1. Ultra-rapid vitrification of mouse oocytes in low cryoprotectant concentrations 
Ho-Joon Lee, Heidi Elmoazzen, Diane Wright, John Biggers, Bo R Rueda, Yun Seok Heo, Mehmet Toner, Thomas L Toth 
Reproductive BioMedicine Online 
Volume 20, Issue 2, Pages (February 2010)
DOI: /j.rbmo
Copyright © 2009 Reproductive Healthcare Ltd. Terms and Conditions

2. Figure 1
Quartz capillary (QC) vitrification device and oocyte loading method. (a) The QC device; (b) schematic illustration of the QC loaded with oocytes; and (c) photomicrograph of oocytes loaded into QC and loaded oocytes (arrowheads). VS, vitrification solution.
Reproductive BioMedicine Online  , DOI: ( /j.rbmo )
Copyright © 2009 Reproductive Healthcare Ltd. Terms and Conditions

3. Figure 2
Oocyte survival rate after vitrification in slush nitrogen in the two different vitrification solutions, 0.5mol/l trehalose+1.5mol/l 1,2-propanediol (PrOH) in HEPES-buffered physiological salt solution containing 20% fetal bovine serum (FHM20) or 0.5mol/l trehalose+2.0mol/l PrOH in FHM20, immediately and 2h after warming.
Reproductive BioMedicine Online  , DOI: ( /j.rbmo )
Copyright © 2009 Reproductive Healthcare Ltd. Terms and Conditions