I must say, it's VERY refreshing to watch a video by someone who is actually teaching the specific reasons behind every step and technique. Sometimes people have the best intentions, im sure, but end up making it appear more complicated with half-explanations, vague (often incorrect) terminology, videos at 3x speed with music playing over parts where they were clearly trying to explain something important (but forgot to edit or add text)... this man however, leaves nothing to the imagination. I'm not left wondering why half of the steps were taken, and actually feel prepared to try it... just pleeeeease post more videos (quality over quantity is just fine). ...and remember "The Six P's" - Prior Planning Prevents Piss-Poor Performance! (I forget where I'd heard it)

Super appreciate the precise and complete explanation without wasting words. Your a quick favorite. Glad I found you

I’ve been looking for this info everywhere, thank you sir! ❤️

Very nice and concise video. Thanks!

I never had a multispore plate like that with no contamination, especially after 8 days. Maybe I should find your video on that lol

Love your videos dude! Thank you so much . Mush love 🍄❤️

Soo helpful, really appreciate these type of videos!! 💯🙌🙌🙏

Nice vid thanks. One thing though that might be confusing to people.. selective rhizo rather than tomentose to transfer has nothing to do with selective isolation. It's only going to help with faster mycelium expansion, but of what, you have no idea. There is no correlation between rhizo myc and good genes in terms of fruits. The only way to selectively isolate and narrow down your genetics is from selecting a fruit, and making a spore print (slight narrowing down) or a clone (maximum narrowing down). Of course after that selecting rhizo over tomentose is going to provid faster colonisation of your next plate. But, again, good rhizo has nothing to do with big/beautiful/strong fruits

really your awesome bro 😍 ,because you clarifying doubts and patience given reply in instagram,youtube comment it's really helpful bro tqq so much😍

I hope the spirits guide you to unbelievable success

So many plates! Love it!

Awsome information thx you

Thanks a million! Your description of how you isolate the leading edge of the mycelium to colonize a plate with singular genetics was super informative and the exact piece of info I was looking for when I clocked on this video! Does it matter how the cut agar piece is laid on the receiving plate? mycelium down or sideways? Or agar up? Mush love

I wish I could’ve seen a follow up video! The results of what you did. I’m brand spanking new to growing and trying to learn :)

If you have 50 different blooms, which should survive if you only need one fruit? Should you isolate the 2-3 rhyzomorphic blooms? The milkiest bloom? The deepest digger? Do you want something that outraces the other myc early on? Or do you want the bloom that reaches the furthest fastest, ignoring how thick and milky it is? Can you tell what will fruit this early or do you need to keep spawning isos until you get a good one?

A thousand times better audio.

Thanks for the video! In your experience, how often do you encounter isolations that are zero or very weak producers? Do you find that isolating from spore is a more efficient path to having desirable traits than is doing a small grow and isolating from clones? Thanks again!

Very helpful. Thank you for the content. I have a few questions if you don't mind. First, can you speak to a method to acquire monokaryotic v. dikaryotic mycelium? Second, why would one want to acquire monokaryotic v. dikaryotic? Finally, any tips on best agar to use specifically for this purpose?

Yep this is what I'll be doing, trying to find the best looking white patch lol. How many times do you need to isolate an agar dish? Will one transfer to agar be sufficient to get dominate genes.

Did you do these transfers in open air without a flow hood or SAB? How did you not get a bunch of contamination?

did you do this in open air?? or is there a laminar flow hood out of frame?

when you say "single isolated strains" you're referring to diploid mycelium, right? In theory you want one set of mixed genetics in order to create a mycelial network that'll produce fruiting bodies., but you did comment on not having mixed genetics - can you confirm what you mean, if what i just said is incorrect? also, when you say "zone of inhibition" i'm assuming you're saying that they are diploid mycelium networks running into other haploid/diploid mycelium networks and not 'mating'... thanks for the video!

After getting spores: How do you germinating them (How long, temperature, time, with or without light?)

Would there be an issue using the orginal multi spore agar, and innocculating a jar or jars with that? Is this a waste of time, it not?

Is it ideal to get a sector from two colonies that have fused together?

Where did u buy ur Petri dishes

Can you do a brf paste video please?