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1 PVDF and P(VDF-TrFE) nano- and micro- structures have be
2 PVDF-HFP exhibits higher degrees of platelet activation-
4 tative activation of both PVDF-CH2-CF2-I and PVDF-CF2-CH2-I chain ends toward the synthesis of well-d
5 t, it was determined that nitrocellulose and PVDF membranes gave significantly lower levels of backgr
7 ferroelectric polymers, especially PVDF and PVDF-based copolymers/blends as potential components in
10 ntly, in the quantitative activation of both PVDF-CH2-CF2-I and PVDF-CF2-CH2-I chain ends toward the
11 ration, samples could be collected onto both PVDF for traditional N-terminal sequencing and PE or Tef
12 nst E. coli as compared with that of control PVDF, while aged Ti3C2Tx membrane showed over 99% growth
16 des directly onto polyvinylidene difluoride (PVDF) membrane for automated N-terminal sequence analysi
17 ), transferred to polyvinylidene difluoride (PVDF) membrane, and the 37-kd protein-AA spot was digest
20 of peptides from polyvinylidene difluoride (PVDF)-bound proteins is performed in the presence of non
21 poly(vinylidene fluoride)/dimethylformamide (PVDF/DMF) was used to coat the tip of each fiber to incr
22 nylidene fluoride-co-hexafluoropropylene) (e-PVDF-HFP) was used as the dielectric layer, despite a th
23 odified poly(vinylidene fluoride) (PVDF) (Er-PVDF) film is developed for converting both mechanical a
24 +) acts to enhance heat transfer into the Er-PVDF film due to its excellent infrared absorbance, whic
25 he use of ferroelectric polymers, especially PVDF and PVDF-based copolymers/blends as potential compo
28 ic polymers such as polyvinylidene fluoride (PVDF) have been widely used for membrane distillation (M
29 ntibodies from aged polyvinylidene fluoride (PVDF) immunoblots at room temperature without removing s
30 re excised from the polyvinylidene fluoride (PVDF) membrane blots, hydrolyzed in 20% trifluoroacetic
31 onto amino modified polyvinylidene fluoride (PVDF) membrane has generated a new type of nano-carbon f
32 tration unit with a polyvinylidene fluoride (PVDF) membrane of 40 nm nominal pore size was used to st
37 as retrofitted with polyvinylidene fluoride (PVDF) microfiltration membrane units, each of which was
38 ve skin formed on a polyvinylidene fluoride (PVDF) porous nanofiber scaffold via electrospinning.
40 re carried out with polyvinylidene fluoride (PVDF) ultrafiltration (UF) membranes and bovine serum al
41 flon, refrigerants, polyvinylidene fluoride (PVDF), fire-extinguishing agents, and foams, is a potent
44 nitrocellulose and polyvinylidine fluoride (PVDF) membranes without being permanently fixed to the m
45 e Er(3+) modified poly(vinylidene fluoride) (PVDF) (Er-PVDF) film is developed for converting both me
49 e transition in a poly(vinylidene fluoride) (PVDF) thin film by leveraging its photothermal effect.
50 e titanate (PZT), poly(vinylidene fluoride) (PVDF), 2D materials, and composite materials are introdu
51 nd a fluoropolymer (polyvinylidene fluoride, PVDF) were analyzed in powder raw material forms as well
52 t calculation, a sandwich microstructure for PVDF-BaTiO3 nanocomposite is designed, where the upper a
55 olyvinylidene fluoride-co-hexafluoropropene (PVDF-HFP)-coated surfaces were evaluated in this study.
56 the average bacterial log removal of the ICE-PVDF increased by approximately 1 log compared to the co
58 anes were eliminated by introducing an inert PVDF separator of 50 mum diameter that was coiled around
59 t the relative flux drop over GOQDs modified PVDF is 23%, which is significantly lower than those ove
62 A concentration from 34.8 by weight% in neat PVDF to 53.9 by weight% in PVDF with 15 by weight% of si
65 rth ion, Er(3+) with the ferroelectricity of PVDF provides a new and robust approach for delivering s
66 rix solution, peptide-mass fingerprinting of PVDF-bound proteins by MALDI-TOF can be obtained in the
68 particles enhanced the thermal stability of PVDF/SiO2 membranes; increasing the decomposition temper
69 is demonstrated, which has the structure of PVDF nanowires-PDMS composite film/indium tin oxide (ITO
71 .84 kDa) it was possible to immobilize it on PVDF by using glutaraldehyde to conjugate the peptide to
72 k of rectangular polyvinylidene fluoride (or PVDF) membranes having 0.22 mum pores housed within a mo
73 m/indium tin oxide (ITO) electrode/polarized PVDF film/ITO electrode, and which can individually/simu
75 significantly lower than those over pristine PVDF (86%) and GO-sheet modified PVDF (62%) after 10 h o
78 mbrane consists of a superhydrophobic silica-PVDF composite selective skin formed on a polyvinylidene
80 from 0 to 1 mM, there was a decrease in the PVDF-BSA and BSA-BSA electrostatic repulsion forces, res
81 lsion forces, which caused a decrease in the PVDF-BSA and BSA-BSA interaction forces accompanied by a
82 -93% lower on the ICE anode than that on the PVDF after filtration, and BW further reduced the densit
83 tected the presence of OPBM displayed on the PVDF and correctly identified the RPLC fraction containi
86 aining tagged amino acids are visible on the PVDF membrane and can be excised for direct sequence ana
87 ll amount of peptide that passed through the PVDF membrane during a collection of peptides for N-term
90 e charge was imparted to an alkaline-treated PVDF membrane by aminosilane functionalization, which en
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