Відео

Nice explanation ma’am ❤

❤

Amazing video

Thank youu very much you saved my lifeee

very clear explanation. thanks!

thank you very much! great explanation! helped a lot! :)

what is the difference between upstream activating sequence and enhancer?

this helped so much thank you!!!

thank you very much, you helped me a lot!

My test in 5min did i beat the world record

Thanks so much But i have a question, is this the same as finding their frequencies

i love you tysm omfg

Perfect video, both as first time learning and as quick refresher before exams.

💯 ❤

Thank god for ur channel😭

Straight to the point Thank you so much 🙌🏾

Amaizing explanation 🎉

Literally saving my life on my genetics final thank you

NICOLE THE GOAT🐐🙏

you taught me more in less than 5 minutes than my teacher has in 2 whole lessons

perfect explanations, thank you so much!

this is an amazing video, thank you sm

اموت عليج 🩷😔

Helpful 🙂 thank you 🙏💯

Thanks

your the best thank you so much!

thank you so much! can you do a video on how positive or negative blood types factor in?

Muito bom

thank you for this:)

Wow thanks big time

Thank you

It took me days, no actually months to understand the whole pedigree thing for an olympiad. This saved me. Thank You So Much this Means alot

thank you!

Thanks

If that day Mendel's became unlucky then today we all are very lucky iykyk

Thanks a lot this was really helpful ❤

good~!!!

Why didn't u make gal operon and arabinose operon 😭

Im confused, if you do the punnet square twice than how are you supposed to know which of the crosses is the right one??

blesss❤ this is so helpful

been looking for a video that was easier to understand considering i’m on 2 hours of sleep and just cannot focus. This video was perfect, thank you.

Finally found a good explanation. TYSM btw 18:25 In this example here it has skipped generations on left so can not it be dominant?

Question 1: what are restriction enzymes used for by bacteria? Q. 2: check your diagram from the textbook to make sure you drew how EcoRI cuts DNA correctly (minute 1:30). Fix your diagram if you had it wrong. Q 3: what are “sticky ends”? How many bases are they? Q 4: what do sticky ends make it easy to do? Q 5: how many molecules does molecule 1 get “cleaved” into? Q 6: why would molecule 2 be cleaved in only one place? Write out the bases on the 2 strands that were mutated. Q 7: how many pieces (fragments) would molecule 2 be cut into Q 8: how can you use gel electrophoresis once the molecules are cut?

Thank you so muchhh!!

Thank you!!

Thank you!!

Thanks alot this helps me alot i have no words❤

thank you this was so helpful you dont even know

Just made a five question flowchart after watching your video mam....sadly cant share pics on youtube... wd hv been super fun

Preparatory Year/syria Pre9❤