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Titin Kit ELISA

Ce kit ELISA Humain Titin est un kit ELISA Colorimetric conçu pour quantifier Humain Titin.
N° du produit ABIN454416

Aperçu rapide pour Titin Kit ELISA (ABIN454416)

Antigène

Voir toutes Titin (TTN) Kits ELISA
Titin (TTN)

Reactivité

  • 3
  • 1
  • 1
Humain

Méthode de détection

Colorimetric

Type de méthode

Sandwich ELISA

Gamme de detection

0.312 ng/mL - 20 ng/mL

Application

ELISA

Type d'échantillon

Cell Culture Supernatant, Plasma, Serum, Tissue Homogenate, Urine
  • Seuil minimal de détection

    0.312 ng/mL

    Fonction

    This immunoassay kit allows for the in vitro quantitative determination of human Titin , concentrations in serum, Plasma, Urine, tissue homogenates and Cell culture supernates.

    Analytical Method

    Quantitative

    Specificité

    This assay recognizes recombinant and natural human Anti-titin Ab.

    Réactivité croisée (Details)

    No significant cross-reactivity or interference was observed.

    Sensibilité

    0.138 ng/mL

    Attributs du produit

    Homo sapiens,Human,Titin,Connectin,Rhabdomyosarcoma antigen MU-RMS-40.14,TTN,2.7.11.1

    Ingrédients

    Reagent (Quantity): Assay plate (1), Standard (2), Sample Diluent (1x20ml), Assay Diluent A (1x10ml), Assay DiluentB 1 x 10ml Detection Reagent A (1x120µl), Detection Reagent B (1x120µl), Wash Buffer(25 x concentrate) (1x30ml), Substrate (1x10ml), Stop Solution (1x10ml)
  • Volume d'échantillon

    100 μL

    Plaque

    Pre-coated

    Préparation des réactifs

    Bring all reagents to room temperature before use. Wash Buffer - If crystals have formed in the concentrate, warm to room temperature and mix gently until the crystals have completely dissolved. Dilute 30 mL of Wash Buffer Concentrate into deionized or distilled water to prepare 750 mL of Wash Buffer. Standard - Reconstitute the Standard with 1.0mL of Sample Diluent. This reconstitution produces a stock solution of 20ng/mL. Allow the standard to sit for a minimum of 15 minutes with gentle agitation prior to making serial dilutions (Making serial dilution in the wells directly is not permitted). The undiluted standard serves as the high standard (20ng/mL) The Sample Diluent serves as the zero standard (0ng/mL). Detection Reagent A and B - Dilute to the working concentration using Assay Diluent A and B (1:100), respectively.

    Prélèvement de l'échantillon

    Serum - Use a serum separator tube (SST) and allow samples to clot for 30 minutes before centrifugation for 15 minutes at approximately 1000 x g. Remove serum and assay immediately or aliquot and store samples at -20 °C or -80 °C. Plasma - Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples for 15 minutes at 1000 x g at 2 - 8 °C within 30 minutes of collection. Store samples at -20 °C or -80° 2 C. Avoid repeated freeze-thaw cycles. Other biological fluids - Remove particulates by centrifugation and assay immediately or aliquot and store samples at -20 °C or -80 °C. Avoid repeated freeze-thaw cycles. Note: Serum, plasma, and cell culture supernatant samples to be used within 7 days may be stored at 2-8C, otherwise samples must stored at -20 °C (≤ 3 months) or -80 °C (≤ 6 months) to avoid loss of bioactivity and contamination. Avoid freeze-thaw cycles. When performing the assay slowly bring samples to room temperature. It is recommended that all samples be assayed in duplicate.

    Calcul des résultats

    Average the duplicate readings for each standard, control, and sample and subtract the average zero standard optical density. Create a standard curve by reducing the data using computer software capable of generating a four parameter logistic (4-PL) curve-fit. As an alternative, construct a standard curve by plotting the mean absorbance for each standard on the y-axis against the concentration on the x-axis and draw a best fit curve through the points on the graph. The data may be linearized by plotting the log of the ANTI-TITIN AB concentrations versus the log of the O.D. and the best fit line can be determined by regression analysis. This procedure will produce an adequate but less precise fit of the data. If samples have been diluted, the concentration read from the standard curve must be multiplied by the dilution factor.

    Précision du teste

    Intra-AssayCV: < 3.9%Inter-AssayCV: < 6.2%

    Restrictions

    For Research Use only
  • Conseil sur la manipulation

    1. The kit should not be used beyond the expiration date on the kit label.
    2. Do not mix or substitute reagents with those from other lots or sources.
    3. If samples generate values higher than the highest standard, further dilute the samples with the Assay Diluent and repeat the assay. Any variation in standard diluent, operator, pipetting technique, washing technique,incubation time or temperature, and kit age can cause variation in binding.
    4. This assay is designed to eliminate interference by soluble receptors, ligands, binding proteins, and other factors present in biological samples. Until all factors have been tested in the Immunoassay, the possibility of interference cannot be excluded.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    The Standard, Detection Reagent A, Detection Reagent B and the 96-well strip plate should be stored at -20 °C upon being received. The other reagents can be stored at 4 °C.
  • Antigène Voir toutes Titin (TTN) Kits ELISA

    Titin (TTN)

    Autre désignation

    TTN

    Classe de substances

    Antibody
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