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FABP4 Kit ELISA

FABP4 Reactivité: Humain Colorimetric Competition ELISA 62.5 pg/mL - 4000 pg/mL Plasma, Serum
N° du produit ABIN6975911
  • Antigène Voir toutes FABP4 Kits ELISA
    FABP4 (Fatty Acid Binding Protein 4, Adipocyte (FABP4))
    Reactivité
    • 16
    • 14
    • 10
    • 6
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Humain
    Méthode de détection
    Colorimetric
    Type de méthode
    Competition ELISA
    Gamme de detection
    62.5 pg/mL - 4000 pg/mL
    Seuil minimal de détection
    62.5 pg/mL
    Application
    ELISA
    Fonction
    For the quantitative determination of human fatty acid binding protein 4 (FABP-4) concentrations in serum, plasma.
    Type d'échantillon
    Plasma, Serum
    Analytical Method
    Quantitative
    Specificité
    This assay has high sensitivity and excellent specificity for detection of human FABP-4. No significant cross-reactivity or interference between human FABP-4 and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between human FABP-4 and all the analogues, therefore, cross reaction may still exist.
    Sensibilité
    15.6 pg/mL
    Ingrédients
    • Assay plate
    • Standard
    • HRP-conjugate (100 x concentrate)
    • Sample Diluent
    • HRP-conjugate Diluent
    • Wash Buffer (25 x concentrate)
    • TMB Substrate
    • Stop Solution
    • Adhesive Strip
  • Stop Solution
  • Adhesive Strip
  • Top Product
    Discover our top product FABP4 Kit ELISA
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Volume d'échantillon
    50 μL
    Durée du test
    1 - 4.5 h
    Plaque
    Pre-coated
    Protocole
    1. Prepare reagents, samples and standards as instructed.
    2. Set a Blank well without any solution.
    3. Add 50 µL standard or sample to each well.
    4. Add 50 µL HRP-conjugate (1x) to each well (Not to Blank well).
    5. Incubate 1 hour at 37 °C
    6. Aspirate and wash 5 times.
    7. Add 90 μL of TMB Substrate to each well. Incubate for 20 minutes at 37 °C. Protect from light.
    8. Add 50 µL Stop Solution to each well. Read at 450 nm within 5 minutes.
    Préparation des réactifs
    1. HRP-conjugate (1x) - Centrifuge the vial before opening. HRP-conjugate requires a 100-fold dilution. A suggested 100-fold dilution is 10 μL of HRP-conjugate + 990 μL of HRP-conjugate Diluent.
    2. Wash Buffer(1x)- If crystals have formed in the concentrate, warm up to room temperature and mix gently until the crystals have completely dissolved. Dilute 20 mL of Wash Buffer Concentrate (25 x) into deionized or distilled water to prepare 500 mL of Wash Buffer (1 x).
    3. Standard Centrifuge the standard vial at 6000-10000rpm for 30s. Reconstitute the Standard with 1.0 mL of Sample Diluent. Do not substitute other diluents. This reconstitution produces a stock solution of 4000 pg/mL. Mix the standard to ensure complete reconstitution and allow the standard to sit for a minimum of 15 minutes with gentle agitation prior to making dilutions. Pipette 150 μL of Sample Diluent into each tube (S0-S6). Use the stock solution to produce a 2-fold dilution series (below). Mix each tube thoroughly before the next transfer. The undiluted Standard serves as the high standard (4000 pg/mL). Sample Diluent serves as the zero standard (0 pg/mL).
    Note:
    • Kindly use graduated containers to prepare the reagent. Please don't prepare the reagent directly in the Diluent vials provided in the kit.
    • Bring all reagents to room temperature (18-25 °C) before use for 30 min.
    • Prepare fresh standard for each assay. Use within 4 hours and discard after use.
    • Making serial dilution in the wells directly is not permitted.
    • Please carefully reconstitute Standards according to the instruction, and avoid foaming and mix gently until the crystals have completely dissolved. To minimize imprecision caused by pipetting, use small volumes and ensure that pipettors are calibrated. It is recommended to suck more than 10 μL for once pipetting.
