Ive never read a protocol that uses charcoal. I love that youve brought this to my attention. Is the paper or source i can learn more about the process? Thanks
@IggyJReilly19808 күн бұрын
Whatever happened with this experiment?
@cactifanatici6 күн бұрын
@@IggyJReilly1980 very slow grower but I still have it growing in tissue culture and optimizing the media each subculture
@IggyJReilly19806 күн бұрын
@@cactifanatici Would you share the hormones and amounts in your latest media? My present plan is to use 1.0 mg/L BAP and 0.5 mg/L IAA, MS, PPM, Sucrose, Agar.
@marcellinofresquez421314 күн бұрын
I love this lol!
@doolittle697715 күн бұрын
do u prefer charcoal in your media?
@cactifanatici15 күн бұрын
@@doolittle6977 yes always
@KeithKreider18 күн бұрын
Media composition?
@cactifanatici17 күн бұрын
@@KeithKreider full details on my patreon but it’s MS based
@andrewbob300218 күн бұрын
Unfortunately I sold off my flow hood years ago. how practical would it be to use a SAB to propagate cactus cuttings? The wash looks like it would be problematic with a SAB.
@cactifanatici17 күн бұрын
@@andrewbob3002 no problem at all
@dragonsimon118 күн бұрын
What does the charcoal in your media do to help your cultures?
@cactifanatici17 күн бұрын
@@dragonsimon1 helps with toxin accumulation
@chetmanley246219 күн бұрын
How much faster are those bioreactors w/ liquid media as opposed to gel culture media?
@cactifanatici19 күн бұрын
@@chetmanley2462 depends on the purpose. They are very fast for multiplying but other stages better done in agar
@jordanbarrs218528 күн бұрын
Thank you so much for your videos
@jacobgarcia359729 күн бұрын
hey man, what lights are you using on your arios? are those lights sufficient for them to bloom?? im curious because i want to make a set up just like yours. thanks
@miztoya3646Ай бұрын
I have some sweet potato callus that I would like to turn into shoot, any advice?
@chetmanley2462Ай бұрын
How old
@BearMeat4DinnerАй бұрын
Walio . Thanks! I am a new subscriber!!!❤
@michaelmurray214Ай бұрын
I found this channel from the plants in jars channel. What I'm most interested in is TC in the Euphorbia species. Do you know if anyone is doing this?
@cactifanaticiАй бұрын
@@michaelmurray214 I’ve only done euphorbia obesa but I know some others that have been done in academic papers. I think the latex is annoying to deal with probably lol
@cactifanaticiАй бұрын
This graft failed lol😂 No update!! Pereskiopsis is a much better option and auxccrss with TC grafts
@HoangHuy-vh2gp2 ай бұрын
can you tell me about tissue culture anubias nana petite what dosage of medium is needed i am trying many times but all failed, the plant does not sprout and grow with: Ms: 2.4g Kinetine: 0.15g Agar: 4g sugar: 15g look forward to your feedback
@cactifanaticiАй бұрын
@@HoangHuy-vh2gp is that using a full media recipe? Have you tried MS with Vitamins 30g sugar. No hormones. Or just 1 mg BAP is where I’d start
@HoangHuy-vh2gpАй бұрын
@@cactifanatici no kinetin just MS, sugar and agar right you?
@cactifanaticiАй бұрын
@@HoangHuy-vh2gp MS with vitamins but yea
@drakeweddner2 ай бұрын
Did yiu ever do s update
@rhysezfpv2 ай бұрын
Is this the one that clumps ? Is it also psychoactive ?
@yibofan68552 ай бұрын
Thank you for posting this. It seems like an open flame that torches the containers' brims was unnecessary and it's okay to hover over the explants. I was taught with these cautions in school but I want to improve my efficiency by simplifying the process. This video is informative.
@Primitivemycology2 ай бұрын
Microwaves are a great way to have non sterile media and a low success rate, buy a pressure cooker for more consistent results. The microwave will work for a beginner that is not yet serious about this craft.
