초록 ▼

Hydrophilic membrane particularly suited for blotting applications, preferably Western blotting. A pre-wet hydrophobic membrane substrate, preferably made of PVDF, is contacted with a monomer solution and subjected to a UV-initiated free radical polymerization step to render the substrate permanentl

Hydrophilic membrane particularly suited for blotting applications, preferably Western blotting. A pre-wet hydrophobic membrane substrate, preferably made of PVDF, is contacted with a monomer solution and subjected to a UV-initiated free radical polymerization step to render the substrate permanently hydrophilic. The resulting membrane exhibits low background fluorescence, high protein binding, excellent retention of protein sample spot morphology, and extended dynamic range (high signal-to-noise ratio, enhanced sample detectability). The membrane demonstrates comparable or higher performance in Western blotting applications than conventional nitrocellulose Western blotting membranes, particularly for protein detection at low sample concentrations, and is directly water-wettable, eliminating the need for an alcohol pre-wet step prior to use.

대표청구항 ▼

1. A Western blot immunodetection assay for detecting target proteins in a protein sample, comprising: electrophoretically separating said target proteins from said protein sample;transferring the separated target proteins onto a porous polymeric substrate having its surface modified with a crosslin

1. A Western blot immunodetection assay for detecting target proteins in a protein sample, comprising: electrophoretically separating said target proteins from said protein sample;transferring the separated target proteins onto a porous polymeric substrate having its surface modified with a crosslinked polymeric coating comprising acrylamide and methylene-bis-acrylamide, said coating rendering said surface hydrophilic;blocking said substrate to prevent nonspecific binding of antibodies to said substrate surface;incubating said substrate with a primary antibody capable of binding to said target proteins;incubating said substrate with a labeled secondary antibody capable of complexing with an enzyme of said primary antibody to provide a measurable signal; anddetecting said signal. 2. The Western blot immunodetection assay of claim 1, wherein the measurable signal is detected by visual, chemiluminescent or fluorescent detection. 3. The Western blot immunodetection assay of claim 1, wherein said porous polymeric substrate having its surface modified has a protein binding capacity as measured by an IgG binding test of about 250-325 μg/cm2. 4. The Western blot immunodetection assay of claim 1, wherein the average total organic carbon level of said porous polymeric substrate is below 1.5 ug/cm2, and wherein extractable monomer levels, as determined by HPLC, are below 0.02 ug/cm2 for acrylamide, and below 0.15 ug/cm2 for methylene-bis-acrylamide. 5. The Western blot immunodetection assay of claim 1, wherein said porous polymeric substrate has a background fluorescence value, and wherein said substrate modified with said polymeric coating exhibits a background fluorescence of about twice that of said substrate background fluorescence value under identical measurement conditions. 6. The Western blot immunodetection assay of claim 1, wherein said substrate comprises polyvinylidene fluoride. 7. The Western blot immunodetection assay of claim 1, wherein the ratio of acrylamide to methylene-bis-acrylamide is about 1:1 (mass/mass). 8. The Western blot immunodetection assay of claim 1, wherein the overall monomer concentration of the acrylamide:methylene-bis-acrylamide monomer reactant solution used to coat said surface is between 0.5% and 1.5% by mass.