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1 ximately 50 pmol per zone for both Coomassie Brilliant Blue and Amaranth dyes; these values were 0.4
2 end-point, cells were stained with Coomassie brilliant blue and area was determined using image analy
5 uantitation of tartrazine in the presence of brilliant blue and sunset yellow FCF as possible interfe
7 ing ARPE-19 for 10 minutes with trypan blue, brilliant blue, bromophenol blue, fast green, light gree
8 ate (SDS) upon the response of the Coomassie Brilliant Blue (CBB) and Pyrogallol Red-molybdate (PRM)
12 ), Amaranth (E123), Sunset Yellow (E110) and Brilliant Blue (E133) were extracted from soft drinks us
13 Patent Blue V (E131), Indigo Carmine (E132), Brilliant Blue (E133), Green S (E142), Fast Green (E143)
14 exin 1 channels using carbenoxolone (CBX) or Brilliant Blue FCF (BB-FCF) (1-100 mum, intravesically),
15 luminescence as the reporter system, the dye Brilliant Blue FCF as the signal-masking reagent, and bu
16 , the structurally related food-coloring dye Brilliant Blue FCF had very little effect at concentrati
17 istration of the pannexin channel antagonist Brilliant Blue FCF increased bladder capacity, whereas i
20 king agents BAY 11-7082 (30 mg/kg, i.p.) and Brilliant Blue G (BBG) (45.5 mg/kg, i.p.) in a mouse mod
22 systemically administered P2X7R antagonist, Brilliant blue G (BBG), in a weight-drop model of thorac
24 riodate oxidised ATP (OxATP: 100 microM) and brilliant blue G (BBG: 1 microM), but not by suramin (10
25 led area, but were matched to the area where brilliant blue G accidentally entered the subretinal spa
26 and microperimetry indicate that subretinal brilliant blue G might cause focal macular damage with a
27 nal changes in his right eye associated with brilliant blue G migration into the subretinal space dur
29 hosphate-6-azophenyl-2',4'-disulphonic acid, Brilliant Blue G or periodate oxidized ATP dialdehyde to
33 ) permeability to Na+, and (e) inhibition by Brilliant Blue G, Cu2+, and pyridoxal phosphate-6-azophe
34 -5-phosphate-6-azo-2',4'-disulfonic acid and Brilliant Blue G, with half-maximal inhibition at 3, 0.2
35 Bradford reagent, comprised of the Coomassie Brilliant Blue G-250 dye, methanol, and phosphoric acid,
38 P and BzATP and inhibited by zinc, Coomassie Brilliant Blue-G, and KN-62, demonstrating activation of
40 ing species of Begonia(5), notable for their brilliant blue iridescence, have a photonic crystal stru
41 Addition of contrast agents (trypan blue or brilliant blue R) improve the signal-to-noise ratio by q
43 w/v) solution of the protein stain Coomassie Brilliant Blue R-250 for 16 to 24 h and then destained.
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