Phil Kyriakakis
@breakliquid.bsky.social
Senior Research Scientist at Stanford Bioengineering | Taking apart and building biology.🧪
Another cool pipette rack pattern!
February 3, 2026 at 3:56 AM
Another cool pipette rack pattern!
Saw this today and nicely explains it why we need to keep speaking up.
February 2, 2026 at 11:01 PM
Saw this today and nicely explains it why we need to keep speaking up.
Another 3d printed pipette rack
February 1, 2026 at 7:33 AM
Another 3d printed pipette rack
It hooks onto the earthquake bar on the bench.
January 24, 2026 at 4:32 AM
It hooks onto the earthquake bar on the bench.
My new pipette holder
January 24, 2026 at 4:31 AM
My new pipette holder
This figure really grabs your attention!
January 23, 2026 at 1:47 AM
This figure really grabs your attention!
I hope their antibodies are better than their legos. The design is very flimsy, but I enjoyed the challenge.
January 7, 2026 at 3:59 AM
I hope their antibodies are better than their legos. The design is very flimsy, but I enjoyed the challenge.
Update, I grabbed 10 colonies and combined into one @plasmidsaurus.bsky.social reaction. All of them were too small and most were the same, the TE inserted in the same place. So screening colonies won't likely work.
November 22, 2025 at 5:10 AM
Update, I grabbed 10 colonies and combined into one @plasmidsaurus.bsky.social reaction. All of them were too small and most were the same, the TE inserted in the same place. So screening colonies won't likely work.
I tried to post it here
November 21, 2025 at 5:27 PM
I tried to post it here
Has anyone had this show up in their plasmid, and how to prevent it? "E. Coli IS10L Transposon"
November 19, 2025 at 6:27 AM
Has anyone had this show up in their plasmid, and how to prevent it? "E. Coli IS10L Transposon"
AI can mess things up real fast! 😭
November 15, 2025 at 1:22 AM
AI can mess things up real fast! 😭
I tried to "squeeze gel purify" DNA, sent it for sequencing, and it worked!
~Protocol:
1) cut out band
2) poke hold in small tube, put gel in it, put in big tube
3) Spin for 2-3 seconds
4) sequence the liquid in the bottom tube
This may not always work, but cool! @plasmidsaurus.bsky.social
~Protocol:
1) cut out band
2) poke hold in small tube, put gel in it, put in big tube
3) Spin for 2-3 seconds
4) sequence the liquid in the bottom tube
This may not always work, but cool! @plasmidsaurus.bsky.social
November 6, 2025 at 6:33 AM
I tried to "squeeze gel purify" DNA, sent it for sequencing, and it worked!
~Protocol:
1) cut out band
2) poke hold in small tube, put gel in it, put in big tube
3) Spin for 2-3 seconds
4) sequence the liquid in the bottom tube
This may not always work, but cool! @plasmidsaurus.bsky.social
~Protocol:
1) cut out band
2) poke hold in small tube, put gel in it, put in big tube
3) Spin for 2-3 seconds
4) sequence the liquid in the bottom tube
This may not always work, but cool! @plasmidsaurus.bsky.social
iGEM is not your typical scientific conference! @igemcommunity.bsky.social
October 29, 2025 at 7:12 AM
iGEM is not your typical scientific conference! @igemcommunity.bsky.social
I really want to use "behooves me" in this writing (grant), but Grammarly doesn't want me to!
September 26, 2025 at 5:42 PM
I really want to use "behooves me" in this writing (grant), but Grammarly doesn't want me to!
Lalo says happy whatever day it is
September 21, 2025 at 12:05 AM
Lalo says happy whatever day it is
Mr Kitten says happy Saturday
September 20, 2025 at 11:47 PM
Mr Kitten says happy Saturday
If only it fixed my PCR.
September 15, 2025 at 9:46 PM
If only it fixed my PCR.
Your gel running in the IR!
September 15, 2025 at 9:45 PM
Your gel running in the IR!
September 6, 2025 at 9:53 PM