Great video! Are you doing philodendrons straight into multiplication media now? You mentioned BA and NAA in this one, although in small concentration. Earlier you recommended to go first into normal media to get established first. What is the latest recommendation to start with philodendrons?
The explant contains multiple types of differentiated and undifferentiated cells, does this matter? Since most plant cells retain totipotency, couldn't you use any part of the plant? Is it faster to use differentiated vs. undifferentiated cells?
To culture the same plant you can use the same process. But for different plants, you might need to find a procedure suitable for that, as different plants have different requirements. About the starter kit, you can use it to culture any plant.
I have a mature Birkin that I kinda abandoned when it completely stopped growing. It's still green but looks pretty sad. Would cutting it all back down to the piece you did in the video be a viable menas of rescuing and propagating this plant?
Hey David, You can cut all the leaves that had already yellowed and are dying (these might tend toward the bottom of the plant as it grows the new leaves from the top start white part and they get green over time and then yellow when it's dying). After cutting, transfer the plant to leca balls so they are consistently in water. You might observe the growth of new leaves after this!
will this work with a Philodendron Caramel Marble? Second question: did you make out of one plant, 3 plants (because the initial plant splits in 3 leaves)?
You can try the recipe. However, media components and concentration differs based on the plant species. And, the division is based on the shoots. so, if you have more shoots in numbers or longer shoots, you can divide them accordingly.
Do you use 1% Clorox for sterilization? For example, in 100mL of distilled water add 1mL of Clorox? What is the concentration of sodium hypochlorite in Clorox? 5.25%?
Yes, definitely! You can refer to our article on the tissue culture of Cassava: www.plantcelltechnology.com/blog/the-application-of-cassava-tissue-culture/
For now, you can refer to our blogs, youtube videos, and books to learn about tissue culture. If we create any tissue culture courses we will notify on our channel!
In our lab we use the following media formulation: For multiplication: Full MS media 25 g of sucrose 3-5 ml/l of BAP 0.3-0.5 ml/l of NAA 1 ml/l of PPM 6 g of Agar or 3 g of Gellan gum For rooting: Full MS media 25 g of sucrose 3-5 ml/l of NAA 0.3-0.5 ml/l of BAP 1 ml/l of PPM 6 g of Agar or 3 g of Gellan gum
i have an expensive tissue culture coming in the mail(hopefully), curious your thoughts on how much light to give them. i have a sealed terrarium cabinet with grow lights but have read the small tissue cultures don’t respond well to those lights immediately. Hoping do not botch a pretty expensive experiment, so your thoughts are appreciated
Hi Brennan, The duration and intensity of light given to the plants depend on the plant species. So, based on which plant are you trying to introduce in tissue culture, follow a particular procedure of tissue culture of the plant to get better results with lesser efforts.
Thanks bro for sharing a Very nice video. Can you make a video on philodendron burle Marx tissue culture? It would be great if you let us know that what composition of soil is best to grow Philodendron Florida Beauty variegated.
🌟@5:00 --->> I'm a NEWB...can someone explain to me when giving the ratio's for the PGRs.....why is he saying they are measured in ml per liter?? The PGRs come in a dry powder form. I know they can be purchased or produced in a solution as well....but he doesn't state the ratio's/dilution for the solution...that I found anyway. Again, I'm just a beginner and so I mean nothing insulting here...I'm ignorant. I think he meant to say mg per liter? I really do appreciate this content. 😍😍 Just ordered my ppm today 🧪🧫
Ok sorry....I think I got it....the measurements you gave was measured in ml per liter as it came from your stock solution that was already prepared with a set ratio. I found your other videos on this 😀. Let me know if I'm still misunderstanding please...thank you for content!!
Sir, i have watch and understand your sterilization protocol. My question is .. Is it ok for after treatment of hydrogen peroxide + vinegar we could wash explant several time with sterile distilled water to remove traces of sterilizing agent and dried for few seconds before inoculation.?
@@PlantCellTechnology ok 👍...Sir what about use of 70% alcohol for explant and seed surface sterilization .. i read in some research papers but is it necessary ??
