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Also known as "double immobilization" [ 13], these systems are wonderfully designed to work under harsh nonaqueous conditions as they contain an aqueous core (for solubilizing enzymes and water soluble substrates), a surfactant interface (for surface active enzymes), and a nonaqueous continuous phase (for hydrophobic substrates).
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After ultrasonic DNA shearing, size-selection is carried out via double solid phase reversible immobilization (dSPRI) using carboxyl coated magnetic beads (Figure 1).
The DNA was fragmented by nebulisation, followed by a double Solid Phase Reversible Immobilization (SPRI) bead capture size selection with Ampure beads (Agencourt Bioscience) to generate DNA fragments of 400 1,500 bp in length.
Time courses of immobilization of double-tagged GlcNAc 2-epimerase on Q Sepharose were similar to those for immobilization of double-tagged Neu5Ac aldolase on SP Sepharose.
Immobilization of double-stranded DNA onto nonwoven cellulose fabric by UV irradiation and utilization of DNA-immobilized cloth were examined.
A new electrochemiluminescent (ECL) disposable biosensor for uric acid was manufactured by immobilization in a double-layer design of luminol as a copolymer with 3,3′,5,5′-tetramethylbenzidine 3,3′,5,5′-tetramethylbenzidinen chiTMBandon gold screen-printhe cenzyme
DNA pull-down assays were carried out in three steps, i) immobilization of biotinylated double-stranded DNA molecules using a Streptavidin Mutein Matrix (Roche), ii) incubation of immobilized DNA with protein, and iii) elution of DNA-protein complex followed by infrared detection of interacting IFP fusion protein in microtiter plates, by in-gel detection and western blot analysis.
An amperometric glucose biosensor was developed using an anionic clay matrix (layered double hydroxide (LDH), Ni/Al NO3) for the immobilization of glucose oxidase (GOx).
After immobilization of calf thymus double stranded DNA (ctDNA), or short DNA oligonucleotide (DNA ODN) onto the surface of dendrimer modified electrode, an enhanced sensor response was recorded using G2-PS/PGEs in contrast to one of unmodified PGEs.
The designed end-point nucleotide composition contains a few guanines or cytosines, and ssDNA immobilization of the SAM by dehybridizing immobilized double-stranded DNA (dsDNA) can improve the hybridization efficiency.
Greater immobilization was also observed by doubling the amount of mature residue incorporated in the soil.
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