IL-13 Kit ELISA (Interleukin 13)

Details for Product IL13 ELISA Kit No. ABIN924771, Fournisseur: Connectez-vous pour afficher
Antigène
  • IL13
  • IL-13
  • P600
  • Il-13
  • L13
  • interleukin 13
  • IL13
  • Il13
Reactivité
Humain
Alternatives
Kits with alternative reactivity to:
60
34
23
14
11
10
9
6
5
5
4
3
3
2
2
2
Méthode de détection
Colorimetric
Type de méthode
Sandwich ELISA
Gamme de detection
125-5000 pg/mL
Seuil minimal de détection
125 pg/mL
Application
ELISA
Options
Fournisseur
Connectez-vous pour afficher
N° du produit (Fournisseur)
Connectez-vous pour afficher
Fonction The OmniKine? Human IL-13 ELISA Kit contains the components necessary for quantitative determination of natural or recombinant Human IL-13 concentrations within any experimental sample including cell lysates, serum and plasma. This particular immunoassay utilizes the quantitative technique of a "Sandwich" Enzyme-Linked Immunosorbent Assay (ELISA) where the target protein (antigen) is bound in a "sandwich" format by the primary capture antibodies coated to each well-bottom and the secondary detection antibodies added subsequently by the investigator. The capture antibodies coated to the bottom of each well are specific for a particular epitope on Human IL-13 while the user-added detection antibodies bind to epitopes on the captured target protein. Amid each step of the procedure, a series of wash steps must be performed to ensure the elimination of non- specific binding between proteins to other proteins or to the solid phase. After incubation and "sandwiching" of the target antigen, a peroxidase enzyme is conjugated to the constant heavy chain of the secondary antibody (either covalently or via Avidin/Streptavidin-Biotin interactions), allowing for a colorimetric reaction to ensue upon substrate addition. When the substrate TMB (3, 3', 5, 5'-Tetramethylbenzidine) is added, the reaction catalyzed by peroxidase yields a blue color that is representative of the antigen concentration. Upon sufficient color development, the reaction can be terminated through addition of Stop Solution (2 N Sulfuric Acid) where the color of the solution will turn yellow. The absorbance of each well can then be read by a spectrophotometer, allowing for generation of a standard curve and subsequent determination of protein concentration.
Marque OmniKine™
Type d'échantillon Cell Lysate, Serum, Plasma
Analytical Method Quantitative
Méthode de détection Colorimetric
Specificité The Human IL-13 ELISA Kit allows for the detection and quantification of endogenous levels of natural and/or recombinant Human IL-13 proteins.
Réactivité croisée (Details) The Human IL-13 ELISA is capable of recognizing both recombinant and naturally produced Human IL-13 proteins. The antigens listed below were tested at 50 ng/mL and exhibited 100% cross reactivity. Human: IL-13 Variant The antigens listed below were tested at 50 ng/mL and did not exhibit significant cross reactivity or interference. Human: IL-4, sIL-4Rα, IL-5, IL-6, IL-6Rα, IL-10 Murine: IL-4, IL-13 Rat: IL-4, IL-13
Attributs du produit The Human IL-13 ELISA Kit allows for the detection and quantification of endogenous levels of natural and/or recombinant Human IL-13 proteins within the range of 125-5000 pg/mL.
Ingrédients
  • Microstrips Coated w / Capture Antibody: 12 x 8-Well Microstrips
  • Protein Standard: Lyophilized (100 ng), Red container
  • Biotinylated Detection Antibody: Lyophilized, Yellow container
  • 400x Streptavidin-HRP: 30 μL, Blue container
  • Wash Buffer (10x): 50 mL, Clear containter
  • Assay Diluent: 50 mL, Clear container
  • Ready-to-Use Substrate: 12 mL, Brown container
  • Stop Solution: 12 mL, Clear container
  • Adhesive Plate Sealers: 4 Sheets
  • Technical Manual 1 Manual
Matériel non inclus The following materials and/or equipment are NOT provided in this kit but are necessary to successfully conduct the experiment:
Microplate reader able to measure absorbance at 450 nm (with correction wavelength set to 540 nm or 570 nm)
Micropipettes with capability of measuring volumes ranging from 1 μl to 1 mL
Deionized or sterile water
Squirt bottle, manifold dispenser, multichannel pipette reservoir or automated microplate washer
Graph paper or computer software capable of generating or displaying logarithmic functions
Absorbent paper or vacuum aspirator
Test tubes or microfuge tubes capable of storing ≥1 mL
Bench
top centrifuge (optional)
Bench
top vortex (optional)
Orbital shaker (optional)
Plasmids, Primers & others Plasmids, Primers & others IL-13 products on genomics-online (e.g. as negative or positive controls)
Antigène
Autre désignation IL-13 (IL13 ELISA Kit Extrait)
Sujet Human IL-13, also known as Interleukin-13, is a 146 amino acid cytokine protein expressed from the IL13 gene located at locus 5q31 on chromosome 5. After initial synthesis, the IL-13 pre-protein undergoes proteolytic cleavage, thus separating the 24 residue signal sequence from the actual 122 residue IL-13 protein, allowing for proper folding and maturation of the cytokine. IL-13, an immunoregulatory cytokine, is produced primarily by activated Th2 cells and is involved in several stages of B-cell maturation and differentiation. It up-regulates CD23 and MHC class II expression while promoting IgE isotype switching of B-cells. IL-13 also down-regulates macrophage activity, thereby inhibiting the production of proinflammatory cytokines and chemokines. In addition, this particular cytokine is found to be critical to the pathogenesis of allergen-induced asthma but operates through mechanisms independent of IgE and eosinophils. The IL13 gene along with IL3, IL5, IL4 and CSF2 form a cytokine gene cluster on chromosome 5q, with this gene particularly close to IL4. From an epidemiological standpoint, defects in IL-13 may cause susceptibility to allergic rhinitis (ALRH), a common disease of complex inheritance and is characterized by mucosal inflammation caused by allergen exposure. Source: Entrez Gene: IL13 interleukin 13 [Homo sapiens], Swiss-Prot: P35225
ID gène 3596
UniProt P35225
Pathways Signalistation JAK/STAT, Positive Regulation of Immune Effector Process, Production of Molecular Mediator of Immune Response, Proton Transport
Plaque Pre-coated
Protocole This particular immunoassay utilizes the quantitative technique of a Sandwich Enzyme-Linked Immunosorbent Assay (ELISA) where the target protein (antigen) is bound in a sandwich format by the primary capture antibodies coated to each well-bottom and the secondary detection antibodies added subsequently by the investigator. The capture antibodies coated to the bottom of each well are specific for a particular epitope on the Human IL-13 cytokine while the user-added detection antibodies bind to epitopes on the captured target protein. Amid each step of the procedure, a series of wash steps must be performed to ensure the elimination of non-specific binding between proteins to other proteins or to the solid phase. After incubation and sandwiching of the target antigen, a peroxidase enzyme is conjugated to the constant heavy chain of the secondary antibody (either covalently or via Avidin/Streptavidin-Biotin interactions), allowing for a colorimetric reaction to ensue upon substrate addition. When the substrate TMB (3, 3’, 5, 5’- Tetramethylbenzidine) is added, the reaction catalyzed by peroxidase yields a blue color that is representative of the antigen concentration. Upon sufficient color development, the reaction can be terminated through addition of Stop Solution (2 N Sulfuric Acid) where the color of the solution will turn yellow. The absorbance of each well can then be read by a spectrophotometer, allowing for generation of a standard curve and subsequent determination of protein concentration.
Préparation de l'échantillon