@@amtd3808 You should follow only a specific protocol serial-wise. Don't try n mix two protocols. If you are following the complete procedure from explant collection to acclimation from the research paper, follow it critically. Don't mix the steps of the two or more protocols. They are specifically designed with some specific combination of chemicals.
Awesome video, keep these coming. You have inspired me to build a lab. Omg, I can't wait to start. Can one order all the supplies from your website. Will this method work to grow rose seeds. Francisco, one question. I saw on another video, can't remember which video where the person claims that tissue culture plants are weaker, and when grown should be labeled as such, so to inform the buys what they have purchased. Can you, comment on this or elaborate on this subject. As I believe that tissue culture plants when full established are as strong as any other form of p propagated plant.
This sounds great, we would be really grateful to work with you! Check out our website for our contact info! Link: www.plantcelltechnology.com/contact-us/
Great video! Are you doing philodendrons straight into multiplication media now? You mentioned BA and NAA in this one, although in small concentration. Earlier you recommended to go first into normal media to get established first. What is the latest recommendation to start with philodendrons?
Would this work the same way using a node or do you need to use the bottom part/rhizome?
Was this a node?
The explant contains multiple types of differentiated and undifferentiated cells, does this matter? Since most plant cells retain totipotency, couldn't you use any part of the plant? Is it faster to use differentiated vs. undifferentiated cells?
the peroxide melted the gellan gum , but not the agar in my case
what is that syringe tool called that you used to suck up the peroxide? cheetrs
micropipette
Can you please tell me about the media composition? Difficult to hear from the video
Sure:
For multiplication:
Full MS media
25 g of sucrose
3-5 ml/l of BAP
0.3-0.5 ml/l of NAA
1 ml/l of PPM
6 g of Agar or 3 g of Gellan gum
@@PlantCellTechnology Thank you very much. So for initiation of culture, what do you use
@@amalnathgm8950 Just remove plant hormones from the above recipe and that's what we use to initiate cultures.
I can use this same process to TC my own plants using your starting kit, right?
To culture the same plant you can use the same process. But for different plants, you might need to find a procedure suitable for that, as different plants have different requirements.
About the starter kit, you can use it to culture any plant.
What, if any, sterilization would you do to small tissue cultured plant if you were starting with it rather than with a node?
I have a mature Birkin that I kinda abandoned when it completely stopped growing. It's still green but looks pretty sad. Would cutting it all back down to the piece you did in the video be a viable menas of rescuing and propagating this plant?
Hey David,
You can cut all the leaves that had already yellowed and are dying (these might tend toward the bottom of the plant as it grows the new leaves from the top start white part and they get green over time and then yellow when it's dying).
After cutting, transfer the plant to leca balls so they are consistently in water. You might observe the growth of new leaves after this!
can i do it with philodendron brasil?
will this work with a Philodendron Caramel Marble? Second question: did you make out of one plant, 3 plants (because the initial plant splits in 3 leaves)?
You can try the recipe. However, media components and concentration differs based on the plant species.
And, the division is based on the shoots. so, if you have more shoots in numbers or longer shoots, you can divide them accordingly.
Do you use 1% Clorox for sterilization? For example, in 100mL of distilled water add 1mL of Clorox?
What is the concentration of sodium hypochlorite in Clorox? 5.25%?
I would love to see a video on hibiscus. So many TC videos are focusing on indoor plants. I am going to be doing TC on hibiscus 🌺
Sure! we'll try to bring something in near future soon. OR even if we create a blog on the tissue culture of the plant, we'll notify you!
Thank you very much . I have a question about cassava or yuca. Will it be possible to tissue culture?
Yes, definitely! You can refer to our article on the tissue culture of Cassava: www.plantcelltechnology.com/blog/the-application-of-cassava-tissue-culture/
@@PlantCellTechnology thank you god bless you
How to learn tissue culture ? Do you have book or materials to learn step by step ?
