Pu•MA System ELISA: Mouse Interleukin-10
Mouse IL-10 (Interleukin-10), initially referred to as cytokine synthesis inhibiting factor (CSIF), is a multifunctional cytokine that plays a large in role in various inflammatory processes. IL-10 is secreted by several activated hematopoietic cell types, keratinocytes, and placental cytotrophoblasts. Secretion by macrophages is stimulated by endotoxins, TNFα (Tumor necrosis factor-alpha), catecholamines, and IL-1. IL-10 controls several inflammatory processes such as inhibiting expression of proinflammatory cytokines, adhesion molecules, antigen-presenting and costimulatory molecules in several immune cells. Conversely, it increases production of anti-inflammatory molecules such as IL-1RA and soluble TNFα receptors. IL-10 plays an essential role in the control of viral infections as well as allergic and autoimmune inflammatory reactions.
The workflow for the Pu•MA System cytokine immunoassay is shown in Figure 1. All assay reagents are prepared in advance and then loaded into Pu•MA System flowchips using single or 8-channel pipettes. The wells are conveniently located on standard 384 multiwell plate spacings. The flowchips are now ready to be loaded into the Pu•MA System for “hands-off” processing. The ELISA steps are automatically performed by the system using pre-loaded protocols. Once the assay is complete, absorbance results are read on your Plate Reader.
Pu•MA System Complete Workflow: 2-3 hours “hands-off”
Figure 1. Schematic Pu•MA System assay workflow.
The adaption of existing ELISA kits and/or antibody pairs is straightforward with the Pu•MA System. Assay buffers optimized for the Pu•MA System flowchips are provided for sample and antibody dilutions. Blocking solutions and wash buffers are also provided. The Mouse IL-10 assays are adapted from BioLegend ELISA Max Kits (p/n 431411). The reagents required for the assay are shown in the table.
Assay reagents were prepared according to the dilutions shown in the Table using Pu•MA Assay Buffer (PAB). IL-10 standards were reconstituted according to instruction provided by BioLegend. A 1:2 serial dilution series of Mouse IL-10 Standard was prepared starting at 100 pg/well using PAB. 20 μl of each reagent was added to the appropriate wells (see Fig 3) except for the Stop Solution where 10 μl was dispensed. Four replicates were run per concentration. The flowchips were loaded into a Pu•MA System and processed using the IL-10 Assay Protocol. Plates were read within 5 min of completion on an absorbance plate reader at 450nm (Tecan Spectrafluor Plus).
|Capture Ab||Mouse IL-10 Capture Antibody (1:25)||BL|
|Block||Pu•MA Blocking Buffer||PFI|
|Sample||Mouse IL-10 Standard||BL|
|1°Ab||Mouse IL-10 Primary
|Wash||Pu•MA Wash Buffer||PFI|
|Stop||Pu•MA Stop Solution||PFI|
Pu•MA System Mouse IL-10 Standard Curve
Figure 2. Response of Cytokine Standards for ELISA run on Pu•MA System. ELISA antibody pairs and standards were obtained from BioLegend. Absorbance was read at 450 nm. OD values shown are background subtracted.
How It Works
The Pu•MA Flowchip and System uses established antibody pairs to perform an automated ELISA. All assay reagents are loaded into reservoirs and then moved one at a time through the “Assay Channel” by the Pu•MA System. Preloaded protocols execute all fluid transfer and incubation steps The system incorporates patented valve-less fluidic switching (VLFS) to precisely control fluid movement in a flowchip. Use of microfluidics reduces
both incubation times and reagent volumes.
Reagent Loading Setup
- Low sample/reagent usage: < 20 μl/well)
- Enhanced kinetics: Faster Assay Results
- Effi cient fl uid removal: Less Wash Required
Figure 3. Pu•MA Flowchip reagent loading setup.
Microfluidic Assay Workflow
- Compact benchtop system
- Easy top-loading of flowchips
- Precision pneumatic control
- Touchscreen-driven interface
- Preloaded assay protocols
- Simple Select and Run operation
Reagents & Flowchips
- Validated immunoassays
- Open platform for existing Ab pairs
- Works with standard pipettors & tips