#181
Posted 22 December 2010 - 12:13 AM
Here is the proposal on Google Docs.
Share and enjoy!
Nason
#182
Posted 27 December 2010 - 07:01 PM
Rather, I have pointed out that I am not in the area, and feel that any "oversight" worthy of the name is not possible remotely.
I have offered to make a statement that in my judgement there is no risk of unethical on incompetent behavior on Nason's part. I hereby make that statement.
This should not be construed as agreement to oversee the project in any way other than making the above statement.
However, if anyone has specific requests for me about what else I could do, I will be glad to hear them out.
Can we count you in to review Nasons bookwork once a month? I can see what you mean in that remote oversight might not be oversight at all. I agree with your statement that there is little to no risk of unethical or incompetent behavior. Do or dont call it oversight though, part of the idea would be to get more eyes on the data for potential (probable) added perspective.
#183
Posted 28 December 2010 - 03:52 AM
#184
Posted 16 January 2011 - 10:48 PM
Nason
#185
Posted 26 January 2011 - 08:43 PM
#186
Posted 11 February 2011 - 03:53 PM
Nason
#187
Posted 13 February 2011 - 11:16 AM
#188
Posted 16 March 2011 - 01:55 PM
Nason
#189
Posted 21 March 2011 - 07:13 PM
Lab Notes on Google Docs
3-21-2011, 2:00 PM
Started age-synchronized plates:
2 plates of N2, 40+ eggs each
2 plates of DA1116, 40+ eggs each
#190
Posted 28 March 2011 - 09:20 PM
#191
Posted 28 March 2011 - 09:26 PM
Edited by Mind, 28 March 2011 - 09:35 PM.
#192
Posted 28 March 2011 - 09:30 PM
#193
Posted 30 March 2011 - 06:01 PM
Here's the latest update on what's going on in the lab:
Most of the eggs on the DA1116 plates were nonviable. I’ve been collecting all viable worms of this strain for breeding purposes. I went back and read up on the genetics a little bit, and the first few generations will have large numbers of nonviable offspring, since they are outcrossed with wild type and still have lots of homozygocity in many deleterious, recessive alleles. The outcrossing is designed to provide genetic diversity while keeping the desired traits. In a nutshell that means it will take awhile longer to get usable numbers of DA1116 worms. I will probably begin an N2-only experiment in the next few days, since I have the extra time.
#194
Posted 04 April 2011 - 10:25 PM
#195
Posted 05 April 2011 - 01:08 AM
#196
Posted 06 April 2011 - 01:37 AM
The fluorescence scope may or may not be purchased for this project, depending on how our financial situation pans out on this end. It may end up being budgeted as part of a future project proposal instead; but we can cross that bridge when we get there.
I'll let everyone know as soon as the worm zapping begins.
Nason
#197
Posted 11 April 2011 - 10:10 PM
Edited by Mind, 11 April 2011 - 10:11 PM.
#198
Posted 22 April 2011 - 06:53 AM
Edited by Mind, 22 April 2011 - 06:54 AM.
#199
Posted 26 April 2011 - 07:08 PM
Nason
#200
Posted 26 April 2011 - 10:17 PM
It is possible that well tissue has chiral molecular tendencies whereas unwell tissue might have a different profile That strengthens the idea that laser modification of molecules could benefit tissue longevity
Reading Wikipedia suggests lipofuscin is a group of molecules rather than a specific I think many of these are chirally or possible circular polarizationally addressable
A super twisty beam of light has been created that can distinguish between left and right-handed molecules with unprecedented precision.
http://www.newscient...from-right.html
#201
Posted 11 May 2011 - 01:00 AM
#202
Posted 11 May 2011 - 01:00 AM
#203
Posted 21 June 2011 - 07:49 PM
I chunked worms today - I plan to get Exp 1 restarted this week...
So how are things going now? I cant wait to find out how each stage turns out.
