CXCL10 Kit ELISA (Chemokine (C-X-C Motif) Ligand 10)

Details for Product CXCL10 ELISA Kit No. ABIN625117, Fournisseur: Connectez-vous pour afficher
Antigène
  • CXCL10
  • C7
  • IFI10
  • INP10
  • IP-10
  • SCYB10
  • crg-2
  • gIP-10
  • mob-1
  • CRG-2
  • IP10
  • Ifi10
  • Scyb10
  • C-X-C motif chemokine ligand 10
  • C-X-C motif chemokine 10
  • chemokine (C-X-C motif) ligand 10
  • CXCL10
  • cxl10
  • Cxcl10
Reactivité
Souris
Alternatives
Kits with alternative reactivity to:
43
33
18
11
10
9
5
4
4
4
2
2
2
2
2
1
Méthode de détection
Colorimetric
Type de méthode
Sandwich ELISA
Gamme de detection
15-2000 pg/mL
Seuil minimal de détection
15 pg/mL
Application
ELISA
Options
Fournisseur
Connectez-vous pour afficher
N° du produit (Fournisseur)
Connectez-vous pour afficher
Fonction Mouse CRG-2 ELISA Kit for cell culture supernatants, plasma, and serum samples.
Type d'échantillon Serum, Plasma, Cell Culture Supernatant
Analytical Method Quantitative
Méthode de détection Colorimetric
Specificité This ELISA kit shows no cross-reactivity with any of the cytokines tested: Mouse CD30, L CD30, T CD40, CTACK, CXCL16, Eotaxin , Eotaxin-2, Fas Ligand, Fractalkine, GM-CFS, IFN- gamma, IGFBP-3, IGFBP-5, IGFBP-6, IL-1 alpha, IL-1 beta, IL-2, IL-3, IL-3 Rb, IL-4, IL-5, IL-6, IL-9, IL-10, IL-12 p40/p70, IL-12 p70, IL-13, IL-17, KC, Leptin R, LEPTIN(OB), LIX, L-Selectin, Lymphotactin, MCP-1, MCP-5, M-CSF, MIG, MIP-1 alpha, MIP-1 gamma, MIP-2, MIP-3 beta, MIP-3 alpha, PF-4, P-Selectin, RANTES, SCF, SDF-1 alpha, TARC, TCA-3, TECK, TIMP-1, TNF-alpha, TNF RI, TNF RII, TPO, VCAM-1, VEGF.
Sensibilité < 15 pg/mL
Attributs du produit
  • Strip plates and additional reagents allow for use in multiple experiments
  • Quantitative protein detection
  • Establishes normal range
  • The best products for confirmation of antibody array data
Ingrédients
  • Pre-Coated 96-well Strip Microplate
  • Wash Buffer
  • Stop Solution
  • Assay Diluent(s)
  • Lyophilized Standard
  • Biotinylated Detection Antibody
  • Streptavidin-Conjugated HRP
  • TMB One-Step Substrate
Matériel non inclus
  • Distilled or deionized water
  • Precision pipettes to deliver 2 μL to 1 μL volumes
  • Adjustable 1-25 μL pipettes for reagent preparation
  • 100 μL and 1 liter graduated cylinders
  • Tubes to prepare standard and sample dilutions
  • Absorbent paper
  • Microplate reader capable of measuring absorbance at 450nm
  • Log-log graph paper or computer and software for ELISA data analysis
Plasmids, Primers & others Plasmids, Primers & others CXCL10 products on genomics-online (e.g. as negative or positive controls)
Antigène
Autre désignation CRG2 (CXCL10 ELISA Kit Extrait)
Sujet The Mouse CRG-2 ELISA (Enzyme-Linked Immunosorbent Assay) kit is an in vitro enzyme-linked immunosorbent assay for the quantitative measurement of mouse CRG-2 in serum, plasma, cell culture supernatants and urine. This assay employs an antibody specific for mouse CRG-2 coated on a 96-well plate. Standards and samples are pipetted into the wells and CRG-2 present in a sample is bound to the wells by the immobilized antibody. The wells are washed and biotinylated anti-mouse CRG-2 antibody is added. After washing away unbound biotinylated antibody, HRP-conjugated streptavidin is pipetted to the wells. The wells are again washed, a TMB substrate solution is added to the wells and color develops in proportion to the amount of CRG-2 bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm. Reproducibility: Intra-Assay: CV<10% Inter-Assay: CV<12%.
ID gène 15945
UniProt P17515
Indications d'application Recommended Dilution for serum and plasma samples2 fold
Volume d'échantillon 100 μL
Plaque Pre-coated
Protocole
  1. Prepare all reagents, samples and standards as instructed in the manual.
  2. Add 100 μL of standard or sample to each well.
  3. Incubate 2.5 h at RT or O/N at 4 °C.
  4. Add 100 μL of prepared biotin antibody to each well.
  5. Incubate 1 h at RT.
  6. Add 100 μL of prepared Streptavidin solution to each well.
  7. Incubate 45 min at RT.
  8. Add 100 μL of TMB One-Step Substrate Reagent to each well.
