Methods in cell separations

被引:61
作者
Dainiak, Maria B.
Kumar, Ashok
Galaev, Igor Yu.
Mattiasson, Bo
机构
[1] Lund Univ, Dept Biotechnol, Ctr Chem & Chem Engn, S-22100 Lund, Sweden
[2] Protista Biotechnol AB, IDEON, S-22370 Lund, Sweden
[3] Indian Inst Technol, Dept Biol Sci & Bioengn, Kanpur 208016, Uttar Pradesh, India
来源
CELL SEPARATION: FUNDAMENTALS, ANALYTICAL AND PREPARATIVE METHODS | 2007年 / 106卷
关键词
cell separation; purity; recovery; throughput; surface antigen; antibodies; stem cells;
D O I
10.1007/10_2007_069
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Research in the field of cell biology and biomedicine relies on technologies that fractionate cell populations and isolate rare cell types to high purity. A brief overview of methods and commercially available products currently used in cell separations is presented. Cell fractionation by size and density and highly selective affinity-based technologies such as affinity chromatography, fluorescence-activated cell sorting (FACS) and magnetic cell sorting are discussed in terms of throughput, yield, and purity.
引用
收藏
页码:1 / 18
页数:18
相关论文
共 78 条
[41]   Autologous transplantation of CD133 selected hematopoietic progenitor cells in a pediatric patient with relapsed leukemia [J].
Koehl, U ;
Zimmermann, S ;
Esser, R ;
Sörensen, J ;
Grüttner, HP ;
Duchscherer, M ;
Seifried, E ;
Klingebiel, T ;
Schwabe, D .
BONE MARROW TRANSPLANTATION, 2002, 29 (11) :927-930
[42]  
Krause DS, 1996, BLOOD, V87, P1
[43]   Affinity binding of cells to cryogel adsorbents with immobilized specific ligands:: effect of ligand coupling and matrix architecture [J].
Kumar, A ;
Rodríguez-Caballero, A ;
Plieva, FM ;
Galaev, IY ;
Nandakumar, KS ;
Kamihira, M ;
Holmdahl, R ;
Orfao, A ;
Mattiasson, B .
JOURNAL OF MOLECULAR RECOGNITION, 2005, 18 (01) :84-93
[44]   Affinity fractionation of lymphocytes using a monolithic cryogel [J].
Kumar, A ;
Plieva, FM ;
Galeav, IY ;
Mattiasson, B .
JOURNAL OF IMMUNOLOGICAL METHODS, 2003, 283 (1-2) :185-194
[45]   Transplantation of a combination of CD133+ and CD34+ selected progenitor cells from alternative donors [J].
Lang, P ;
Bader, P ;
Schumm, M ;
Feuchtinger, T ;
Einsele, H ;
Führer, M ;
Weinstock, C ;
Handgretinger, R ;
Kuci, S ;
Martin, D ;
Niethammer, D ;
Greil, J .
BRITISH JOURNAL OF HAEMATOLOGY, 2004, 124 (01) :72-79
[46]  
Law P, 1993, J Hematother, V2, P247, DOI 10.1089/scd.1.1993.2.247
[47]   Concomitant mobilization of plasma cells and hematopoietic progenitors into peripheral blood of multiple myeloma patients: Positive selection and transplantation of enriched CD34(+) cells to remove circulating tumor cells [J].
Lemoli, RM ;
Fortuna, A ;
Motta, MR ;
Rizzi, S ;
Giudice, V ;
Nannetti, A ;
Martinelli, G ;
Cavo, M ;
Amabile, M ;
Mangianti, S ;
Fogli, M ;
Conte, R ;
Tura, S .
BLOOD, 1996, 87 (04) :1625-1634
[48]   Transplantation of allogeneic CD34(+) blood cells [J].
Link, H ;
Arseniev, L ;
Bahre, O ;
Kadar, JG ;
Diedrich, H ;
Poliwoda, H .
BLOOD, 1996, 87 (11) :4903-4909
[49]   G-CSF alone mobilizes sufficient peripheral blood CD34(+) cells for positive selection in newly diagnosed patients with myeloma and lymphoma [J].
Mahe, B ;
Milpied, N ;
Hermouet, S ;
Robillard, N ;
Moreau, P ;
Letortorec, S ;
Rapp, MJ ;
Bataille, R ;
Harousseau, JL .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 92 (02) :263-268
[50]  
Mammen M, 1998, ANGEW CHEM INT EDIT, V37, P2755