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Procedures for derivation and characterisation of human embryonic stem cells from Odense, Denmark.

Methods in molecular biology (Clifton, N.J.) (2012-04-25)
Linda Harkness, Moustapha Kassem
RÉSUMÉ

In 1998, a development occurred in stem cell biology with the first report of the derivation of a human embryonic stem cell (hESC) line. Since then a number of techniques have been used to derive and characterise hESCs. Here, we describe the derivation methods used by our laboratory for isolation of the ICM by immunosurgery and outgrowth of the whole blastocyst. We have added protocols for routine culture, passaging and cryopreservation of our hESC lines as well as the methods we have used for characterisation (flow cytometry, karyotyping, immunocytochemistry, in vitro and in vivo differentiation). Additionally, we have included gene sequences for PCR and an antibody list for immunocytochemistry.

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Albumine de sérum bovin, cold ethanol fraction, pH 5.2, ≥96%
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Mitomycine C from Streptomyces caespitosus, powder, BioReagent, suitable for cell culture
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Complement sera from guinea pig, lyophilized powder
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Anti-Human IgG (whole molecule) antibody produced in rabbit, IgG fraction of antiserum, buffered aqueous solution
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Anti-TRA-1-85 Antibody, blood group Antigen Ok(a), clone TRA-1-85, clone TRA-1-85, Chemicon®, from mouse