Beijing Sizhengbai Biotechnology MRN1210-50 RNA Extraction Kit User Manual

The manual provides storage conditions, component list, and step‑by‑step protocol for extracting total RNA from Gram‑positive and Gram‑negative bacteria…


Beijing Sizhengbai Biotechnology MRN1210-50 RNA Extraction Kit User Manual - cover page
Brand
北京四正柏生物科技有限公司
Category
Other
Document type
User Manual
Language
Chinese
Pages
2
File format
PDF
File size
303 KB
Published
05 October, 2026
Updated
05 October, 2026
MD5 checksum
73528A54C656B865A25424FAE220F24B

About this manual

The MRN1210-50 bacterial RNA extraction kit is designed for rapid isolation of total RNA from a wide range of Gram‑negative and Gram‑positive bacteria. The kit includes Solution A (30 ml), Solution B (20 ml), 50 spin‑adsorption columns, 50 ml universal wash buffer, 10 ml RNA elution buffer, and a user manual.

The protocol outlines preparation of fresh lysis solution (mix A and B 1:1), sample lysis, phase separation with chloroform, binding to the column, washing, and elution of RNA. Critical steps include centrifugation at 12 000‑15 000 g for specified times, careful handling of the aqueous phase to avoid DNA/protein contamination, and optional DNase treatment. Extracted RNA can be stored at –80 °C or used immediately for downstream applications. This manual is written in Chinese.

What's inside

  • Product Description
  • Specifications and Components
  • Storage Conditions and Shelf Life
  • Usage Instructions

Specifications

Solution A volume30 ml
Solution B volume20 ml
Typical OD260/OD280 of extracted RNA≈2.0
RNA purity range (OD260/OD280)1.8‑2.1

Frequently asked questions

How should the lysis solutions be prepared?

Mix Solution A and Solution B in a 1:1 ratio to make fresh lysis solution, and use it immediately.

What centrifugation speed and time are required for the binding step?

Centrifuge at 12 000‑15 000 g at room temperature for 3‑5 minutes to bind the lysate to the column.

How should the extracted RNA be stored?

The RNA eluate can be used immediately or stored at –80 °C for later use.

What is the recommended method to check RNA integrity?

Run the RNA on a formaldehyde‑denaturing agarose gel; non‑denaturing gels cannot separate all RNA molecules.

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