SV Total RNA Isolation System by Promega Corp.

Manufacturer Promega Corp.  |   Model: Z3101
5.0
/
5.0
  |  2 reviews
Extracts RNA from Tissues, Cultured Cells and White Blood Cells


SV Total RNA Isolation System by Promega Corp. product image
SV Total RNA Isolation System
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Average Rating: 5.0
2 Scientists have reviewed this product

5 out of 5
Ease of use
5 out of 5
After sales service
5 out of 5
Value for money


Best kit for RNA isolation
Rating: 5.0

  • Application Area: RNA isolation

"For RNA isolation, this will be the best kit as it gives the purified RNA. This kit is free from phenols and other lysis methods, which makes this kit at first stand. As this kit uses column based method, amount of contamination is very less and gives a good yield of RNA."

Review date: 24 Oct 2017 | SV Total RNA Isolation System
  • Status:

    Reviewer

  • Member since: 2016

  • Organization: NATIONAL POLITECHNIQUE INSTITUTE



  • Ease of use
    5 out of 5
    After sales service
    5 out of 5
    Value for money
    5 out of 5
Good results, not to much time needed
Rating: 5.0

  • Application Area:Gene expression of plants

"The SV total RNA Isolation system is an easy and fast way to obtain good quality RNA, the previous preparation of some of the reagents is not complicated. It takes around thirty minutes to complete the protocol, but for someone with plenty experience could achive it in less time. The integrity of the RNA is enough to use in PCR protocols and in the synthesis of cDNA. The protocol include some suggestions that helps to the user."

Review date: 23 Oct 2017 | SV Total RNA Isolation System

Isolate RNA with a Simple, 1-hour Procedure

The SV Total RNA Isolation System provides a fast and simple technique for preparation of intact total RNA from tissues, cultured cells and white blood cells in as little as one hour. Using this membrane-based purification system, up to 60mg of tissue can be processed per purification, depending on tissue type. The system incorporates a DNase treatment step directly on the minicolumn membrane. This step substantially reduces genomic DNA contamination, which can interfere with amplification-based methodologies. Purification is achieved without the use of phenol:chloroform extractions or ethanol precipitations, and there is no DNase carryover in the final RNA preparation.