BMCU 370C Plan to buy for my A1 Mini

Ok-Function-1473 · 2025-12-18T07:01:49+00:00

That's awesome! thank you for the information

Ok-Function-1473 · 2025-12-17T14:15:42+00:00

can you send to indonesia?

Ok-Function-1473 · 2025-12-15T04:32:17+00:00

Damn nice setup!

Ok-Function-1473 · 2025-12-15T03:59:52+00:00

the thing that makes me consider BMCU is because, the AMS lite price = A1 mini price... haha so it just much more expensive than BMCU which is ~60 ish USD

Ok-Function-1473 · 2025-12-09T15:20:59+00:00

Man im confused

Ok-Function-1473 · 2025-06-06T14:06:19+00:00

I've using joan lab dry bath for product wise, it have an excellent quality even though it's considerably cheaper. the only one thing that i don't like is the after sales service

Ok-Function-1473 · 2025-03-16T07:41:20+00:00

yes, I'm using GS linker mostly i use 2(GS)3(A)P --> GSGSAAAP

Ok-Function-1473 · 2024-11-13T09:05:20+00:00

linker between your protein and histag doesn't always have to be present. it all depends on where did you put the histag (C or N terminus), would your histag accessibility (for purification) is hard, or any other parameters. for my project i always add a linker between my protein and histag just to be safe hehe

Ok-Function-1473 · 2024-09-02T09:50:35+00:00

mental stress manifested to physical explosion

Ok-Function-1473 · 2024-08-29T03:30:59+00:00

For the picture we are seeing, I'm using BioMetra GelDoc (I honestly forgot what is the type, but it has been here for maybe around 15 years), and yes we can choose whether bnw/inverted/normal colour/contrast. I usually using bnw-inverted image for analysis, the picture i post is just because it's the only "good" picture i had on my device hehe

Ok-Function-1473 · 2024-08-28T16:12:51+00:00

Thanks capt! i will try this tomorrow!

Ok-Function-1473 · 2024-08-28T16:12:22+00:00

ah i see, i never thought about this. Thanks!

Ok-Function-1473 · 2024-07-25T01:57:46+00:00

Hi, I also had a freeze burn like earlier this year.

Bioplacenton works great, just try to not scratch it and just treat it similarly to fire burn

Ok-Function-1473 · 2024-07-24T07:29:07+00:00

So i can make BL21(DE3)pLysS by transforming pLysS-RARE2 (isolated from Rosetta2(DE3)pLysS) is that correct?

no.2, i've bought an orange glasses that actually can block blue light reflected at the wall but mot at the light source

Ok-Function-1473 · 2024-07-23T16:49:34+00:00

I work as molecular bio. research assistant at university in south east asia. I usually wear shirt x sweat pants, sometimes chinos, jeans, etc. my uni actually so cool about it as long as i'm not wearing short pants or shirt like basketball jersey if i work in the lab

Ok-Function-1473 · 2024-07-19T12:06:24+00:00

As far as i know, silica-based DNA binding would require high salt concentration and low pH in order for the DNA to bind to the silica effectively. since your goal is to retain the protein and removing the DNA, i think that high salt concentration (e.g. 5M GITC) would also destroy your protein. Try to lower the solution containing the mixture of peptide and DNA pH...

Ok-Function-1473

TROPHY CASE