Results 321 to 330 of about 240,931 (342)
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2007
Microcystin-based affinity matrices have been utilized to demonstrate the association of signaling proteins with protein phosphatases and for the purification of low-abundance microcystin-sensitive protein phosphatases. Here, we describe the procedure for the synthesis and use of microcystin-Sepharose and microcystin-biotin-Sepharose.
Moorhead, Greg B.G. +2 more
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Microcystin-based affinity matrices have been utilized to demonstrate the association of signaling proteins with protein phosphatases and for the purification of low-abundance microcystin-sensitive protein phosphatases. Here, we describe the procedure for the synthesis and use of microcystin-Sepharose and microcystin-biotin-Sepharose.
Moorhead, Greg B.G. +2 more
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Cholesterol immobilization via ether-linked Sepharose gels
The Analyst, 1992Cholesterol has been immobilized on Sepharose-6B via oxyether linkages to the 3- or 25-position. The 3- or 25-hydroxysterol methanesulfonates were coupled with epoxy-Sepharose-6B at 80 degrees C for 24 h. Approximately 2% of the ligand was incorporated into the gel.
R K, Satsangi, G E, Mott
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Chromatography of vWF on dextran sulphate sepharose
Thrombosis Research, 1987A relatively simple and reproducible chromatographic separation using Dextran Sulphate (DS) Agarose is described for the purification of vWf:Ag from cryoprecipitate or plasma source material. The elution profiles suggest high affinity of vWf for the matrix permitting resolution from Fibrinogen, IgG and the unbound Albumin.
R H, Saundry, P, Harrison, G F, Savidge
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MICROFLUOROMETRIC IMMUNOASSAYS WITH ANTIGENS BOUND TO SEPHAROSE BEADS
Annals of the New York Academy of Sciences, 1975Sepharose beads, to which protein had been coupled, were used in the development of two types of microfluorometric immunoassays. The first is an inhibition assay: a fixed amount of antiserum was absorbed with different amounts of antigen. This was accomplished in both direct and indirect incubation schemes.
Haaijman, J.J. +2 more
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Purification of Immunoglobulins Using Protein A-Sepharose
2003Most immunochemical techniques used in molecular biology rely on a specific class of antibodies, immunoglobulin G (IgG). In mammals, IgG antibodies are produced during the secondary humoral response and contribute about 80% of the serum immunoglobulin. Factors affecting the experimental production of antibodies have been discussed in detail (1).
N J, Kruger, J B, Hammond
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Binding of immune complexes to IgA-Sepharose 4B
Journal of Immunological Methods, 1984A method for the determination and removal of circulating immune complexes in pathological sera was developed using human secretory or dimeric myeloma IgA covalently bound to Sepharose 4B. IgA-Sepharose 4B was able to selectively bind heat or antigen-aggregated human IgG (circulating immune complexes) but not monomeric IgG.
G, Moţa, M A, Dobre
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Interferon-sepharose: Induction of the antiviral state
Biochemical and Biophysical Research Communications, 1974Summary Mouse (L cell) interferon has been covalently attached to Sepharose beads. The interferon-Sepharose beads induce resistance in L cells to virus replication. It is concluded that interferon induces resistance to viral replication from the cell surface only without entry into the cell.
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Sepharose-bound trypsin and activated sepharose-bound trypsinogen
Archives of Biochemistry and Biophysics, 1974Ralph J. Knights, Albert Light
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Immobilization of human intestinal mucosa enzymes on sepharose
Analytical Biochemistry, 1977Abstract Digestive enzymes from human intestinal mucosa were solubilized by Triton X-100 and papain and covalently bound to eyanogen bromide-activated Sepharose 4-B gel. Triton X-100 solubilized most of the activities, and 39.1 to 63.5% were immobilized on the carrier. The other enzymes, still bound on the microvilli, were subsequently solubilized by
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