Advanced Western Blotting Solutions for Cancer & Immuno-Oncology
Accelerate your cancer & immuno-oncology research. Our next-generation cancer research equipment allows you to uncover new views into the role of proteins in cancer and accelerate your ability to develop and analyze protein-based therapeutics. Simple Western™ can help you reveal new insights and advance cancer & immuno-oncology research through the study of proteins, their function and signaling, through reliable, quantitative, and automated workflows.
Simple Western
Simple Western
Simple Western™ systems provide fully automated, hands-free Western blotting analysis, giving you highly quantitative and reproducible results, and using less sample in the process.
Quantification
Simple Western provides fully quantitative results and has a wider dynamic range than a traditional Western blot.
Reproducibility
Reproducibility
Simple Western eliminates the unavoidable variation of traditional Western blotting, producing intra-assay CV’s <15%.
Limited Sample
Limited Sample
Quantitation of protein expression via Simple Western only requires input volumes of 3 µL, so the majority of your sample remains available for other characterization methods.
Sensitivity
Sensitivity
Simple Western has chemiluminescence and industry-leading NIR/IR detection that is 100X more sensitive than the closest competitive traditional Western blot fluorescence imaging system.
Speed
Speed
Simple Western tests up to 25 samples in 3 hours or 96 samples overnight and allows for the multiplex detection of multiple proteins per sample.
From Your Peers in Cancer Research
"[Simple Western] is easy to use, convenient, and gives answers quickly. The throughput and system automation is a definite advantage."
- Jane Gray, Ph.D., Head of Research Instrumentation, Cancer Research UK Cambridge
"I was able to screen various antibodies in a single run within half a day. This had previously taken weeks and months using traditional Western blotting methods."
- Krishna C. Yalla, Ph.D., Postdoctoral Research Scientist, Institute of Cancer Science
Simple Western offers highly specific, sensitive, and reproducible quantification of important immuno-oncology targets in human cells. These targets are detected simultaneously with total protein in your sample for accurate total protein normalization. Immune checkpoint proteins: PD1, PD-L1, CTLA-4, and TIGIT; Hypoxic markers: HIF-1α, VEGFR-2, TGF-β, and ANG2; CAR T-Cell Target: CD19
Methodologies like flow cytometry have limitations such as off-target binding of variants or isoforms and difficulties in finding validated antibodies. Simple Western and Single-Cell Western systems partner to get you critical answers on the immune cell populations found in the tumor microenvironment, offering both population level views and single-cell level perspectives on cell subtypes.
Simple Western requires only a few microliters of precious samples like laser capture microdissection (LCM) sample to generate multiple data points. Simple Western also has high sensitivity multiplex detection of low abundance proteins that are difficult to detect by traditional Western blot. And it’s all wrapped up in a simple workflow that minimizes your hands-on time.
In Simple Western assays, proteins are immobilized after separation, reducing variability and enabling quantitative measurements of protein abundance. High-sensitivity multiplexing is easy using multiple detection channels or RePlex to enable phospho/total measurements in the same capillary. Measure total protein in your sample for accurate total protein normalization.
- Virtual Poster Presentation “Novel approach for automated sequential immunoassay for quantitation and characterization of PI3K/AKT pathway proteins” by Dr. Jessica Dermody
- Virtual Poster Presentation “Determination of antibody’s specificity towards phosphorylated protein targets with automated in-capillary enzyme treatment and immunoassay” by Dr. Daryl Taketa
- Virtual Poster Presentation “Multiplexed Protein and RNA Quantification on a Single Instrument Harmonizes Multi-omic Analyses of Biomarkers for Immunotherapies and Targeted Therapies in Non-Small Cell Lung Cancer” by Dr. Chris Heger
Heterogeneity and single-cell resolution. Single-Cell Western on Milo™ adds single cell resolution and heterogeneity information to cell signaling studies traditionally done with conventional Western blotting and simplifies challenging phospho-flow assays done with flow cytometry.
Milo Adds Single-Cell Resolution and Heterogeneity Information
The Milo Single-Cell Western system helps detect discrete cell signaling states by measuring multiple phospho-proteins in individual cells within a population. Because cells are lysed in Single-Cell Westerns, membrane permeabilization is not required and both intracellular and intranuclear proteins are accessible for antibody probing, making it possible to use phospho-antibodies validated for Western blotting and simplifying some challenging intracellular flow assays.
Tumor Landscape Mapping of Chemo-Resistant Cancer
In this webinar, Dr. Kyeung Min Joo, from Sungkyunkwan University School of Medicine, Seoul, South Korea describes their findings from the use of single-cell analysis technologies including Single-Cell Westerns to depict the tumor landscape of a single case of chemo-resistant metastatic, muscle-invasive urothelial bladder cancer (MIUBC).
Epigenetic Alterations in Single Nuclei
Epigenetic alterations play important roles to drive the cancer phenotype. Use Single-Cell Westerns to investigate histone modifications in single nuclei and understand epigenetic regulation of gene expression at the single-cell level.
High-Impact Peer-Reviewed Cancer Research
Simple Western systems have been involved in breakthrough immunotherapies, including those involving immune checkpoint inhibitors, CAR T-cell therapy, bispecific antibodies, and macrophage switching. Single-Cell Westerns provide insight into population heterogeneity at the protein level and has been used to study the molecular underpinnings of malignant cell transformation with unprecedented detail.