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IKK alpha Kit ELISA

High Sensitivity CHUK Reactivité: Humain Colorimetric Sandwich ELISA 3.12 pg/mL - 200 pg/mL Cell Lysate, Tissue Homogenate
N° du produit ABIN6999499
  • Antigène Voir toutes IKK alpha (CHUK) Kits ELISA
    IKK alpha (CHUK) (conserved Helix-Loop-Helix Ubiquitous Kinase (CHUK))
    Reactivité
    • 4
    • 2
    • 2
    • 1
    • 1
    Humain
    Méthode de détection
    Colorimetric
    Type de méthode
    Sandwich ELISA
    Gamme de detection
    3.12 pg/mL - 200 pg/mL
    Seuil minimal de détection
    3.12 pg/mL
    Application
    ELISA
    Fonction
    The kit is a high sensitivity sandwich enzyme immunoassay for in vitro quantitative measurement in various sample types.
    Type d'échantillon
    Cell Lysate, Tissue Homogenate
    Analytical Method
    Quantitative
    Specificité
    This assay has high sensitivity and excellent specificity for detection of Conserved Helix Loop Helix Ubiquitous Kinase.
    Sensibilité
    1.11 pg/mL
    Classe de qualité
    High Sensitivity
    Ingrédients
    • Pre-coated, ready to use 96-well strip plate, flat buttom
    • Plate sealer for 96 wells
    • Reference Standard
    • Standard Diluent
    • Detection Reagent A
    • Detection Reagent B
    • Assay Diluent A
    • Assay Diluent B
    • Reagent Diluent (if Detection Reagent is lyophilized)
    • TMB Substrate
    • Stop Solution
    • Wash Buffer (30 x concentrate)
    • Instruction manual
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    Discover our top product CHUK Kit ELISA
  • Volume d'échantillon
    100 µL
    Durée du test
    3 h
    Plaque
    Pre-coated
    Protocole
    1. Prepare all reagents, samples and standards,
    2. Add 100μL standard or sample to each well. Incubate 1 hours at 37 °C,
    3. Aspirate and add 100μL prepared Detection Reagent A. Incubate 1 hour at 37 °C,
    4. Aspirate and wash 3 times,
    5. Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37 °C,
    6. Aspirate and wash 5 times,
    7. Add 90μL Substrate Solution. Incubate 10-20 minutes at 37 °C,
    8. Add 50μL Stop Solution. Read at 450nm immediately.
    Préparation des réactifs
    1. Bring all kit components and samples to room temperature (18-25 °C) before use. If the kit is not used up all at once, remove only the strips and reagents for the current experiment and leave the remaining strips and reagents in the desired condition.
    2. Standard - Reconstitute the standard with the Standard Diluent, keep it at room temperature for 10 minutes and shake it gently (do not let it foam). Please prepare tubes with Standard Diluent and make a dilution series. Mix each tube thoroughly before the next transfer. The last tube with Standard Diluent is the blank as 0 mg/mL.
    3. Detection Reagent A and Detection Reagent B - Spin or centrifuge the stock of Detection Reagent A and B briefly before use. Dilute to working concentration (1:100) with Assay Diluent A or B, respectively.
    4. Wash Solution - Dilute 20 mL of Wash Solution Concentrate (30x) with 580 mL of deionized or distilled water to make 600 mL of Wash Solution (1x).
    5. TMB Substrate - Aspirate the required amount of solution with sterile tip and do not return the residual solution back into the vial.

    Note:

    1. Serial dilution directly in the wells is not recommended.
    2. Prepare standard within 15 minutes before assay. Do not dissolve the reagents directly at 37 °C.
    3. Detection Reagent A and B are sticky solutions, so pipette them slowly to reduce volume errors.
    4. Reconstitute Standard or working solutions of Detection Reagent A and B carefully according to instructions, avoiding foaming and mixing gently until crystals are completely dissolved. To minimize inaccuracy caused by pipetting, use small volumes and ensure pipettes are calibrated. It is recommended to aspirate more than 10 µL for one-time pipetting.
    5. The reconstituted Standard, Detection Reagent A and B can only be used once.
    6. When crystals have formed in the Wash Solution concentrate (30x), warm it to room temperature and mix gently until the crystals are completely dissolved.
    7. Contaminated water or preparation containers affect 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).
    Précision du teste
    Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level of target were tested 20 times on one plate, respectively.
    Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level of target were tested on 3 different plates, 8 replicates in each plate.
    CV(%) = SD/meanX100
    Intra-Assay: CV < 10%
    Inter-Assay: CV < 12%
    Restrictions
    For Research Use only
  • Stock
    4 °C/-20 ° C
    Stockage commentaire
    1. For unopened kit: All reagents should be stored according to the labels on the vials. The Standard, Detection Reagent A, Detection Reagent B, and 96-well Strip Plate should be stored at -20 °C upon receipt, while the other reagents should be stored at 4 °C.
    2. For opened kits: the remaining reagents must be stored according to the above storage conditions. In addition, please return the unused wells to the foil pouch containing the desiccant and seal the foil pouch with the zipper.
    Date de péremption
    6 months
  • Antigène Voir toutes IKK alpha (CHUK) Kits ELISA
    IKK alpha (CHUK) (conserved Helix-Loop-Helix Ubiquitous Kinase (CHUK))
    Autre désignation
    Conserved Helix Loop Helix Ubiquitous Kinase (CHUK Produits)
    Synonymes
    ikk Kit ELISA, ikk1 Kit ELISA, ikka Kit ELISA, ikkalpha Kit ELISA, CHUK Kit ELISA, IKBKA Kit ELISA, IKK-alpha Kit ELISA, IKK1 Kit ELISA, IKKA Kit ELISA, NFKBIKA Kit ELISA, TCF16 Kit ELISA, AI256658 Kit ELISA, Chuk1 Kit ELISA, Fbx24 Kit ELISA, Fbxo24 Kit ELISA, Ikka Kit ELISA, zgc:56539 Kit ELISA, conserved helix-loop-helix ubiquitous kinase S homeolog Kit ELISA, conserved helix-loop-helix ubiquitous kinase Kit ELISA, chuk.S Kit ELISA, CHUK Kit ELISA, Chuk Kit ELISA, chuk Kit ELISA
    Sujet
    TCF16, IKK1, IKK-alpha, IkBKA, NFKBIKA, IKKA, Inhibitor of nuclear factor kappa-B kinase subunit alpha, Transcription factor 16, I-kappa-B kinase 1
    Pathways
    Signalisation PI3K-Akt, Signalisation NF-kappaB, Signalisation RTK, TCR Signaling, Signalisation TLR, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway, Activation of Innate immune Response, Hepatitis C, Toll-Like Receptors Cascades, BCR Signaling, Ubiquitin Proteasome Pathway, S100 Proteins
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