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Estradiol Kit ELISA

Reactivité: Différentes espèces Colorimetric Competition ELISA 12.35 pg/mL - 1000 pg/mL Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
N° du produit ABIN6574085
  • Antigène Voir toutes Estradiol Kits ELISA
    Estradiol
    Reactivité
    • 5
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Différentes espèces
    Méthode de détection
    Colorimetric
    Type de méthode
    Competition ELISA
    Gamme de detection
    12.35 pg/mL - 1000 pg/mL
    Seuil minimal de détection
    12.35 pg/mL
    Application
    ELISA
    Fonction
    The kit is a competitive inhibition enzyme immunoassay technique for the in vitro quantitative measurement of E2 in serum, plasma, tissue homogenates, cell lysates, cell culture supernates.

    We offer validation data (WB) for the kit components. So you can be sure to order a reliable ELISA kit product composed of high quality reagents.
    Type d'échantillon
    Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
    Analytical Method
    Quantitative
    Specificité
    This assay has high sensitivity and excellent specificity for detection of Estradiol (E2)
    Réactivité croisée (Details)
    No significant cross-reactivity or interference between Estradiol (E2) and analogues was observed.
    Sensibilité
    4.93 pg/mL
    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
  • Commentaires

    Information on standard material:
    The standard might be recombinant protein or natural protein, that will depend on the specific kit. Moreover, the expression system is E.coli or yeast or mammal cell. There is 0.05% proclin 300 in the standard as preservative.

    Information on reagents:
    The stop solution used in the kit is sulfuric acid with concentration of 1 mol/L. And the wash solution is TBS. The standard diluent contains 0.02 % sodium azide, assay diluent A and assay diluent B contain 0.01% sodium azide. Some kits can contain is BSA in them.

    Information on antibodies:
    The provided antibodies and their host vary in different kits.

    Volume d'échantillon
    50 μL
    Durée du test
    2 h
    Plaque
    Pre-coated
    Protocole
    1. Prepare all reagents, samples and standards,
    2. Add 50μL standard or sample to each well.
      Then add 50μL prepared Detection Reagent A immediately.
      Shake and mix. Incubate 1 hour at 37 °C,
    3. Aspirate and wash 3 times,
    4. Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37 °C,
    5. Aspirate and wash 5 times,
    6. Add 90μL Substrate Solution. Incubate 10-20 minutes at 37 °C,
    7. Add 50μL Stop Solution. Read at 450 nm immediately.
    Préparation des réactifs
    1. Bring all kit components and samples to room temperature (18-25 °C) before use. If the kit will not be used up in one time, please only take out strips and reagents for present experiment, and leave the remaining strips and reagents in required condition.
    2. Standard - Reconstitute the Standard with 2.0mL of Standard Diluent, kept for 10 minutes at room temperature, shake gently (not to foam). The concentration of the standard in the stock solution is1,000pg/mL. Prepare 5 tubes containing 0.6mL Standard Diluent and produce a triple dilution serie. Mix each tube thoroughly before the next transfer. Set up 5 points of diluted standard such as 1,000pg/mL, 333.33pg/mL, 111.11pg/mL, 37.04pg/mL, 12.35pg/mL, and the last tube with Standard Diluent is the blank as 0pg/mL.
    3. Detection Reagent A and Detection Reagent B - If lyophilized reconstitute the Detection Reagent A with 150μL of Reagent Diluent, kept for 10 minutes at room temperature, shake gently (not to foam). Briefly spin or centrifuge the stock Detection A and Detection B before use. Dilute them to the working concentration 100-fold with Assay Diluent A and B, respectively.
    4. Wash Solution - Dilute 20 mL of Wash Solution concentrate (30x) with 580 mL of deionized or distilled water to prepare 600 mL of Wash Solution (1x).
    5. TMB substrate - Aspirate the needed dosage of the solution with sterilized tips and do not dump the residual solution into the vial again.

    Note:

    1. Making serial dilution in the wells directly is not permitted.
    2. Prepare standard within 15 minutes before assay. Please do not dissolve the reagents at 37 °C directly.
    3. Detection Reagent A and B are sticky solutions, therefore, slowly pipette them to reduce the volume errors.
    4. Please carefully reconstitute Standards or working Detection Reagent A and B according to the instruction, and avoid foaming and mix gently until the crystals are completely dissolved. To minimize imprecision caused by pipetting, use small volumes and ensure that pipettors are calibrated. It is recommended to suck more than 10μL for one pipetting.
    5. The reconstituted Standards, Detection Reagent A and Detection Reagent B can be used only once.
    6. If crystals have formed in the Wash Solution concentrate (30x), warm to room temperature and mix gently until the crystals are completely dissolved.
    7. 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).
    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
  • Précaution d'utilisation
    The Stop Solution suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.
    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
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    Santos, Lapa Neto, Santos, Marinho, Nascimento, Alves, Teixeir, Wanderley-Teixeira: "Immunohistochemical and histophysiological study of prolonged use of nandrolone on reproductive organs and fertility." dans: Biotechnic & histochemistry : official publication of the Biological Stain Commission, pp. 1-19, (2020) (PubMed).

    Cavalcante, Ferreira, Pereira, Moraes, Simas, Sannomiya, Breithaupt-Faloppa, Moreira: "Acute administration of oestradiol or progesterone in a spinal cord ischaemia-reperfusion model in rats." dans: Interactive cardiovascular and thoracic surgery, Vol. 26, Issue 2, pp. 196-201, (2019) (PubMed).

