Skip to content
Molekula

Application

Electrophoresis & blotting

Running buffers, stains, and transfer reagents for SDS-PAGE, native PAGE, and Western blotting.

Protein and nucleic-acid electrophoresis runs in a Tris-glycine or Tris-acetate buffer, separates by size in a polyacrylamide or agarose gel, and is visualised with Coomassie, silver, or fluorescent stain. Molekula supplies electrophoresis-grade Tris, glycine, SDS, acrylamide, TEMED, and APS.

What's in this workflow

Running buffers
Tris-glycine (SDS-PAGE), Tris-tricine (low-MW peptides), TAE/TBE (agarose nucleic acid).
Gel monomers
Acrylamide, bis-acrylamide, TEMED, ammonium persulfate (APS).
Detergents & denaturants
SDS, urea.
Stains
Coomassie Brilliant Blue R-250 / G-250, silver nitrate.
Transfer
Methanol-Tris-glycine, semi-dry / wet-tank.

Products from our catalogue

Live matches from the Molekula catalogue — request a quote on any product page.

Related products

FAQ

What percentage acrylamide gel should I use?

12% is a good default for 10–80 kDa proteins; 8% resolves larger proteins; 15% for small peptides. Use Tris-tricine for proteins below 20 kDa.

How is APS used in PAGE gels?

APS (ammonium persulfate) is the radical initiator; TEMED accelerates the polymerization. Standard recipe is 0.05% APS + 0.05% TEMED in the gel mix.

Need a custom grade or pack size?

Talk to a chemist — we run process chemistry from grams up to multi-kilogram campaigns.

Get a quote
Request a quote
Tell us what you need and our sales team will come back with pricing and lead times.
Full name
Company
Email
Phone (optional)
Product
Message
Buy now
Leave your details and we'll be in touch shortly.
Full name
Company
Email
Phone (optional)
How many packs?
Message