For now, you can refer to our blogs, youtube videos, and books to learn about tissue culture. If we create any tissue culture courses we will notify on our channel!
could you write list of media ingredient i know you say but i couldn't make out a few of them
In our lab we use the following media formulation:
For multiplication:
Full MS media
25 g of sucrose
3-5 ml/l of BAP
0.3-0.5 ml/l of NAA
1 ml/l of PPM
6 g of Agar or 3 g of Gellan gum
For rooting:
Full MS media
25 g of sucrose
3-5 ml/l of NAA
0.3-0.5 ml/l of BAP
1 ml/l of PPM
6 g of Agar or 3 g of Gellan gum
i have an expensive tissue culture coming in the mail(hopefully), curious your thoughts on how much light to give them. i have a sealed terrarium cabinet with grow lights but have read the small tissue cultures don’t respond well to those lights immediately. Hoping do not botch a pretty expensive experiment, so your thoughts are appreciated
Hi Brennan,
The duration and intensity of light given to the plants depend on the plant species. So, based on which plant are you trying to introduce in tissue culture, follow a particular procedure of tissue culture of the plant to get better results with lesser efforts.
Thanks bro for sharing a Very nice video.
Can you make a video on philodendron burle Marx tissue culture?
It would be great if you let us know that what composition of soil is best to grow Philodendron Florida Beauty variegated.
Sure! Currently, many videos are lined up but we will try to create a video on this as well, very soon!
🌟@5:00 --->> I'm a NEWB...can someone explain to me when giving the ratio's for the PGRs.....why is he saying they are measured in ml per liter?? The PGRs come in a dry powder form. I know they can be purchased or produced in a solution as well....but he doesn't state the ratio's/dilution for the solution...that I found anyway. Again, I'm just a beginner and so I mean nothing insulting here...I'm ignorant. I think he meant to say mg per liter? I really do appreciate this content. 😍😍 Just ordered my ppm today 🧪🧫
Ok sorry....I think I got it....the measurements you gave was measured in ml per liter as it came from your stock solution that was already prepared with a set ratio. I found your other videos on this 😀. Let me know if I'm still misunderstanding please...thank you for content!!
@@MiniatureChickenChannel Yeah, right! We prepare the stock solution of these hormone, which we use for our further experiments.
@@PlantCellTechnology Got it...thank you!
Sir, i have watch and understand your sterilization protocol. My question is .. Is it ok for after treatment of hydrogen peroxide + vinegar we could wash explant several time with sterile distilled water to remove traces of sterilizing agent and dried for few seconds before inoculation.?
Washing several times is not required. However, 2-3 gentle washes with distilled water will work to remove the traces of chemicals.
@@PlantCellTechnology ok 👍...Sir what about use of 70% alcohol for explant and seed surface sterilization .. i read in some research papers but is it necessary ??
@@amtd3808 You should follow only a specific protocol serial-wise. Don't try n mix two protocols. If you are following the complete procedure from explant collection to acclimation from the research paper, follow it critically. Don't mix the steps of the two or more protocols. They are specifically designed with some specific combination of chemicals.
@@PlantCellTechnology 👍👍👍..ok..Got it...👍👍
Would love to see a Tissue culture from corms like Ranunculus or bulbs like Calla Lily.
We will see if we can make this happen! Happy culturing!
Chan you do pink princess please??
We can try if we get our hands on the plant. thanks!
Awesome video, keep these coming. You have inspired me to build a lab. Omg, I can't wait to start. Can one order all the supplies from your website. Will this method work to grow rose seeds.
Francisco, one question. I saw on another video, can't remember which video where the person claims that tissue culture plants are weaker, and when grown should be labeled as such, so to inform the buys what they have purchased.
Can you, comment on this or elaborate on this subject. As I believe that tissue culture plants when full established are as strong as any other form of p propagated plant.
Yes, we will have content around this subject coming out soon!
Can you do philodendron pink princess please???
Sure! we'll do it as we get our hands on the plant.
I have a fairly large house plant collection and I’d be happy to donate some cuttings to the project:)
This sounds great, we would be really grateful to work with you! Check out our website for our contact info!
Link: www.plantcelltechnology.com/contact-us/
If you were in Europe I’d donate a bunch of plants!!
We appreciate that, good luck with your culturing!