sepharose and Leukemia

sepharose has been researched along with Leukemia* in 6 studies

Other Studies

6 other study(ies) available for sepharose and Leukemia

ArticleYear
Isolation and Characterization of a Phaseolus vulgaris Trypsin Inhibitor with Antiproliferative Activity on Leukemia and Lymphoma Cells.
    Molecules (Basel, Switzerland), 2017, Jan-23, Volume: 22, Issue:1

    A 17.5-kDa trypsin inhibitor was purified from

    Topics: Animals; Cell Line, Tumor; Cell Proliferation; DEAE-Cellulose; Fungi; Humans; Leukemia; Lymphoma; Mice; Phaseolus; Seeds; Sepharose; Trypsin; Trypsin Inhibitors

2017
An antifungal defensin from Phaseolus vulgaris cv. 'Cloud Bean'.
    Phytomedicine : international journal of phytotherapy and phytopharmacology, 2011, Jan-15, Volume: 18, Issue:2-3

    An antifungal peptide with a defensin-like sequence and exhibiting a molecular mass of 7.3kDa was purified from dried seeds of Phaseolus vulgaris 'Cloud Bean'. The isolation procedure entailed anion exchange chromatography on DEAE-cellulose, affinity chromatography an Affi-gel blue gel, cation exchange chromatography on SP-Sepharose, and gel filtration by fast protein liquid chromatography on Superdex 75. Although the antifungal peptide was unadsorbed on DEAE-cellulose, it was adsorbed on both Affi-gel blue gel and SP-Sepharose. The antifungal peptide exerted antifungal activity against Mycosphaerella arachidicola with an IC(50) value of 1.8 μM. It was also active against Fusarium oxysporum with an IC(50) value of 2.2 μM. It had no inhibitory effect on HIV-1 reverse transcriptase when tested up to 100 μM. Proliferation of L1210 mouse leukemia cells and MBL2 lymphoma cells was inhibited by the antifungal peptide with an IC(50) of 10 μM and 40 μM, respectively.

    Topics: Adsorption; Animals; Antifungal Agents; Antineoplastic Agents, Phytogenic; Cell Line, Tumor; Defensins; Fungi; Inhibitory Concentration 50; Leukemia; Lymphoma; Mice; Neoplasms; Phaseolus; Phytotherapy; Plant Extracts; Seeds; Sepharose; Triazines

2011
A study of leukemic cell migration by an agarose plate method.
    Japanese journal of clinical oncology, 1983, Volume: 13, Issue:2

    By means of inducing random migration of leukemic cells in human peripheral blood by an agarose plate method, a study was made to see how migration distance and cell morphology after migration differed with the type of leukemia. After 3 days of incubation, the distance of random migration in cells of lymphocytic leukemia patients was on the average 0.41 mm for the cells of 13 patients with adult T-cell leukemia/lymphoma and 0.03 mm for the cells of four patients with chronic lymphocytic leukemia which were all of B-cell origin. Thus leukemic cells of T-cell origin migrated farther than those of B-cell origin. In the cases of myelocytic leukemia, the distance of random migration was on the average 0.54 mm for the cells of five patients with acute myelocytic leukemia, 2.42 mm for the cells of three patients with acute myelomonocytic leukemia, 1.69 mm for the cells of four patients with chronic myelocytic leukemia at blastic crisis and 3.78 mm for the cells of one patient with chronic monocytic leukemia. Thus, cells of monocyte origin migrated quite well. Migrating cells differing from cells of smear samples retained their original natural morphology and were considered to serve as an aid in the differentiation of types of leukemia.

    Topics: Adult; Aged; Cell Movement; Female; Humans; Leukemia; Leukocyte Count; Male; Middle Aged; Sepharose

1983
Protein-coated agarose surfaces for attachment of cells.
    In vitro, 1979, Volume: 15, Issue:11

    Plastic dishes were coated with an agarose layer. The layer was modified by covalently binding proteins to it, using the CNBr-method. Cells were seeded on the dishes and the number of attached cells was evaluated. The specificity of the attachment was demonstrated by showing that cells, carrying specific membrane-bound immunoglobulins, attached only to the corresponding anti-immunoglobulins. This indicated that the method could be used for cell sorting. The attachment of cells to proteins was influenced by the amount of bound protein, incubation time, temperature and the degree of trypsinization. Most attached cells were viable for several days and when dying they detached. Detailed morphological and cytochemical analyses of the dynamics of attachment and cytoplasmic spreading on the chemically well-defined surfaces were possible using the new method.

    Topics: Burkitt Lymphoma; Cell Adhesion; Cell Line; Concanavalin A; Glioma; Humans; Leukemia; Lymphoma, Non-Hodgkin; Neuroglia; Polylysine; Polysaccharides; Protamines; Protein Binding; Proteins; Sepharose

1979
Characterization of the target cell receptor for IgE. III. properties of the receptor isolated from rat basophilic leukemia cells by affinity chromatography.
    Journal of immunology (Baltimore, Md. : 1950), 1978, Volume: 120, Issue:2

    Topics: Animals; Basophils; Binding Sites, Antibody; Chromatography, Affinity; Immunoglobulin E; Leukemia; Mice; Rats; Sepharose

1978
The isolation of dihydrofolate reductases by affinity chromatography on folate-sepharose.
    Analytical biochemistry, 1977, May-01, Volume: 79, Issue:1-2

    Topics: Animals; Cell Line; Chromatography, Affinity; Folic Acid; Humans; Lacticaseibacillus casei; Leukemia; Leukemia L1210; Leukocytes; Methotrexate; Mice; Sepharose; Tetrahydrofolate Dehydrogenase

1977