Cat No. Size List Price* Qty  
BIO-52071 10 Preps $60.00
BIO-52072 50 Preps $233.00
BIO-52073 250 Preps $1,020.00
*For more information on pricing please contact us

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ISOLATE II RNA Mini Kit is specially designed for fast and efficient isolation of extremely pure total RNA from a wide variety of samples. The kit is compatible with mammalian tissues, cultured cells, bacterial cells, yeast, bacteria, biological fluids, paraffin embedded tissue, RNAlater® treated samples, as well as other starting materials.

Features & Benefits

  • Rapid protocol - 30 min/6 preps
  • High purity RNA - typical A260/A280 ratio 1.9 - 2.1
  • High quality - RNA integrity number (RIN) >9
  • Filters (shredders) included - to enhance sample homogenization
  • DNase I included - for complete removal of genomic DNA


Isolation of RNA from:

  • Mammalian tissues
  • Eukaryotic cells
  • Bacterial cells
  • Yeast
  • Biological fluids (cell-free)

Isolated RNA is ready for downstream applications such as reverse transcription and one-step real-time PCR.


ISOLATE II RNA Mini Kit is specially designed for fast and efficient isolation of extremely pure total RNA from a wide variety of samples. The kit is compatible with mammalian tissues, cultured cells, bacterial cells, yeast and biological fluids (cell-free). Biological samples which are sometimes difficult to process will yield high-quality RNA i.e. mouse tissue (liver, brain), various tumour cell lines, Streptococcus and Actinobacillus pleuropneumoniae.

The sample is lysed with an optimized lysis buffer containing chaotropic ions, which simultaneously inactivates RNases, preventing degradation of the released RNA. The lysate is then applied to a spin column to selectively remove genomic DNA. RNase-free DNase I is supplied with the kit.

There is no need to perform a separate DNase digestion step. The RNA is bound to the silica membrane, washed and pure, high quality RNA is eluted fig. 1).

The online product manual has protocols for purifying total RNA from cultured cells, tissues, yeast, bacteria, biological liquids, paraffin embedded tissue and RNAlater® treated samples, as well as DNase I treatment of purified RNA and clean-up of RNA from reaction mixtures.

RNA isolated with the ISOLATE II RNA Mini Kit shows excellent performance in downstream applications, such as reverse transcription, one-step real-time PCR (fig. 2), Northern blot analysis, microarrays and RNA protection assays.



10 Reactions

50 Reactions

250 Reactions





ISOLATE II RNA Mini Columns & Collection Tubes




Collection Tubes (2ml)




Collection Tubes (1.5ml)




Lysis Buffer RLY




Wash Buffer RW1




Wash Buffer RW2



3 x 12ml  

Membrane Desalting Buffer MEM




Reaction Buffer for DNase I RDN




DNase, RNase-free (lyophilized)

1 Vial

1 Vial

5 Vials

RNase-free Water




Product Manual




Bench Protocol Sheet




Storage & Stability

All components should be stored dry and at room temperature.

When stored under the recommended conditions and handled correctly, full activity of reagents is retained until the expiry date indicated on the outer box label.

Shipping conditions

Ambient temperature.

Certificates of Analysis (COAs)

Certificates of Analysis for ISOLATE II RNA Mini Kit are grouped by catalogue number and then listed by batch number. Larger pack sizes are listed first. To locate the COA for your product, first find the catalogue number and then the required batch number.

View all 36 COAs for ISOLATE II RNA Mini Kit →

Frequently asked questions

  • The sequencing protocol I am using says that I have to have my DNA suspended in pure water. Do I have to use the elution buffer supplied with the kit?

      The elution buffer is ideal for applications such as restriction enzyme digestion, sequencing and PCR. It is possible to use DNase free water for elution, but you should expect a slightly lower yield
  • I made my PCR product using RANGER DNA polymerase; it is more than 5kb long. Can I still use the ISOLATE II PCR and Gel Kit to purify the product away from the primers?

      Yes, though this may require some optimisation. Warming the elution buffer to 50 or even 70°C before applying it to the column can help to elute long PCR products, but there is the possibility using this adaptation to the protocol that the primers will be eluted too.
  • I have mutagenized my gene of interest using PCR with relatively long primers (> 30bp). Is the ISOLATE II PCR and Gel Kit suitable for removing excess primers and dNTPs from the reaction?

      The ISOLATE II PCR and Gel Kit can be used under standard conditions to separate most PCR primers away from their product. A primer of only 30bp is efficiently separated, but longer mutagenic primers of around 100bp may be separated from the PCR buffer along with the amplicon.
  • My strain of E. coli contains a low copy plasmid. How can I isolate the plasmid DNA?

