| dc.contributor.author | Kaaya Godwin P. | |
| dc.contributor.author | Maxie MG. | |
| dc.contributor.author | Valli VE. | |
| dc.date.accessioned | 2013-06-18T07:47:47Z | |
| dc.date.available | 2013-06-18T07:47:47Z | |
| dc.date.issued | 1981-04 | |
| dc.identifier.citation | Cryobiology. 1981 Apr;18(2):119-24. | en |
| dc.identifier.uri | http://www.sciencedirect.com/science/article/pii/0011224081900833 | |
| dc.identifier.uri | http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/35405 | |
| dc.identifier.uri | www.ncbi.nlm.nih.gov/pubmed/7238066 | |
| dc.description.abstract | Bovine marrow granulocyte/macrophage and erythroid progenitor cells maintained viability after storage in liquid nitrogen for 2 to 4 weeks. The granulocyte/macrophage progenitor cells maintained 100% viability for 4 weeks, while the erythroid progenitor cells maintained 100% viability for at least 2 weeks. The optimum concentration of either DMSO or glycerol was found to be 5–10%. DMSO was superior to glycerol as a cryopreservative of bovine granulocyte/ macrophage progenitor cells. Glycerol was found to be unable to cryopreserve bovine erythroid progenitor cells. | en |
| dc.language.iso | en | en |
| dc.publisher | University of Nairobi. | en |
| dc.title | Cryopreservation of bovine hemopoietic progenitor cells in liquid nitrogen | en |
| dc.type | Article | en |
| local.publisher | School of Biological Sciences | en |
