Gregor

13 May 19:56

We ship cultures on the retail side to Canada and have also shipped to Australia before. It seems pretty strain/country specific though, as Australia didn't allow Lions Mane. Honestly, that method should be fine but may also help to ask the delivery service if they can provide any guidance as shipping biological material is pretty common. Also in a suitcase should be perfectly fine. I have heard some good stories from my old employer of flying with a whole carry on briefcase full of anaerobic cultures ranging from all over the medical field. Also I have a feeling Erik will have some experience in this so i'll give him an ask.

Phillipe Kenny Glad I could help and hey thanks for asking questions as  a lot of these concepts and ideas are new to us as well! By asking questions you're helping us flush out these ideas as well and make sure we are still being honest to the facts or still being open to new ideas. We are all on this journey together and it's nice to bring a community along with ya!

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10 May 18:00

I've really only seen that it helps with Cordycepin production and not too much other data on growth times and what not. Very cool nonetheless, how do the fruit bodies compare in size to your other bathces.

10 May 17:55

This was actually a quote I got from a medical mycology textbook. The fungi when in contact will only send the nucleus across through the septa (which most likely contains some cytoplasm.) The nuclei, are then coexisting in each cell across both colonies by DNA replication. The colonies don't transfer all their cytoplasm among each other they just share that nucleus across the colony. It's like each colony takes it upon itself to replicate and spread the new nucleus genetics across all cells rather than the colonies moving a whole bunch of nuclei over to the compatible partner. So, the nuclei aren't combing until karyogamy like you said they are just existing together in the cells. I'm sure in that bridging cell where the 2 colonies meet there has to be some cytoplasm transfer in order to move the nucleus over to the other cell and test for compatibility but that would be our only transfer. 

Christopher Edgar Awesome that is great to hear! glad I could help and thanks for actually trying to collect some data it really helps to visualize what's going on and draw some better conclusions.

The block wouldn't be considered sterile but it is definitely a high-temp pasteurization that should work great. When cooking our master mix blocks we try to make sure they achieve a temperature of 200F to ensure proper pasteurization. For true sterile the internal temp of the master mix block would need to be at 245-250F for at least 20 minutes, we just do 35 in our autoclave to be safe for spawn.

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BenJamin Harder it's not necessarily inbreeding but if you kept adding new broth indefinitely, senescence would eventually occur. It's more like if you kept expanding out your strain.

Nope no problem at all with pouring the LC instead of injecting it. Just if you are gonna open the lid make sure you are right in front of that flowhood.

That is definitely a possibility. The eventual idea for us is that by letting that mycelium generate in the LC while consistently feeding it new broth, we can create a sort of hockey puck of mycelium forming on the bottom. 

I think Erik is planning on doing another video once we get the cultures up and running about this. This is just what I gathered from talking to him about the LC setup.

12 Apr 15:59

very cool thanks for sharing! Are these albino strains? Also, what are the 3 methods and which pictures correspond to which method?

12 Apr 15:57

So I can't really give a conclusive answer only ideas. The chlorodioxide is fast acting as the chemist says but it does have an oxidation rate that is 2.6 times more powerful than you're run of the mill chlorine bleach. You might be able to ask the chemist if he has any insight on chlorodioxide vs bleach, in terms of it's potency as an antimicrobial. But in my mind due to that greater oxidative power you would want a lower the ppm say 75-100 and then with the 2.6 factor it equals you're total bleach oxidative power. Keep in mind this doesn't always work linearly so that is just a guess.