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Invitrogen™ IL-1RA Equine ELISA Kit
Sandwich ELISA Kit
Brand: Invitrogen™ EEIL1RN
Additional Details : Weight : 0.00400kg
Includes: Pre-coated plate(s), standard, detector antibody, HRP conjugate, diluents, wash buffer, chromogen, stop solution, and plate covers.
Description
The Equine Interleukin-1 Receptor Antagonist (Eq IL-1RA) ELISA quantitates Eq IL-1RA in equine serum, plasma, or cell culture medium. The assay will exclusively recognize both natural and recombinant Eq IL-1RA. Principle of the method The Equine IL-1RA solid-phase sandwich ELISA (enzyme-linked immunosorbent assay) is designed to measure the amount of the target bound between a matched antibody pair. A target-specific antibody has been pre-coated in the wells of the supplied microplate. Samples, standards, or controls are then added into these wells and bind to the immobilized (capture) antibody. The sandwich is formed by the addition of the second (detector) antibody, a substrate solution is added that reacts with the enzyme-antibody-target complex to produce measurable signal. The intensity of this signal is directly proportional to the concentration of target present in the original specimen. Rigorous validation Each manufactured lot of this ELISA kit is quality tested for criteria such as sensitivity, specificity, precision, and lot-to-lot consistency. See manual for more information on validation.
Interleukin 1 receptor antagonist (ILRA) is a protein related to the IL-1 family based on its similarities in amino acid sequence to both IL-1 beta and IL-1 alpha, similarities in gene structure, and collective gene localization. The human gene contains four exons and maps to chromosome 2q13-14. IL-1 RA binds to the IL-1 receptor and blocks IL-1 action through competitive inhibition. In contrast to IL-1, the binding of IL-1RA does not initiate signaling events. The secretion of IL-1 RA is mediated by a classical signal sequence while neither IL-1alpha nor IL-1beta possess such a sequence. The lack of homology between IL-1 RA and IL-1 alpha or IL-1 beta near the N terminus may provide an explanation for the biosynthetic and functional differences between IL-1 RA and the two IL-1 proteins. The production of IL-1RA is stimulated by many substances including adherent IgG, cytokines, and bacterial or viral components. IL-1RA is an important natural anti-inflammatory protein that when missing or just available in inadequate amounts plays a key role in several pathological conditions such as rheumatoid arthritis, colitis, osteomyelitis, periostitis and pustulosis.Specifications
O18999 | |
10 pg/mL | |
Solid-phase sandwich ELISA | |
ELISA Kit | |
Plasma, Serum, Supernatant | |
96 assays | |
ELISA, Protein Assays, Protein Biology, Cancer Biology, Immunology, Neuroscience, Neurobiology, Protein Detection, Protein Analysis | |
100034236 | |
<12% | |
Pre-coated 96 well plate, Standard, Assay Diluent concentrate, Biotinylated Detection Antibody, SAV-HRP, Wash Buffer, Chromogen, Stop Solution, Adhesive Plate Covers | |
96 Tests | |
Extracellular Matrix & Cell Adhesion | |
2°C to 8°C | |
Equine | |
4 hr. 45 min. |
12.29-3000 pg/mL | |
10pg/mL to 3000pg/mL | |
Biotin | |
Cell Structure & Organelle Proteins | |
The sandwich ELISA antibody pair detects Equine IL-1RA. | |
Equine | |
Colorimetric Microplate Reader | |
IL-1RA | |
<10% | |
HRP | |
RUO | |
Plasma, 33 μL; Serum, 33 μL; Supernatant, 100 μL | |
IL-1RA | |
1 hr. 20 min. |