Custom Premix Selecting "Custom Premix" option means that all of the beads you have chosen will be premixed in manufacturing before the kit is sent to you.
The SNAP id 2.0 protein detection system uses a vacuum to drive reagents through the membrane, enabling increased antibody-antigen binding, enhanced washes, and antibody recollection.
The possible causes and potential remedies for challenges encountered during preparation of samples for SDS-PAGE (sodium dodecyl sulfate polyacrylamide gel electrophoresis) and optimizing electrophoresis conditions.
Learn how SNAP id 2.0 protein detection system works, which applications it is compatible with, and how it optimizes westernblotting conditions for reduced workflow.
This page describes common challenges encountered when lysing cells and extracting proteins prior to Westernblotting. Total protein concentration must be determined for these cell lysates. Variables affecting each of these steps are outlined below, as each could affect the sensitivity and reproducibility of the Western blot.
The possible causes and potential remedies for challenges encountered as a result of blocking, washing, antibody incubation, and detection/exposure of Western blots.
We provide a broad selection of chemiluminescent westerns including HRP (horseradish peroxide) substrates, the most sensitive in blotting and premixed for convenience.
We provide a wide portfolio of westernblotting products including optimized reagents for chemiluminescent and fluorescent Western blots, and the SNAP i.d.® 2.0 system.
Discover updated application notes for Westernblotting topics and find useful insights for antibody reuse, triple well blotting, and immunodetection applications.