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Пікірлер: 11
@muratturkbey74083 жыл бұрын
I was looking for like this video for a long. Thank you for sharing with us =)
@Genetex_Antibodies12 жыл бұрын
Thanks, GeneTex appreciate your support!
@user-zb7lh4rf7e11 ай бұрын
It's helping me a lot. Thank you
@thamizh28505 жыл бұрын
Since your lysis buffer have 1% sds, lysate should be viscous. But you didnt say anything how to reduce viscosity.
@delongtsway9534 жыл бұрын
Do you mean the RIPA? The lysate should have been removed during the centrifuge step.
@itssushmita6872 жыл бұрын
How much 2x loading buffer to be added for 5ug/ul of protein?? Please tell me
@Genetex_Antibodies2 жыл бұрын
Thanks for the inquiry. The volume of the 2x loading buffer depends on the loading amount into the well. For example, if you would like to use 30μg/well as the loading amount, it should take out 6μl as a sample from 5ug/ul whole-cell/tissue extract or the recombinant protein. And 2x loading buffer should use 6μl for each sample (2x sample buffer: sample volume is 1:1). Then you can follow Step10 on the video to finish all steps for the sample preparation. We hope it helps. Please feel free to contact us if you have any questions. www.genetex.com/contact
@itssushmita6872 жыл бұрын
@@Genetex_Antibodies thank you so much
@itssushmita6872 жыл бұрын
@@Genetex_Antibodies actually I'm getting different band density for beta actin.... I am loading 20ug of protein concentration for 20ul well.... Can you suggest something
@Genetex_Antibodies2 жыл бұрын
@@itssushmita687 Thanks for sharing the feedback with us. As the result you got, we think the concentration of samples has some problems. You can consider redetermining the concentration of samples by using a BSA standard curve. We hope this information will be of use. Please do not hesitate to contact us if you have any questions. The contact address is support@genetex.com.