I wonder if you'd be open to making a short video guide about labelling, would love to get your perspective and process to go along with this great info about breeding labelling.
going through agar trials now ;from some dried fruits its been a real crapshoot but I have - what i believe -to be one clean monokaryon from a random cube, i'm trying to get a PE swab to take and possibly get a clean pe mono to breed with the other cube sample i'm new to this so i have no gear just checking my plates daily to see if i can get another clean transfer.
Can you take two different Monokaryons from the same fungi to create a new fungi forever or will this loop degrade over time like cloning does? In other terms: Do you regulary _need_ new gen information (Monokaryons) from other fungi to keep your fungi gens healthy? Or can you keep a fungi alive with itself (without having to store the original cultures in culture slants)?
Hi Ed , I just made a Glass Petri Dish out of a Beer Bottle Bottom and it took Me about 30 minutes. Cuttin' the Glass took a Score & about 1 minute of boiling and a split second dip in Ice water and the other 29 minutes was Sanding her Smooth 😎 I figure every one of these I make I save 75 Sackarooski's LoL Yeeee Haw
I just woke up, but I get updates on your videos so I know when u drop a video, love all them, but I especially pay attention to the breeding videos, I don’t have a scope yet, but I am attempting to do the more ghetto version of this for now, just can’t check for clamps yet, I also don’t have high hopes for this experiment but still fun none the less while I’m waiting on being able to purchase the scope I want! I just bought a hood so I gotta wait a little bit!
I think you could do it with two tomentose monos, but not all the monos look so fluffy like the ones in this video. Sometimes, they're more on the pseudo-rhizomorphic side. It's a lot of work to do just to find out later one of the monos was a dikaryon. Then there's the Buller phenomenon, but that's another video...
@@edwardgrand right I’m only doing a couple plates just to FAFO lol but I do plan on getting a scope soon, & that’s what I was thinking as well, but I’ve been looking at a lot of exotic stuff lately these starry night apes are real tomentose looking plus like the shakti & a couple others, but definitely highly respect you and your work! I love watching your videos u really break it down in such an easy digestible way, keep that shit coming I can’t wait to share my results with u here sooner than later, & Man U know what? I wish we could cross stuff like Omni & enigma, I got these 2 beautiful mutants that I’d love to cross but oh well I’ll just appreciate there beauty anyhow, mush love, mush respect ✊
SRYA recipe 3% Sticky Rice powder/flour 2% Agar 0.1% Baker's or Nutritional Yeast Food Coloring (if desired) FOR 500 ml Total volume 15 g sticky rice powder 10 g Agar 0.5 g Baker's Yeast Food Coloring or 1g charcoal if desired. 500 ml tap water - Should make between 20-25 standard size plates.
@@edwardgrandthank you so much . I try to be like everyone else but to me being perfectly sterile and then putting in a stagnant box then into a stagnant closest doesn't make sense to me. Why not do the opposite? Start dirty then put in a prefect atmosphere that you make?
@@gangsterbuilder Because we want to grow one and only one species. Same idea behind planting corn or wheat. We have to prep the field, otherwise we will get a random mix of organisms.
I wonder if you'd be open to making a short video guide about labelling, would love to get your perspective and process to go along with this great info about breeding labelling.
going through agar trials now ;from some dried fruits its been a real crapshoot but I have - what i believe -to be one clean monokaryon from a random cube, i'm trying to get a PE swab to take and possibly get a clean pe mono to breed with the other cube sample i'm new to this so i have no gear just checking my plates daily to see if i can get another clean transfer.
"Here I've got a Dancing.. Uh Tomentose." 😅
Not sure where broski was going with that😂
Probably talking about dancing tiger I hope😂
them pepto bismuth pink plates r cool looking
Ed, you are a great mixture of a human! I'm learning and laughing lots going through all your videos and listening to you on the @mycogeeky podcasts.
that last plate was beautiful!
Man you are crushing content. Love it! Thanks for all your knowledge!
