48,those are dead
49,the others dunked after full colonization
Texan Isolates
Started By
fucgubarn
, Jan 01 2006 05:41 AM
39 replies to this topic
#21
fucgubarn
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Posted 03 January 2006 - 03:33 PM
47,liquid to white rice with horse poo and colonizing
48,those are dead
49,the others dunked after full colonization
48,those are dead
49,the others dunked after full colonization
#22
fucgubarn
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Posted 03 January 2006 - 03:34 PM
at this particular stage i fucked up again,there was noone to care for them,what a waste
#23
Guest_dial8_*
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Posted 03 January 2006 - 03:36 PM
Eeeeeek. Sorry to hear that.
#24
fucgubarn
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Posted 03 January 2006 - 03:36 PM
50,51,52
some of the clones fruting (1&2 flush)
some of the clones fruting (1&2 flush)
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#25
fucgubarn
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Posted 03 January 2006 - 03:39 PM
53,54,55
back to clone No 5,the mushroom from which mycelia grew produced mushrooms again,so some of those were taken and placed on fresh PDA,
from this comes the first post in this thread,
it is a clone from a clone straight from the petri!
:)
back to clone No 5,the mushroom from which mycelia grew produced mushrooms again,so some of those were taken and placed on fresh PDA,
from this comes the first post in this thread,
it is a clone from a clone straight from the petri!
:)
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#26
fucgubarn
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Posted 03 January 2006 - 03:57 PM
well,that is about all,
have saved little liquids of every isolate and clone and hope in the future will have the opportunity to test them :)
hope you enjoy the ride with me :)
have saved little liquids of every isolate and clone and hope in the future will have the opportunity to test them :)
hope you enjoy the ride with me :)
#27
siam_jim
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Posted 03 January 2006 - 03:59 PM
cool fbarn...really like how you show what you did with isolation from the plates..very helpful
thanks
peace
siam
thanks
peace
siam
#28
MurCurY
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Posted 03 January 2006 - 04:42 PM
your pda is so clear.,.,,what recipe are you using and procedure for autoclaving? I'm using MEA and tried pda but both times it always clouds a bit on the bottom.
#29
PeopleCanFly
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Posted 03 January 2006 - 06:01 PM
nice thread :)
interesting to see the separation lines between the substrains in the petris
interesting to see the separation lines between the substrains in the petris
#30
waylitjim
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Posted 03 January 2006 - 06:57 PM
Great thread! Very well documented, and informative.
Archive Material > copied to the Vaults > Agar
Archive Material > copied to the Vaults > Agar
#31
Guest_pcsillypj_*
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Posted 04 January 2006 - 02:40 AM
awsome work...you always put
up good stuff...thnx for sharin mang..;)
up good stuff...thnx for sharin mang..;)
#32
Guest_xxxsevxxx_*
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Posted 04 January 2006 - 04:55 AM
i like the way you put 4 isolates onto one plate , thats saves money in the long run plus its more effective imo . i do the exact same thing . nice work up .
later VII
later VII
#33
Guest_dial8_*
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Posted 04 January 2006 - 09:24 AM
I was just about to archive this thread myself. :)
Again, great work, barn!
Again, great work, barn!
Great thread! Very well documented, and informative.
Archive Material > copied to the Vaults > Agar
#34
fucgubarn
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Posted 07 January 2006 - 05:21 AM
'your pda is so clear.,.,,what recipe are you using and procedure for autoclaving? I'm using MEA and tried pda but both times it always clouds a bit on the bottom.'
do not remember now how much PDA powder for a litter of water it was,will check and let you know,
the autoclaving is supposed to be for 15 minutes but i prefer 10 to 13 minutes with a risk ofcourse,
and if you want clear, pour the agar very thin in the petridish
do not remember now how much PDA powder for a litter of water it was,will check and let you know,
the autoclaving is supposed to be for 15 minutes but i prefer 10 to 13 minutes with a risk ofcourse,
and if you want clear, pour the agar very thin in the petridish
#35
fucgubarn
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Posted 07 January 2006 - 07:50 AM
the same on two cakes,not bad also :)
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#36
Guest_pcsillypj_*
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Posted 07 January 2006 - 10:29 AM
nice flush...have you tried this texan strain
on bulk yet..?
on bulk yet..?
#37
fucgubarn
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Posted 07 January 2006 - 02:44 PM
:)
gues by bulk you mean strawlog or something big?
no,haven't tryed anything different than what you see,besides this is already too much for a lone searcher :)
gues by bulk you mean strawlog or something big?
no,haven't tryed anything different than what you see,besides this is already too much for a lone searcher :)
#38
doobydoobydoo
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Posted 07 January 2006 - 06:52 PM
Very impressive post fucgubarn. Thanks for sharing with us.
:kewl: :bow:
:kewl: :bow:
#39
Guest_xxxsevxxx_*
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Posted 08 January 2006 - 12:00 AM
pouring agar to thin causes it to stick to the sides of jars when trasferd to grain . it is a good way to pour them when your doing agar to agar tranfers . pda is a good recipe for everybody cause all the ingriedents or easy to get .
i like 300gm of taters in 1000ml of h2o boiled for a hour thenstrained threw cheese cloth . added to 20 gm agar and 10 gm dextrose . makes for a beautifull clear agar everytime . also i go for 40-45 min pc at 15pci anything less seems to have a 10-20% contam rate . anything over 45 min at 15pci causes the media sugars to carmalize .
later VII
i like 300gm of taters in 1000ml of h2o boiled for a hour thenstrained threw cheese cloth . added to 20 gm agar and 10 gm dextrose . makes for a beautifull clear agar everytime . also i go for 40-45 min pc at 15pci anything less seems to have a 10-20% contam rate . anything over 45 min at 15pci causes the media sugars to carmalize .
later VII
#40
fucgubarn
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Posted 09 January 2006 - 01:20 AM
:) second flush,
after the first flush the block was washed under running water,drained and put back in the fruiting chaimber,
no dunking,no caseing and not bad for a second flush also :):)
after the first flush the block was washed under running water,drained and put back in the fruiting chaimber,
no dunking,no caseing and not bad for a second flush also :):)
