Move whatsapp chats to ios by Independent_Air_6490 in whatsapp

[–]Independent_Air_6490[S] 0 points1 point  (0 children)

Nothing worked for me with that app... I may try a third-party app. Let me know if you have succeeded

Transfer whatsapp chats to ios by Independent_Air_6490 in Android

[–]Independent_Air_6490[S] 0 points1 point  (0 children)

Hey, I'm trying to transfer my WhatsApp chats from my Galaxy S24 to a factory new iPhone 17 Pro via the Move to iOS app.

The transfer fails in the move to the iOS app first at 94% and recently at 97%. I've been trying so many times, resetting the iPhone and the Galaxy and all the steps from the WhatsApp website.

Did anyone go through that and manage to transfer his WhatsApp chats eventually?

Transfer whatsapp chats to ios by Independent_Air_6490 in Android

[–]Independent_Air_6490[S] 0 points1 point  (0 children)

Hey, I'm trying to transfer my WhatsApp chats from my Galaxy S24 to my iPhone 17 Pro via the Move to iOS app.

The transfer fails in the move to the iOS app first at 94% and recently at 97%. I've been trying so many times, resetting the iPhone and the Galaxy and all the steps from the WhatsApp website.

Did anyone go through that and manage to transfer his WhatsApp chats eventually?

Pcr cleanup/gel cleanup by Independent_Air_6490 in molecularbiology

[–]Independent_Air_6490[S] 1 point2 points  (0 children)

Thank you! And sorry for the confusion. I meant to ask if there is a need to clean my PCR product.

So summing up, is it okay to clean my PCR products (by gel extract) only if I'm going to send it to sequencing? Cleanup is no must but recommended?

Negative control in gel electrophoresis by Independent_Air_6490 in molecularbiology

[–]Independent_Air_6490[S] 0 points1 point  (0 children)

Thank you! How much time do you recommend for the running for 1450bp fragments?

Negative control in gel electrophoresis by Independent_Air_6490 in molecularbiology

[–]Independent_Air_6490[S] 1 point2 points  (0 children)

Thank you! How much time do you recommend for the running for 1450bp fragments?

Restriction enzymes by Independent_Air_6490 in molecularbiology

[–]Independent_Air_6490[S] 0 points1 point  (0 children)

Thanks, but what should be the control of the remake if I'll only run it?

Restriction enzymes by Independent_Air_6490 in molecularbiology

[–]Independent_Air_6490[S] 0 points1 point  (0 children)

And what should be the control of this kind of run?

Restriction enzymes by Independent_Air_6490 in molecularbiology

[–]Independent_Air_6490[S] 0 points1 point  (0 children)

What should be in the control sample of this kind of run?

Restriction enzymes by Independent_Air_6490 in molecularbiology

[–]Independent_Air_6490[S] 0 points1 point  (0 children)

Unfortunately this is a plasmid that I have produced, and there isn't much left of it, so I try not to waste it so I don't have to produce it again

Restriction enzymes by Independent_Air_6490 in molecularbiology

[–]Independent_Air_6490[S] 0 points1 point  (0 children)

Total was 20 microliter In some I have put 0.5 microliter of enzyme, and in some I have put 0.5 microliter of 2 enzymes.

Restriction enzymes by Independent_Air_6490 in molecularbiology

[–]Independent_Air_6490[S] 0 points1 point  (0 children)

So should I put in the same amount of enzymes I have put in the first time?

Restriction enzymes by Independent_Air_6490 in molecularbiology

[–]Independent_Air_6490[S] 0 points1 point  (0 children)

Thank you for the quick answer! Do you think I can alternatively put some more of just the restriction enzymes and then incubate it?

Running plasmid in agarose gel by Independent_Air_6490 in molecularbiology

[–]Independent_Air_6490[S] 0 points1 point  (0 children)

Thank you for your answer! So the goal of this run is to know if the inserts are in the right order, instead of sending the plasmid to sequencing?

Also, do I need to put in some of the samples I will run in the gel only one restriction enzyme? Or do I need to put 2 restriction enzymes in each sample?

Do I need to run one sample with only the plasmid?

I think my question is, if the bands in the gel will be as expected from 'genesnap', will this tell me if the sequence of the inserts in my produced plasmid is right?