๐จ Next MEWE Webinar is in 1 WEEK!!! ๐จ
"Microbial Immigration in Engineered Ecosystems?" with talks by Dr. Bing Guo (.@bingGuo_lab) and Dr. Fangqiong Ling (@h2omics) and moderated by Dr. Marta Vignola (@martavig5). June 21, 2022. Register here: https://t.co/ZR3SBUIdks
Anyone is planning to go to AEESP Conference this Jun28-30? ๐๐ปโโ๏ธ๐๐ปโโ๏ธ๐๐ปโโ๏ธ Can we share a room in the student housing?(Girl only๐)
Looking for students interested in PhDs studying #plastics or #carbon in natural waters @Northeastern. PhDs starting 2022 could be in Marine & Env Science; Chemistry; or Civil @ Env Engineering depending upon your background. Contact me for more details!
Did someone use eppendorf epmotion system and wanna transfer all of liquid from a 96 well pcr plate to another one?
There is always 10uL solution residual as mentioned in the property. My experiment is very sensitive to the volume, any one has some good suggestion for this๏ผ
l used SequalPrep Normalization Plate Kit after PCR and most steps are done on epmotion M5073, but after normalization and cleanup, the DNA yield is really low Around 0.3ng/uL, in their protocol they promised around 1-2ng/uL can yield. Anyone met the same situation before?
Did someone use SequalPrep Normalization Plate Kit before?
l was confused with Step1:Incubate the plate for 1 hour at room temperature to allow binding of DNA to the plate surface.
And how can l know DNA has already attached the wall?๐๐๐