Jacks Lab, Center for cancer research,MIT
http://web.mit.edu/ccr/labs/jacks/protocols/AdenovirusCre.html
|
REAGENTS:
|
| |
MEM (Sigma catalog #M-0268) |
| |
2 M CaCl2 |
| |
*Adenovirus - University of Iowa |
Note*- The University of Iowa facility sends virus at a titer of 10E12 particles/mL which is equal to 10E10 PFU/mL. It is important to minimize freeze/thawing as the titer drops ten-fold each time the virus is frozen. Upon arrival we thaw the virus and aliquot it. Then we thaw an aliquot when we are ready to use it. However, Iowa accounts for one thaw/freeze to aliquot, so no need to adjust for this. Therefore, at the time of infection the titer is actually 10E10 PFU/mL. Ordering info. can be obtained from the following people:
The tech doing the ordering is: Kate Ramsey Research Assistant I University of Iowa Gene Transfer Vector Core 221 EMRB Iowa City, IA 52242 phone: (319) 335-6726 fax: (319) 353-5572 kate-ramsey@uiowa.edu
The director of the facility: Beverly L. Davidson, Ph.D. Roy J. Carver Assoc Prof Internal Medicine Assoc Prof in Neurology and Physiology & Biophysics Director, Gene Transfer Vector Core 200 EMRB University of Iowa College of Medicine Iowa City, IA 52242 (319) 353-5511 beverly-davidson@uiowa.edu
Protocol:
Formation of AdCre:CaPi co-precipitates:
We typically use 2.5 x 10E7 PFU as our standard dose. You can change the titer by altering the amount of virus used, and adjusting the volume of MEM accordingly in order to give a final volume of 125 uL. When less virus is needed, we normally dilute it in MEM and then use 2.5 uL.
Add 2.5 uL of AdCre to 121.9 uL of MEM and mix well. Next add .6 uL of CaCl2 and mix well. Let this mixture sit for ~20 minutes prior to use.
Infection:
1) Anesthetize the mice with avertin, making sure that the mice are fully anesthetized and have no reaction to pain. I test this by pinching their toe with a pair of forceps. If they are not fully anesthetized they will shake their head scattering the virus. 2) Using a protein gel loading tip, take 62.5 uL (half) of the virus mixture and place the pipet tip at the opening of one nostril. It won't fit into the nostril, but that's fine. Slowly expel the virus solution from the tip. Be sure the mouse is indeed inhaling the drop that is forming. If not, stop expelling and wait until it inhales what is there. 3) Let the mouse recover for 5-10 minutes. It will cough for a while after inhaling the virus. Wait until its breathing has returned to normal. 4) Repeat with the remaining 62.5 uL of virus mixture.
Note*- Occasionally, mice don't cope with the avertin very well. It depresses their temperature and breathing rate. If you notice a mouse that is breathing really slowly or shivering, filling a large glove with hot water and placing the mouse on the glove often helps it to recover & survive.
上一篇:Making collagen solution from lyophilized rat tail collagen鼠尾制备胶原蛋白 下一篇:实验动物的给药途径和方法及药量计算方法 |