Easy access to products and protocols for research use only in the identification of 2019-nCoV based on Centers for Disease Control and Prevention (CDC) recommendations
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Avantor supports end-to-end fluid management solutions – including peristaltic pumps and aseptic fluid transfer solutions – that are reliable and customer-centric, helping bioprocessing manufacturers meet their research and production goals.
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New Avantor® J.T.Baker® premium conductive and non-conductive robotic tips deliver superior quality and reliable performance for results you can trust.
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Enzymes accelerate, or catalyze, chemical reactions, and they are known to catalyze more than 5,000 biochemical reaction types. Most enzymes are proteins, although a few are catalytic RNA molecules. Choose specific enzymes for cleaving bonds, removing genomic DNA from RNA preparations, for producing fragments of proteins, or for use in ion exchange chromatography. Enzymes are used in the chemical industry and other industrial applications when extremely specific catalysts are required.
Description:
Modifying enzyme. Sequencing, cDNA synthesis, cDNA cloning. Concentration: 0.5-2 units/uL. Size: 50 units. Packaged in a tamper-evident, clear plastic sealed packet that contains the enzyme tube, its buffer(s) and a lot-specific Promega* Product Information insert. 24-month lifetime.
Description:
Thermolabile USER* II Enzyme, Concentration: 1, 000 units/ml, generates a single nucleotide gap at the location of a uracil residue.It can be 100% inactivated at temperatures >65 deg C, Directional RNA Seq, NEBNext adaptor cleavage, USER cloning, Size: 250 unit
Description:
And Overexpressed In E. Coli. Endo H Cleaves The Chitobiose Core Of High Mannose And A Limited Number Of Hybrid Oligosaccharides From N-Linked Glycoproteins.
Description:
Immobilized Papain, Generate Fc and Fab from IgG, Eliminates contamination with papain enzyme, Can be used in virtually all scenarios using free papain, Size: 25ml resin
Description:
Thermostable FEN1 - 1,600 units Catalyzes the cleavage of 5´ DNA flaps from branched double stranded DNA substrates, creating a 5´ phosphate terminus. FEN1 products can be ligated by DNA ligase to create double stranded DNA.
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