    • Distilled water is recommended to be used to make the preparation for reagents. Contaminated water or container for reagent preparation will influence the detection result.
    Préparation de l'échantillon
    • It is recommended to use fresh samples without long storage, otherwise protein degradation and denaturationmay occur in these samples, leading to false results. Samples should therefore be stored for a short periodat 2 - 8 °C or aliquoted at -20 °C (≤1 month) or -80 °C (≤ 3 months). Repeated freeze-thawcycles should be avoided. Prior to assay, the frozen samples should be slowly thawed and centrifuged toremove precipitates.
    • If the sample type is not specified in the instructions, a preliminary test is necessary to determinecompatibility with the kit.
    • If a lysis buffer is used to prepare tissue homogenates or cell culture supernatant, there is a possibilityof causing a deviation due to the introduced chemical substance.The recommended dilution factor is for reference only.
    • Please estimate the concentration of the samples before performing the test. If the values are not in therange of the standard curve, the optimal sample dilution for the particular experiment has to be determined.Samples should then be diluted with PBS (pH =7.0-7.2).
    Note:
    Recommend to dilute the serum or plasma samples with Sample Diluent(1:100) before test. The suggested 100-fold dilution can be achieved by adding 10 μL sample to 40 μL of Sample Diluent. Complete the 100-fold dilution by adding 15 μL of this solution to 285 μL of Sample Diluent. The recommended dilution factor is for reference only. The optimal dilution factor should be determined by users according to their particular experiments. 6
    Précision du teste
    Intra-assay Precision (Precision within an assay): CV%<8% Three samples of known concentration were tested twenty times on one plate to assess.
    Inter-assay Precision (Precision between assays): CV%<10% Three samples of known concentration were tested in twenty assays to assess.
    Restrictions
    For Research Use only
  • Stock
    4 °C,-20 °C
    Stockage commentaire
    Unopened kit Store at 2 - 8°C. Do not use the kit beyond the expiration date. May be stored for up to 1 month at 2 - 8°C. Coated assay Try to keep it in a sealed aluminum foil bag, plate and avoid the damp. Standard May be stored for up to 1 month at 2 - 8° C. If don't make recent use, better keep it store at HRP-conjugate -20°C. Opened kit HRP-conjugate Diluent Sample Diluent May be stored for up to 1 month at 2 - 8°C. Wash Buffer TMB Substrate Stop Solution *Provided this is within the expiration date of the kit.
    Date de péremption
    6 months
  • Antigène Voir toutes FABP4 Kits ELISA
    FABP4 (Fatty Acid Binding Protein 4, Adipocyte (FABP4))
    Autre désignation
    fatty acid binding protein 4, adipocyte (FABP4 Produits)
    Synonymes
    A-FABP Kit ELISA, AFABP Kit ELISA, ALBP Kit ELISA, aP2 Kit ELISA, LOC100223994 Kit ELISA, FABP Kit ELISA, AP2 Kit ELISA, FABP3 Kit ELISA, FABP4 Kit ELISA, MGC84940 Kit ELISA, fabp4 Kit ELISA, 422/aP2 Kit ELISA, ALBP/Ap2 Kit ELISA, Ap2 Kit ELISA, Lbpl Kit ELISA, Albp Kit ELISA, fatty acid binding protein 4 Kit ELISA, fatty acid-binding protein, adipocyte Kit ELISA, fatty acid binding protein 4, adipocyte Kit ELISA, fatty acid binding protein 4, adipocyte L homeolog Kit ELISA, Fatty acid-binding protein, adipocyte Kit ELISA, adipocyte fatty acid-binding protein Kit ELISA, adipocyte fatty acid binding protein Kit ELISA, FABP4 Kit ELISA, LOC100223994 Kit ELISA, fabp4.L Kit ELISA, fabp4 Kit ELISA, Fabp4 Kit ELISA, LOC100732353 Kit ELISA, LOC100861279 Kit ELISA, LOC100057425 Kit ELISA, LOC395224 Kit ELISA
    Sujet

    Abbreviation: FABP4

    Alias: A-FABP, aP2

    UniProt
    P15090
    Pathways
    Brown Fat Cell Differentiation
Support technique