Video

Once I have done a bradfort assay with my protein, could I use it to do a SDS PAGE analysis

Best explanation indeed Thanks for sharing

Please your English ....

How come Coomassie Blue still have -ve charge, even after donating the lone pair to Protein molecule!?

Where are my Turkish fans ? Only me ? :D

How can one read a plasmid using three different enzymes to cut

Gosh I saw a really good video before that was so clear, she really pooped my understanding here. She explains really well lab procedures but she sucks explaining biomolecular concepts

Her other videos were nice, this one is not good at all

isn't it SYBR Green? or is cyber green another type?

이해하는데 도움이 되었습니다.

I learned a lot about EILSA !! ( 식품영양학과 3학년 이세영 )

동영상을 통해 더 이해가 잘 되었습니다(32223454이인희)

What a helpful media! Thanks for your explanation.(Sang Jae Lee , DKU in Korea)

Very helpful

Very helpful

유익한 영상이였습니다 (32227907 현소율)

Thank you for the clear explanation.

Coding strand is not the one transcribed 8:16, it should be the template/non coding/antisense/transcribed

Nice job!

The best explanation so far... I would not have understood it without this video... God bless the teacher

Thanks for the detailed method of teaching..😊😊😊

Thank youuuuu❤

Probe is specific or primers are specific?

1. The sample is added on the stationary phase 2. The mobile phase is added 3. The mobile phases moves through the stationary phase 4. The components in the sample moves with the moving mobile phase based on their affinity towards stationary and mobile phases. THE STORY ❤: At first, the sample is added into the stationary phase. So, at that point, stationary phase is holding the sample. 😊 But as soon as the mobile phase is added, the mobile phase started to run fast pulling the components in the sample along the way through stationary phase👯‍♀️. So even if they all are standing on the stationary phase, the mobile phase is holding the hand of sample and running forward🥰 until the supply of mobile phase is terminated. But still the mobile phase didn't get his Juliet💔, all the components kept running with him till their affinity lasted stoppedsomewherein between. But sadly there were nobody with him when he ended the race and looked back. Poor mobile phase 😢

Thank you ❤

Very explanatory, thanks. please do another video to explain the 10 lasers an detectors

Thank u so much , perfect explanation

you do all :salut

It was great

best explanation. Appreciate it!

The color white of Calico cat causes by epistasis the gene 🧬

Thanks a lot. i didnt find these lessons who teach better than you.

How will B+ on anion exchange resin get replaced by our protein of interest?

❤❤❤

Incredibly helpful! Thank you 🙌

ty, this video helpme in the exam

Thank you for your clear explanation! 😊

Beautiful explanation! Love this ❤

thanks

Outclass and outstanding

türk aksanı mı bu acep

What about fused Telomeres...Genetic Tampering ?

I really2 want the slide presentation. I wanto teach in another language with my student

Very informative video. I think the P regions should be the promoter regions not the primer regions

thank you so much maam, for your wonderful explanation of Principle of Agarose gel electrophoresis.

Tomorrow is my exam This helped me sooooo much I was not able to understand from many videos or google but here I've understood everything very well 😄

Rna primer is needed in the leading strand too at the beginning of replication..then why dont leading strand end face the same problem as there wont be a hydroxyl group available there too??

Loved it.

Dear lady i cannot thank you enough. ❤❤❤❤❤

you just saved a soul. God bless u