Katharine Hubbard

Пікірлер

@UrPretty123 3 сағат бұрын

YOURE AMAZING!!! Godsend 💕💓 beautiful explanation, perfectly understood!

@vsuresh2020 2 күн бұрын

What was the use of the 255 number in the normalisation formula?

@RashadSaleh92 9 күн бұрын

Thanks very much.

@RashadSaleh92 9 күн бұрын

Amazing video thank you very much

@RashadSaleh92 9 күн бұрын

Thank you so much that was so very well explained and straight to the point.

@ahmetenginpzc 14 күн бұрын

Thats perfect!!!

@JacksonSeibert 15 күн бұрын

Truly well done, thank you for your insight!

@Ombrenoirs 16 күн бұрын

Amazing, thank you so much!!!

@chandramoulikaponnam9174 20 күн бұрын

how to design primers if we want to add a tag to protein?

@samcumdi 22 күн бұрын

My 6th grader asked me about Spectrophotometer, "what does it do and what is it used for?" Aside from telling him, ''It is a light-related instrument'' - I didn't have much to say about it. What better feedback when he returns from school😊. No School like KZbin, Thanks Katharine Hubbard.

@AlissonCruzRivas 22 күн бұрын

TY SM , DOING GODS WORK

@drchauhanrps 28 күн бұрын

Thank you for this great video! Very informative!

@sergiumitrea6437 29 күн бұрын

Hello from România, i havent 110 apple tree with agrobacterium tumefaciens, i remove all trees , after how much years i cant plant apple tree in that soil near 2meter to the tree how have agrobacterium. Thanks a lot. And how i cant clean the soil...thanks...a lot

@asarhh Ай бұрын

Awesome explanation 🎉

@hellfrr Ай бұрын

Thank you so much for posting your videos. Very very clear explanation, great for understanding and for easy review later. You're saving me a lot of time and confusion. You're a wonderful woman

@szxnv Ай бұрын

@rrobat Ай бұрын

Great tutorial! And about the volume of the reaction? Do you think we should consider it?

@vidhiverma7306 Ай бұрын

Please can you tell the tool to design this type of primers?

@shenya2057 Ай бұрын

Thank you so much ma'am, this video really helped me a lot :)

@MarcusElonNesonc Ай бұрын

Thankyoy

@Geezweez788 Ай бұрын

This is Varsity stuff but How i wish KZbin was around when I was in high school 😢

@XinyunQiu Ай бұрын

Here is a general structure of a primer combining these components: 5' - Leading Sequence - Restriction Site - Gene-Specific Sequence - 3' When designing primers for cloning, amplification, or mutagenesis, it's important to include specific sequences that ensure the primer's proper function. Below are the key components to consider when designing primers for these purposes: The primer above includes: Leading sequence: GCG (3 bases to enhance restriction enzyme efficiency) Restriction site: GAATTC (EcoRI) Gene-specific sequence: ATGACTGACTGACTGAC

@user-ce4li4fj6h Ай бұрын

Thank you very much for your videos! They are very well structured and helpful (from a chemist who learns bio)

@ZahidKhyzer Ай бұрын

very nice , can you please help tell , can i use this for Gems Spectrometer

@rotemzilberman2035 2 ай бұрын

I guess after watching this video I just HAVE TO subscribe to this channel

@evaramos7332 2 ай бұрын

You are adding in the reverse primer (when you write It 3'-5') the sequence of the MCS in 3'-5' but that sequence that you added is actually the MCS written in 5'-3' (i ve searched the sequence). So, do you have to change the order of the MCS into 3'-5', dont you?

@SARATHATHEVIUPM 2 ай бұрын

AMAZING.. WONDERFUL CLEAR EXPLANATION

@Glacierlune 2 ай бұрын

Just imagine if a cell had a cloraplast and a mitochondria. They would be passing oxygen atoms back and forth.

@katharinehubbard5043 2 ай бұрын

Plant cells have both!

@Glacierlune 2 ай бұрын

@@katharinehubbard5043 Lol I knew that at one time. I wonder why I forgot. I usually don't forget many things about biology. (But I have had some meurcury poisoning that has took a lot of my cognitive functions away, healing now)

@anthonytan6143 2 ай бұрын

Incredible video thank you so much !!!

@xinyuyu6738 2 ай бұрын

You are my hero!

@SamsonAruna-pp2se 2 ай бұрын

You are a life saver. You explanation made it look like a simple thing to know.

@ruthanasreemoe 3 ай бұрын

Can I just use test tube instead of quivet

@katharinehubbard5043 3 ай бұрын

Test tubes might work but you’d have to be a lot more careful about positioning them - the readings you get will be influenced a lot by the curvature of the tube, so unless you are confident the tube is in exactly the right place each time your data might not be very useful. Cuvettes are square so have flat sides that you don’t have to be quite so careful about

@ruggerogabbrielli6831 3 ай бұрын

Did bacteriophages evolved not to have those palindromic sequences?

@arijitmukherjee5846 3 ай бұрын

Can you please explain how to choose the wavelength in the spectrophotometer for calculating absorbance

@domhnall6492 3 ай бұрын

I Lov it

@Huy-tu7mx 3 ай бұрын

Thank you for sharing! Very informative! You're such an effective educator!

@dr.mohamedel-telbany830 3 ай бұрын

Amazing 😍

@MarinaG-f8w 3 ай бұрын

Hello, I'm writing a lab report involving chlorophyll determination but I'm having trouble finding a study that uses these exact conversion factors and formulas. Could you please send me the link of where it was taken from? Thanks!

@harithhazim453 4 ай бұрын

When an expert teaches something, life becomes easy. Thank you!

@vitoriaaraujo3020 4 ай бұрын

This video is gonna save my live in genetic engineering. Thank you!

@mahmoudofficial-e5w 4 ай бұрын

that perfect as hell you must get much much mre mybe if you make playlist according to lippincot or harper , will be ammzing

@akshathabanadka9808 4 ай бұрын

How it g/L equivalent to microgram/mL. Isn't it mg/L?

@eloisepearce7949 4 ай бұрын

Thank you so much! Please could I ask how you would estimate an Amax value based on the experimental data?

@christinaliu3158 4 ай бұрын

very good explanation,watched about 5min and then I know this is what I needed. Also saved another 2 or 3 vedios for my paper (pharmacology😢) Many thanks