What is Salt Precipitation DNA Extraction Kit?
The Salt Precipitation DNA Extraction Kit uses a high-efficiency lysis buffer to release DNA and precipitate it in a high-salt environment. Alcohol is then added for dehydration, and the precipitate is collected by centrifugation. Residual matter is removed and the DNA is re-dissolved.
This kit offers high DNA recovery efficiency and a low per-use cost. The procedure is simple and straightforward, without complex binding and washing steps, making it easy for even novice users to quickly learn. It does not use toxic organic solvents such as phenol and chloroform, eliminating the risk of silica residue and simplifying waste disposal.

Technical Specifications
Model | Method | Sample | Format | Workflow |
---|---|---|---|---|
SP-UNI-20R | Salt Precipitation | Universal | 20R | Manual |
SP-UNI-50R | Salt Precipitation | Universal | 50R | Manual |
SP-UNI-100R | Salt Precipitation | Universal | 100R | Manual |
SP-UNI-200R | Salt Precipitation | Universal | 200R | Manual |
SP-UNI-8R | Salt Precipitation | Universal | 8R | Compatible with semi-automated or fully automated extraction systems |
SP-UNI-24R | Salt Precipitation | Universal | 24R | Compatible with semi-automated or fully automated extraction systems |
SP-UNI-48R | Salt Precipitation | Universal | 48R | Compatible with semi-automated or fully automated extraction systems |
SP-UNI-72R | Salt Precipitation | Universal | 72R | Compatible with semi-automated or fully automated extraction systems |
SP-UNI-96R | Salt Precipitation | Universal | 96R | Compatible with semi-automated or fully automated extraction systems |
Working Principle
The principle behind the Salt Precipitation DNA Extraction Kit is based on the biochemical properties of DNA and its interaction with salts and alcohols. The process begins with cell lysis, where a buffer solution breaks down cell membranes and releases DNA into the solution. Next, a high-salt concentration is added, which causes the DNA to precipitate out of solution by neutralizing the negative charges on the DNA molecules and reducing their solubility. This is followed by the addition of cold ethanol or isopropanol, which further dehydrates the DNA and forms a visible pellet upon centrifugation.
After precipitation, the DNA pellet is washed with ethanol to remove impurities such as proteins, salts, and other cellular debris. Finally, the pellet is resuspended in a buffer or water, resulting in purified DNA ready for use. This method leverages basic chemistry principles, making it easy to understand and perform without complex equipment. It is a classic technique that has been widely adopted due to its effectiveness and low cost, providing a foundational understanding of DNA handling in molecular biology.
Performance
The performance of a Salt Precipitation DNA Extraction Kit is characterized by its ability to yield high-quality DNA with good purity and integrity, though it may not match the efficiency of more advanced methods like spin-column or magnetic bead-based kits. In terms of yield, this kit can effectively extract DNA from moderate sample sizes, producing sufficient quantities for many standard laboratory procedures. The purity of the extracted DNA is generally adequate for applications such as PCR amplification, where contaminants like proteins or salts are minimized through the precipitation steps.
However, the performance may vary depending on the sample type and user technique, as the method involves manual steps that can introduce variability. For instance, over-drying the DNA pellet or incomplete washing might affect the final quality. Despite these potential limitations, the kit excels in educational and low-budget scenarios, offering a reliable and reproducible way to demonstrate DNA extraction principles. It is not typically recommended for high-throughput or clinical applications where maximum purity and yield are critical, but it serves as an excellent starting point for learning and basic research.
Application
Salt Precipitation DNA Extraction Kits find widespread application in educational institutions, research labs, and field studies where simplicity and cost-effectiveness are prioritized. They are commonly used in high school and university biology classes to teach students the basics of DNA isolation, allowing learners to visualize and handle DNA for the first time. In research settings, these kits are employed for preliminary studies or sample screening, especially when working with non-critical samples or in projects with limited funding.
Beyond education, these kits are applicable in basic genetic testing, such as identifying plant species or analyzing animal DNA from hair or saliva samples. They are also useful in environmental monitoring, for example, extracting DNA from soil or water samples to study microbial communities. While not suitable for advanced diagnostics or forensic analysis due to potential impurity issues, the kit's versatility makes it a valuable tool for introductory molecular work and DIY biology projects.
Core Features and Advantages
The core features of a Salt Precipitation DNA Extraction Kit include its simplicity, affordability, and accessibility. It requires minimal equipment—typically just a centrifuge and basic labware—making it ideal for settings with limited resources. The kit components are stable at room temperature and have a long shelf life, reducing storage costs and logistical challenges. Additionally, the method is highly scalable; users can adjust protocols for small or large sample volumes based on their needs.
One of the key advantages is its educational value, as it allows users to observe the entire DNA extraction process visually, from cell breakdown to the formation of a DNA pellet. This hands-on experience reinforces concepts in genetics and biochemistry. Moreover, the kit is environmentally friendly compared to some alternatives, as it often uses less plastic waste and non-toxic chemicals. While it may not offer the highest purity for advanced applications, its cost-effectiveness and ease of use make it a popular choice for teaching, basic research, and field applications where portability and simplicity are essential.