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91.
M. A. Livrea A. Bongiorno L. Tesoriere C. Nicotra A. Bono 《Cellular and molecular life sciences : CMLS》1987,43(5):582-586
Summary 11-cis retinaldehyde binding analysis was performed on a bovine retinal pigment epithelium preparation of cellular retinaldehyde binding protein (CRALBP), whose purity degree was estimated as 75%. Equilibrium binding studies were carried out measuring the replacement of tritium-labeled with unlabeled 11-cis retinaldehyde at 25°C. Analysis of the experimental data both by a direct curve-fitting procedure utilizing a non linear least square regression analysis and by a conventional Scatchard plot revealed a single non-interacting binding site with an apparent equilibrium constant of 0.9×10–7 M.A binding stoichiometry of approximately 1 mol of 11-cis retinaldehyde/mol of binding protein can be calculated from the experimental data. Competition studies carried out in the presence of unlabeled trans and cis isomers of Vitamin A derivatives confirm the high degree of specificity of the 11-cis retinaldehyde binding. 相似文献
92.
MSI and MSII made on ribosome in idling step of protein synthesis 总被引:56,自引:0,他引:56
93.
The significance of glycosylated proteins 总被引:15,自引:0,他引:15
94.
Growth of the bacterial cell 总被引:56,自引:0,他引:56
95.
96.
RNA-DNA hybrids at the cytological level 总被引:37,自引:0,他引:37
97.
RNA synthesis during early development of the mouse 总被引:5,自引:0,他引:5
98.
Incorporation of tritiated thymidine by teleost epidermal cells 总被引:1,自引:0,他引:1
R C Henrikson 《Experientia》1967,23(5):357-358
99.
100.
G. Deby-Dupont J. Pincemail A. Thirion C. Deby M. Lamy P. Franchimont 《Cellular and molecular life sciences : CMLS》1991,47(9):952-957
In order to obtain a radioimmunoassay (RIA) technique for the measurement of human plasma myeloperoxidase (MPO), we purified the enzyme from polymorphonuclear granulocytes (neutrophils), and compared three methods of labeling it with125Iodine: chloramine T, lactoperoxidase, and an original technique of self labeling based on the ability of the enzyme to oxidize and bind125I in the presence of H2O2. The chloramine T technique produced a degraded protein, as well shown by a high non-specific binding of tracer to antibody. The lactoperoxidase technique did not succeed in labeling MPO with an adequate specific activity. In contrast, the self-labeling method gave a stable tracer with a specific activity of 23 Ci/gmg MPO (85 MBq), a satisfactory level of immunoreactivity, and a low-specific binding (3%). After labeling, purification of tracer was achieved by gel filtration chromatography in phosphate buffer (0.05 M; pH7) to which 0.1% poly-L-lysine was added. The labeled molecule remained stable for 40 days and could be used for RIA with a polyclonal antibody raised in rabbits. 相似文献