Multi Block Thermal Cycler Real Time PCR Machine Equipment ODM AC100V To 240V

Laboratory Equipment ForeAmp-SD696 PCR machines China Multi-Block Thermal Cycler
 

Description:

PCR (Polymerase Chain Reaction) uses DNA to become single-stranded when denatured at a high temperature of 95°C in vitro. At low temperature (often around 60°C), the primers and the single-strand are combined according to the principle of base complementary pairing, and then adjusted. The temperature reaches the optimum reaction temperature of DNA polymerase (about 72°C), and DNA polymerase synthesizes complementary strands along the direction of phosphate to five-carbon sugar (5'-3'). The PCR instrument based on polymerase is actually a temperature control device, which can be well controlled between the denaturation temperature, the renaturation temperature and the extension temperature.

 
Feature
 

♦ Adaptive pressure heating allows it to cool and tighten one step.
♦ The air passages are located at the front and rear and are installed on the Chinese side.
♦ It is the Android operating system and 10. 1 inch capacitive touch screen. It has a graphical navigation interface and is very simple to operate.
♦ Built-in 11 standard program file templates for quick editing
Required documents.
♦ The running program and remaining time can be displayed in real time, allowing editing of files while the program is running.
♦ The one-button rapid incubation function can meet the experimental requirements of denaturation, enzyme digestion/enzyme linkage, ELISA, etc
♦ High temperature and high temperature operating modes can meet the needs of different experiments.

 
Specification

Application

1. Gene amplification for research and clinical use
2. Qualitative PCR Gene Amplification
3. Fluorescence/enzyme-free endpoint quantitative DNA gene amplification
4. Gene amplification for other genetic analysis applications, such as microarrays
5. Applicable to domestic and foreign infectious diseases (various hepatitis viruses, Mycobacterium tuberculosis, sexually transmitted diseases, prenatal and postpartum care, mycoplasma, chlamydia, parasites, etc.), tumors (P53, Helicobacter pylori, etc.), scientific research (gene Identification, bacterial virus typing, etc.) various PCR kits

Elements of PCR

Basic PCR must have

1. The DNA template to be copied Template

2. Primers that define both ends of the replication range.

3. DNA polymerase Taq. Polymerase

4. Synthetic raw materials (four deoxynucleotides) and water

The working principle of PCR machine

The DNA is denatured by heating, the double-stranded DNA is melted by restriction endonuclease, and the single-strand is replicated into double-strand under the action of polymerase, so as to achieve the purpose of gene replication