Scientist Solutions: Life Science Discussions
 Refer a Friend    Link To Us    Bookmark Us       

      
 » Home » Cell Based Assays / Tissue Culture - NEW! » Transfection and Assay Development » G2 Phase Block with Hoechst 33342 for Cell Synchronization

Other Topics
11/22/2008 04:29 PM
Blasticidine gene cDNA
11/20/2008 12:49 PM
transfection of HEK293 ce ...
11/15/2008 10:15 AM
MTT assay
8/6/2008 10:37 AM
What is lipofectamine 200 ...
7/30/2008 10:32 AM
transfection doubts
7/29/2008 02:17 AM
Separation of nuclei, cyt ...
6/30/2008 11:49 AM
calium ion estimation
6/18/2008 10:08 AM
Benfotiamine
5/24/2008 04:24 AM
comet assay
3/24/2008 09:45 AM
karyotyping
3/13/2008 02:12 PM
does H2O2 interfere with ...
2/28/2008 07:44 PM
ATP depletion
2/18/2008 09:19 AM
nEUTARL RED ASSAY
2/3/2008 04:13 AM
In vitro Ubiquitination a ...
2/3/2008 04:27 AM
In-vitro Ubiquitination
12/21/2007 08:41 PM
Botulinum toxin A in MCF- ...
6/8/2007 03:48 PM
Tissue digestion for expl ...
4/20/2007 07:03 AM
comet assay
4/19/2007 01:05 PM
plant comet assay
3/15/2007 06:28 PM
Amaxa
2/28/2007 07:54 PM
Q10 on MCF-7
2/10/2007 04:12 PM
drug that block exocytosi ...
11/29/2006 12:08 AM
Lysosome isolation from R ...
11/13/2006 12:22 AM
Fugene Transfection Proto ...
10/19/2006 10:19 PM
subcellu;ar fractionation
7/6/2006 09:53 PM
Easy "no ethanol" cell cy ...
5/15/2006 02:54 PM
Methods for Enhancing Lip ...
1/29/2006 08:07 PM
Desferal - DFO - Administ ...
1/23/2006 04:18 PM
Ion channel screening by ...
1/18/2006 11:08 PM
Nuclear HeLa extract
Subscribet to topic
Add Reply  Add New Topic  Add New Poll
bottom of page RSS Feed 

Topic Feed

 

G2 Phase Block with Hoechst 33342 for Cell Synchronization

 [View Printable]
trook

Frog Laureate

See
Similar
Scientists





Group: Member
Posts: 337
Joined: Jan 17, 2005







 Send a personal messsage to trook Reply with a quote from this post Go to the top of the page


Please find the following protocol:

G2 Phase Block with Hoechst 33342 for Cell Synchronization


Procedure:

1. Presynchronize cells at G0 by serum starvation. Add Low Serum Medium to cells at 70% confluency and allow cells to grow in this medium for 2 days. he amounts of Aphidicolin and Hoechst (and the times of exposure) may vary depending on the cell line you are working with. Also, different cell lines use different media, thus "Complete Medium" may be different for your cell line than what is described here. This protocol was developed to work with Swiss 3T3 Cells.

2. Stimulate the cells to reenter the cell cycle by replacing the Low Serum Medium with Complete Medium containing 4 μg/ml Aphidicolin and allow the cells to grow in this medium for 14 hr.

3. Alternatively, add Aphidicolin to exponentially growing cells to 4 μg/ml for 24 hr.

4. Remove the Aphidicolin-Containing Medium and rinse the cell culture with 10 ml PBS. Replace PBS with Complete Medium with Hoechst 33342. Allow the cells to grow for 12 hr in this medium. The actual time may vary depending on the cell line used and should be determined empirically.

5. Remove the Hoechst-containing medium and rinse the cells with PBS. Replace the PBS with Complete Medium. The cells should now be synchronized in the cell cycle. This can be easily checked by Propidium Iodide staining followed by flow cytometry.


Solutions:

Complete Medium with Hoechst 33342
Dulbecco's Modified Eagle's Medium
0.5 to 1 μg/ml Hoechst 33342
(should be determined empirically for each cell line)
100 Units/ml Penicillin
100 μg/ml Streptomycin
10% (v/v) Calf Serum

Complete Medium with Aphidicolin
Dulbecco's Modified Eagle's Medium
100 Units/ml Penicillin
4 μg/ml Aphidicolin
100 μg/ml Streptomycin
10% (v/v) Calf Serum

Low Serum Medium
20 mM HEPES
0.5% (v/v) Calf Sserum
100 Units/ml Penicillin
100 μg/ml Streptomycin
DMEM

