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Exp Biol Med (Maywood) ; 232(11): 1470-6, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18040072

ABSTRACT

We depleted reticulocytes from erythrocytes of both sickle cell disease (SCD) subjects and healthy controls by four methods: fluorescence-activated cell sorting (FACS), Miltenyi immunomagnetic depletion (MACS), a combination of these methods (FACS + MACS) and Percoll density separation. The efficiency of these methods was assessed by new methylene blue staining and manual enumeration of the reticulocytes. FACS sorted erythrocytes from reticulocytes based on size and granularity, as well as the absence of dsDNA staining. MACS depleted reticulocytes from erythrocytes based on the immunoaffinity to CD36 and CD71. Reticulocytes from healthy controls were depleted to

Subject(s)
Anemia, Sickle Cell , Cell Fractionation , Erythrocytes , Reticulocytes , Cell Fractionation/methods , Humans , Proteomics/methods
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