    Ding, Gong, Li, Fu, Jin, Zhang, Gao, Sun: "Rcan2 and estradiol independently regulate body weight in female mice." dans: Oncotarget, Vol. 8, Issue 29, pp. 48098-48109, (2018) (PubMed).

    Wei, Song, Zhifen: "Molecular mechanism and functional role of macrophage colony‑stimulating factor in follicular granulosa cells." dans: Molecular medicine reports, Vol. 16, Issue 3, pp. 2875-2880, (2018) (PubMed).

    Mao, Fan, Yu, Luo, Wu, Tang, Kang, Tang: "Abnormality of Klotho Signaling Is Involved in Polycystic Ovary Syndrome." dans: Reproductive sciences (Thousand Oaks, Calif.), Vol. 25, Issue 3, pp. 372-383, (2018) (PubMed).

    Ding, Tan, Song, Ma, Xiao, Zhang: "Effect of controlled ovarian hyperstimulation on puberty and estrus in mice offspring." dans: Reproduction (Cambridge, England), Vol. 154, Issue 4, pp. 433-444, (2018) (PubMed).

    Hua, Cao, Wang, Sun, Chen: "Exposure of Pregnant Mice to Triclosan Causes Insulin Resistance via Thyroxine Reduction." dans: Toxicological sciences : an official journal of the Society of Toxicology, Vol. 160, Issue 1, pp. 150-160, (2018) (PubMed).

    Zhao, Zhou, Chen, Liu, Chu, Zhang: "Beneficial effects of Heqi san on rat model of polycystic ovary syndrome through the PI3K/AKT pathway." dans: Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences, Vol. 25, Issue 1, pp. 21, (2018) (PubMed).

    Wang, Wang, Lu, Cui, Li, Li, Zhang, Zhang, Liu: "The Combination of icariin and constrained dynamic loading stimulation attenuates bone loss in ovariectomy-induced osteoporotic mice." dans: Journal of orthopaedic research : official publication of the Orthopaedic Research Society, Vol. 36, Issue 5, pp. 1415-1424, (2018) (PubMed).

    He, Wang, Guo et al.: "Postnatal separation prevents the development of prenatal stress-induced anxiety in association with changes in oestrogen receptor and oxytocin immunoreactivity in female mandarin vole (Microtus ..." dans: The European journal of neuroscience, Vol. 47, Issue 1, pp. 95-108, (2018) (PubMed).

    Wang, Wang, Liang, He, Xia, Shen, Wang, Gao, Wang: "DHEA-induced ovarian hyperfibrosis is mediated by TGF-β signaling pathway." dans: Journal of ovarian research, Vol. 11, Issue 1, pp. 6, (2018) (PubMed).

    Cao, Hua, Xiong, Zhu, Zhang, Chen: "Impact of Triclosan on Female Reproduction through Reducing Thyroid Hormones to Suppress Hypothalamic Kisspeptin Neurons in Mice." dans: Frontiers in molecular neuroscience, Vol. 11, pp. 6, (2018) (PubMed).

    Tang, Yin, Zhang, Chen, Jin, Liu: "Prenatal exposure to polychlorinated biphenyl and umbilical cord hormones and birth outcomes in an island population." dans: Environmental pollution (Barking, Essex : 1987), Vol. 237, pp. 581-591, (2018) (PubMed).

    Li, Wang, Zhou, Shuang, Zhao, Chen: "Up-Regulation of Long Noncoding RNA SRA Promotes Cell Growth, Inhibits Cell Apoptosis, and Induces Secretion of Estradiol and Progesterone in Ovarian Granular Cells of Mice." dans: Medical science monitor : international medical journal of experimental and clinical research, Vol. 24, pp. 2384-2390, (2018) (PubMed).

    Liu, Xiong, Wang, Yang, Wang, Liu, Wu, Li, Ou, Zhang, Zhu: "Effects of water extract from epimedium on neuropeptide signaling in an ovariectomized osteoporosis rat model." dans: Journal of ethnopharmacology, Vol. 221, pp. 126-136, (2018) (PubMed).

    Ferreira, Armstrong-Jr, Kudo, de Jesus Correia, Dos Reis, Sannomiya, Breithaupt-Faloppa, Moreira: "Differential Effects of Brain Death on Rat Microcirculation and Intestinal Inflammation: Female Versus Male." dans: Inflammation, Vol. 41, Issue 4, pp. 1488-1497, (2018) (PubMed).

    Zhang, Li, Li, Wang, Zhu, Su, Letcher, Liu: "Exposure to tris(1,3-dichloro-2-propyl) phosphate for Two generations decreases fecundity of zebrafish at environmentally relevant concentrations." dans: Aquatic toxicology (Amsterdam, Netherlands), Vol. 200, pp. 178-187, (2018) (PubMed).

    Olatunji, Olaniyi, Usman, Abolarinwa, Achile, Kim: "Combined oral contraceptive and nitric oxide synthesis inhibition synergistically causes cardiac hypertrophy and exacerbates insulin resistance in female rats." dans: Environmental toxicology and pharmacology, Vol. 52, pp. 54-61, (2017) (PubMed).

    Cao, Hua, Wang, Chen: "Exposure of pregnant mice to triclosan impairs placental development and nutrient transport." dans: Scientific reports, Vol. 7, pp. 44803, (2017) (PubMed).

  • Antigène Voir toutes Estradiol Kits ELISA
    Estradiol
    Abstract
    Estradiol Produits
    Classe de substances
    Hormone
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