#204
Posted 10 August 2011 - 09:14 PM
Nason
#205
Posted 01 September 2011 - 04:16 PM
#206
Posted 02 September 2011 - 09:34 AM
In case you still try from time to time: I have worked with C elegans a little, I'm really not a pro but here are some tips against contamination: in a worm lab usually the microscope is on a glass surface that can be cleaned with alcohol very regularly, and on that glass surface, 5 to 10 cm away from the microscope, one uses a candle (oil-based candle generally, as it is rechargeable) that is lighted during worm manipulation (= opening the plates, sterilizing the metal stick in the flamme, transfering the worms from an old plate to a new plate, closing the new plate).Do you need specific contacts for people who know specific techniques that you are a bit discovering?
Have you used similar techniques? Briefly, how have you prepared the plates? (agar, feeding bacteria)
In case you don't try from time to time: are you going to send your equipment to a worm lab that might try the laser ablation of lipofuscin? Could it be a good idea to send it to someone from LongeCity willing to try his hands on C elegans, at home? If so, how much would it cost per month for that person to try to set up some lifespan experiment? Have you been in contact with people willing to try at home?
From far your idea of laser pulse to potentially increase C elegans lifespan still seems very interesting, mechanistically speaking at least.
Edited by AgeVivo, 02 September 2011 - 09:36 AM.
#207
Posted 29 October 2011 - 10:57 AM
What laser will be used - wavelength, power, jauls per squaire centimeters
Over what cells / tissues / organs / or the whole body
Will it be over people or over animals, and which exactly animals
Do You have a methodics for the laser procedures or this has to be determined
Where will You get lipofuscine
I am asking that, because I have an access to two surgical lasers and two low power lasers for low energy treatment, and since I work with human individuals, I may eventually be of service and thus to save You some dollars by doing some of the needed things cheeper. Also, I know of a relatively cheap animal experimentation center, that will allow me to work with the animals and thus saving some money if the research must be done on animals. I am certified from the American laser association of laser dentistry and from the World Federation of Laser Dentistry, that allows me to use lasers for medical uses. I don't mind not to take money for my work and only for consumatives and for the tax for the usage of the lasers and taxes for other needs of the research.
#208
Posted 29 October 2011 - 12:46 PM
S123 talked to a professor at his University in Belgium and the professor said laser ablation would never work because there are cells in the gut that will absorb the same laser light that is absorbed by lipofuscin, and the gut cells will be destroyed (this is the condensed cliif-notes version) and the worms will die. Considering that when Nason actually did some minor work on this project when he was at the SENS RC, and the worms did not immediately die, I have not yet written laser ablation off 100%.
Seivtcho, you should talk to S123 to get the full explanation why his professor thinks the project would not work. Also, thanks so much for offering your expertise. If something does go forward with this, make sure to stay in touch with AgeVivo for tips on raising c.elegans. In fact, we have several members who have done research with worms that would be able to help you get set up.
Edited by Mind, 29 October 2011 - 12:49 PM.
#209
Posted 29 October 2011 - 12:55 PM
It is really possible the power of the laser needed to destroy the lipofuscin to be
powerful enough to destroy the cell itself.
I'll try to do some prelimenary research (without being sponsored) to see if with
the two high power and the two low power lasers actually are cappable to destroy
lipofuscin and if the power neede is close to the ablation of the whole cell, then this
idea has a really big problem.
#210
Posted 29 October 2011 - 03:37 PM
S123 talked to a professor at his University in Belgium and the professor said laser ablation would never work because there are cells in the gut that will absorb the same laser light that is absorbed by lipofuscin, and the gut cells will be destroyed (this is the condensed cliif-notes version) and the worms will die. Considering that when Nason actually did some minor work on this project when he was at the SENS RC, and the worms did not immediately die, I have not yet written laser ablation off 100%.
His main point was that these fluorescent granules are NOT lipofuscin. He recently tested them (publication is still in progress) and found that they were NOT composed of lipofuscin.
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