Product nameHuman Cytokines FirePlex®-HT Panel 1
Sample typeCell culture supernatant, Serum, Plasma, Heparin Plasma, EDTA Plasma, Citrate Plasma
Species reactivityReacts with: Human
Human Cytokines FirePlex®-HT Panel 1 (ab234897) uses FirePlex® particle technology to quantify IL-8, IFN gamma, IL-4, IL-1 beta, MCP1, TNF alpha, IL-10, IL-17A, IL-2, IL-6 from 6.25 µl of sample input in 384-well plate format.
Assays are validated in serum, plasma, and cell culture supernatant with 175 samples in duplicate per 384-well plate.
The two-step workflow and no-wash assay format limit hands-on time and are amenable to automation, thus making FirePlex-HT ideally suited for high-throughput screening studies. Assay readout is conducted on high-content imagers with data analysis using the FirePlex® Analysis Workbench software.
Users should note that assay performance data supplied in the accompanying Product Datasheet is a representative dataset, and is not lot-specific. For lot-specific assay performance data, please refer to the product's certificate of analysis, which can be found here.
FirePlex® is a registered trade mark in certain territories (including Europe and the United States) and is an unregistered trade mark elsewhere
This product is currently only supported for customers in North America and Europe, if you are outside these areas please contact us.
The following table provides the sensitivity, dynamic range, and CVs for Human Cytokines FirePlex®-HT Panel 1 *.
IL-8 5.72 13.7 - 3,333 7.4% IFN-gamma 72.48 123.4 - 10,000 11.5% IL-4 19.96 41.1 - 10,000 5.9% IL-1 beta 4.54 4.5 - 3,333 16.1% MCP1 2.43 4.5 - 3,333 13.3% TNF-alpha 18.03 41.1 - 10,000 4.7% IL-10 22.75 41.1-10,000 9.0% IL-17A 7.04 13.7-10,000 13.4% IL-2 13.51 13.7 - 10,000 5.2% IL-6 3.06 4.5 - 10,000 8.4%
*representative dataset, not lot-specific. For lot-specific assay performance data, please refer to the product's certificate of analysis, which can be found here.
Storage instructionsPlease refer to protocols.
Components 1 units 3 units 384 Well Imaging Plate 1 x 384 tests 3 x 384 tests 384 Well Imaging Plate Lid 1 unit 3 units 384 Well Imaging Plate Seal 2 units 6 units FirePlex-HT 1X PBS 1 x 8ml 3 x 8ml FirePlex-HT- 5X Capture Particle Mix 1 x 700µl 3 x 700µl FirePlex-HT Human Protein Standard Mix HTA 1 x 7 tests 3 x 7 tests FirePlex-HT Reagent Diluent R1 1 x 8ml 3 x 8ml FirePlex-HT Sample Diluent S1 1 x 25ml 3 x 25ml FirePlex-HT - Imaging Dye Concentrate 1 x 875µl 3 x 875µl FirePlex-HT 35X Detector Antibody Mix 1 x 110µl 3 x 110µl
Cellular localizationTNF alpha: Secreted and Cell membrane. IL-8: Secreted. MCP1: Secreted. IL-6: Secreted. IL-10: Secreted. Interferon gamma: Secreted. IL-1 beta: Cytoplasm, cytosol. Lysosome. Secreted, exosome. Cytoplasmic vesicle, autophagosome. Secreted. The precursor is cytosolic. In response to inflammasome-activating signals, such as ATP for NLRP3 inflammasome or bacterial flagellin for NLRC4 inflammasome, cleaved and secreted. IL1B lacks any known signal sequence and the pathway(s) of its secretion is(are) not yet fully understood (PubMed:24201029). On the basis of experimental results, several unconventional secretion mechanisms have been proposed. 1. Secretion via secretory lysosomes: a fraction of CASP1 and IL1B precursor may be incorporated, by a yet undefined mechanism, into secretory lysosomes that undergo Ca(2+)-dependent exocytosis with release of mature IL1B (PubMed:15192144). 2. Secretory autophagy: IL1B-containing autophagosomes may fuse with endosomes or multivesicular bodies (MVBs) and then merge with the plasma membrane releasing soluble IL1B or IL1B-containing exosomes (PubMed:24201029). However, autophagy impacts IL1B production at several levels and its role in secretion is still controversial. 3. Secretion via exosomes: ATP-activation of P2RX7 leads to the formation of MVBs containing exosomes with entrapped IL1B, CASP1 and other inflammasome components. These MVBs undergo exocytosis with the release of exosomes. The release of soluble IL1B occurs after the lysis of exosome membranes (By similarity). 4. Secretion by microvesicle shedding: activation of the ATP receptor P2RX7 may induce an immediate shedding of membrane-derived microvesicles containing IL1B and possibly inflammasome components. The cytokine is then released in the extracellular compartment after microvesicle lysis (PubMed:11728343). 5. Release by translocation through permeabilized plasma membrane. This may occur in cells undergoing pyroptosis due to sustained activation of the inflammasome (By similarity). These mechanisms may not be not mutually exclusive. IL-2: Secreted. IL-4: Secreted. IL-17A: Secreted.
ab234897 has not yet been referenced specifically in any publications.