@HappinessForUsTFC2 ай бұрын
This looks so fun! Kudos brother, I'm going to follow your path and try this when I get my laminar flow cabinet. Thanks for sharing. Those boxes look great to use.
@ChipsandIcecream372 ай бұрын
super glad to see you posting again !!!!
@Akashic_Monk2 ай бұрын
Fire 🔥
@mcactus62102 ай бұрын
Wow seem amazing
@leevermaak90282 ай бұрын
Looking fire how old are they
@jacobg1472 ай бұрын
Do the successful tissue cultures have a similar growth rate to new seedlings?
@cactifanatici2 ай бұрын
@@jacobg147 faster if in optimal conditions
@CannaGro812 ай бұрын
Thanks for tje knowledge 🙏
@CannaGro812 ай бұрын
Awesome. I'm just getting into Lophophora
@shawnbutcher11532 ай бұрын
Damn the things I would do for a flow good😭
@TheRootedPepper.Slugwell3 ай бұрын
@cactiFanatic do you have a list of hormones and where to get them. Such as a package deal where I can buy them all? I’m not tech savy so I don’t really know much out online stuff. Took me forever to find this video again. And another couple days to figure out how to comment on KZbin. Do you have an email?
@cactifanatici3 ай бұрын
Yeah email me at [email protected] My patreon has that list and info
@sailanabila46054 ай бұрын
How long will the cactus grow in this media?
@cactifanatici3 ай бұрын
As long as it needs to. I usually transfer every 1-3 months as needed but can stay forever
@nickygrobler29794 ай бұрын
Could you lease send a link for your patreon account
@cactifanatici4 ай бұрын
www.patreon.com/Cactifanatici?
@monicabasson79364 ай бұрын
What tissue culture media do you use
@cactifanatici4 ай бұрын
I specify specifically on my patreon recipes but it’s MS based
@machankinson17954 ай бұрын
Best Asmr ever
@Mycoheterotroph4 ай бұрын
Do you use PGRs in your media? I’m about to start a large tissue culture operation of palo santo but definitely want to branch out into xerophiles and carnivores, and for the palo santo I will be trying somatic embryogenesis and from there using a bunch of pgrs to pump shoots, etc
@cactifanatici4 ай бұрын
Sometimes on my patreon I go more into the hormones and when I’m using them
@Mycoheterotroph4 ай бұрын
🙏🏼🙏🏼
@escapeRC85 ай бұрын
Sir how about auxin and cytokinin how many milliliter or ppm per liter
@cactifanatici5 ай бұрын
To anyone wondering I’ve already explained this is a horrible graft and did not work. First and last time. San Pedro and pereskioposis are my go to stocks with almost 100
@jerryribyat14815 ай бұрын
Why did you hack the hell out of your grafting stock go back to grafting 101
@cactifanatici5 ай бұрын
Yeah lol …. This video is old. First and last time I ever did this
@joeysurge40695 ай бұрын
what is media recipe u use for callus and seeds
@josephwilliamcosta5 ай бұрын
Do you have a video or pictures of the results of this?
@cactifanatici5 ай бұрын
Death lol
@dragonsimon15 ай бұрын
Have you found these to be efficacious for most of the plants you work with?
@cactifanatici5 ай бұрын
Yes TIB systems al has do better but the crop can be lost easier also
@dragonsimon15 ай бұрын
@@cactifanatici How so? You mean contamination rates are higher?
@cactifanatici5 ай бұрын
It’s easier to spread the contam yes
@Frankiemind5 ай бұрын
Can you use agar to start the from seeds as well?
@dutchvonderlinde16935 ай бұрын
RIP to the rootstock and scion, there is no way this worked lmao
@cactifanatici5 ай бұрын
Facts lol!!!!
@dutchvonderlinde16935 ай бұрын
how do you germinate seeds on this type of media? can you just put them on it and wait and leave it in the cup for a while? do you have a vid' about it ? cheers
@Alproverse6 ай бұрын
Thank you for sharing this🤝🏽
@brandonbernard41716 ай бұрын
Awesome videos. Thanks for just being straight up and not dressing it up like most other videos on the topic