Ever wondered how 🥔 haploid inducers induce 🥔 haploids? Then check out my second
chapter, now out in @ThePlantCell
https://t.co/AXVENw4Mrg
Or just read this 🧵:
Latest episode of #No_Time_To_Read podcast!
It was a wonderful discussion with @KirkAmundson Kirk about his recent @ScienceMagazine article.
Podcast: https://t.co/kNBr8zQL45
Article: https://t.co/WsIbYB0XaX
Plant developmental genes share functions & expression, but align orthologs' promoters and often… no conservation. Or is there?
In our new preprint, we show that conservation exists and is ancient, but was just obscured by genome complexity.
https://t.co/yY3MS5pgxA
Made amoeba cookies for my exit seminar!
It's at 4pm tomorrow, December 9th in 1022 Green Hall. DM for a zoom link if you'd like to see a lot of microscopy of my weird #Rhizaria#syncytial#protist!
Did you know some 🍄 have extremely low mutation rates? So where is their population's genetic diversity coming from? In this new @PNASNews ms we show that a fairy-ring #mushroom has differential genome stability depending on the life-cycle stage! 1/n
https://t.co/MqEl8FDYSn
We have a postdoctoral research opening in my group on the topic of meiotic recombination - please get in touch if of interest! @plantsci#meiosis#Arabidopsis#genetics#epigenetics
https://t.co/HcYdCcRzho
The UC Davis Dept. of Plant Biology is recruiting an Assistant Professor in Plant Developmental Biology! Please consider applying and RT! For those of you in the know... this was the home of Katherine Esau - and I vouch for excellent potential colleagues: https://t.co/rdPriuw7wf
We are hiring an Assistant/Associate Professor of Potato Breeding and Genetics TT position to lead our potato breeding, genetics and variety development program! 🥔🌱 #potatobreeding@UMaine@UMainePotato -- details in a short thread below 1/x
@J_SaizPerez @LabSchnittger Brief explanation: Resuspend the pellet from 3-4 ml Agro culture into 3 ml of transformation buffer (5% sucrose and 0.02% Silwet-77). Add transformation buffer in droplet on the closed flowers using pipette. Keep in the dark for at least 24h.
Have fun! 😉
@MitchFeldmann If you only need to type that 1 marker, you can run a size diff PCR with a small piece of tissue in the rxn, then gel to check size. Quick and def dirty, but no DNA extraction or library prep needed.