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ICAM1 Kit ELISA

Kit ELISA ICAM1 Rat, Colorimetric test pour la quantification de Rat ICAM1 et a été mentionné dans 2+ publications.
N° du produit ABIN625195
565,77 €
Plus frais de livraison 40,00 € et TVA
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour ICAM1 Kit ELISA (ABIN625195)

Antigène

Voir toutes ICAM1 Kits ELISA
ICAM1 (Intercellular Adhesion Molecule 1 (ICAM1))

Reactivité

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Rat

Méthode de détection

Colorimetric

Type de méthode

Sandwich ELISA

Gamme de detection

20 pg/mL - 7000 pg/mL

Application

ELISA

Type d'échantillon

Plasma, Cell Culture Supernatant, Serum
  • Seuil minimal de détection

    20 pg/mL

    Fonction

    Rat ICAM-1 (CD54) ELISA Kit for cell culture supernatants, plasma, and serum samples.

    Analytical Method

    Quantitative

    Specificité

    This ELISA kit shows no cross-reactivity with the following cytokines tested: rat CINC-2, CINC-3, CNTF, Fractalkine, IL-1 alpha, IL-1 beta, IL-4, IL-6, IL-10, GM-CSF, IFN-gamma, Leptin, Lix, MCP-1, MIP-3 alpha, beta- NGF, TIMP-1, TNF-alpha.

    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
    ,
    • 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
  • Indications d'application

    Suggested Plasma Dilution: 20 - 200 fold

    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: 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 cell culture supernates. Suggested dilution for normal serum/plasma: 20-200 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 before use.
      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 supernates) into Item C vial to prepare a 50 ng/mL standard. Dissolve the powder thoroughly by a gentle mix. Add 70 µL ICAM-1 standard (50 ng/mL) from the vial of Item C, into a tube with 430 µL Assay Diluent A or 1x Assay Diluent B to prepare a 7,000 pg/mL standard solution. Pipette 400 µL Assay Diluent A or 1x Assay Diluent B into each tube. Use the 7,000 pg/mL 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). 70 µL standard + 430 µL 200 µL 200 µL 200 µL 200 µL 200myl 7,000 2,333 777.8 259.3 86.42 28.81 0 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) and pipette up and down to mix gently before use. HRP-Streptavidin concentrate should be diluted 400-fold with 1x Assay Diluent B. For example: Briefly spin the vial (Item G) and pipette up and down to mix gently . Add 30 µL of HRP-Streptavidin concentrate into a tube with 12 ml 1x Assay Diluent B to prepare a 400-fold diluted HRP- Streptavidin solution (don't store the diluted solution for next day use). 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 Rat ICAM-1 concentrations (pg/mL) O D =4 50 n m 0.01 0.1 1 10 10 100 1,000 10,000 Assay Diluent B Rat ICAM-1 concentrations (pg/mL) O D =4 50 n m 0.01 0.1 1 10 10 100 1,000 10,000
    Sensitivity: The minimum detectable dose of ICAM-1 is typically less than 20 pg/mL.
    Recovery: Recovery was determined by spiking various levels of rat ICAM-1 into serum, plasma and cell culture media. Mean recoveries are as follows: Sample Type Average % Recovery Range ( %) Serum 89.42 80-101 Plasma 85.54 76-95 Cell culture media 98.54 89-107
    Linearity: Sample Type Serum Plasma Cell Culture Media 1:2 Average % of Expected 102.3 99.71 103.4 Range ( %) 93-112 91-107 92-110 1:4 Average % of Expected 108.2 108.8 105.0 Range ( %) 96-117 98-117 95-114
    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
  • Zhang, Zhang, Tsui: "Mesenteric lymph duct drainage attenuates acute lung injury in rats with severe intraperitoneal infection." dans: Inflammation, Vol. 38, Issue 3, pp. 1239-49, (2015) (PubMed).

    Zhang, Yang, Gong, Yang, Chen, Cai, Zheng, Yang, Xia: "Cordyceps sinensis extracts attenuate aortic transplant arteriosclerosis in rats." dans: The Journal of surgical research, Vol. 175, Issue 1, pp. 123-30, (2012) (PubMed).

  • Antigène Voir toutes ICAM1 Kits ELISA

    ICAM1 (Intercellular Adhesion Molecule 1 (ICAM1))

    Autre désignation

    ICAM-1

    Classe de substances

    Viral Protein

    Sujet

    Gene Symbols: ICAM1, ICAM-1

    Protein Name (Synonyms): Intercellular adhesion molecule 1 (ICAM-1) (CD antigen CD54)

    ID gène

    25464

    UniProt

    Q00238

    Pathways

    Cellular Response to Molecule of Bacterial Origin, Regulation of Actin Filament Polymerization, Carbohydrate Homeostasis, Regulation of Leukocyte Mediated Immunity, Thromboxane A2 Receptor Signaling
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