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IL-6 Kit ELISA

Le kit ELISA IL-6 (ABIN5523461) Souris est un kit ELISA Colorimetric conçu pour quantifier Souris IL-6. Ce kit ELISA a été cité dans 1 publication.
N° du produit ABIN5523461
481,54 €
Plus frais de livraison 40,00 € et TVA
96 tests
Destination: France
Envoi sous 11 à 15 jours ouvrables

Aperçu rapide pour IL-6 Kit ELISA (ABIN5523461)

Antigène

Voir toutes IL-6 (IL6) Kits ELISA
IL-6 (IL6) (Interleukin 6 (IL6))

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Souris

Méthode de détection

Colorimetric

Type de méthode

Sandwich ELISA

Gamme de detection

15.625 pg/mL - 1000 pg/mL

Application

ELISA

Type d'échantillon

Cell Culture Supernatant, Cell Samples, Plasma, Serum, Tissue Lysate
  • Seuil minimal de détection

    15.625 pg/mL

    Fonction

    Mouse IL-6 (Interleukin 6) ELISA Kit

    Analytical Method

    Quantitative

    Specificité

    Specifically binds with IL-6 , no obvious cross reaction with other analogues. Recommended Sample Dilution Ratio The following table shows the recommended dilution ratios for this kit for a limited number of samples for your reference only. (The matrix components in serum/plasma will affect the test results, which it need to be diluted at least 1/2 with Sample Dilution Buffer before testing! When the content of other samples is very low, the original solution can be added without dilution, but it is necessary to ensure that the pH is between 6.8 and 8.0, and it does not contain more than 10 % organic solvents or high-concentration protein denaturants.) 1. Common sample validation: Sample Type Recommended Dilution Ratio Content Normal mouse serum/plasma (EDTA, Citrate , heparin) (n=16) 1/2 dilution ND-42pg/mL Normal mouse were intraperitoneally injected with 50 μg LPS, and the serum was detected 12 hours later (n=3) 1/2-1/5 dilution 856-1856pg/mL Mouse spleen tissue homogenates undiluted 133pg/1 mg (total protein) RAW 264.7 cells were cultured with 5 %FBS + 1640 + double antibody for 7 hours 1/2 dilution 21pg/mL RAW 264.7 cells were cultured with 5 %FBS+ 1640 + double antibody +100 ng/mL LPS, and the cell culture supernatant was detected after 7 hours 1/2 dilution 657pg/mL 2. KD sample validation (Detect IL-6-KD RAW 264.7 cells): Sample Type Dilution Ratio Content Wild RAW 264.7 cells were stimulated with 100 ng/mL LPS for 7 hours to detect cell culture supernatant 1/2 dilution 857pg/mL RAW 264.7 cells (+siRNA) were stimulated with 100 ng/mL LPS for 7 hours to detect cell culture supernatants 1/2 dilution ND RAW 264.7 cells (+siRNA) were treated with 100 ng/mL LPS for 7 hours and then cultured with 300 ng/mL Brefeldin A (BFA) for 3 hours. Add cell lysis buffer(Catalogue No.:E050), collect the lysate solution (total protein concentration measured by BCA assay: 1.69 mg/mL) to detect. 1/2 dilution 29pg/mg(total protein) Note:ND is lower than the sensitivity of the kit and was not detected 3. Antibody by WB KD validation (Detect IL-6-KO RAW 264.7 cells):

    Sensibilité

    9.375 pg/mL

    Ingrédients

    • ELISA Microplate(Dismountable)
    • Lyophilized Standard
    • Biotin-labeled Antibody
    • HRP-Streptavidin Conjugate(SABC
    • 100X)
    • TMB Substrate
    • Sample Dilution Buffer
    • Stop Solution
    • Plate Sealer
    • Product Description

    Matériel non inclus

    • Microplate reader (wavelength: 450nm)
    • 37 °C incubator (CO2 incubator for cell culture is not recommenced.)
    • Automated plate washer or multi-channel pipette/5 mL pipettor
    • Precision single (0.5-10μL
    • 5-50μL
    • 20-200μL
    • 200-1000μL) and multi-channel pipette with disposable tips(Calibration is required before use.)
    • Sterile tubes and Eppendorf tubes with disposable tips
    • Absorbent paper and loading slot
    • Deionized or distilled water
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Commentaires

    Sandwich ELISA, Double Antibody

    Volume d'échantillon

    100 μL

    Durée du test

    4 h

    Plaque

    Pre-coated

    Protocole

    Step 1: Add 100 µL standard or sample into each well, seal the plate and statically incubate for 90 minutes at 37 °C. Washing: Wash the plate twice without immersing. Step 2: Add 100 µL biotin-antibody working solution, seal the plate and statically incubate for 60 minutes at 37 °C. Washing: Wash the plate three times and immerse for 1 min each time. Step 3: Add 100 µL HRP-Streptavidin Conjugate (SABC) working solution, seal the plate and statically incubate for 30 minutes at 37 °C. Washing: Wash the plate five times and immerse for 1 min each time. Step 4: Add 90 µL TMB substrate solution, seal the plate and statically incubate for 10-20 minutes at 37 °C. (Accurate TMB visualization control is required.) Step 5: Add 50 µL stop solution. Read at 450nm immediately and calculate.

    Restrictions

    For Research Use only
  • Conseil sur la manipulation

    Avoid direct light exposure to antibody solutions

    Stock

    4 °C

    Stockage commentaire

    Store sealed Kit at 2-8° C. Do Not Cryopreserve. Store ELISA Microplate for 1 month at 2-8°C, Store for 12 month at -20°C. Put the leftover strips into a sealed foil bag with the desiccant

    Date de péremption

    12 months
  • Twayana, Chaudhari, Ravanan: "Prolonged lipopolysaccharide exposure induces transient immunosuppression in BV2 microglia." dans: Journal of cellular physiology, Vol. 234, Issue 2, pp. 1889-1903, (2019) (PubMed).

  • Antigène Voir toutes IL-6 (IL6) Kits ELISA

    IL-6 (IL6) (Interleukin 6 (IL6))

    Autre désignation

    IL-6

    Sujet

    Interleukin-6, IL-6, B-cell stimulatory factor 2, BSF-2, CTL differentiation factor, CDF, Hybridoma growth factor, Interferon beta-2, IFN-beta-2, IL6, IFNB2

    UniProt

    P08505

    Pathways

    Signalisation TLR, Hormone Transport, Negative Regulation of Hormone Secretion, Myometrial Relaxation and Contraction, Positive Regulation of Immune Effector Process, Production of Molecular Mediator of Immune Response, Regulation of Carbohydrate Metabolic Process, Autophagy, Cell RedoxHomeostasis, Cancer Immune Checkpoints, Inflammasome
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