  9. Incubate 30 min at RT.
  10. Add 50 μL of Stop Solution to each well.
  11. Read at 450 nm immediately.
Préparation des réactifs
  1. Bring all reagents and samples to room temperature (18 - 25 °C) before use.
    2. Sample dilution: If your samples need to be diluted, Assay Diluent A (Item D) should be used for dilution of serum/plasma samples. 1x Assay Diluent B (Item E) should be used for dilution of culture supernatants. Suggested dilution for normal serum/plasma: 2 fold. Please note that levels of the target protein may vary between different specimens. Optimal dilution factors for each sample must be determined by the investigator.
    3. Assay Diluent B should be diluted 5-fold with deionized or distilled water.
    4. Preparation of standard: Briefly spin the vial of Item C and then add 400 µL Assay Diluent A (for serum/plasma samples) or 1x Assay Diluent B (for cell culture medium) into Item C vial to prepare a 0.1 myg/mL standard. Dissolve the powder thoroughly by a gentle mix. Add 20 µL CRG-2 standard from the vial of Item C, into a tube with 980.0 µL Assay Diluent A or 1x Assay Diluent B to prepare a 2,000 pg/mL stock standard solution. Pipette 300 µL Assay Diluent A or 1x Assay Diluent B into each tube. Use the stock standard solution to produce a dilution series . Mix each tube thoroughly before the next transfer. Assay Diluent A or 1x Assay Diluent B serves as the zero standard (0 pg/mL). 200 µL 200myl 200 µL 200 µL 200 µL 200 µL 20 µL standard + 980 µL 2000 800 320 128 51.2 20.48 8.20 0 pg/mL pg/mL pg/mL pg/mL pg/mL pg/mL pg/mL pg/mL
    5. If the Wash Concentrate (20x) (Item B) contains visible crystals, warm to room temperature and mix gently until dissolved. Dilute 20 ml of Wash Buffer Concentrate into deionized or distilled water to yield 400 ml of 1x Wash Buffer.
    6. Briefly spin the Detection Antibody vial (Item F) before use. Add 100 µL of 1x Assay Diluent B into the vial to prepare a detection antibody concentrate. Pipette up and down to mix gently (the concentrate can be stored at 4 °C for 5 days). The detection antibody concentrate should be diluted 80-fold with 1x Assay Diluent B and used in step 4 of Part VI Assay Procedure.
    7. Briefly spin the HRP-Streptavidin concentrate vial (Item G) before use. HRP-Streptavidin concentrate should be diluted 80-fold with 1x Assay Diluent B. For example: Briefly spin the vial (Item G) and pipette up and down to mix gently . Add 125 µL of HRP-Streptavidin concentrate into a tube with 10 ml 1x Assay Diluent B to prepare a 80 fold diluted HRP- Streptavidin solution. Mix well.
Procédure de l'essai
  1. Bring all reagents and samples to room temperature (18 - 25 °C) before use. It is recommended that all standards and samples be run at least in duplicate.
    2. Add 100 µL of each standard (see Reagent Preparation step 2) and sample into appropriate wells. Cover well and incubate for 2.5 hours at room temperature or over night at 4 °C with gentle shaking.
    3. Discard the solution and wash 4 times with 1x Wash Solution. Wash by filling each well with Wash Buffer (300 myl) using a multi-channel Pipette or autowasher. Complete removal of liquid at each step is essential to good performance. After the last wash, remove any remaining Wash Buffer by aspirating or decanting. Invert the plate and blot it against clean paper towels.
    4. Add 100 µL of 1x prepared biotinylated antibody (Reagent Preparation step 6) to each well. Incubate for 1 hour at room temperature with gentle shaking.
    5. Discard the solution. Repeat the wash as in step
    6. Add 100 µL of prepared Streptavidin solution (see Reagent Preparation step 7) to each well. Incubate for 45 minutes at room temperature with gentle shaking.
    7. Discard the solution. Repeat the wash as in step
    8. Add 100 µL of TMB One-Step Substrate Reagent (Item H) to each well. Incubate for 30 minutes at room temperature in the dark with gentle shaking.
    9. Add 50 µL of Stop Solution (Item I) to each well. Read at 450 nm immediately.
Calcul des résultats

