Preparation of honey bee (Apis mellifera L.) primary cell culture by enzymatic disaggregation and planting minced tissues methods | ||
| تحقیقات دامپزشکی و فرآوردههای بیولوژیک | ||
| Article 13, Volume 29, Issue 1, March 2016, Pages 101-109 PDF (4.44 M) | ||
| Document Type: Full Research Paper | ||
| DOI: 10.22034/vj.2016.105751 | ||
| Authors | ||
| R. Fallahi* 1; MR., Ghalenoee,2 | ||
| 1Member of Scientific Board; Razi Vaccine and Serum Research Institute, Alborz, Iran. | ||
| 2Member of Scientific Board; Agricultual Research Education & Extention Organization | ||
| Abstract | ||
| In this study, in order to preparation of primary cell culture of honey bees, some samples were collected from larval and pupal honey bee and were prepared according to standard guidelines. For preparing of primary culture, the short-time enzymatic disaggregation (three-phase, 10 min), long-time (18 h) and planting minced tissues methods were used. For growth of obtained cells in various methods, the Grac'e medium enriched with fetal bovine serum (FBS) to a value of 15% was used in the temperature 28oC. Cells obtained in various methods, had good status in number and rate of growth of living cells and have reached in full confluency after 2-5 weeks and several successive subcultures were prepared. In enzymatic disaggregation method the best result was obtained from long-time trypsinization of pupa stage. The result of planting minced tissues method in the larval and pupal stages were similar and both were great. | ||
| Keywords | ||
| Primary Cell Culture; honey bee; Enzymatic disaggregation; Planting minced tissues | ||
| References | ||
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1- Bergem, M., Norberg, K. and Aamodt, R. M. (2006) Long-term maintenance of in vitro cultured honeybee (Apis mellifera) embryonic cells, BMC Developmental Biology,6:17. | ||
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