Description :

Introduction

This fast and reliable kit is designed to recover DNA from agarose gels, and purify DNA fragments from PCR, RFLP, phosphorylation, labeling, ligation, hybridization and other enzymatic reactions. DNA fragments from 100 bp to 20 kb can be purified using the ezBind^TM mini column with over 80-90 % recovery.

Storage and Stability

All components can be stored at room temperature. All kit components are guaranteed for 12 months from the date of purchasing.

Kit Contents

Safety Information

Buffer GC contains acidic acid and chaotropic salts, which may form reactive compounds when combines with bleach. Do not add bleach or acidic solutions directly to the preparation waste.

Before Starting

Prepare all components and get all necessary materials ready by examining this instruction booklet and become familiar with each steps.

Important

•  Add 8 mL (DC3511/DC3514-00) or 60 mL(DC3511/DC3514-01) or 96 mL (DC3511/DC3514-02) or 60 mL (DC3511/DC3514-03) 100% ethanol to DNA Wash Buffer before use.
•  A gel slice of 100 mg equals to a volume of 100 µL.
•  Buffer GC may form precipitates under cool ambient condition. Warm up the buffer at 37°C to dissolve before use.
•  Pre-warm aliquots of Elution Bufer or ddH₂O at 55-60°C waterbath.

 Materials supplied by users

•  Tabletop microcentrifuge and 1.5 mL microtubes.
•  55-60°C waterbath.
•  Vacuum manifold if use vacuum protocol.
•  96~100 % ethanol.
•  Isopropanol for DNA fragment less than 200 bp.

Perform all steps including centrifugation at room temperature!

Trouble Shooting Guide

* FOR RESEARCH USE ONLY.

Operating protocal