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Model | SONOL20-1000 | SONOL20-500 | SONOL28-300 | SONOL40-100 |
Frequency | 20±0.5 KHz | 20±0.5 KHz | 28±0.5 KHz | 40±0.5 KHz |
Power | 1000 W | 500 W | 300 W | 100 W |
Voltage | 220/110V | 220/110V | 220/110V | 220/110V |
Temperature | 300 ºC | 300 ºC | 300 ºC | 300 ºC |
Pressure | 35 MPa | 35 MPa | 35 MPa | 35 MPa |
Max Capacity | 8 L/Min | 5 L/Min | 1L/Min | 0.5 L/Min |
Cell Disruptor ( or Ultrasonic Homogenizer) offers precision engineering with all the features necessary for ultrasonic disruption. This product can disintegrate or shear most cells - cell lysing, bacteria, spores, and DNA/Chromatin.
Cell disruption is a technique or process used to release and isolate biological molecules from inside a cell. Ultrasonication is a highly efficient method to perforate and disrupt cell walls and membranes so that the intracellular material and the targeted biomolecules are released into the solvent. As a non-thermal, mild , yet highly efficient technique, ultrasonic disruptors are used in lab and industry to lyse cells and to produce superior extracts. Ultrasonic cell disruptors are used to prepare DNA and RNA as well as to extract bioactive compounds such as vitamins, polyphenols or natural pigments.
Ultrasonic cell breaker is an important equipment used in biological laboratories, and its main function is to quickly and effectively break biological samples. This kind of equipment crushes samples by high-frequency oscillating ultrasonic waves. It has the advantages of simple operation, high crushing efficiency, and little damage to samples. Therefore, it has been widely used in the fields of biology, medicine, and pharmaceuticals. This article will introduce the working principle, application fields and purchase points of the ultrasonic cell disruptor to help readers better understand the scientific value of this instrument.
The working principle of ultrasonic cell disruptor
The Ultrasonic Cell Disruptor utilizes the high-frequency oscillation force of ultrasonic waves to crush biological samples. Ultrasonic transducers convert electrical signals into mechanical vibrations, which are then transmitted into the sample through an ultrasonic probe. Due to the extremely fast vibration speed, which can reach tens of thousands of times per second or even higher, tiny cavitation bubbles can be generated in the sample. Under a certain pressure difference, these cavitation bubbles will collapse rapidly, thereby generating a powerful microjet, causing the membrane on the surface of the sample to be destroyed and the cells to be broken.