Promega LS1040 Eastep Super Total RNA Extraction Kit User Manual

The Promega LS1040 Eastep Super Total RNA Extraction Kit manual provides step‑by‑step instructions, reagent preparation, storage guidelines and…


Promega LS1040 Eastep Super Total RNA Extraction Kit User Manual - cover page
Brand
Promega
Category
Other
Document type
User Manual
Language
Chinese
Pages
16
File format
PDF
File size
725 KB
Published
29 September, 2026
Updated
29 September, 2026
MD5 checksum
240227028021E03605C99A1D7F5361E6

About this manual

This technical manual describes the Eastep® Super Total RNA Extraction Kit (LS1040) from Promega. It outlines the kit components, storage conditions, reagent preparation, and detailed protocols for extracting total RNA from animal tissues, cultured cells, plant material and bacteria.

The document also includes guidelines to prevent RNase contamination, recommended sample starting amounts, a complete purification workflow, yield data for different sample types, and a troubleshooting section with solutions to common problems such as low A260/A230 ratios or RNA degradation. This manual is written in Chinese.

What's inside

  • Product description
  • Kit components
  • Storage conditions
  • Reagent preparation
  • RNase contamination prevention
  • Cell disruption methods
  • Sample starting amounts
  • RNA purification workflow
  • Extraction from animal tissue
  • Extraction from cells

Specifications

Number of extractions per kit50
RNA lysis buffer (SR220A)40 ml
RNA dilution buffer (SR221A)30 ml
RNA wash buffer (SR222A)40 ml
10X DNAse I buffer (SR223A)0.3 ml
1‑Thioglycerol (SR224A)1 ml

Frequently asked questions

How many RNA extractions can be performed with one LS1040 kit?

One LS1040 kit provides enough reagents for 50 total RNA extractions from tissues, cells or bacteria.

What are the recommended storage conditions for the kit reagents?

The 10X DNAse I buffer and 1‑thioglycerol should be stored at 4 °C; other components at 15 °C–30 °C; the prepared DNAse I solution at –20 °C; RNA lysis buffer with 1‑thioglycerol at +4 °C for up to 6 months.

What should be done if the RNA yield is low or the A260/A230 ratio is below 1.8?

Add NaCl to a final concentration of 0.1 M, then add 2.5 × volume of anhydrous ethanol, incubate at –20 °C for 30 min, centrifuge at 10 000 g, and resuspend the RNA in RNase‑free water.

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