MinElute procedure.
MinElute procedure.
Higher DNA concentrations.
Higher DNA concentrations.
MinElute membrane assembly.
MinElute membrane assembly.
pH Indicator Dye.
pH Indicator Dye.
Spin column handling options — D.
Spin column handling options — D.
Spin column handling options — E.
Spin column handling options — E.
Spin column handling options — C.
Spin column handling options — C.
Spin column handling options — B.
Spin column handling options — B.
Spin column handling options — A.
Spin column handling options — A.
MinElute procedure. The simple bind-wash-elute procedure ensures greater convenience.
Higher DNA concentrations. A 500 bp and a 1000 bp fragment purified using the MinElute Gel Extraction Kit and three different silica-based DNA purification kits from the indicated suppliers. Two microliters of each eluate was loaded onto a 1.5% agarose gel. M: markers.
MinElute membrane assembly. MinElute spin column in cross section, showing the unique membrane assembly (utility model pending).
pH Indicator Dye. pH indicator dye in the solubilization and binding buffer allows easy visual determination of optimal pH for DNA adsorption (pH ≤7.5). An incorrect binding-mixture pH can occur if the agarose gel electrophoresis buffer was frequently used or incorrectly prepared. In this case, the pH can be easily adjusted by addition of 10 µl 3 M sodium acetate, pH 5.0.
Spin column handling options — D. QIAvac 24 plus.
Spin column handling options — E. QIAcube.
Spin column handling options — C. Manifold with luer connectors.
Spin column handling options — B. QIAvac 24.
Spin column handling options — A. Microcentrifuge.