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LAWSON20-A ultrasonic DNA disruptor

Product ID:SHGCxbps074

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Supply Ability:50 SETS/MON
Port:SHENZHEN
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  • Product Introduction
  • Consulting
  • Model NumberLAWSON20-A
    Brand NameNINGBOLUOSHANG
    Payment TermsTT,PAYPAL
    LAWSON20-A ultrasonic DNA disruptor

    Introduction:
    The LAWSON20-A ultrasonic DNA disruptor uses an isothermal, non-contact method to break, homogenize, and mix the sample. Used for aseptic, ultra micro fragmentation, and can break chromosomes through centrifuge tubes. Tailored for the pre-treatment of second-generation sequencing DNA samples and chromatin immunoprecipitation experiments. Compared to traditional probe ultrasonic crushers, the probe is in direct contact with the sample and can only process one sample at a time, resulting in a longer experimental cycle. For over a thousand samples, it is necessary to repeatedly use the same probe, which can easily cause cross contamination of the samples. Non contact samples can be crushed in a closed container without producing infectious flying mist. The ultrasound probe does not come into contact with the sample to avoid cross contamination. For laboratories that process multiple or valuable samples every day, non-contact ultrasonic DNA crushers have advantages such as high throughput, low sample loss, and no cross contamination. Gradually becoming an indispensable standardized tool for ChlP (chromatin immunoprecipitation) and DNA splicing research platforms.
    Features:
    1. No aerosol production - enhances biological safety (such as mycobacteria, viruses, etc.)
    2. Eliminated the risk of sample cross contamination
    3. Eliminated the traditional phenomenon of probe wear and slag dropping
    4. Can handle multiple types of samples, with a wide range of sample processing capabilities
    5. Suitable for various standard containers
    6. Can be used to process trace samples, with a minimum of 5ul
    7. The automatic continuous rotation of the centrifuge tube makes the energy distribution of ultrasound more uniform
    8. Optional high and low temperature constant temperature water bath, customized Eppendorf tube crushing and rotating base with various diameters according to customer needs
    Technical parameters:
    Model: LAWSON20-A Single Channel
    Power: 10-1000W continuously adjustable
    Sample processing quantity: 30 * 0.1ml, 20 * 0.65ml, 11 * 2ml, and 5 5-15ml centrifuge tubes
    Ultrasonic sample volume: above 2ml or below 5 µ L
    Single ultrasound time: 0.1-99.9S
    Single interval time: 0.1-99.9S
    Total time (ultrasound+gap): 1-99H59M59S
    Frequency range: 20-40KHz
    Cooling system - temperature control range: portable constant temperature bath host (compressor refrigeration) 2-40
    Temperature reading accuracy: ± 0.1
    Compressor power: 600W
    Ultrasonic water tank volume: 15 * 14 * 10cm
    Adapter material: 316 stainless steel material
    Noise level:<55dB
    Imported original multi frequency ultrasonic transducers: 3 sets
    Power supply (optional 110V): 220V/110V/50Hz/60Hz

  • Introduction:
    The LAWSON20-A ultrasonic DNA disruptor uses an isothermal, non-contact method to break, homogenize, and mix the sample. Used for aseptic, ultra micro fragmentation, and can break chromosomes through centrifuge tubes. Tailored for the pre-treatment of second-generation sequencing DNA samples and chromatin immunoprecipitation experiments. Compared to traditional probe ultrasonic crushers, the probe is in direct contact with the sample and can only process one sample at a time, resulting in a longer experimental cycle. For over a thousand samples, it is necessary to repeatedly use the same probe, which can easily cause cross contamination of the samples. Non contact samples can be crushed in a closed container without producing infectious flying mist. The ultrasound probe does not come into contact with the sample to avoid cross contamination. For laboratories that process multiple or valuable samples every day, non-contact ultrasonic DNA crushers have advantages such as high throughput, low sample loss, and no cross contamination. Gradually becoming an indispensable standardized tool for ChlP (chromatin immunoprecipitation) and DNA splicing research platforms.
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