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Karyotype analysis of cryopreserved mononuclear cells from cord blood
Journal of Genetic Medicine ; : 55-60, 2008.
Article Dans Coréen | WPRIM | ID: wpr-62800
ABSTRACT

PURPOSE:

The ability to perform chromosome analysis of cryopreserved cord blood mononuclear cells is important for future retrospective studies. We compared the karyotypes of cryopreserved cells with cells before cryopreservation.

METHODS:

One cord blood (CB) sample was obtained from normal healthy volunteer. Karyotype analysis was performed before cryopreservation. After mononuclear cell separation with Ficoll-Hypaque, the mononuclear cells were cryopreserved by programmed controlled-rate freezer and then transferred into the liquid nitrogen (-196 degrees C) for 3 days. After rapid thawing, cytogenetic analysis was performed as the same method for each sample by different conditions. The samples were divided by three groups. The first group was no culture before cryopreservation, the second group was 72 hours culture before cryopreservation, but no 24 hours culture after thawing and the third group was 72 hours culture before cryopreservation and 24 hours culture after thawing.

RESULTS:

The chromosome analysis was successful in the second and third groups of CB sample.

CONCLUSION:

The successful result from CB samples may suggest the usefulness of long-term cryopreservation for retrospective study in various clinical settings including hematologic malignancies.
Sujets)

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Cryoconservation / Séparation cellulaire / Études rétrospectives / Analyse cytogénétique / Sang foetal / Caryotype / Azote Type d'étude: Étude observationnelle langue: Coréen Texte intégral: Journal of Genetic Medicine Année: 2008 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Cryoconservation / Séparation cellulaire / Études rétrospectives / Analyse cytogénétique / Sang foetal / Caryotype / Azote Type d'étude: Étude observationnelle langue: Coréen Texte intégral: Journal of Genetic Medicine Année: 2008 Type: Article