I cannot stress how helpful this is ... no other video explain this process with this much clarity. Definitely helping me on MCAT test

Thank you for a this great explination! Im going to use this technique in my bachelors thesis and this video clarified a lot of things for me!

Hi Dr, you explained everything so clearly! I have watched nearly every video you posted! Thank you so much!

I havent finished watching this video yet and boy you are doing a great job. I have been looking for someone who explains the protocol and the theory behind it and this is exactly what i need. Please keep posting 👍👍👍😘😘😘😘

@joelarnoldngassa8720

3 жыл бұрын

She's a girl

first time I understand it .. thanks millions.

The videos on this channel are great and helped me a lot to better understand the techniques. Your teaching method is excellent, and it is very useful to explain the reason for using each substance and solution. I hope you continue this great videos. Thank you so much!

Thank you very much, I'm a med student preparing for my Microbiology exam and this helped a lot!! :))

thank you for your easily explanation it's help me very well ... please don't stop these interesting videos

well explained!! the graphs are really clear to understand !!

Very well explained and extremely helpful, thanks so much!

THANK YOU!!! ♥ You helped me a lot. Greetings from Argentina (:

This was explained so well. Thank you so much!

Thank you very much... You are explanes amazingly.... Pleas complete this video

Thank you very much for this informative and detailed video. I enjoyed it very much.

Thank you madam. Your videos are making the concepts very easier

Very helpful video!!! Thanks so much

Very useful video thank you so much!

you're simply ... Professional

Thank you for this informative video, finally I'm able to understand WB :)

Thank you. This was very helpful.

Awesome video.. it helped me a lot to understand the principle of western blotting.

Very informative. Thank you

Simply amazing! Thank you 🙏

thanks for such an explainatory video

thank you so much for your explanation. Very nice

great work and well explained

ugh so good thanks for enlightening me on western blotting

Thank you so much for the video, helped me a lot!!! Appreciate it.Greetings from an italian student ;-)

@biomedicalandbiologicalsci4989

6 жыл бұрын

This makes me happy .. thank you :)

thankyou for the explanation... it is easier to understand :)

You are amazing, thank you so much!

so clear simple and useful thanks

Amazing video!

Thank you. powerful video

well explained in a simplified way

Really Amazing There Is video about native electrophoresis plz?

Short question.: Why do all proteins move to the anode if you prevent SDS-binding with methanol? Whithout SDS-binding some basic/alkaline proteins would be positively charged, wouldnt they?

@biomedicalandbiologicalsci4989

6 жыл бұрын

Hei, proteins here are already bound to SDS, because as I said; before applying the western blotting technique we applied the SDS-PAGE in which all the proteins were bound to SDS. So the Methanol is added to the transfer buffer in only 20%, so during the run, methanol will lightly detach the SDS from the proteins (not completely) in order to enhace their ability to bind to the membrane.

How do we determine the precise Time and Voltage required for our protein of interest? Can we look it up somewhere, or is this something that requires some trial and error? Also, if for example, we have 10 different proteins of interest that we are looking for in our samples, does each protein have their own optimal Time and Voltage (I am assuming yes)? If yes, how can we optimize the Time and Voltage so that we get ALL of our 10 proteins of interest on to the membrane without having some of them being left behind in the gel or in the filter paper?

Nice explanation mam...likes your videos

great explanation

Perfect explanation thank youuu

Such a nice presentation..😘😘

You are very very very wonderful thank you very much teacher

OK. So I have questions. 1) Is there a "ladder" for SDS-PAGE? Otherwise I don't see how can I determine specific molecular weight numbers 2) SDS denatures proteins, would that interfere with the primary antibodies from recognizing the protein of interest given that it is denatured? 3) The "sandwich" is placed in PLASTIC container. Why use plastic, a non-conductor, when we are going to electrically push the proteins? Does the transfer buffer gets into the plastic bag, or stay completely outside?

"...from the mouse or from the rat or from the rabbit or whatever!" 😀 Anyway, I'm moving from SDS-PAGE to Western Blotting in my research lab, and this video was very informative, helping me understand the technique and protocol!

This is awesome! Thanks! :)

you are amazing thank you so much

Could to please made a video for developing a blot in chem doc which consists of dos n donts

Thank you so much.

Muchas gracias!

it was very helpfull

Thank you!

finally i understand WB, good bless u 😭🌹🌹🌹🌹🌹🌹🌹🌹🌹🌹🌹🌹🌹

Thank you so much

omg finally i understand this!!!

THANK YOU SO MUCH

I have a question regarding the secondary AB. if the first Ab is mouse anti-human why isnt the secondary let’s say goat anti-mouse? Isnt it a mistake? Thanks

Very much thankful ☺️

Really you are very good .... Actually this video helped me 😄

@Biomeducated

5 жыл бұрын

Do you have a control protein blotted as well? I assume your proteins of interest are from a cell lysate, no? A housekeeping protein like GADPH, or something like Actin? Or some bacterial protein if you have expressed the poteins to have them purified later on? If the band size/intensity of the Controls is the same in each condition, then you indeed have expression differences between wild-type and mutant.

