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.
Excellent exposition.
Thank you s much. Hope you talk about RNA RIN value as well. Thanks
Fantastic material, many thanks!
amazing video, so helpful! thank you!
Thank you! It helped me a lot
Very well presented. thank you very much
Excellent video mate.
Great Video Man! Keep up the good work !
That's a great and very helpful video! Congrats!
Awesome video! Would love more.
such a great video!!
Fantastic video! Thank you so much.
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).
Love it, thanks!
excellent
Great, thanks!
Excellent sir thanks
why is the latter separated into peaks, while the sample is a single peak?
Very helpul thank you
AWESOME!
This rocks!
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! :)
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
非常感谢
Garu of love and Light...🤔🙃
cool
In