Superplex Your Western Blots
Superplex assays on Jess™ go far beyond traditional multiplex assays on Western blot and other protein analysis systems, so we named it something else. Jess automates the protein separation and immunodetection of traditional Western blotting, eliminating tedious and error-prone steps. With both fluorescent and chemiluminescent detection capabilities combined with in-capillary protein normalization, you can efficiently develop an assay to get more data points out of one sample.
What is Superplex?
Multiplex Up To Three Channels
Superplexing using Jess’s infrared (IR), near-infrared (NIR) and chemiluminescence channels helps you identify and differentiate relative protein expression between samples while built-in Protein Normalization gives you the confidence you need in your results all in one shot. Your sample, antibodies, and Protein Normalization and other reagents are loaded automatically, and all steps of a Superplex immunoassay take place in a single capillary. Jess first detects the total amount of protein present in your sample with the Protein Normalization Module, and then probes for your targets of interest in order of fluorescence-based detection first, followed by chemiluminescence.
- Run multiplexed chemiluminescence and fluorescence assays on the same sample at the same time
- Look at multiple targets and parameters simultaneously
- Get info on protein abundance, isoform and size all at once
- Throw in total protein without giving up a detection channel
- Detect high and low abundance proteins in the same sample, even when they have identical molecular weights
- Save time—your multiplexed, normalized, quantitative, size-based data will be ready in 3.5 hours
- Conserve precious samples—Jess only needs 3 µL/sample
Superplexing is Simple
All you have to do is load your samples, antibodies and reagents into a plate, insert the plate and capillary cartridge and press Start! Then enjoy 3 hours of handsfree run time to focus on your science, product development, or project deadline. When Jess is done, come back to fully analyzed and quantitative results! Compass for Simple Western automatically analyzes the data when the run is complete, including normalizing target data.
More Western Blot Data in Less Time
When you Superplex with Jess, one tiny 3 µL sample gives you at least 4 data points. Not to mention the time you save with your Western blots by doing four things at once, and that it only takes 3.5 hours to do them. But those aren't the only pros of Superplexing. Because each of those data points gets captured in the same capillary, you're not spending time comparing, infering and interpreting data across runs, samples, or lanes either. That means you get to make more informed, confident conclusions about your Western blot test results.
Figure caption: Protein normalization reveals comparable p-Akt signals across increasing concentrations of Jurkat + Calyculin A lysate. Comparative data showing p-Akt protein expression detected on Jess’s chemiluminescence channel and total Akt detected by the NIR channel as a measure of raw peak area shown in orange bars and separate-channel normalization for the normalized peak area shown in blue bars. As expected, normalization of the raw data results in similar peak area across all three lysate concentrations. Values plotted are mean protein peak areas for samples run in triplicate.
Simple Western Multiplex Assay Compatibility Chart
Simple Western™ has several assay types for multiplex analysis. See how they are compatible in the table below. You can also build your own assay using the Simple Western Kit Builder.
Assay Type |
Instrument |
Detection Channels |
Separation Module |
Detection Modules |
|
---|---|---|---|---|---|
Jess and Abby |
• Chemi |
• Chemi Detection Modules or Total Protein Detection Module (DM-TP01) |
Yes | ||
Jess |
• Chemi • Fluor |
• Chemi Detection Modules or Total Protein Detection Module (DM-TP01) • NIR / IR Detection Modules |
Yes | ||
Jess |
• Chemi • Fluor |
• Protein Normalization Module (DM-PN02) • Chemi Detection Modules • NIR / IR Detection Modules |
No | ||
Jess |
• Chemi • Fluor |
• Chemi Detection Modules or Stellar Total Protein Detection Module (DM-TP03) • Stellar NIR / IR Detection Modules |
No |
- Separation Modules include all MW ranges (2-40, 12-230, 66-440 kDa) and capillary cartridge formats (2 x and 8 x of 13 and 25 capillary cartridges)
- NIR/IR Detection Modules include Anti-Mouse and Anti-Rabbit Modules
- Chemi Detection Modules include Anti-Mouse, Anti-Rabbit, Anti-Goat, Anti-Human, Biotin Modules, and No-Secondary Detection Modules
Multiplex Western Blotting vs Simple Western
Simple Western lets you keep everything you like about multiplexing with Western blots and eliminate what you don't.
Western Blot |
Simple Western |
---|---|
Cannot multiplex across chemiluminescence and fluorescence channels | Multiplex across chemiluminescence and NIR/IR fluorescence channels with simultaneous total protein detection |
Tedious and heavily hands-on traditional Western blot workflow | Fully automated Western analysis following a simple sample preparation |
Challenging to detect low abundance proteins | Industry-leading fluorescence detection sensitivity with Stellar NIR/IR Modules |
Gel-to-membrane transfer variability | No gel-to-membrane transfer variability, highly reproducible |
Up to 50 µL sample required | 3 µL sample required |
Semi-quantitative | Fully quantitative |
>12 hours to results | 3 hours to results (5 hours with RePlex) |
No single-step total protein detection | Automated total protein normalization with multiple total protein detection methods |
Laborious strip and re-probe procedure often results in signal loss and/or interference | RePlex automates sequential Western analysis with no signal loss or interference because samples are covalently bound to the capillary |
Higher cost per run compared to Simple Western | Lower cost per run compared to Western blot |
Challenging to resolve high MW proteins | Resolve and quantify high MW proteins like Dystrophin |