Thank you ❤️❤️❤️

Please do upload videos on biological technique

Thank you !!

Thank you a lot

Has ethanol the same principle as methanol? We use a commercial "turbo buffer" which is recommended to use ethanol instead methanol!

Fentastic !!! Thanks a lot..

@biomedicalandbiologicalsci4989

6 жыл бұрын

You are welcome :)

awesome

thank you !

Can anyone explain that why proteins are negatively charged to me?

Excelente!

You told methanol removes SDS from protein, then how it is still negatively charged?

I have a preformed a WB and im comparing a wildtype and mutant protein and the results show that we have more intensity in the mutant samples than the wildtype samples. The only thing this tells me is that we have more of the protein of interest in the mutant compared to the wildtype right i.e. it doenst give me any other information?

@Biomeducated

5 жыл бұрын

Do you have a control protein blotted as well? I assume your proteins of interest are from a cell lysate, no? A housekeeping protein like GADPH, or something like Actin? Or some bacterial protein if you have expressed the poteins to have them purified later on? If the band size/intensity of the Controls is the same in each condition, then you indeed have expression differences between wild-type and mutant.

Hi can I please know what is the reason for using glycine ? is it like a driver molecule for the proteins to separate ?

@julianomachado7050

3 жыл бұрын

I am also interested in this potential explanation!

I have a question... I understand that the primary Ab is extracted from something other than a human (such as a mouse or rabbit). I also understand that the secondary antibody is made anti- whatever the species used to make the primary antibody. However, how is the secondary antibody produced? For instance, if you have a human protein, a mouse primary antibody, then would you need to synthesis the secondary antibody in another animal such as a rabbit? What happens if you synthesis the secondary antibody in a human or mouse?

@biomedicalandbiologicalsci4989

7 жыл бұрын

Hello ... The secondary antibody is an IgG that has a specific affinity to the proteins of a certain species such as mouse or rabbit or sheep. It is also produced in an animal by hyper-immunizing (injecting a high concentration of immunoglobulins) the animal with purified immunoglobulin fractions from a normal mouse (or any other animal) serum to produce High-affinity antibodies. Yes, usually the secondary Ab is produced in another animal because you cannot produce anti-mouse secondary Ab in a mouse because if you inject mouse immunoglobulins into a mouse then the mouse will not produce Ab against them. On the other hand, you can produce anti-mouse Ab in humans but usually, we dont produce Ab in humans (ethically). However, if you are studying sheep proteins for example and you use mouse primary Ab you better not use sheep secondary Ab to prevent unspecific binding. So usually for example, if we are studying human proteins we use mouse anti-human primary Ab and rabbit anti-mouse secondary Ab.

Thanks

how can i know how much time and voltage i need to my proteins? it depends on what? how can i know if my proteins run away from the membrane or some stayed on the gel?

@Biomeducated

5 жыл бұрын

If you have included your 'protein ladder/standard' in SDS-PAGE (as you should! ;)), then you will see it on your blot (the colours of the ladder are seen)...if not, well, then your samples have migrated into the solution and you can start all over again :p point is, you cannot see it during the run. Make sure you get it right immediately, and stick to your own routine, always, when preparing the cassette! Time and voltage depends. Anyway, you should be careful with higher voltages, as this might increase temperature, and maybe decrease the quality and resolution of your blot. As I remember, we used 25V for 'overnight' (ca. 16h) (and put the whole setup in an ice filled bin!), if you start blotting at the end of the day, OR 45V for intraday (ca. 4h). This worked fine, but ideally you should optimize for your own equipment yourself :)

THANK YOU MA'AM ! PLEASE UPLOAD VIDEO ON HPLC

@biomedicalandbiologicalsci4989

6 жыл бұрын

kzread.info/dash/bejne/nGqokrxmpqycm9o.html go to this link .. and subscribe the channel so you can see all the new videos :)

Very I formative

Good

so great ..go on

@biomedicalandbiologicalsci4989

7 жыл бұрын

Thank you ... stay around many interesting videos are coming up :)

You are too good mam

What 's the filter papers and sponges for?

@bhagyashreejadhav8757

4 жыл бұрын

To compress nitrocellulose membrane tightly on gel..

Thanks a lot, :)

@biomedicalandbiologicalsci4989

6 жыл бұрын

Welcome :)

Sounds like my one professor

So helpful more details and immunofluorescence,imuunochemistry,immunodiffusion,emsa,

Thanks gurl

Mam plz start teaching

Post something daily

Protein isolation

what-ever

ˇ治郅治郅治郅

Very useful Video thank you!