If samples are to be used within 24 hours, aliquot and store at 4 °C. If samples are to be used over a long period of time, aliquot and store between -20 °C and -80 °C, depending on the duration of storage.
Note: Samples containing a visible precipitate or pellet must be clarified prior to use in the assay.
Caution: Avoid repeated freeze/thaw cycles to prevent loss of biological activity of proteins in experimental samples.

  • Cell Lysate and Supernatants:
    Remove large cell components via centrifugation and perform the assay. Cell lysates and supernatants require a dilution using Assay Diluent. A serial dilution may be performed to determine a suitable dilution factor for the sample. For future use of the sample, follow the sample storage guidelines stated above.
  • Serum:
    Allow samples to clot in a serum separator tube (SST) for 30 minutes. After sufficient clotting, centrifuge at 1000 x g for 15 minutes and remove serum from SST in preparation for the assay. Serum samples require at least a 1:50 dilution using Assay Diluent. For future use of the sample, follow the storage guidelines above.
  • Plasma:
    Use heparin, citrate or EDTA as an anticoagulant to gather plasma from original biological sample. After collection of the plasma, centrifuge for 15 minutes at 1000 x g. This step must be performed within 30 minutes of plasma collection. Plasma samples require at least a 1:50 dilution using Assay Diluent. Afterwards, perform the assay or for future use of the sample, follow the storage guidelines stated above.

Procédure de l'essai

Note: If possible, all incubation steps should be performed on an orbital shaker to equilibrate solutions when added to the microplate wells. Also, all provided solutions should be at ambient temperature prior to use.
Note: Avoid adding solutions into wells at an angle, always keep pipette tip perpendicular to plate bottom.

Reconstitution of Provided Materials:

    1. Reconstitute the Biotin-Conjugated Detection Antibody in 67 µL of ddH₂O for a concentration of 180 µg/ml.
    2. Reconstitute the Protein Standard in 100 µL of ddH₂O for a concentration of 340 ng/ml.
    3. Dilute the 50 mL of 10x Wash Buffer in 450 mL of ddH2O for 500 mL of 1x Wash Buffer.
Addition of Known Standard and Unknown Sample to Immunoassay:
    The OmniKine™ Human CD163 ELISA Kit allows for the detection and quantification of endogenous levels of natural and/or recombinant Human CD163 proteins

Calcul des résultats

Generation of Standard Curve and Interpretation of Data
1. Average the duplicate or triplicate readings for each standard, control and sample and subtract the average zero standard optical density.
2. Generate a standard curve by using Microsoft Excel or other computer software capable of establishing a 4- Parameter Logistic (4-PL) curve fit. If using Excel or an alternative graphing tool, plot the average optical density values in absorbance units (y-axis) against the known standard concentrations in pg/ml (x-axis). Note: Only use the values in which a noticeable gradient can be established. Afterwards, generate a best fit curve or trend-line through the plotted points via regression analysis.

Restrictions For Research Use only
Précaution d'utilisation Reagents provided in this kit may be harmful if ingested, inhaled or absorbed through the skin. Please carefully review the MSDS for each reagent before conducting the experiment.
Stop Solution contains 2 N Sulfuric Acid (H2SO4) and is an extremely corrosive agent. Please wear proper eye, hand and face protection when handling this material. When the experiment is finished, be sure to rinse the plate with copious amounts of running water to dilute the Stop Solution prior to disposing the plate.
Conseil sur la manipulation This ELISA kit is intended for research purposes only, NOT diagnostic or clinical procedures of any kind.
Materials included in this kit should NOT be used past the expiration date on the kit label.
Reagents or substrates included in this kit should NOT be mixed or substituted with reagents or substrates from any other kits.
Variations in pipetting technique, washing technique, operator laboratory technique, kit age, incubation time or temperature may cause differences in binding affinity of the materials provided.
The assay is designed to eliminate interference and background by other cellular macromolecules or factors present within any biological samples. However, the possibility of background noise cannot be fully excluded until all factors have been tested using the assay kit.

Reagents provided in this kit may be harmful if ingested, inhaled or absorbed through the skin. Please carefully review the MSDS for each reagent before conducting the experiment.
Stop Solution contains 2 N Sulfuric Acid (H2SO4) and is an extremely corrosive agent. Please wear proper eye, hand and face protection when handling this material. When the experiment is finished, be sure to rinse the plate with copious amounts of running water to dilute the Stop Solution prior to disposing the plate.
Stock 4 °C
Stockage commentaire Note: If used frequently, reagents may be stored at 4 °C.
  • Unopened Kits: Store at 4 °C for 6 months.
  • Microstrips Coated w/ Capture Antibody, 400x Streptavidin-HRP Wash Buffer (10x), Assay Diluent Ready-to-Use Substrate, Stop Solution: 6 Months at 4 °C
  • Protein Standard, Biotinylated Detection Antibody: Lyophilized: 6 Months (if Reconstituted: 1 Month) at 4 °C
Images (Fournisseur)
ELISA image for Interleukin 13 (IL13) ELISA Kit (ABIN924771) This is an example of what a typical standard curve will look like. You must make you...
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