Calculate the mean absorbance for each set of duplicate standards, controls and samples, and subtract the average zero standard optical density. Plot the standard curve on log-log graph paper or using Sigma plot software, with standard concentration on the x-axis and absorbance on the y-axis. Draw the best-fit straight line through the standard points.
Typical Data: These standard curves are for demonstration only. A standard curve must be run with each assay. Assay Diluent A Mouse CRG2 concentration (pg/mL) O D =4 50 n m 0.01 0.1 1 10 0 10 100 1,000 10,000 Assay Diluent B Mouse CRG2 concentration (pg/mL) O D =4 50 n m 0.001 0.01 0.1 1 10 0 10 100 1,000 10,000
Sensitivity: The minimum detectable dose of CRG-2 is typically less than 15 pg/mL.
Recovery: Recovery was determined by spiking various levels of Mouse CRG-2 into Mouse serum, plasma and cell culture media. Mean recoveries are as follows: Sample Type Average % Recovery Range ( %) Serum 97.68 86-106 Plasma 96.42 85-104 Cell culture media 98.86 88-107
Linearity: Sample Type Serum Plasma Cell culture media 1:2 Average % of Expected 96 93 97 Range ( %) 88-104 86-105 85-106 1:4 Average % of Expected 96 95 96 Range ( %) 89-105 87-106 90-106
Reproducibility: Intra-Assay: CV<10 % Inter-Assay: CV<12 %

Précision du teste Intra-Assay: CV< 10 % Inter-Assay: CV< 12 %
Restrictions For Research Use only
Conseil sur la manipulation Avoid repeated freeze-thaw cycles.
Stock -20 °C
Stockage commentaire The entire kit may be stored at -20°C for up to 1 year from the date of shipment. Avoid repeated freeze-thaw cycles. The kit may be stored at 4°C for up to 6 months. For extended storage, it is recommended to store at -80°C.
Date de péremption 6 months
Images (Fournisseur)
ELISA image for Chemokine (C-X-C Motif) Ligand 10 (CXCL10) ELISA Kit (ABIN625117) Chemokine (C-X-C Motif) Ligand 10 (CXCL10) ELISA Kit
Produit citée dans: Bocian, Urbanowitz, Owens, Iozzo, Götte, Seidler: "Decorin potentiates interferon-γ activity in a model of allergic inflammation." dans: The Journal of biological chemistry, Vol. 288, Issue 18, pp. 12699-711, 2013

Bocian, Urbanowitz, Owens, Iozzo, Götte, Seidler: "Decorin potentiates interferon-? activity in a model of allergic inflammation." dans: The Journal of biological chemistry, Vol. 288, Issue 18, pp. 12699-711, 2013 (PubMed).

Avez-vous cherché autre chose?