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Advanced western blotting solutions

Our mission is to empower scientists with advanced and cost-effective tools that enhance productivity and reproducibility for protein analysis.

G-BLOT BENEFITS

With the G-Blot, you can achieve up to 10X the throughput of traditional gels without changing your western blotting workflow. It’s fully compatible with the reagents you already know and trust, allowing your lab to boost productivity and efficiency effortlessly.

tube

Easy to Use

Use your existing reagents, protocols, and power supplies.

Fast

Save Time

Reduce redundancy by running 96 samples in 1 gel instead of 10 gels.

moneyxl

Reduce Costs

Spend less money on pre-cast gels, membranes, and antibodies when your run 1 gel instead of 10. No need to buy expensive new equipment.

Dupleicate

Reproducibility & Quantitation

Eliminate gel-to-gel variability, run replicates, and standard curves in the same blot, with equivalent sensitivity to regular western.

Plug & Play

Easily Integrate Into Your Workflow

The G-Blot seamlessly integrates with standard western blotting reagents for running denaturing polyacrylamide gels, 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. It is compatible with standard power supplies, sample types (e.g. Laemmli buffer), and transfer systems, and wet transfer is recommended. Both nitrocellulose and PVDF membranes are supported.

Procedure

Traditional Western Blot

Traditional Western Blot

G-Blot

G-Blot

Equivalent Sensitivity to Regular Western

Traditional Western Blot

G-Blot

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.

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Procedure

Traditional Western Blot

G-Blot

Equivalent Sensitivity to Regular Western

Traditional Western Blot

G-Blot

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.

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