Why switch to the G-Blot?
Easy to Use
Use your existing reagents, protocols, and power supplies.
Save Time
Reduce redundancy by running 96 samples in 1 gel instead of 8 gels.
Reduce Costs
Spend less money on precast gels membranes, and antibodies when you run 1 gel instead of 8. No need to buy expensive new equipment.
Improve Quantitation
Eliminate gel to gel variability, run replicates, and standard curves in the same blot.
Easily Integrate Into Your Workflow
The G-Blot seamlessly integrates with standard reagents for running denaturing gels, using Tris-HCl for the gel and running buffer, and Laemmli buffer for sample preparation. Compatible with standard power supplies and wet transfer systems, the G-Blot supports both nitrocellulose and PVDF membranes. It also works with existing blocking and washing buffers, antibodies, and detection chemistries, making it a versatile choice for streamlined lab workflows.
Traditional Western Blot Procedure
G-Blot Procedure
Equivalent Sensitivity for Chemiluminescence
Serial dilutions of recombinant alpha tubulin were loaded into a traditional western blot gel and a G96 gel, separated, transferred to a nitrocellulose membrane, incubated with the same antibodies, and detected with the same chemiluminescent substrate. More details here (see Figure 4D).
