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SV TOTAL RNA

Isolation System

 
Component Listing for Z3100

10 x 5ea/pack
1 x 50ml
1 x 20ml
1 x 2ml
1 x 3,850u
1 x 250µl
1 x 25ml
1 x 5.3ml
1 x 58.8ml
1 x 13ml

Spin Column Assemblies and Elution Tubes
SV RNA Lysis Buffer
SV RNA Dilution Buffer
B-Mercaptoethsnol (48.7%)
Dnase I (Iyophilized)
MnCl2, 0.09M
Yellow Core Buffer
SV Dnase Stop Solution (concentrated)
SV RNA Solution Solution (concentrated)
Nuclease-Free Water

Description: The SV Total RNA Isolation System(a.b) provides a fast and simple technique for the preparation of purified and intact total RNA from tissues, cultured cell and white blood cell in as little as one hour. Using this membrane-based purification system, up to 60mg of tissue. The system incorporates a Dnase treatment step directly on the membrane of the minicolumn. This substantially reduces genomic DNA contamination, wich 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.

Features

• Safe and efficient: Rapid isolation of high yields of total RNA without the use of hazardous compounds like phenol.
• Versatile: Isolation directly from blood, cells or tissue.
• Flexible: Two methods available for purification: microcentrifugation (spin) or vacuum.
• Highly Pure: Purified RNA is suitable for all routine molecular biology applications, including RT-PCR and Northern blotting.

Protocol
Technical Manual #TM048

Storage Conditions: Store at 22-25ºC.

Notes: The Miniprep Vaccum Adapters (Cat.# A1331) are required for the vacuum format of the SV Total RNA Isolation System and must be purchased separately. The Vac-Man® (Cat# A7231) and the Vac-Man® Jr. (Cat.# A7660) Laboratory Vacuum Manifolds can be used with the SV Total RNA Isolation System and are available separately.

a) Cat.# Z3100. Z3101, Z3141 and Z3051 For Laboratory Use.

b) U.S. Pat. No. 6, 218, 531 and other patents pending.

   
   
RNA was isolated from 1ml of human blood using the SV Total RNA Isolation System. RT-PCR was performed using the indicated volumes of eluted RNA and primers complementary to human B-actin or human Adenomatous Polyposis Coli (APC) gene with the Promega Access RT-PCR System (Cat.# A1250).
   
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