Jacob K

38 posts

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Jacob K

Jacob K

@jay_clicks

Graduate student // Pasta connoisseur // Running enthusiast https://t.co/yaH17DwPtH

Boston, MA Katılım Ocak 2016
184 Takip Edilen91 Takipçiler
Jay Tan
Jay Tan@JayXiaojunTan·
Lysosomes are essential for cellular quality control, but how about the quality control of the lysosome itself? Online now @TrendsCellBio, we reviewed the molecular mechanisms of four major lysosomal quality control pathways: TFEB/Lysophagy/ESCRT/PITT. authors.elsevier.com/a/1gVEr3QxxSr6…
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Jacob K
Jacob K@jay_clicks·
@DrlxReina At a quick glance it seems like all the wells with the foam at the top aren't running. I'd check to make sure there's enough buffer to cover all the wells which should displace the foam. My bet is that the foam is hindering conductance which is why those samples aren't running
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Reina Desrouleaux
Reina Desrouleaux@DrlxReina·
Hello! What would cause my gel to run like this? Is the cassette bad? (The other gel is running just fine! )
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Jacob K
Jacob K@jay_clicks·
@IrisMontes19 @noellneuro TBH people panic and buy out all the bread and milk when there's less than a foot too. But I'm not going to work tomorrow... Pretty sure the T will be closed and roads undrivable
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Iris D. Montes
Iris D. Montes@IrisMontes19·
@noellneuro I wasn’t worried until I saw the panic in the grocery stores 😅
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Noell Cho
Noell Cho@noellneuro·
I’ve lived in Boston since 2018. Wondering if I’m not taking this blizzard warning as seriously as I should since I’m still planning to go to lab tomorrow. who’s laughing at me #islandgirl
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Jacob K
Jacob K@jay_clicks·
@D_HellerTrulli Hmmm, adding more classes to burnt out residents didn't help. Surprising. Maybe if they add mandatory yoga sessions after overnights🤔🤔🤔
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Jacob K retweetledi
Malavika Raman
Malavika Raman@MaliRamanLab·
Check out a new paper from the lab! New role for p97 at organelle contact sites: The p97-UBXD8 complex modulates ER-Mitochondria contact sites by modulating membrane lipid saturation and composition biorxiv.org/content/10.110…
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Jacob K
Jacob K@jay_clicks·
@avtytla Isn't it based on surface area instead of volumes? IE 1:3 pass is taking whatever cells are in 1 cm^2 and putting into 3 cm^2. So for replating into the same dish, it's 1/3 of the cells but if replating into a dish 3x the size, use all the cells. This is wrinkling my brain
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Jacob K
Jacob K@jay_clicks·
@oldladyscience Were just not photogenic enough to be featured 😭😭
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Jacob K
Jacob K@jay_clicks·
Where are the Boston fireworks? No sign of them
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Pablo Munoz
Pablo Munoz@pablo_jack·
@jay_clicks @AnoopArunagiri Indeed! I think that only icy software has something to measure dispersion. BTW, I tried the macro but I found some problems with line182 and with bioformat line when I choose setup.
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Jacob K
Jacob K@jay_clicks·
@pablo_jack @AnoopArunagiri That's an interesting challenge. AggreCount can capture ROIs of nuclei, cell borders, and puncta. Theoretically it could calc the distance between cell borders and puncta using the same methodology it uses now for nuc->puncta distance.
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Pablo Munoz
Pablo Munoz@pablo_jack·
@jay_clicks @AnoopArunagiri Oh that is great! I was waiting long time for something like this. Now I am trying to find a way to measure aggregation from nucleus to cell periphery, as a distance map for puncta dispersion. Maybe aggrecount 2.0 in the future :)
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Jacob K
Jacob K@jay_clicks·
@pablo_jack @AnoopArunagiri Absolutely! We actually started using it to quantify peroxisomes in our lab. In its essence, AggreCount isolates and quantifies bright puncta and then measures the distance between the puncta and a nucleus. So anything with punctate staining may be quantified. LMK how it works
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Pablo Munoz
Pablo Munoz@pablo_jack·
@AnoopArunagiri This is great! DO you think that I can adjust the parameters and use it to quantify vesicles or organelles accumulation?
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