lysis in A Sentence

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    Lysis & cell disruption,

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    2

    Cell Lysis(e.g. disruption and extraction of cells).

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    3

    Botanicals Extraction(e.g. by ultrasonic cell Lysis).

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    Ultrasonic homogenizers are a common tool for successful cell Lysis.

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    Ultrasonic tissue homogenizers and cell lysers are very efficient tools for cell disruption, Lysis and extraction.

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    6

    After chemotherapy, there is often a rapid amount of cellular destruction, and tumor Lysis syndrome may occur.

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    7

    Commonly used detergents in Lysis buffers are mostly nonionic or zwitterionic, e.g. CHAPS, deoxycholate, Triton™ X-100, NP40, and Tween 20.

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    8

    The goal of Lysis is to disrupt parts of the cell wall or the complete cell to release biological molecules.

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    9

    When bone tissue is damaged by pathogenic microorganisms, leukocytes migrate to inflamed areas, which secrete Lysis enzymes that decompose bone.

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    10

    The disintegration of cell structures(Lysis) by means of ultrasound is used for the extraction of intra-cellular compounds or for the microbial inactivation.

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    Besides its outstanding extraction yield and efficiency, sonication is well-established and reliable for cell Lysis and the extraction of intracellular matter.

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    12

    Ultrasonic homogenization, Lysis and extraction is performed with an ultrasonic homogenizer such as the UP200Ht or UP200St, equipped with an micro-tip sonotrode.

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    13

    Ultrasonic Lysis and extraction is a reliable and long-time established method for the disruption of cells and the subsequent release of viruses, viral proteins, DNA, and RNA.

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    14

    Ideally, samples should be kept ice-cold during Lysis, but for most samples it sufficient if the temperature does not rise above the temperature of culture or tissue source.

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    15

    Lysis buffer must be chosen in accordance to the cell material or tissue(tissue culture, plant, bacteria, fungi, etc.), and whether the cells are in a structure and the type of structure.

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    16

    While heparin does not break down clots that have already formed(unlike tissue plasminogen activator), it allows the body's natural clot Lysis mechanisms to work normally to break down clots that have formed.

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    17

    Immediately before ultrasonic extraction, ice cold Lysis buffer(with protease inhibitors DTT, leupeptin and aprotinin) is rapidly added into the sample tube(per ~10 mg of tissue approx. ~600 μL of buffer are recommended). Approx.

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