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1 harged carboxylates causes red shifts of the absorption maximum.
2 nt in the QD excitation near the J-aggregate absorption maximum.
3 re involved in fine-tuning the chromophore's absorption maximum.
4 ted acyl group, and a large red shift in the absorption maximum.
5 395 nm and 460 nm) on either side of the PYP absorption maximum (446 nm) were undertaken using 100-fs
7 e found that the resulting enzyme is a blue (absorption maximum 590 nm) complex containing MnxE, MnxF
8 crograms of phosphorescence probe (Green 2W; absorption maximum 636 nm) was injected into the tail ve
10 le chromophore can be manipulated to have an absorption maximum across such an extended spectral regi
11 isible light-absorbing pigment with a 534 nm absorption maximum and approximately 100 nm half-bandwid
13 ve cytoplasmic transducer protein shifts the absorption maximum and strongly decreases the rate of da
14 lectron's radius of gyration and its optical absorption maximum, and extrapolating to the bulk limit
15 O-like in its C-C stretch bands, but has an absorption maximum apparently close to that of unphotoly
16 he nature of the assay product, which has an absorption maximum around 470 nm, had not been determine
17 light inactivation and a red-shifted visible absorption maximum as compared with the more extensively
20 redshift of its absorption spectrum from an absorption maximum at 267 nm in thymidine to 363 nm in 2
23 of oxidized C. tepidum Rd exhibited a unique absorption maximum at 385 nm and a shoulder at 420 nm.
26 teinylglycine [NO2ZGly(S-NBD)CysGly] with an absorption maximum at 423 nm is readily hydrolyzed by an
27 mperature, the X. laevis violet opsin has an absorption maximum at 426 nm when generated with 11-cis-
28 intermediate has a significantly red-shifted absorption maximum at 440 nm, suggesting that the retiny
29 roteins bind heme and exhibit the ferrous-CO absorption maximum at 444 nm characteristic of thiolate
30 rmation of an Fe(II)-CO complex with a Soret absorption maximum at 448.5 nm, which collapses (at 0.24
34 nitial (or spectrally similar) state with an absorption maximum at 501 nm upon illumination with 380-
36 pectrum to yield a 28% greater intensity, an absorption maximum at 520 nm, and distinct shoulders at
38 lation, forms a light-sensitive pigment with absorption maximum at 560 nm upon reconstitution with 11
39 Concentrated samples of native PALcc have an absorption maximum at 560 nm, suggestive of a phenolate-
41 arotenoid cation radical is formed having an absorption maximum at 898 nm, an 85 nm blue shift relati
42 prepared zinc arylsulfanyl TPyzPzs showed an absorption maximum at a Q-band over 650 nm, fluorescence
43 ark and the batho intermediates) that has as absorption maximum at approximately 470 nm, and thermall
45 urther decrease in pH from 2 to 0 shifts the absorption maximum back to 575 nm when HCl is used (acid
46 components were used to predict their plasma absorption maximum, based on molecular mass and lipophil
47 date, with Chl f having the most red-shifted absorption maximum because of a C2(1)-formyl group subst
48 cular framework shows that the excited-state absorption maximum can be extensively modulated [lambdam
49 of the solvent on the position of the UV-vis absorption maximum, can be determined via a linear Hamme
50 d to account for the 30 nm blue shift of its absorption maximum compared to that of the green pigment
54 ring and consequently to a red shift of its absorption maximum from 446 nm to 457 and 458 nm in the
55 e Glu46Gln mutation shifted the ground state absorption maximum from 446 to 462 nm, indicating that t
56 W265Y, A292S, A295S, and A299C) shifted the absorption maximum from 500 to 438 nm, accounting for 2,
57 ge of pH from 6.5 to 2 causes a shift of the absorption maximum from 568 to 600 nm (acid blue bR) and
60 the S65G and S72A mutations which shift the absorption maximum from the 395 nm of wild-type GFP clos
61 viscosity coordinating solvents, the initial absorption maximum further red shifts between 2 and 10 p
