High-performance liquid chromatography of biopolymers.
暂无分享,去创建一个
[1] O. Mikeš,et al. Rapid chromatographic separation of technical enzymes on spheron ion exchanges , 1978 .
[2] T. Atkinson,et al. High-performance liquid affinity chromatography of proteins on Cibacron Blue F3G-A bonded silica , 1981 .
[3] M. Rubinstein. Preparative high-performance liquid partition chromatography of proteins. , 1979, Analytical biochemistry.
[4] F. Regnier,et al. High-performance anion-exchange chromatography of oligonucleotides , 1983 .
[5] Y. Kato,et al. High-speed gel filtration of proteins in 6 M guanidine hydrochloride on TSK-GEL SW columns , 1980 .
[6] E. Nice,et al. Hydrophobic high-performance liquid chromatography of hormonal polypeptides and proteins on alkylsilane-bonded silica. , 1979, Journal of chromatography.
[7] L. McLaughlin,et al. The use of high-performance liquid chromatography in the isolation and analysis of oligoribonucleotides synthesized by the T4 RNA ligase reaction. , 1982, Analytical biochemistry.
[8] J. Rivier. Evaluation of triethylammonium phosphate and formate-acetonitrile mixtures as eluents for high-performance gel permeation chromatography , 1980 .
[9] K. Gibson,et al. Supports for reverse-phase high-performance liquid chromatography of large proteins. , 1980, Analytical biochemistry.
[10] K. Unger,et al. Structure and properties ofn-alkyldimethylsilyl bonded silica reversed-phase packings , 1978 .
[11] H. Khorana,et al. Partial primary structure of bacteriorhodopsin: sequencing methods for membrane proteins. , 1979, Proceedings of the National Academy of Sciences of the United States of America.
[12] K. Mosbach,et al. High performance liquid affinity chromatography (HPLAC) and its application to the separation of enzymes and antigens , 1978, FEBS letters.
[13] F. Regnier,et al. High-performance liquid chromatography of proteins. , 1980, Analytical biochemistry.
[14] B. Sproat,et al. Rapid synthesis of oligodeoxyribonucleotides. VII. Solid phase synthesis of oligodeoxyribonucleotides by a continuous flow phosphotriester method on a kieselguhr-polyamide support. , 1982, Nucleic acids research.
[15] W. D. Bostick,et al. Liquid-chromatographic separation and on-line bioluminescence detection of creatine kinase isoenzymes. , 1980, Clinical chemistry.
[16] O. Mikeš,et al. Chromatography of biopolymers and their fragments on ion-exchange derivatives of the hydrophilic macroporous synthetic gel spheron. , 1976, Journal of chromatography.
[17] C. Cramers,et al. Synthesis of a nonpolar, chemically bonded stationary phase with low residual hydroxyl group content , 1980 .
[18] R. R. Walters. High-performance affinity chromatography. pore-size effects , 1982 .
[19] Y. Kato,et al. High-speed gel filtration of proteins in sodium dodecyl sulphate aqueous solution on TSK-GEL SW type , 1980 .
[20] A. Pingoud,et al. Comparison of several high-performance liquid chromatography techniques for the separation of oligodeoxynucleotides according to their chain lengths , 1983 .
[21] F. Regnier,et al. High-performance cation-exchange chromatography of proteins. , 1983, Analytical biochemistry.
[22] K. Wilson,et al. Comparison of the high-performance liquid chromatography of peptides and proteins on 100- and 300-Å reversed-phase supports , 1982 .
[23] H. Jennissen. Multivalent interaction chromatography as exemplified by the adsorption and desorption of skeletal muscle enzymes on hydrophobic alkyl-agaroses. , 1978, Journal of chromatography.
[24] S. Shaltiel,et al. Hydrocarbon-coated sepharoses. Use in the purification of glycogen phosphorylase. , 1972, Biochemical and biophysical research communications.
[25] F. Regnier,et al. Reversed-phase supports for th resolution of large denatured protein fragments. , 1981, Journal of chromatography.
[26] F. Regnier,et al. Variables in the high-performance anion-exchange chromatography of proteins. , 1980, Analytical biochemistry.
[27] G. Guiochon,et al. Introduction to reversed-phase high-performance liquid chromatography , 1977 .
[28] S. Hjertén. Some general aspects of hydrophobic interaction chromatography , 1973 .
[29] E. Nice,et al. Comparison of short and ultrashort-chain alkylsilane-bonded silicas for the high-performance liquid chromatography of proteins by hydrophobic interaction methods , 1981 .
[30] A. D. Kelmers,et al. Improved separation of transfer RNA's on polychlorotrifuoroethylene-supported reversed-phase chromatography columns. , 1971, Biochimica et biophysica acta.
[31] F. Regnier,et al. Preparation of a porous microparticulatee anion-exchange chromatography support for proteins , 1979 .
[32] F. Regnier,et al. The importance of silica type for reverse-phase protein separations. , 1982, Analytical biochemistry.
[33] Heinz Engelhardt,et al. Chemically bonded stationary phases for aqueous high-performance exclusion chromatography , 1977 .
[34] W. Gilbert,et al. A new method for sequencing DNA. , 1977, Proceedings of the National Academy of Sciences of the United States of America.
[35] J. Meek,et al. Factors affecting retention and resolution of peptides in high-performance liquid chromatography , 1981 .
[36] B. Karger,et al. Distribution phenomena of mobile-phase components and determination of dead volume in reversed-phase liquid chromatography , 1980 .
[37] F. Regnier,et al. High-performance liquid chromatography of proteins. , 1976, Methods in enzymology.
[38] B. Karger,et al. High performance liquid chromatography of proteins on a diol-bonded silica gel stationary phase , 1980 .
[39] I. Halasz,et al. Preparation and properties of reversed phases , 1976 .
[40] P. Borer,et al. Separation of oligo-RNA by reverse-phase HPLC. , 1979, Nucleic acids research.
[41] F. Regnier,et al. Glycerolpropylsilane bonded phases in the steric exclusion chromatography of biological macromolecules. , 1976, Journal of chromatographic science.
[42] J. Porath,et al. Salting-out in Amphiphilic Gels as a New Approach to Hydrophobia Adsorption , 1973, Nature.