      The high quality of the columns used in the ISOLATE II kits, including the miniprep kit, allow larger volumes of culture media to be used as starting material. The exact volume to be used depends on the strain and plasmid used in the experiment, but the miniprep columns will cope with the biomass from 5ml of E. coli grown in LB to an OD600 of around 3. When using larger volumes of culture medium, it is important to ensure that as much spent medium as possible is removed from above the biomass pellet after spinning down the culture. If care is taken, up to 15ml of bacterial culture medium can be used as a starting material, which should give a better yield of low copy plasmid DNA. However, double the volumes of buffers P1, P2 and P3 should be used compared to the standard protocol.
  • My plasmid yield from using the ISOLATE II Plasmid Mini Kit is very low, what could be the cause of this?

      The most frequent cause of low yield is that the biomass pellet is not resuspended properly prior to lysis. Clumps of bacteria mean that the lysis solution cannot access all the cells and these unlysed cells are then spun down later in the process. Low yield can also be caused by incomplete transfer of the cleared lysate to column, especially when the white precipitate made on the addition of buffer P3 is loose, making it hard to retrieve the maximum amount of lysate. Counterintuitively, very high biomass concentrations can lead to low plasmid yield. This can be because the column becomes overloaded, so the yield per mg biomass is less than expected. However use of rich media such as SOC or TY instead of LB can give high biomass but very low plasmid concentration.
  • Another lab has sent me a plasmid, but the purity looks low. Can I use your ISOLATE II Plasmid Mini Kit to clean up the plasmid?

      The ISOLATE II Plasmid Mini Kit can be used to both purify and concentrate naked plasmid DNA. The DNA can be loaded directly onto a fresh column then the remaining washing, drying and elution steps followed as for the standard protocol. The sample can be concentrated by reducing the elution volume in the final stage. However, a better recovery can be obtained by using the ISOLATE II PCR and Gel Kit and treating the plasmid sample as though it were a PCR product.
  • Can I use a gel to quantify RNA isolated using the ISOLATE II RNA kits?

      Agarose gel analysis of RNA samples can be both valuable and misleading. The pattern of bands on the gel can be indicative of the quality of the sample, but equally it can also only indicate that the gel tank, buffer or agarose is contaminated with RNase. A safer measure is to use a spectrophotometer (ideally a microfluidic one) to determine the ratio of A260 to A280 for purity determination. Some microfluidic devices can also give an estimate of the integrity of the RNA. All these methods give an idea of the quality of total RNA which tends to be dominated with rRNA and tRNA. It is not uncommon for an agarose gel to show an abundance of 18S and 23S rRNA but on analysis for there to be little of the transcript of interest. Ideally RNA quality control should include an assessment of the presence of common transcripts (from reference genes, such as GAPDH) using RT-PCR or RT-qPCR.

      If the yield of RNA is low, it is best to first check that all the solutions used and the equipment employed is largely free of RNase. Solutions should be prepared with the highest quality reagents available, preferably ones that have a certificate of analysis to show that they are free of DNase, and RNase. If there is confidence that RNase contamination is at a minimum then it may be worth ensuring that the sample is properly homogenised before lysis, and to check a sample of the lysed material under a light microscope to ensure that all the cells are disrupted.

      RNA samples that have been contaminated with RNase (either during processing or those that have been sent from another lab) can be purified using the ISOLATE II RNA Micro Kit.
  • Can I use columns or solutions from one kit in another one?

      The columns supplied with the ISOLATE II kits are superficially similar, but each type has been optimized to work within the buffer system supplied with the corresponding kit. The swapping of columns (or buffers) between kits may lead to no recovery of nucleic acid whatsoever, or at the very least severely impaired purification.

Customer Testimonials

I recently used the ISOLATE II RNA Mini kit. I had some cultured cells which are derived after FACS, which are not very many, to extract RNA from. Because I had a small starting quantity (<1E6 cells), I wasn’t expecting an extremely high yield. However, I attained a relatively good yield from that small amount of starting sample. What also impressed me was the 260/280 and 260/230 ratios. I have been having trouble getting a good 260/230 ratio lately, probably because of residual guanidine not being washed off properly. With the kit, both ratios were well above 2.0.
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We have been utilizing ISOLATE II RNA Mini Kit from Bioline and have found that the RNA yield, concentrations and purity have been consistently good. From 40,000 liver cancer (mouse and human) cells we are able to get 200-600ng/ul yield of RNA.
"I find that the 260/280 and 260/230 ratios with this kit (ISOLATE II RNA Mini Kit) are excellent and reproducible. I previously used the Qiagen RNeasy kit, but the Bioline kit is both cheaper and gives better quality RNA."

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