64 lower frequency upon deprotonation, and the absorption maximum in the UV-visible spectrum shifts to
65 ntal spectrum of the blue form in DsRed (the absorption maximum is 408 nm or 3.04 eV) and mTagBFP (40
66 ong-wave subfamily of cone pigments, but its absorption maximum is 508 nm, similar to that of the rho
68 e flavin domain and a species with a similar absorption maximum is also seen during reduction of the
70 s retinal as does the N state of BR, but its absorption maximum is red-shifted relative to PR (like t
72 ing two Se atoms for S gave a shorter band I absorption maximum (lambda(max) of 695 nm) and a smaller
74 in the bandwidth closest to the indicator's absorption maximum (lambdamax) at pHs above the indicato
75 trix-isolated 1 at lambda = 222 nm (near its absorption maximum) led to the corresponding 2H-azirine
77 487 nm absorption maximum to a species with absorption maximum near 350 nm (M) followed by a species
79 e among the archaeal rhodopsins in having an absorption maximum near 500 nm, blue shifted roughly 70
81 ual high-potential haem c with a red-shifted absorption maximum, not unlike that of certain eukaryoti
82 At room temperature, mouse UV opsin has an absorption maximum of 357 nm, while at 70 K, the pigment
84 nm when generated with 11-cis-retinal and an absorption maximum of 415 nm when generated with 9-cis-r
85 obenzene-3, 4'-disulfonic acid, which has an absorption maximum of 489 nm and an extinction coefficie
88 sin, a retinal-protein intermediate, with an absorption maximum of about 430 nm, has been identified.
89 the fluorescent drug-tubulin complex at the absorption maximum of anthranilate, yields a covalent ad
92 strate that the longitudinal surface plasmon absorption maximum of GNRs is correlated with the effect
93 btained at a wavelength corresponding to the absorption maximum of liquid water of about 2.94 mum.
94 itted fluorescence of azido-ATP-EDANS at the absorption maximum of S135C-EMA and a corresponding 50%
95 ively causes (1) a bathochromic shift in the absorption maximum of the B band (405 to 426 nm) and (2)
96 , progressively causes (1) a redshift in the absorption maximum of the B band (405-436 nm) and the Q(
97 erved for the GFP emission, excited near the absorption maximum of the BFP, is very low due to depola
98 as about equal to the difference between the absorption maximum of the bullfrog and newt pigments, 44
101 the complex to protein causes a shift in the absorption maximum of the dye-metal complex from 450 to
102 The first determination of the absolute absorption maximum of the human blue cone visual pigment
104 urface plasmon resonance wavelength with the absorption maximum of the NIR dye to maximize the plasmo
105 e accompanied by a hypsochromic shift of the absorption maximum of the photoinduced form, whereas no
107 the host protein, enabled regulation of the absorption maximum of the pigment in the range of 425 to
108 hat observed for the analogous excited-state absorption maximum of the PZnE-EPZn benchmark; these dat
111 gradual blue-shift in the wavelength of the absorption maximum of their visual pigments with increas
112 In the case of the basic form of E113Q, the absorption maximum of this intermediate was at 408 nm.
113 n is observed for 1-7 with the lowest-energy absorption maximum (Q band) varying little as a function
114 or the 70- to 80-nanometer blue shift of its absorption maximum relative to those of haloarchaeal tra
118 and broader and with lower extinction at the absorption maximum than either the human blue or salaman
120 hway from the unphotolyzed state with 487 nm absorption maximum to a species with absorption maximum
121 itterions of amino acids in DMSO, and its UV absorption maximum undergoes a significant red shift in
123 fraction contained BR in a lattice form: its absorption maximum was blue-shifted by < or = 4 nm relat
125 s in a significantly smaller redshift in the absorption maximum, which depends sensitively on the pos
126 cence emission and a 45 nm blue shift of the absorption maximum with an increase in the pH from 5 to
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