Find Tissue Culture Protocols for Any Plant!
Find Tissue Culture Protocols for Any Plant!
Our lab director Francisco answers one of the most asked questions about finding protocols for tissue culture. Having been in the field for so long, he shows you how he finds them! Get 10%OFF the tissue culture products you need using my code: https://www.plantcelltechnology.com/?ref=FP10
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39 minutes !!! WTF 😂 Thx a lot
PS : I love your new hair cut 😜
Francisco, how do i get a college degree in plant tissue culture?
I was trying to find the protocol for fancy Gloxinia. …. I thought it interesting that the protocol you found said the AGE OF LEAF was very important
Que bueno que tienes éstos momentos tan bello como das tus comentarios y millones de bendiciones
Thank you so much for all of your videos!! You are amazing and I am so excited to do a consultation call once I get my lab set up. One question on the “half strength MS” in the recipe- do you have a video where you explain what half strength would be? Does it have to be ordered that way or is it a dilution ratio? Thank you so much!
Just found you’re page and so thankful!
You’re the best man, thank you.
Thank you so much Francisco, I love plants they are my favourite hobby and the best things for my mental health. tissue culture growing is all I want to do, I aspire to make a living like you here in north of England where it’s dark and gloomy for most of the year. The knowledge is priceless to me and I really appreciate you sharing your knowledge ❤ I’m most interested in self heading philodendrons because they are beautiful and I have far too many haha
Can we use water agar for tissue culture? If we can use agar water then how much amount of agar agar is used in water??
Can you guide me with a protocol for ginger (for surface sterilization) please? And also having trouble of how to isolate the meristem from rhizome sprouts?
Thank you for posting 🙂
I said the Goodyera, and I deliberately did not pick a species to not limit it and give more chance, the reason I told this one is because I try to search for it every few weeks and there are papers related to seed germination, which is useless because Goodyera seeeds is pretty much impossible to come by, pollinating them is also not an option. There is none that works with anything other than seeds and even most of those are related to european temperate species. The video is not over but I’ll be super suprised if you found one.
Sir What is the media for cymbidium orchid?
In 1983 I was propagating orchids in tissue culture. We just blended banana, potato and agar with a few hormones. Great for all cymbidiums.
Are they protocols for fruit trees too?
21:20 so what you’re saying is every protocol regarding tissue culture are not compatible with the same species?
what about the cold plasma treatment
Evaluate the potential of tissues culture on endangered plant apeciss
What does that mean they use a banana
Can u tell me how much time the tissue culture of nicotiana Benthamiana take ?
boss u r great
please make another content for astarica potato tissue culture
full system and many more details
what is the recipe for canna?
Please tell me the best media for potato tissue culture, tell me the exact amount that makes up to a litre please
May I ask your protocol for nepenthes seeds? Thanks
Thank you for this video. Can you tell me if anyone is allowed to use protocols on plants that they purchase from stores if these plants have a license or patent. I don’t know if I am using the correct terminology
Thanks Francisco for another great video. My plant is the family Costaceae which I had been unable to find in the literature until I tried Google Scholar and found a couple of papers which I hope to get from a botanist friend in India. I have also found some good information on the sister family Zingiberaceae but not sure it would be applicable. What I would like to know is whether or not there is a source with GENERAL information about the different protocols for different types of explant material – differentiated cells vs. non-differentiated cells. Seeds, leaves, meristems, etc., are there general requirements like starting in the dark vs. the light, using auxins vs. cytokinins, or both and in what general ratio? That would at least give me a starting point if I want to experiment with leaves, for example. Are seeds normally started at lower strength MS? – that kind of question. Do you know a good reference source to get that generalized information?