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1  extension at its amino terminus relative to allophycocyanins.
2               Fluorescence from phycocyanin, allophycocyanin, allophycocyanin-B/terminal emitter, and
3       We developed a new class of FP from an allophycocyanin alpha-subunit (APCalpha).
4 e complex after incubation with streptavidin-allophycocyanin and a LANCE-conjugated anti-GST allowed
5 mal amount of phycobilisome cores containing allophycocyanin and other phycocyanobilin-bearing core p
6 ents such as biotinylated dUTP, streptavidin-allophycocyanin, and streptavidin-europium.
7 ify nuclear import of a heterologous protein allophycocyanin (APC) in standard import assays in digit
8 a reveal the ratio of phycocyanin (C-PC) and allophycocyanin (APC) in the antenna complex, the subuni
9 uence-fitness landscape for aptamers binding allophycocyanin (APC) protein via a novel Closed Loop Ap
10 s on the monomer-to-trimer transformation of allophycocyanin (APC), an important antenna protein in c
11 and incubated with the following antibodies: allophycocyanin (APC)-conjugated PDGFR-alpha, FITC-conju
12 an important photosynthetic antenna protein, Allophycocyanin (APC).
13 lyase was also tested with recombinant apoHT-allophycocyanin (aporHT-AP) and PCB in vitro.
14 orescence from phycocyanin, allophycocyanin, allophycocyanin-B/terminal emitter, and chlorophyll a wa
15 ching for all types of PBs takes place on an allophycocyanin bilin emitting at 660 nm (APC(Q)(660)) w
16 ively quench the excited state of one of the allophycocyanin bilins.
17 CD34+ cells were immunophenotyped using CD34-allophycocyanin, CD38-fluorescein isothiocyanate, and Th
18  bind chromophores but fail to adopt typical allophycocyanin conformations.
19  via the phycobilisome, which consists of an allophycocyanin core and six radiating rods, each with t
20 suggested that OCP binds to one of the basal allophycocyanin cylinders.
21  of real DNA oligomers binding to a protein (allophycocyanin), data we derived from experimental eval
22 nergy acceptor molecules (SPA beads for SPA, allophycocyanin for HTRF) were in close proximity, both
23 nce energy transfer (FRET) pair europium and allophycocyanin for measuring BACE1 enzymatic activity i
24 omplex is subsequently formed by addition of allophycocyanin-labeled streptavidin ([XL665]SA), which
25  of PCB to allophycocyanin subunits in vivo, allophycocyanin levels were significantly reduced in all
26 ach of these proteins, which have been named allophycocyanin-like (Apl) proteins, apparently contains
27 proteins that is most closely related to the allophycocyanin members of the phycobiliprotein superfam
28  pMHC tetramers and dextramers and with PE-, allophycocyanin-, or FITC-based reagents.
29  hexamers of the coloured phycobiliproteins, allophycocyanin, phycocyanin and phycoerythrin (PE).
30 bated with streptavidin-coupled cross-linked allophycocyanin (SA-XL665).
31 U are also required for attachment of PCB to allophycocyanin subunits in vivo, allophycocyanin levels
32          Recombinant apo-phycocyanin and apo-allophycocyanin subunits were used as the substrates for
33 led from chromophore-bearing phycocyanin and allophycocyanin subunits, nonpigmented linker proteins a
34 hotyrosine antibody and streptavidin-labeled allophycocyanin were added as detection reagents for SPA
35 rgy transfer using streptavidin labeled with allophycocyanin ([XL665]SA).

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