicular Spermatozoa and Spermatogonia
Citation	Life 2023.
Authors	Margo Williems, Celine Devriendt, Catharina Olson, Ben Caljon, Toon Janssen, Inge Gies, Veerle Vloeberghs, Herman Tournaye, Dorien Van Saen and Ellen Goossens

Title	Real-Time PCR Quantification of 87 miRNAs from Cerebrospinal Fluid: miRNA Dynamics and Association with Extracellular Vesicles after Severe Traumatic Brain Injury
Citation	International Journal of Molecular Sciences 2023.
Authors	Seršic LV, Alic VK, Biberic M, Zrna S, Jagoic T, Tarcukovic J and Grabušic K,

Title	Biomarker Potential of Urine miR-451 at Different Stages of Diabetic Nephropathy
Citation	Journal of Diabetes & Metabolism 2016.
Authors	Sayilar EI, Gullulu M, Tuncel E, Peynirci H, Alemdar A, et al

Title	Comparison of MicroRNA Content in Plasma and Urine Indicates the Existence of a Transrenal Passage of Selected MicroRNAs
Citation	Circulating Nucleic Acids in Serum and Plasma - CNAPS 2016.
Authors	Pazourkova, E., Pospisilova, S., Svobodova, I., Horinek, A., Brisuda, A., Soukup, V., ... & Babjuk, M

Title	Expression Levels of PIWI-interacting RNA, piR-823, Are Deregulated in Tumor Tissue, Blood Serum and Urine of Patients with Renal Cell Carcinoma
Citation	Anticancer Research 2016.
Authors	ILIEV, R., FEDORKO, M., MACHACKOVA, T., MLCOCHOVA, H., SVOBODA, M., PACIK, D., ... & SLABY, O

Title	Live Cell MicroRNA Imaging Using Exonuclease III-Aided Recycling Amplification Based on Aggregation-Induced Emission Luminogens
Citation	ACS Appl. Mater. Interfaces 2016.
Authors	Min, X., Zhang, M., Huang, F., Lou, X., & Xia, F

Title	MicroRNAs in urine supernatant as potential non-invasive markers for bladder cancer detection
Citation	Neoplasma 2016.
Authors	HANUS, T., MARES, J., KORABECNA, M., & BABJUK, M

Urine microRNA Purification Kit