Human IL-3 XL Luminex® Performance Assay
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Human IL-3 XL Luminex® Performance Assay Summary
| Panel | Luminex Performance Human XL Cytokine Panel |
| Assay Type | Magnetic bead-based multiplex assay for the Luminex® platform |
| Format | 1 x 96-well microplate and Magnetic antibody-coated beads |
| Species | Human |
| Analytes Detected | Please see analyte list in assay customization tool below. |
| Performance Validation | Our Luminex High Performance Assays undergo our most extensive validation testing. All Luminex High Performance Assay Panels are validated for use with serum and plasma samples. Some High Performance Assays are additionally validated for cell culture supernatants, milk, saliva, or urine, as indicated on the individual product data sheets. Luminex High Performance Assays are tested for sensitivity (three-quarters the low standard), intra-assay precision, inter-assay precision, and to ensure assay linearity for validated sample types. Recovery values for individual samples in validated sample types are also tested. Validation data for each analyte can be found in the product datasheet. View Luminex High Performance Human XL validation data. |
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Magnetic Luminex High Performance Assays are flexible bead-based multiplex assays. They allow up to 50 user-defined target analytes to be simultaneously profiled using cell culture supernates, serum, or plasma samples. Some panels are also validated with human milk, saliva, and/or urine samples.
- Simultaneously profile Human IL-3 with up to analytes of your choice in one sample
- Magnetic format allows for easier wash steps
- Undergoes similar validation testing as Quantikine® ELISA Kits
- Precise and Specific
- Requires a small sample volume (<50 µL)
- Run your assay in just 3-5 hours
- Mass-calibrated standards for consistent results with every new lot of material
- Enough reagents for one 96-well plate
- Premixed cocktail of biotinylated detection antibody
- Standard Cocktail(s)
- Bead Diluent
- Biotin Antibody Diluent
- Calibrator Diluent
- Wash Buffer
- Streptavidin-PE
- One flat-bottom 96-well Microplate
- Foil Plate Sealers (4)
- Mixing Bottle
- Standard Value Card**
- High and low controls with Control Mean Value Card
**A standard curve must be generated each time an assay is run, utilizing values from the Standard Value Card included in the Base Kit.
- User-mix antibody-coated Magnetic beads in individual vials
Recommended Sample Types: Cell culture supernates, serum, EDTA plasma, and heparin plasma
Components: Human IL-3 Magnetic Microparticles (Part 898808) is supplied as a 100X concentrated stock (0.075 mL) with preservatives.
Other Supplies Required: Magnetic Luminex® Performance Assay Human XL Discovery Base Kit (R&D Systems®, Catalog # LUXLM000).
Sensitivity: The Minimum Detectable Dose (MDD) was determined by adding two standard deviations to the mean MFI of twenty zero standard replicates and calculating the corresponding concentration.
Six assays were evaluated, and the MDD of human IL-3 ranged from 1.21-9.05 pg/mL. The mean MDD was 2.63 pg/mL.
Correlation: This assay has been correlated to the Quantikine® ELISA Kit.
Specificity: This assay recognizes natural and recombinant human IL-3.
Bead Region: 56
Precision
|
Intra-assay Precision (precision within an assay) - Two samples of known concentration were tested twenty times on one plate to assess intra-assay precision. |
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| Intra-Assay Precision | Inter-Assay Precision | |||
|---|---|---|---|---|
| Sample | 1 | 2 | 1 | 2 |
| n | 20 | 20 | 30 | 30 |
| Mean (pg/mL) | 204 | 1942 | 209 | 1,951 |
| Standard deviation | 6.71 | 77.2 | 26.0 | 143 |
| CV (%) | 28.9 | 97.5 | 12.4 | 32.9 |
Recovery
|
Samples containing and/or spiked with human IL-3 were evaluated for recovery. |
||||||
| Sample Type | Average % Recovery | Range (%) | ||||
|---|---|---|---|---|---|---|
| Cell culture supernate | 108 | 96.7-115 | ||||
| Serum | 77.7 | 58.0-100 | ||||
| EDTA plasma | 84.6 | 65.6-109 | ||||
| Heparin plasma | 82.1 | 63.4-98.2 | ||||
| Plaelet-poor EDTA | 83.2 | 70.2-94.5 | ||||
| Platelet-poor Heparin | 82.7 | 65.6-97.9 | ||||
Linearity
|
Samples containing and/or spiked with human IL-3 were serially diluted to evaluate assay linearity. |
||||||||||||
| Cell culture supernate | Serum | EDTA plasma | Heparin plasma | Platelet-poor EDTA | Platelet-poor Heparin | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1:2 | Average % of Expected | 100 | 117 | 114 | 114 | 118 | 114 | |||||
| Range (%) | 95.6-104 | 112-120 | 112-118 | 105-123 | 113-124 | 110-118 | ||||||
| 1:4 | Average % of Expected | 95.7 | 119 | 113 | 112 | 123 | 121 | |||||
| Range (%) | 89.5-101 | 110-129 | 110-118 | 104-121 | 118-126 | 118-127 | ||||||
| 1:8 | Average % of Expected | 99.2 | 128 | 118 | 117 | 134 | 122 | |||||
| Range (%) | 92.0-103 | 116-142 | 111-126 | 110-127 | 125-151 | 116-129 | ||||||
| 1:16 | Average % of Expected | 99.6 | 126 | 117 | 114 | 134 | 121 | |||||
| Range (%) | 93.3-105 | 112-143 | 101-134 | 99.3-131 | 131-138 | 110-133 | ||||||
Assays for the Luminex platform are offered as High Performance Assays or Assays. The Luminex High Performance Assays are fully validated panels with a focused selection of analytes. They are available in We Mix, You Mix, and Predetermined formats. The Luminex Assays allows for the maximum number of analytes in a multiplex and is supplied as a premixed kit. View a table comparing the features and benefits of these bead-based multiplex assays.
