The Journal of Visualized Experiments (JoVE) is a peer reviewed, PubMed-indexed video journal. Our mission is to increase the productivity of scientific research.

Recommend to Librarian

Automatic Translation

This translation into Turkish was automatically generated through Google Translate.
English Version | Other Languages

 JoVE General

Flaş Dondurma ve E12.5 Fare Beyin Cryosectioning

,

Department of Developmental and Cell Biology, University of California, Irvine (UCI)

You must be subscribed to JoVE to access this content.

This article is a part of   JoVE General. If you think this article would be useful for your research, please recommend JoVE to your institution's librarian.

Recommend JoVE to Your Librarian

Current Access Through Your IP Address

You do not have access to any JoVE content through your current IP address.

IP: 23.22.252.150, User IP: 23.22.252.150, User IP Hex: 387382422

Current Access Through Your Registered Email Address

You aren't signed into JoVE. If your institution subscribes to JoVE, please or create an account with your institutional email address to access this content.

 

Video Article Chapters

Cite this Article: Flaş Dondurma ve E12.5 Fare Beyin Cryosectioning

Currle, D. S., Monuki, E. S. Flash Freezing and Cryosectioning E12.5 Mouse Brain. J. Vis. Exp. (4), e198, doi:10.3791/198 (2007).

Protocol: Flaş Dondurma ve E12.5 Fare Beyin Cryosectioning

  1. Istenilen zaman için PBS içinde% 4 paraformaldehid doku sabitleyin.
  2. Sakkaroz demlenmeye doku (cryoprotection)
    1. 2059 tüp PBS w / v% 30 sakaroz çözeltisini olun.
    2. PBS içinde doku 3x sallanan ile durulayın (~ 5 dk).
    3. % 30 sukroz solüsyonu yerleştirin doku. Doku lavabo olmaz.
    4. Batırdı, 4 ° C gecede kadar veya doku yerleştirin.
  3. Etiket uygun boyutu, bilgi ve yönlendirme ile cryomold.
  4. (Baloncuklar önlemek) OCT ile cryomold doldurun.
  5. Ekim banyo ve OCT ile kat doku transferi
  6. Cryomold OCT doku aktarın.
  7. Orient mikroskop altında doku.
  8. Plastik Petri kabı içine sıvı nitrojen dökün.
  9. Hızlı ve dikkatli bir şekilde azot içine cryomold doku düşüktür. (Üst cryomold daldırın.)
  10. OCT beyaz katı olduğunda, -80 ° C derin dondurucu saklama için dondurulmuş doku içine yerleştirin.
  11. ~ 20 ° C arası en az 30 dakika süreyle doku dengelenmesi. önce kesit.

Subscription Required. Please recommend JoVE to your librarian.

Disclosures: Flaş Dondurma ve E12.5 Fare Beyin Cryosectioning

Materials: Flaş Dondurma ve E12.5 Fare Beyin Cryosectioning

Name Company Catalog Number Comments
Tissue-Tek Cryomold Ted Pella, Inc. 27181
O.C.T. Ted Pella, Inc. 27050
Sucrose solution 30% sucrose solution in PBS w/v
paraformaldehyde 4% paraformaldehyde in PBS

Ask the Author: Flaş Dondurma ve E12.5 Fare Beyin Cryosectioning

11 Comments

This is one application almost all labs use either for some immuno or insitu experiments and seeing the procedure to this level of detail, I think will enable people to achieve better results with less trial and error.

1

Reply

Posted by: AnonymousJuly 6, 2007, 9:41 PM

awesome

2

Reply

Posted by: AnonymousJuly 18, 2007, 10:42 PM

great! thanks a lot.

3

Reply

Posted by: AnonymousSeptember 25, 2007, 2:01 PM

The presentation was wonderful and I learned more from this video than what my conservative collegues in the lab explained me.

Thanks a lot

4

Reply

Posted by: #3May 29, 2008, 4:58 PM

I'm having some issues washing off the OCT with BPS from the slides. - I did some retrograde staining of peripheral nerves and I cross sectioned the spinal cord of mice-
the problem is that as I add PBS drop by drop, or as I place the slide into plate with PBS liquid layer my samples keep falling off the slide..
Any ideas? because I'm running out of them
e-mail me please: jccs_85@hotmail.com

5

Reply

Posted by: CarlosJuly 2, 2009, 9:35 AM

This is a great video demonstrating how to cryosection brain that will certainly help me with my future studies. I was wondering, is it always necessary and/or desirable to fix the brain with paraformaldahyde prior to cryoprotecting with sucrose? I seem to recall hearing for some applications, such as IHC, paraformaldahyde fixation may disrupt the antibody/antigen interaction for certain antibodies used. Would someone be willing to comment on this?

6

Reply

Posted by: Shelly July 8, 2009, 8:18 PM

send me an e-mail at spencer.currle@stjude.com

6.1

Reply

Posted by: AnonymousJuly 9, 2009, 10:32 AM

This is a great video demonstrating how to cryosection brain that will certainly help me with my future studies. I was wondering, is it always necessary and/or desirable to fix the brain with paraformaldahyde prior to cryoprotecting with sucrose? I seem to recall hearing for some applications, such as IHC, paraformaldahyde fixation may disrupt the antibody/antigen interaction for certain antibodies used. Would someone be willing to comment on this?

7

Reply

Posted by: Shelly July 9, 2009, 4:42 PM

I have the same question as Shelly. Some applications require fixing tissue after cryosectioning. Do you have a protocol for this?

8

Reply

Posted by: SueSeptember 20, 2010, 3:03 PM

Hello, my name is Xiang Weng, I am a student in Long Island University, department of Biomedical Science, I want to learn cryosectioning, thank you.

9

Reply

Posted by: Xiang W.October 5, 2012, 11:24 AM

Hello, my name is Xiang Weng, I am a student in Long Island University, department of Biomedical Science, I want to learn cryosectioning, thank you.

10

Reply

Posted by: Xiang W.October 5, 2012, 11:35 AM

I have looked all over for the answer but I cannot find it: How many seconds (or how long in general) does it take to flash freeze a serum lab sample using ethanol and dried ice? Thanks!

11

Reply

Posted by: Michele K.April 3, 2013, 8:51 PM

Post a Question / Comment / Request

You must be signed in to post a comment. Please or create an account.

Waiting
simple hit counter