I have heard of people putting the peice of tissue straight to grain. I remember hearing that it takes quite a while for it to start colonizing however sine the points of contact are very small. Straight to liquid solution would be better. Dont forget to "mince" the peice of tissue (kinda chop it up with the razor) before dropping it in. Good luck!
How are those 20 jars doin'?
Vinegar : re DirtyCloneAttempt
Started By
smegma
, Mar 04 2005 08:33 AM
27 replies to this topic
#22
smegma
-
- Free Member
- 484 posts
Mycotopiate
Posted 07 March 2005 - 10:25 AM
I have heard of people putting the peice of tissue straight to grain. I remember hearing that it takes quite a while for it to start colonizing however sine the points of contact are very small. Straight to liquid solution would be better. Dont forget to "mince" the peice of tissue (kinda chop it up with the razor) before dropping it in. Good luck!
How are those 20 jars doin'?
All are showing SOLID to OK growth.
None are showing VISIBLE contams SO FAR.
Hopefully I got lucky.
FWIW - The Karo jars I did with the same clone juice still look clean and are growing VERY fast. Again, hopefully luck is on my side.
I am still working on this digital camera thing... soon my friends.
#23
sandman
-
- Honorary Former Staff
- 3,814 posts
BACTERIA!
Posted 07 March 2005 - 10:29 AM
yes, there have indeed been people that succeeded with the h202/blender tek. Like 1 or 2 that I have heard of at least. Luck may be on your side! I sure hope it works out man. Got a camera?
#24
smegma
-
- Free Member
- 484 posts
Mycotopiate
Posted 07 March 2005 - 10:35 AM
yes, there have indeed been people that succeeded with the h202/blender tek. Like 1 or 2 that I have heard of at least. Luck may be on your side! I sure hope it works out man. Got a camera?
Just to clarify for anyone else following this, I did NOT blend in H2O2, I dipped the donor tissue in it for around 30 sec. then dropped in 100ml sterilized, distilled H2O with the metal blender parts and gasket sterilized with it.
Don't know if this helped or hurt me yet.
My main issue is that I did not take a clean core sample and some of the outter "skin" of the donor chunk got blenderized.
#25
Hippie3
-
- Founders
-
- 40,642 posts
DUNG DEALER
Posted 08 March 2005 - 10:03 AM
None are showing VISIBLE contams
one rarely sees visible contams in liquid culture
but they're there....
#26
smegma
-
- Free Member
- 484 posts
Mycotopiate
Posted 08 March 2005 - 01:55 PM
Update: One jar "somehow" has wetspot.
5% gone...
Also lost 4 trays of Texas Oysters to trich. I am assuming the rest of the trays in the Martha will have it right soon. At least I got 1 flush from all trays and 2 from some. :(
5% gone...
Also lost 4 trays of Texas Oysters to trich. I am assuming the rest of the trays in the Martha will have it right soon. At least I got 1 flush from all trays and 2 from some. :(
#27
Hippie3
-
- Founders
-
- 40,642 posts
DUNG DEALER
Posted 22 April 2005 - 02:01 PM
how'd this end up anyway smeg ?
#28
Lazlo
-
- Honorary Former Staff
- 7,620 posts
old hand
Posted 23 April 2005 - 12:35 AM
If you don't mind me interupting. Mine came out like jewel. :D
