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ImmunoArrayᵀᴹ Antiphospholipid Syndrome (APS) and Neutrophil Extracellular Traps (NETs) Related Native Protein Autoantibody Detection Service (CAT#: NA-0726-FY17)
Developed by Creative Biolabs, the APS and NETs-Related Native Protein Autoantibody Detection Service utilizes an advanced, high-sensitivity protein microarray platform to profile autoantibodies against 120 literature-backed antigens. By immobilizing native form proteins onto a nitrocellulose membrane surface, this high-throughput, low-sample-rate service allows researchers to precisely evaluate autoimmune signatures linked to APS, NETosis, and systemic diseases. It serves as a powerful translational medicine tool, aiding in the discovery of clinically valuable antibody biomarkers, deciphering disease pathogenesis, and establishing multi-parametric models for early diagnostics, prognosis, and treatment monitoring.
| Specifications | |
|---|---|
| Size | 16-sample format per slide; features advanced multiplexing capable of profiling>120 targets per well (encompassing the 120 specific disease-related antigens). |
| Throughput Level | High-throughput (processes 16 samples per slide simultaneously, with support for parallel operations across multiple slides). |
| Protein Count | Up to 120 types of native form proteins. |
| Proteome Coverage | Focused panel consisting of 120 native form proteins thoroughly reviewed in literature and established as being explicitly associated with systemic autoimmune diseases, specifically targeting Antiphospholipid Syndrome (APS), Rheumatoid Arthritis (RA), and Systemic Lupus Erythematosus (SLE). |
| Arraying Technology | High-sensitivity antigen microarray technology (protein microarray) where native form proteins are orderly immobilized as ligands onto the nitrocellulose membrane surface of glass slides; molecular interactions are captured via fluorescent labeling and quantified using a fluorescence scanner. |
| Features | High Multiplexing: Screens>120 autoantibodies simultaneously in a single well, far outperforming traditional single-target ELISA methods. Native Conformation: Proteins are immobilized in their native forms on a nitrocellulose membrane surface to ensure accurate immune recognition. Ultra-low Sample Volume: Requires only 5 μL of serum or other body fluids, heavily conserving clinical specimens. High Flexibility: Dynamically combines diverse antigen matrices (proteins, peptides, nucleic acids) to detect distinct antibody types and subclasses. High Sensitivity & Wide Dynamic Range: Yields a broad signal dynamic range spanning from 1 to 65000. Cost-Effective: Delivers massive profiling capabilities at less than 1/10 of the cost of traditional ELISA kits. Semi-Quantitative: Supports relative quantification derived from established standard curves. |
| Application Fields | APS, NETs & Systemic Autoimmunity: High-efficiency screening and biomarker profiling for Antiphospholipid Syndrome (APS), Rheumatoid Arthritis (RA), Systemic Lupus Erythematosus (SLE), diabetes, MCTD, Sjögren's syndrome, scleroderma, polymyositis, dermatomyositis, etc. Translational & Clinical Research: Large-scale immune profiling across allergic diseases, infectious diseases, neurological impairments/brain nerve disorders, oncology (cancer biomarkers), vaccine R&D/post-vaccination monitoring (e.g., SARS-CoV-2, RSV, influenza), organ transplantation evaluation, drug screening, and clinical trials. |
For Research Use Only | Not For Clinical Use
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