Good morning Ed. Good night Ed! Mushlove
Can you take two different Monokaryons from the same fungi to create a new fungi forever or will this loop degrade over time like cloning does? In other terms: Do you regulary _need_ new gen information (Monokaryons) from other fungi to keep your fungi gens healthy? Or can you keep a fungi alive with itself (without having to store the original cultures in culture slants)?
Hi Ed , I just made a Glass Petri Dish out of a Beer Bottle Bottom and it took Me about 30 minutes. Cuttin' the Glass took a Score & about 1 minute of boiling and a split second dip in Ice water and the other 29 minutes was Sanding her Smooth 😎
I figure every one of these I make I save 75 Sackarooski's LoL
Yeeee Haw
I was able to isolate one by just tapping the tip of my scalpel on a spore print, then tapping it on agar.
Missing your vids Mr Grand! Hope you are well. Looking forward to the next one.
I'll make some more soon. Been busy with work.
'I Love the Smell of ISO in the Morning', and Ed videos! ❤ ( and I like to shower with ISO! ) 💙
Thanks for the dope video! Do you think youll do a video in the future about dedikaryotization?
I just woke up, but I get updates on your videos so I know when u drop a video, love all them, but I especially pay attention to the breeding videos, I don’t have a scope yet, but I am attempting to do the more ghetto version of this for now, just can’t check for clamps yet, I also don’t have high hopes for this experiment but still fun none the less while I’m waiting on being able to purchase the scope I want! I just bought a hood so I gotta wait a little bit!
I think you could do it with two tomentose monos, but not all the monos look so fluffy like the ones in this video. Sometimes, they're more on the pseudo-rhizomorphic side. It's a lot of work to do just to find out later one of the monos was a dikaryon. Then there's the Buller phenomenon, but that's another video...
@@edwardgrand right I’m only doing a couple plates just to FAFO lol but I do plan on getting a scope soon, & that’s what I was thinking as well, but I’ve been looking at a lot of exotic stuff lately these starry night apes are real tomentose looking plus like the shakti & a couple others, but definitely highly respect you and your work! I love watching your videos u really break it down in such an easy digestible way, keep that shit coming I can’t wait to share my results with u here sooner than later, & Man U know what? I wish we could cross stuff like Omni & enigma, I got these 2 beautiful mutants that I’d love to cross but oh well I’ll just appreciate there beauty anyhow, mush love, mush respect ✊
Thanks doc Grand Slam🎉
Thank you Ed!!
Thanks for the videos. I was wandering is it recommended to swob then go right to agar or should you wait a few days after swobbing?
I go directly to agar. The don't need the maturation period like seeds. Just make sure they are dry before you store them.
Hey man so if I was gonna follow along with your videos about mating where would I start? And are they in a kind of an order?
There's not really any order. I didn't really have a plan when I started making videos. I'll try to fill in the gaps later or make a Playlist.
Quick flow hood question: Do you run your flow hood at full power? I heard some only run it at about 150 pascal, just wanted to check what is best.
I need more friends like this guy lol
What is your agar recipe?
SRYA recipe
3% Sticky Rice powder/flour
2% Agar
0.1% Baker's or Nutritional Yeast
Food Coloring (if desired)
FOR 500 ml Total volume
15 g sticky rice powder
10 g Agar
0.5 g Baker's Yeast
Food Coloring or 1g charcoal if desired.
500 ml tap water
- Should make between 20-25 standard size plates.
@@edwardgrand Thank you for not being a gate keeper! Thank you for sharing this recipe you are the best !
🎉😊
Do they all look like fluffy clouds? Because if so I have lots and lots and lots and know what stops the clamps 😂
Some are not fluffy. Occasionally, I get a monkaryon that is pseudo-rhizomorphic. That's when you really need to scope them.
@@edwardgrandthank you so much . I try to be like everyone else but to me being perfectly sterile and then putting in a stagnant box then into a stagnant closest doesn't make sense to me. Why not do the opposite? Start dirty then put in a prefect atmosphere that you make?
@@gangsterbuilder Because we want to grow one and only one species. Same idea behind planting corn or wheat. We have to prep the field, otherwise we will get a random mix of organisms.
🕺🪩🙏🏼