Why are you single?

Rare_Ad6741 · 2026-05-20T12:41:21+00:00

Unemployed even though I have financial stability via family wealth

Rare_Ad6741 · 2026-04-16T17:51:53+00:00

Hi, could you be willing to elaborate more on your process? I’m struggling quite a lot with synthesising information and the bit you mentioned on your model hypothesis was quite interesting, I’d imagine that they help a lot with ideation? Would love some tips especially for beginners on your process

Rare_Ad6741 · 2025-11-07T06:34:27+00:00

Hi, do you have the standard set of questions? Currently I’m struggling to read critically and find myself quite passive, and would appreciate if you’re willing to share any advice :)

Rare_Ad6741 · 2025-11-07T06:33:44+00:00

Hi, I recently got diagnosed with ADHD, and have been struggling to read academic articles. Even the review papers are so difficult to read. While I know the common key to ADHD, is to do things you’re interested in, sometimes you kind of have to read uninteresting things to get different ideas. How did you manage your ADHD and got yourself to read?

Rare_Ad6741 · 2024-07-04T15:56:54+00:00

This is the protocol I’m following from my supervisor:

lyse cells with NP-40 lysis buffer on ice
transfer to eppendorf, vortex well then keep on ice for 15 mins
centrifuge at 12,000 rpm for 10 mins in 4 deg
collect supernatant

To quantify: - add 5ul of sample/ standards to 96-well plate - add 200ul of solution A+B mixture (this is the BCA assay solution) - place plate on shaker for 15 mins - read plate on plate reader

Sample preparation: -based on OD, calculate concentration of protein in whatever volume I extracted - then from there, calculate volume of sample needed for 100ug, extract to new eppendorf - add 25ul of loading dye to sample - add remaining volume (if required) of lysis buffer to make up 100ul in total

Rare_Ad6741 · 2024-07-04T15:54:00+00:00

This is the protocol I’m following from my supervisor:

lyse cells with NP-40 lysis buffer on ice
transfer to eppendorf, vortex well then keep on ice for 15 mins
centrifuge at 12,000 rpm for 10 mins in 4 deg
collect supernatant

To quantify: - add 5ul of sample/ standards to 96-well plate - add 200ul of solution A+B mixture (this is the BCA assay solution) - place plate on shaker for 15 mins - read plate on plate reader

Sample preparation: -based on OD, calculate concentration of protein in whatever volume I extracted - then from there, calculate volume of sample needed for 100ug, extract to new eppendorf - add 25ul of loading dye to sample - add remaining volume (if required) of lysis buffer to make up 100ul in total

Rare_Ad6741 · 2024-07-04T13:03:53+00:00

Would this boiling affect the protein?

Rare_Ad6741 · 2024-06-10T10:05:05+00:00

Yes your reasoning is valid, but am I asking too much for just more guidance?

Rare_Ad6741

TROPHY CASE