ZR RNA MicroPrep™

Quick (15 minute) RNA isolation from a variety of sources using Fast-Spin column technology.
RNAlater™ compatible.
Omits the use of organic denaturants and proteases.

Product Name Size Catalog # Price Qty
ZR RNA MicroPrep™ 50 Preps. R1060
$191.00
ZR RNA MicroPrep™ 200 Preps. R1061
$611.00
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About ZR RNA MicroPrep™

The ZR RNA MicroPrep™ provides a quick method for high quality total RNA isolation from cells, needle biopsies, and tissue. The product isolates both large and small RNA species without the use of reducing agents or phenol. Small RNAs (e.g., tRNAs, microRNAs) can be recovered with a simple adjustment of the RNA isolation protocol. Eluted RNA is suitable for use in RT-PCR and other RNA-based procedures.


Format Spin Column
Processing Time 15 min (does not account for in-column DNase I treatment (~20 min))
Equipment Microcentrifuge
Sample Sources Cells from culture or small amounts of solid tissue.
Storage ≤-70ºC. The addition of RNase inhibitors is optional but highly recommended for prolonged storage.
RNA Purity High quality RNA (A260/A280>1.8, A260/A230>1.8) is recovered.
RNA Recovery RNA can be eluted into small volumes, ≥ 6 µl allowing for a highly concentrated sample. Maximum RNA binding capacity of provided column is ~5 µg.
Sample Size 101 - 105 cells in suspension or solid form.

DNA Elimination Step Included Included None
Minimal Elution Volume 6 µl 25 µl 30 µl
Wash Residue Carryover No No Yes
Cost per Prep. (USD) $3.62 $3.62 $4.54

 



Recovery of small RNA. Total RNA isolated using the ZR RNA MicroPrep™ was resolved in an agarose gel (2-4) and small RNAs from the same sample were also resolved in a native polyacrylamide gel (6-7). Input = 105 yeast cells spiked with 1 µg ZR small-RNA™ Ladder (Zymo Research)

PCR amplification of ß-actin transcript post-RT (353 bp fragment shown): Total RNA from human epithelial cells (HCT 116) was isolated using the ZR RNA MicroPrep™.

Step 1

Cell homogenization/sample preparation2:

a. Cell samples:  Isolate cells by gentle centrifugation and remove the supernatant.  Resuspend the pelleted cells in 400 µl RNA Lysis Buffer.

b. Tissue samples:  Add 400 µl RNA Lysis Buffer directly to the sample and mechanically homogenize up to 10 mg fresh or frozen tissue.

c. Liquid samples/suspensions:  Add 4 volumes RNA Lysis Buffer to the sample and mix well (e.g., 320 µl buffer added to 80 µl sample)Adjust the reagents volume proportionally as needed.

Step 2

Centrifuge the sample mixture at ≥12,000 × g for 1 minute.

Step 3

Transfer the lysate (i.e., the supernatant from Step 2) to a Zymo-Spin™ IIIC Column in a Collection Tube.  Centrifuge at 8,000 × g for 30 seconds.  Save the flow-through!

Step 4

Add 0.8 volume ethanol (95‑100%) to the flow-through in the Collection Tube and mix well (e.g., 320 µl ethanol added to 400 µl flow-through)For quantitative small RNA recovery, use 2 volumes ethanol (95‑100%)3.

Step 5

Transfer the mixture to a Zymo-Spin™ IC Column4 in a Collection Tube.  Centrifuge at ≥12,000 × g for 1 minute5.  Discard the flow-through.

Step 6

Add 400 µl RNA Prep Buffer to the column.  Centrifuge at ≥12,000 × g for 1 minute.  Discard the flow-through and replace the Zymo-Spin™ IC Column back into the Collection Tube.

Step 7

Add 800 µl RNA Wash Buffer to the column.  Centrifuge at ≥12,000 × g for 30 seconds.  Discard the flow-through and place the Zymo-Spin™ IC Column back into the Collection Tube. Repeat the wash step with 400 µl RNA Wash Buffer.

Step 8

Centrifuge Zymo-Spin™ IC Column at ≥12,000 × g for 2 minutes in the emptied Collection Tube to ensure complete removal of the wash buffer.

Step 9

Place the Zymo-Spin™ IC Column into an RNase-free tube.  Add ≥6 µl DNase/RNase-Free Water directly to the column matrix and let stand at room temperature for 1 minute.

Step 10

Centrifuge at 10,000 × g for 30 seconds to elute the RNA from the column.  RNA can be used immediately or stored at ≤-70 oC.

For specific notes and additional information, please see the product protocol PDF.
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Featured Citations

In a study that compared the ability of six commercially available RNA purification kits to extract miRNA from Gyrodactylus salaris, a parasite of freshwater fish such as the Atlantic salmon, the Quick-RNA MicroPrep kit from Zymo Research was shown to result in both the highest yield of miRNA and the best miRNA/total RNA ratio (note: the Quick-RNA MicroPrep kit is an updated version of the ZR RNA MicroPrep kit, which was used in this study).  The kit from Zymo Research outperformed the mirVana Kit (Ambion) and the Trizol Plus Kit (Invitrogen). 


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