Foregene PCR Machines Multi Block Thermal Cycler 96 Well

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
 

♦ Self-adaptingpressurehotlidmakesclosinglidand tighteninglidinonestep.

♦ Airchannelisinfrontandbackanditallowsmachineplaced sidebyside .

♦IthasAndroidoperationsystemand10 . 1inchcapacitive touchscreen.Ithasgraphicalmenunavigationinterfaceand operationisverysimple .

♦Built- in11standardprogramfiletemplate,canquicklyedit

therequiredfiles .

♦The running program and left time can be displayed in real time , allow to edit file when program is running .

♦ One-click quick incubation function can meet experiment’s needs such as denaturation , enzyme cutting/enzyme- link and ELISA

♦ Hotlidtemperatureandhotlidworkmodecanbesetto meetdifferentexperiment’sneed .

 
Specification

Application

1.Gene amplification for research and clinical use

2.Qualitative PCR gene amplification

3.Fluorescent/Enzyme-Free Endpoint Quantitative DNA Gene Amplification

4.Gene amplification for other gene analysis applications such as microarrays

5.Suitable for various PCR kits at home and abroad for infectious diseases (various hepatitis viruses, Mycobacterium tuberculosis, STD sexually transmitted diseases, prenatal and postnatal care, mycoplasma, chlamydia, parasites, etc.), tumors (P53, Helicobacter pylori, etc.), scientific research (Genetic identification, bacterial virus typing, etc.)

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