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  2. N-Ethylbuphedrone - Wikipedia

    en.wikipedia.org/wiki/N-Ethylbuphedrone

    N-Ethylbuphedrone (also known as NEB) is a stimulant of the cathinone class that has been sold as a designer drug. [1] [2] [3] ...

  3. Molecular-weight size marker - Wikipedia

    en.wikipedia.org/wiki/Molecular-weight_size_marker

    Specific restriction endonucleases are used to digest DNA. The RFLP molecular marker is specific to a single fragment. Along with alleic RFLP markers, a molecular-weight size marker, in this case a DNA marker, [30] is also included on an electorphoresed agarose gel. The DNA marker allows for the size of the restriction fragments to be estimated.

  4. Restriction digest - Wikipedia

    en.wikipedia.org/wiki/Restriction_digest

    Restriction digest is most commonly used as part of the process of the molecular cloning of DNA fragment into a vector (such as a cloning vector or an expression vector).The vector typically contains a multiple cloning site where many restriction site may be found, and a foreign piece of DNA may be inserted into the vector by first cutting the restriction sites in the vector as well the DNA ...

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  6. New England Biolabs - Wikipedia

    en.wikipedia.org/wiki/New_England_Biolabs

    New England Biolabs (NEB) is an American life sciences company which produces and supplies recombinant and native enzyme reagents for life science research. [2] It also provides products and services supporting genome editing , synthetic biology and next-generation sequencing . [ 3 ]

  7. TEV protease - Wikipedia

    en.wikipedia.org/wiki/TEV_protease

    TEV protease (EC 3.4.22.44, Tobacco Etch Virus nuclear-inclusion-a endopeptidase) is a highly sequence-specific cysteine protease from Tobacco Etch Virus (TEV). [1] It is a member of the PA clan of chymotrypsin-like proteases. [2]

  8. Restriction site associated DNA markers - Wikipedia

    en.wikipedia.org/wiki/Restriction_site...

    In 2012 a modified RAD tagging method called double digest RADseq (ddRADseq) was suggested. [10] [11] By adding a second restriction enzyme, replacing the random shearing, and a tight DNA size selection step it is possible to perform low-cost population genotyping.

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