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1 extension at its amino terminus relative to allophycocyanins.
2 lication to the ultrafast dynamics of single allophycocyanin, a light-harvesting protein from cyanoba
6 e complex after incubation with streptavidin-allophycocyanin and a LANCE-conjugated anti-GST allowed
8 shown how a purified phycocyanin (mixture of allophycocyanin and c-phycocyanin) disassembled and dena
9 mal amount of phycobilisome cores containing allophycocyanin and other phycocyanobilin-bearing core p
10 compare this structure to the structures of allophycocyanin and smURFP mutants to identify the struc
12 og of the light-harvesting phycobiliprotein, allophycocyanin (AP), that strongly absorbs far-red ligh
13 ify nuclear import of a heterologous protein allophycocyanin (APC) in standard import assays in digit
14 a reveal the ratio of phycocyanin (C-PC) and allophycocyanin (APC) in the antenna complex, the subuni
15 uence-fitness landscape for aptamers binding allophycocyanin (APC) protein via a novel Closed Loop Ap
16 s on the monomer-to-trimer transformation of allophycocyanin (APC), an important antenna protein in c
17 and incubated with the following antibodies: allophycocyanin (APC)-conjugated PDGFR-alpha, FITC-conju
20 orescence from phycocyanin, allophycocyanin, allophycocyanin-B/terminal emitter, and chlorophyll a wa
21 ching for all types of PBs takes place on an allophycocyanin bilin emitting at 660 nm (APC(Q)(660)) w
23 CD34+ cells were immunophenotyped using CD34-allophycocyanin, CD38-fluorescein isothiocyanate, and Th
25 arge-transfer character of the bilins in the allophycocyanin-containing segments localizes the excita
26 via the phycobilisome, which consists of an allophycocyanin core and six radiating rods, each with t
29 of real DNA oligomers binding to a protein (allophycocyanin), data we derived from experimental eval
30 nergy acceptor molecules (SPA beads for SPA, allophycocyanin for HTRF) were in close proximity, both
31 nce energy transfer (FRET) pair europium and allophycocyanin for measuring BACE1 enzymatic activity i
32 SDITRPGGNMYTTR (SR18), linked to the pigment allophycocyanin, had very strong antioxidant properties
34 omplex is subsequently formed by addition of allophycocyanin-labeled streptavidin ([XL665]SA), which
35 of PCB to allophycocyanin subunits in vivo, allophycocyanin levels were significantly reduced in all
36 ach of these proteins, which have been named allophycocyanin-like (Apl) proteins, apparently contains
37 proteins that is most closely related to the allophycocyanin members of the phycobiliprotein superfam
39 g how bilin binding in the alpha-subunits of allophycocyanin paralogs can modify the bilin-binding si
40 verning the dynamics of the pyrrole rings of allophycocyanin, particularly influenced by solvents and
43 U are also required for attachment of PCB to allophycocyanin subunits in vivo, allophycocyanin levels
45 led from chromophore-bearing phycocyanin and allophycocyanin subunits, nonpigmented linker proteins a
46 ws comparisons with other previously studied allophycocyanins to gain insights into how phycocyanobil
48 the arrangement of the numerous red-shifted allophycocyanin variants and the probable locations of t
49 f a phycobiliprotein core complex comprising allophycocyanin variants that absorb far-red light durin
50 hotyrosine antibody and streptavidin-labeled allophycocyanin were added as detection reagents for SPA