| CONTENTS | OVERHEADS | GLOSSARY | REFERENCES | SKILLS | CLASSIC |
9/11/97
ZERO CALCIUM SEAWATER:
See zero calcium seawater in MODIFIED SEAWATERS.
PRE-ISOLATION MIX:
To make 100ml of mix, must mix fresh daily:
|
Amount |
Sigma cat # |
Potassium Gluconate |
7.0 g |
G4500 |
Glycine |
2.4 g |
G2879 |
Magnesium Chloride, 2M stock |
0.1 ml |
104-20 (this is a 4.9 M stock solution) |
KEGTA (pH6.6) 0.2M stock |
1.0 ml |
E3889 (use potassium hydroxide to neutralize) |
To make 100 ml of 2M MgCl2 from the 4.9M stock take 41 ml of the 4.9M stock and dilute to 100ml with distilled water.
To make KEGTA, 0.2M, take 7.6g of EGTA and add to 80 ml of distilled water. While stirring add one pellet at a time, potassium hydroxide. It will take approximately 25-30 pellets to bring the pH up to 6.6. This takes awhile! Be patient. It is best to use a pH meter, but paper will do. When it gets closer, as evidenced by the fact that most of the EGTA is dissolved, you may want to switch to a KOH solution instead of the pellets. A 2N solution should work fine. Finally bring the volume up to 100ml. This solution will keep at room temperature in a stoppered bottle for several months.
ISOLATION MIX:
You will need a chemical called Triton X100 from Sigma Chemical Co. cat# X-100
Make up the PRE-ISOLATION MIX and remove 10 ml. To this add 0.1 ml of Triton X100. This will be a little hard to dissolve. Be patient. Gentle rocking seems to work best.
To embryos at or near metaphase: (or any stage you wish to view)
<- live vs. isolated ^ |
Like the information on the Carnoy's fixative, this is a technique that allows you to see into the embryo better than with the live specimen. Do see Mitosis & Centrosomes!
EXAMPLE:
After one treatment, the isolated mitotic apparatus looked very different than the above control. Note that the microtubules have grown longer than the cell could accommodate, resulting in a "spiral" array of microtubules. |