UltraBind™ Affinity Membrane
Modified polyethersulfone (PES) membrane for covalent protein binding
- Proteins can be efficiently attached without prior membrane derivatization.
- ELISA
- Affinity separation
Media
Modified polyethersulfone with aldehyde surface chemistryPore Size
0.45 µmTypical Thickness
152 µm (6 mils)Typical IgG Binding Capacity
135 µg/cm2UltraBind Membrane Binds and Retains Proteins

Membrane discs (13 mm) were soaked in a protein solution and washed to determine the capacity and strength of protein binding. Discs were soaked in radioactively-labeled IgG and BSA (200 µg unlabeled protein with 100,000 cpm of 125I-labeled tracer) for 60 minutes with agitation, rinsed, and either read in a scintillation counter or stripped using a 1% SDS/2 M Urea wash. Biodyne B membrane (charged nylon transfer membrane) and Bio-Inert membrane (modified Nylon 6,6 membrane) were used as high and low binding capacity controls respectively. UltraBind membrane efficiently bound protein and retained it after the SDS/Urea wash.
Antigen Detection (dot blot ELISA) with UltraBind Membrane

Dilutions of human serum albumin (hSA) ranging 2000 to 0.5 pg/spot were applied to UltraBind membrane using a 96-pin transfer tool on a Matrix PlateMate* Liquid Handling Station. The membrane was then blocked with 0.5% Hammersten-grade casein in PBS. hSA was detected with rabbit anti-hSA antibody followed with alkaline phosphatase conjugated goat anti-rabbit IgG. Signal was generated by reaction with BCIP/NBT substrate allowing detection of as little as 0.5 pg hSA.
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