Sentence examples for blocks were prepared by from inspiring English sources
Tissue blocks were prepared by routine histological methods after 12 and 24 weeks after the surgery.
A series of peptides, varied by the position of the MMP-2 hexapeptide substrate and the length of RADA blocks, were prepared by parallel synthesis.
Block copolymers of various compositions, consisting of poly(4-vinylpyridine)(P4VP) and poly(dimethylsiloxane) (PDMS) blocks, were prepared by anionic polymerization.
Further, the fibrillar PODB crystals comprised of the helical and the non-helical blocks were prepared by the on-off switching of the helical morphology with the changing the temperature and the concentration of the polymerization.
Three diblock copolymers of poly[N- 2-hydroxypropyl)methacrylamide] (poly[N- 2-hydroxypropylbutyl acrylate) (poly[N- 2-hydroxypropyllengths of blocks were prepared by atomethacrylamideical polymerization.
In this study, poly 2-hydroxyethyl methacrylate-co-glycidyl methacrylate)-block- poly 2-hydroxyethyl methacrylate-co-glycidyl-Gmethacrylate -blocks with a uniformethacrylate -block-co-GMA) layer and a gradient thickness of poly 2-hydroxyethylrepoly 2-hydroxyethylace-initiated atomethacrylateadical P HEMA-co-GMA -b-PHEMAynamically controlled P HEMA-co-GMA -b-PHEMA.
Paraffin embedded blocks was prepared by the Histology Core at The Mayo Clinic and 4-micron thick sections were cut for hematoxylin eosin (H&E) staining and for immuno-staining.
An MgCl2-KCl eutectic salt was used as the PCM, and its EG-based composite PCM block was prepared by this process, in which the optimal mass fraction of the eutectic was determined to be around 85%.
To explain in further detail, the block was prepared by transferring a cylinder of 3 mm diameter from each of the paraffin-embedded tissue samples using a microarrayer (KIN-1, Azumaya, Tokyo, Japan), as previously described [ 23].
Briefly, the PHis block was prepared by a ring-opening polymerization method using amine-containing small molecules, N-Boc-1,4 butanediamine, as an initiator, and the number-average molecular weight (MW) of PHis was determined to be 3.7 kDa by its H NMR spectrum.
From each tumor block, two 1.5-mm cores were obtained using tissue arraying instrument (Beecher Instruments; Silver Spring, MD) TMA blocks were prepared using previously described protocol by Kononen et al[ 24].
