Teaching a Beginner How to Make Liquid Tissue Culture Media

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Teaching a Beginner How to Make Liquid Tissue Culture Media

Рет қаралды 10,948

Күн бұрын

Our lab director, Francisco, teaches our Digital Marketing Manager (a plant tissue culture beginner), Rachel, how to make liquid tissue culture media step by step. Watch now to follow along and learn how to make it yourself! Get 10%OFF the tissue culture products you need to follow along: www.plantcellt...
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Пікірлер: 36

@thetruthserum2816 Жыл бұрын

Cool video! Here are my notes: General Multiplication Tissue Culture Medium: To 800 ml of Distilled water add: 30 grams Sucrose Sugar (for Carbohydrates) 4.54 grams of MS Salts Media (for Micro and Macronutrients) Using a Micropipettor add: 1 ml PPM Plant Preservative Mixture (Biocide to prevent contaminants) Plant Growth Regulators: 1 ml Benzylaminopurine/BA/BAP (cytokinin for shoot initiation) 0.1 ml Naphthaleneacetic Acid / NAA (rooting agent) Then add distilled water to bring total volume to 1L Calibrate the pH to 5.8: (Store your probes in 3 Mol KOH, rinse in distilled water) To go Higher (more basic), use Sodium Hydroxide To go Lower (more acidic), use Hydrochloric Acid Optional; Add gel medium: (more gel medium makes a more firm medium) If using Agar - 7-10 grams depending on firmness desired If using gellan gum 2-4 grams depending on firmness desired 500 ml Half Batch Calculator: Liters of Water: 0.5 Agar (g): 3.5 MS Media (g): 2.27 PPM (ml): 0.5

@PlantCellTechnology Жыл бұрын

Wonderful. Thanks for sharing it here in the comments. It will be useful for other culturists like you. :)

@hafsabibi8557 Жыл бұрын

@@PlantCellTechnologybut why don't Francisco add BAP or NABP?regulators in media

@PlantCellTechnology Жыл бұрын

@@hafsabibi8557 The establishment media is generally free of tissue culture hormones. Whereas the multiplication media contain hormones for organ development. We hope this resolves your query.

@hafsabibi8557 Жыл бұрын

With the same proportions my media is not solidifying

@PlantCellTechnology Жыл бұрын

@@hafsabibi8557 Check out the concentration and quality of your gelling agent. Read this article to further learn about other factors that cause the situation: www.plantcelltechnology.com/pct-blog/gelling-agents-what-to-look-for/

@anyadevine4094 Жыл бұрын

Can we get more of these? Theyre super informative, maybe one on sterilisation and placing the plants in the media. Very helpful for beginners 😊

@PlantCellTechnology Жыл бұрын

We already have some videos on surface sterilization of explants and acclimation. Do check them on our channel.

@pflanzensucht6173 Жыл бұрын

Hello Fransisco , great videos im consuming them all since several Days. For me as a wannabe hobby wanna be Tissue culture starter i still got several questionmarks. One of them is , what plant material excatly do i add and when can i multiply these , because for me it just sound like you put a node wait till new grow and take that new node , which makes 2-3 Plants. But obviously thats not the quantity people are Producing with Tissue culture so how do they do it ? And also there must be some kind of gathering for atleast some recipes right ? Do you guys have a video or a how to on your side that im missing ? Would be awesome if you could answer my first question in particular. Thank you for your time.

@alexuy8201 Жыл бұрын

Can you teach me the protocol for date palm please thank you

@KaruvariFamily-rr6tj 29 күн бұрын

Yes

@MikeLeady 5 ай бұрын

On the point in the video where you stated now would be the time to add agar, is it safe to assume that it will not interfere with your pH, or should I mix it prior to adjusting pH?

@PlantCellTechnology 5 ай бұрын

Can you please pinpoint the time for the reference to the question? If you are asking if it's safe to add agar after adjusting the pH of the media, then the answer is yes. However, the pH will definitely fluctuate a bit. If you add agar before adjusting the pH, it can ruin your pH meter.

@Plantsforlifelove 2 ай бұрын

Hey what is the media for monstera / philodendron ?

@jessikathompson3469 Жыл бұрын

In all of your bio-coupler videos, it appears that you are fully sealing the bio-couplers before autoclaving them. Are you loosely connecting them to avoid pressure and breaking in the autoclave?

@PlantCellTechnology Жыл бұрын

Yes, that's correct!

@BrianBerriosOne Жыл бұрын

What could you use if you dont have a autoclave?

@thetruthserum2816 5 ай бұрын

Instant pot - High Pressure mode...

@dragonsimon1 Жыл бұрын

In my experience, the PH prior to autoclave and PH after autoclave varies slightly, and the final PH Pre-inserting the plant and post removing the plant (eg. measurement of leftover media after two months of plant growth). I get if the PH is too high or too low, it would be detrimental, and even affect gelling ability if swung too high or too low, but in general if it's within 4.5-7 pre autoclave, is PH adjustment really necessary? Thanks for your insight.

@PlantCellTechnology Жыл бұрын

When you adjust the pH of the media, after autoclave there's might be the possibility of it varying a bit. But. it won't be to that extent that it affects your culture. Generally, 5-6 don't affect much. And, yes you need to adjust the pH pre-autoclave if it's between 4.5-7. It'd better be in the range of 5.5-6. or more specifically 5.8.

@dragonsimon1 Жыл бұрын

@@PlantCellTechnology Thanks for the quick response. Okay makes sense! ! I've seen your video about PH calibration pre and post autoclave before but my results varied when I tried the same. Also I found it weird how overtime, the PH of the media would start dropping. I assume there's some chemical interaction from the plant and the media influencing the PH which caused me to wonder my original thought.

@user-iy7dn3eg4p 5 ай бұрын

너무나 좋은 영상이라서 열심히 보고있습니다. 감사합니다. 하지만 저는 한국인인데 영어 발음 때문에 자막이 정확하게 나오지 않습니다 처방전은 자막으로 타이핑해서 화면에 나티나게 해 주면 좋겠습니다

@HinaKhan-wn1wp 11 ай бұрын

Can you make a video for macroalgae propagation through semi liquid media... I actually want video Tortorial for it using PES media

@PlantCellTechnology 11 ай бұрын

Hi Hina, We aren't working on macroalgae for now in our lab. We are mostly into houseplants, carnivorous plants, and fungi tissue culture.

@akasaha3138 Жыл бұрын

Should not we sterilize all the equipment before using preparing the medium????

@PlantCellTechnology Жыл бұрын

In media preparation you don't need to sterilize equipment, just keep them clean. Because after the media is prepared it will be autoclaved for the culturing processes. Yes, whatever equipment you use during the tissue culture process need to be sterilized.

@inking4517 Жыл бұрын

Ok i learned some new stuff as a complete newbie but the the last ingredients wasnt clear and some links doesn’t work

@PlantCellTechnology Жыл бұрын

Last ingredient is 1-Naphthaleneacetic acid (NAA). It's a synthetic auxin-a plant hormone. And about links: Can you share those that aren't working?

@jedz86 6 ай бұрын

what if i add agfar and sset ph after that?

@PlantCellTechnology 6 ай бұрын

You can do that. But, normally the pH is adjusted before adding agar. This is because agar has no significant effect on the pH of the culture medium and the method keeps the pH meter clean.