Magnetic Luminex High Performance Assays are designed for use with the Luminex MAGPIX CCD Imager. Alternatively, kits can be used with the Luminex 100/200™ or Bio-Rad® Bio-Plex®, dual laser, flow-based sorting and detection platforms.
Analyte-specific antibodies are pre-coated onto color-coded microparticles. Microparticles, standards, and samples are pipetted into wells and the immobilized antibodies bind the analytes of interest. After washing away any unbound substances, a biotinylated antibody cocktail specific to the analytes of interest is added to each well. Following a wash to remove any unbound biotinylated antibody, Streptavidin-Phycoerythrin conjugate (Streptavidin-PE), which binds to the biotinylated detection antibodies, is added to each well. A final wash removes unbound Streptavidin-PE and the microparticles are resuspended in buffer and read using the Luminex or Bio-Plex analyzer. One laser is bead-specific and determines which analyte is being detected. A magnet in the analyzer captures and holds the superparaMagnetic microparticles in a monolayer. Two spectrally distinct Light Emitting Diodes (LEDs) illuminate the beads. One LED identifies the analyte that is being detected and the second LED determines the magnitude of the PE-derived signal, which is in direct proportion to the amount of analyte bound. Each well is imaged with a CCD camera. Kits can also be used with Luminex 100/200 or a Bio-Rad Bio-Plex dual laser, flow-based systems.
Scientific Data
Background: IL-3
M-CSF, also known as CSF-1, is a four-alpha-helical-bundle cytokine that is the primary regulator of macrophage survival, proliferation and differentiation. M-CSF is also essential for the survival and proliferation of osteoclast progenitors. M-CSF also primes and enhances macrophage killing of tumor cells and microorganisms, regulates the release of cytokines and other inflammatory modulators from macrophages, and stimulates pinocytosis. M-CSF increases during pregnancy to support implantation and growth of the decidua and placenta. Sources of M-CSF include fibroblasts, activated macrophages, endometrial secretory epithelium, bone marrow stromal cells and activated endothelial cells. The M-CSF receptor (c-fms) transduces its pleotropic effects and mediates its endocytosis. M-CSF mRNAs of various sizes occur. Full length human M-CSF transcripts encode a 522 amino acid (aa) type I transmembrane (TM) protein with a 464 aa extracellular region, a 21 aa TM domain, and a 37 aa cytoplasmic tail that forms a 140 kDa covalent dimer. Differential processing produces two proteolytically cleaved, secreted dimers. One is an N- and O- glycosylated 86 kDa dimer, while the other is modified by both glycosylation and chondroitin-sulfate proteoglycan (PG) to generate a 200 kDa subunit. Although PG-modified M-CSF can circulate, it may be immobilized by attachment to type V collagen. Shorter transcripts encode M-CSF that lack cleavage and PG sites and produce an N-glycosylated 68 kDa TM dimer and a slowly produced 44 kDa secreted dimer. Although forms may vary in activity and half-life, all contain the N-terminal 150 aa portion that is necessary and sufficient for interaction with the M-CSF receptor. The first 223 aa of mature human M-CSF shares 88%, 86%, 81% and 74% aa identity with corresponding regions of dog, cow, mouse and rat M-CSF, respectively. Human M-CSF is active in the mouse, but mouse M-CSF is reported to be species-specific.
Product Datasheets
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