When you said you are adding gel/dye mix to other 3 gel wells but you already added 1 out of 3 gel well the gel/dye mixture for priming. Do you have to add gel/dye mixture again on that well?
I use the RNA Pico Kit but I´m wondering about your gel preparation. In my instructions it says to centrifuge the gel (spin filter) and add the dye AFTER (centrifuge again).
Thank you very much for this video. It helps a lot! However, may I check on the reagents (especially all related to the dye) because as what I read in the Agilent High Sensitivity DNA Kit Guide, I understand that the reagents are light-sensitive. But in this video, it does not seem that way. Can anyone help in this matter? Thank you in advance.
Hi Lilian, I use this instrument daily for my job in cancer research and in our lab we always store the reagents in a dark box due to it being light sensitive especially the dye that gets mixed with the gel as well as the other reagents.
Hello everyone, how are you? I wondered how much it would be necessary to pay for a small lab capable of doing NGS? Can anyone help me? Thanks in advance! :)
This video has been very helpful for me. Thank you for producing this well organized and thorough tutorial!
Very good presentation! Thank you! The only missing detail for beginners is proper storage of gel and other chemicals after opening kit.
Pages 12-13
www.agilent.com/cs/library/usermanuals/Public/G2938-90321_SensitivityDNA_KG_EN.pdf
Dr. Eric Chou Explanations are very nice.
Thank you s much. Hope you talk about RNA RIN value as well. Thanks
Excellent exposition.
Thank you! It helped me a lot
When you said you are adding gel/dye mix to other 3 gel wells but you already added 1 out of 3 gel well the gel/dye mixture for priming. Do you have to add gel/dye mixture again on that well?
Fantastic material, many thanks!
Great Video Man! Keep up the good work !
amazing video, so helpful! thank you!
That's a great and very helpful video! Congrats!
Excellent video mate.
Very well presented. thank you very much
I use the RNA Pico Kit but I´m wondering about your gel preparation. In my instructions it says to centrifuge the gel (spin filter) and add the dye AFTER (centrifuge again).
Awesome video! Would love more.
such a great video!!
Fantastic video! Thank you so much.
excellent
Love it, thanks!
why is the latter separated into peaks, while the sample is a single peak?
Great, thanks!
AWESOME!
Excellent sir thanks
Thank you very much for this video. It helps a lot! However, may I check on the reagents (especially all related to the dye) because as what I read in the Agilent High Sensitivity DNA Kit Guide, I understand that the reagents are light-sensitive. But in this video, it does not seem that way. Can anyone help in this matter? Thank you in advance.
Hi Lilian, I use this instrument daily for my job in cancer research and in our lab we always store the reagents in a dark box due to it being light sensitive especially the dye that gets mixed with the gel as well as the other reagents.
Hello everyone, how are you? I wondered how much it would be necessary to pay for a small lab capable of doing NGS? Can anyone help me? Thanks in advance! :)
Very helpul thank you
This rocks!
3:20 13:20 Software.
5:00 Hardware.
I am a beginner, we are doing sequencing but is not show sequences like atcatcgatgc
this is not sequencing, it is pre analysis of sample that will be sequenced
Garu of love and Light...🤔🙃
非常感谢
cool
In