Fractionation of normal and leukemic T-cells by lectin-affinity column chromatography.
Fractionation of normal and leukemic T-cells by lectin-affinity column chromatography.
复制标题
通过凝集素亲和柱层析分离正常和白血病 T 细胞。
DOI:
10.1016/s0304-3835(02)00207-0
复制
发表时间:
2002
期刊:
影响因子:
9.7
通讯作者:
O. Nakamura
中科院分区:
文献类型:
--
作者:
H. Ohba;R. Bakalova;S. Moriwaki;O. Nakamura
A method for rapid fractionation of normal and leukemic T-cells (Jurkat, RPMI-8402, MOLT-4), using lectin-affinity column chromatography, is described. CNBr-activated Sepharose 6MB was used as a non-mobile phase. The gel was covalently conjugated with Dolichos biflorus agglutinin (DBA) over 24 h. The normal cells were eluted by phosphate buffered saline (Ca2+and Mg2+free), while the leukemic T-cells, interacting with DBA, were removed by N-acetyl-d-galactosamine or by low-concentrated acetic acid as a mobile phase. The cell fractions were detected spectrophotometrically at 600 nm. The rate of cell elution decreased in the order: normal>leukemic T-cells. The viability and the type of separated T-cell fractions were characterized by flow cytometry, using adequate fluorescent antibodies. The interactions between leukemic T-cells and DBA-saturated Sepharose beads were examined by fluorescent microscopy, using fluorescent isothiocyanate-DBA as a fluorescent marker.
DOI:
--
发表时间:
1987
期刊:
Cancer biochemistry biophysics
影响因子:
--
作者:
Forsberg,LS;Macher,BA
通讯作者:
Macher,BA