PBS
pH 7.2
2.7 mM KCl
4.3 mM Sodium Phosphate Dibasic (Na2HPO4)
1.8 mM Potassium Phosphate Monobasic (KH2PO4)
137 mM NaCl

Complete Medium
100 Units/ml Penicillin
Dulbecco's Modified Eagle's Medium (DMEM)
100 μg/ml Streptomycin
10% (v/v) Calf Serum


Bioreagents and Chemicals:

DMSO
Potassium Phosphate, Monobasic
Sodium Phosphate, Dibasic
Potassium Chloride
Sodium Chloride
Streptomycin
Penicillin
Hoechst 33342
Aphidicolin
Calf Serum
Dulbecco's Modified Eagle's Medium (DMEM)
Propidium Iodide


Reference Link:

http://www.bio.com/protocolstools/protocol.jhtml?id=p9005

.........................

 Posted Dec 01, 2006, 18:37 PM
gurunatc

Frog Egg

See
Similar
Scientists





Group: Member
Posts: 1
Joined: Nov 06, 2007







 Send a personal messsage to gurunatc Reply with a quote from this post Go to the top of the page

Hi,
I was wondering what percentage of cells hare synchronized ater the Hoechst addition?
Also if I were to use NIH3T3 and Hydroxyurea, what changes would you suggest be made?

gurunatc



trook said:

Please find the following protocol:

G2 Phase Block with Hoechst 33342 for Cell Synchronization


Procedure:

1. Presynchronize cells at G0 by serum starvation. Add Low Serum Medium to cells at 70% confluency and allow cells to grow in this medium for 2 days. he amounts of Aphidicolin and Hoechst (and the times of exposure) may vary depending on the cell line you are working with. Also, different cell lines use different media, thus "Complete Medium" may be different for your cell line than what is described here. This protocol was developed to work with Swiss 3T3 Cells.

2. Stimulate the cells to reenter the cell cycle by replacing the Low Serum Medium with Complete Medium containing 4 μg/ml Aphidicolin and allow the cells to grow in this medium for 14 hr.

3. Alternatively, add Aphidicolin to exponentially growing cells to 4 μg/ml for 24 hr.

4. Remove the Aphidicolin-Containing Medium and rinse the cell culture with 10 ml PBS. Replace PBS with Complete Medium with Hoechst 33342. Allow the cells to grow for 12 hr in this medium. The actual time may vary depending on the cell line used and should be determined empirically.

5. Remove the Hoechst-containing medium and rinse the cells with PBS. Replace the PBS with Complete Medium. The cells should now be synchronized in the cell cycle. This can be easily checked by Propidium Iodide staining followed by flow cytometry.


Solutions:

Complete Medium with Hoechst 33342
Dulbecco's Modified Eagle's Medium
0.5 to 1 μg/ml Hoechst 33342
(should be determined empirically for each cell line)
100 Units/ml Penicillin
100 μg/ml Streptomycin
10% (v/v) Calf Serum

Complete Medium with Aphidicolin
Dulbecco's Modified Eagle's Medium
100 Units/ml Penicillin
4 μg/ml Aphidicolin
100 μg/ml Streptomycin
10% (v/v) Calf Serum

Low Serum Medium
20 mM HEPES
0.5% (v/v) Calf Sserum
100 Units/ml Penicillin
100 μg/ml Streptomycin
DMEM

PBS
pH 7.2
2.7 mM KCl
4.3 mM Sodium Phosphate Dibasic (Na2HPO4)
1.8 mM Potassium Phosphate Monobasic (KH2PO4)
137 mM NaCl

Complete Medium
100 Units/ml Penicillin
Dulbecco's Modified Eagle's Medium (DMEM)
100 μg/ml Streptomycin
10% (v/v) Calf Serum


Bioreagents and Chemicals:

DMSO
Potassium Phosphate, Monobasic
Sodium Phosphate, Dibasic
Potassium Chloride
Sodium Chloride
Streptomycin
Penicillin
Hoechst 33342
Aphidicolin
Calf Serum
Dulbecco's Modified Eagle's Medium (DMEM)
Propidium Iodide


Reference Link:

http://www.bio.com/protocolstools/protocol.jhtml?id=p9005

.........................

Posted Nov 06, 2007, 17:57 PM
Sum

Frog Egg

See
Similar
Scientists





Group: Member
Posts: 9
Joined: Oct 22, 2007







 Send a personal messsage to Sum Reply with a quote from this post Go to the top of the page

A very stupid question.. Addition of the Hoechst 33342 in culture alters the radioresistance of the cells considerably, so won't this protocol change the nature of the cells one is working with ?
But I suppose that's only in the case of cancer-therapy studies that one cannot follow this protocol.

.........................

Posted Jan 14, 2008, 4:04 AM
top of page Add Reply  Add New Topic  Add New Poll

Forum Jump