R1011-1-50, RAD Buffer (RNA Agarose Dissolving Buffer) (50 ml)
R1011, Zymoclean™ Gel RNA Recovery Kit (50 Preps) w/ Zymo-Spin™ IC Columns (Capped)
1.047,20 RON
The Zymoclean Gel RNA Recovery Kit provides a quick and efficient purification method for recovery of RNA fragments from agarose gels. The procedure combines a unique, single-step agarose dissolving/RNA binding buffer with Zymo-Spin column technology to yield high quality, purified RNA in just minutes. The purified RNA is eluted into small volumes of DNase/RNase-free water for highly concentrated samples suitable for subsequent RNA-based manipulations. Compatible with MOPS, TAE, and TBE buffered agarose gels (formaldehyde up to 2.0%).
Quick and Reliable: 30 minute recovery of purified RNA fragments from agarose gels.
Concentrated: Up to 10 µg sample in ≥ 6 µl elution.
High Recovery: ≥ 80% recovery for RNA > 500 nt.
DESCRIPTION
The Zymoclean Gel RNA Recovery Kit provides a quick and efficient purification method for recovery of RNA fragments from agarose gels. The procedure combines a unique, single-step agarose dissolving/RNA binding buffer with Zymo-Spin column technology to yield high quality, purified RNA in just minutes. The purified RNA is eluted into small volumes of DNase/RNase-free water for highly concentrated samples suitable for subsequent RNA-based manipulations. Compatible with MOPS, TAE, and TBE buffered agarose gels (formaldehyde up to 2.0%).
TECHNICAL SPECIFICATIONS
Equipment
Microcentrifuge, 37°C-65°C heat source
Purity
RNA is ready for all subsequent analysis and molecular manipulation
Sample Source
Single- or double-stranded RNA fragments (≥200 nt) resolved in TAE TBE, and MOPS buffered agarose gels. Compatible with formaldehyde to 2.0% (final conc.)
Quick and Reliable: 30 minute recovery of purified RNA fragments from agarose gels.
Concentrated: Up to 10 µg sample in ≥ 6 µl elution.
High Recovery: ≥ 80% recovery for RNA > 500 nt.
DESCRIPTION
The Zymoclean Gel RNA Recovery Kit provides a quick and efficient purification method for recovery of RNA fragments from agarose gels. The procedure combines a unique, single-step agarose dissolving/RNA binding buffer with Zymo-Spin column technology to yield high quality, purified RNA in just minutes. The purified RNA is eluted into small volumes of DNase/RNase-free water for highly concentrated samples suitable for subsequent RNA-based manipulations. Compatible with MOPS, TAE, and TBE buffered agarose gels (formaldehyde up to 2.0%).
TECHNICAL SPECIFICATIONS
Equipment
Microcentrifuge, 37°C-65°C heat source
Purity
RNA is ready for all subsequent analysis and molecular manipulation
Sample Source
Single- or double-stranded RNA fragments (≥200 nt) resolved in TAE TBE, and MOPS buffered agarose gels. Compatible with formaldehyde to 2.0% (final conc.)