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ROTI®Prep RNA MINI, 50 preparations

for molecular biology
Examples of effect: Damage metals and burn body tissues; may cause serious eye damage. Safety: Avoid contact; wear safety spectacles and gloves. In the event of contact with eyes and skin, rinse with water.
Examples of effect: Lead to damage to heath, cause irritation to eyes, skin or respiratory organs. Are fatal in larger quantities. Safety: As previously stated, in the event of skin irritation or contact with eyes, rinse with water or a suitable medium.
i harmful if swallowed, in contact with skin or if inhaled, causes severe skin burns and eye damage, harmful to aquatic life with long lasting effects
P280 P303+P361+P353 P305+P351+P338 P312
i wear protective gloves/protective clothing/eye protection/face protection, IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water [or shower], IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing, call a POISON CENTRE/doctor if you feel unwell
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Pack Qty.
Density (D) 1,13 g/cm³
Storage temp. +15 to +25 °C
Transport temp. ambient temp.
UN-Nr. 3316

Kit for RNA isolation from eukaryotic cells, tissues, bacteria, biopsies.
Preparation of up to 100 μg whole RNA from up to 20 mg tissue or cells per column.

Roti®Prep RNA MINI has been developed for the isolation of total RNA from various sources.
The isolation is carried out through the proven and reliable spin column technique, which is very easy to handle and needs only few steps.
Product details

€269.30/Pack Qty. 

excl. VAT. | 1 kit per Pack Qty.

Art. No. 8485.2

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from 24 Pack Qty. €242.37/Pack Qty.
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Product details

ROTI®Prep RNA MINI for molecular biology

Roti®Prep RNA MINI has been developed for the isolation of total RNA from various sources.
The isolation is carried out through the proven and reliable spin column technique, which is very easy to handle and needs only few steps.

  • Preparation by well-known mini spin-column system
  • Fast, easy and efficient
  • Use of DNase not necessary
  • Preparation in approx. 15 to 40 minutes
  • Yields up to 100 μg RNA, depending on source material
  • Elution in 30-80 μl

One of the critical points in RNA extraction is the presence of endogenous RNases, which can lead to high losses very early in extraction of the (in comparison to DNA) very sensitive RNA. Therefores the lysis buffer has been specially optimised to inactivate RNases, with highest efficiency, already at the early stage of the extraction.
Furthermore, in order to get a high-pure total RNA, one particularly for this purpose developed prefilter is used. This filter exclusively serves for binding and targeted removal of DNA impurities, and is discarded after use with the bound DNA. Thus, it is possible to omit application of DNase I.
Total RNA is then obtained from the DNA-free eluate through a simple “Binding-Washing-Elution” process.
In each preparation, up to 100 μg highly pure total RNA may be isolated. One preparation takes (excluding lysis) approx. 10 mins.
Isolated RNA is free of DNA and enzyme inhibitors, and may directly be applied to RT-PCR or other downstream applications.

Possible basic material:
  • Tissues (up to 20 mg)
  • Eukaryotic cells (up to 5x106)
  • Bacteria Gram + and Gram - (up to 1x109)
  • Biopsies

The kit contains

Lysis Buffer LSR, Washing Buffer WSA, Washing Solution WSL, RNase-free Water, spin filters (blue), spin columns (violet), collection tubes, elution tubes, detailed instructions-for-use.
Contents of this Kit may not be bought separately.

Please order ethanol 99,8 % (p.a., Art. No. 9065) and 70 % (p.a., Art. No. T868) separately.

Not a medical device / Not an IVD product
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Art. No. Pack Qty. Pack. Packaging Price Quantity
8485.1 1 kit cardboard 10 preparations


8485.2 1 kit cardboard 50 preparations


8485.3 1 kit cardboard 250 preparations


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