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DF100 Gel and PCR DNA Fragment Extraction Kit 100 Preps

SKU: DF100
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16,260.00
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Streamline your molecular biology workflow with the DF100 DNA Extraction Kit. Designed for high-yield, high-purity recovery from agarose gels and PCR reactions, this kit ensures your downstream applications like sequencing and cloning proceed without interference. Experience reliable, rapid, and consistent results for 100 essential laboratory preps.

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Disclaimer: The product shown in the image is for reference purposes only. The actual product may vary slightly due to manufacturing batches, packaging, lighting, or screen settings.

Description

Introduction

The DF100 Gel and PCR DNA Fragments Extraction Kit provides a high-efficiency solution for isolating DNA from both agarose gels and reaction mixtures. This optimized system minimizes loss while effectively removing impurities such as salts, enzymes, and primers, ensuring your DNA is ready for sensitive applications.

Key Features

– High recovery efficiency for DNA fragments ranging from 100 bp to 10 kb.

– Rapid spin-column protocol completes in under 20 minutes.

– Excellent purity levels suitable for direct sequencing, ligation, and transformation.

– Compatible with both TAE and TBE agarose gel buffers.

– Comprehensive kit includes all buffers and spin columns for 100 preps.

– No phenol-chloroform extraction required for safer laboratory handling.

Benefits

This kit solves common laboratory bottlenecks by providing a fast and reliable purification method. By ensuring high DNA recovery rates and superior purity, you eliminate the need for repeat experiments caused by contaminated samples. Its user-friendly protocol saves valuable time, allowing researchers to focus on analysis rather than time-consuming extraction procedures. The consistent results provided by the DF100 kit enhance the reproducibility of your data, making it an essential tool for any busy molecular biology lab.

Usage / How to Use

The DF100 kit is ideal for researchers performing gel electrophoresis or PCR amplification. To use, excise the DNA fragment from the agarose gel or take the PCR reaction mixture and add the provided binding buffer. After loading the mixture into the spin column and performing the necessary wash steps to remove contaminants, the purified DNA is eluted in a small volume of elution buffer or water, ready for immediate use in downstream molecular cloning or genetic analysis workflows.

Why Choose This Product

– Proven reliability in academic and industrial molecular research settings.

– Highly optimized buffer chemistry ensures maximum yields even with low starting concentrations.

– Streamlined workflow significantly reduces hands-on preparation time.

– Trusted by researchers for consistent performance across diverse DNA fragment sizes.

– Full technical support and high-quality components ensure successful experiments every time.

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