Mouse Embryonic Stem Cell Adipogenesis Kit
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Mouse Embryonic Stem Cell Adipogenesis Kit´Â mouse ES cellÀ» Áö¹æ¼¼Æ÷(adipocytes)·Î ºÐȽÃ۱â À§ÇÑ reagent¸¦ Á¦°øÇÕ´Ï´Ù. |
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| Merck Millipore |
- mouse ES cellÀ» adipocyte·Î ºÐȽÃ۱âÀ§ÇØ ÇÊ¿äÇÑ reagent¸¦ Á¦°øÇÕ´Ï´Ù.
- ºÐÈµÈ adipocyteÀÇ ¾çÀ» ÃøÁ¤ÇϱâÀ§ÇÑ Oil Red O stain, wash, dye extraction solutionµîÀÌ °°ÀÌ Á¦°øµË´Ï´Ù.
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- Embryoid Body (EB) Formation Medium - 500 mL
- Accutase Cell Dissociation Solution - 100 mL
- Inducer A Solution - 200 uL
- Inducer A Solution - 200 uL
- 3,3¡Ç,5-Triiodo-L-thyronine (T3) Solution - 200 uL
- 0.1% Gelatin Solution - 100 mL
- Oil Red O Solution - 60 mL
- Wash Solution - 250 mL
- Dye Extraction Solution - 30 mL
Figure 1. Undifferentiated mouse ES cells (Catalogue No. SCR012) display the characteristic tight round colonies with a high nuclear to cytoplasmic ratio, (A, 40 X magnification) and stain positively for mouse ES cell marker SSEA-1 (B, 40 X magnification).
Figure 2. Formation of embryoid bodies (EB) after the culture of dissociated mouse ES cells in EB Formation Medium for 2 days (A). Morphology of EBs after treatment with Inducer A Solution for 3 days (B). 10 X magnification.
Figure 3. 26-day differentiation of mouse ES cells to Oil Red O positive adipocytes (A) bright-field image, 20X magnification. (B, C) Oil Red O stained images, 10 and 20 X magnification, respectively).
Figure 4. Differentiation of mouse ES cells via T3 and insulin (induced) produced approximately twice the amount of oil red O stained adipocytes as compared to spontaneous differentiation (uninduced).
Blank represents the background staining of the plate (no cells included) due to absorbance of plates to the oil red O stain.