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Caspase 3 Kit ELISA

CASP3 Reactivité: Rat Colorimetric Sandwich ELISA 0.31 ng/mL - 20 ng/mL Cell Culture Supernatant, Plasma, Serum
N° du produit ABIN6963116
  • Antigène Voir toutes Caspase 3 (CASP3) Kits ELISA
    Caspase 3 (CASP3)
    Reactivité
    • 11
    • 9
    • 8
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Rat
    Méthode de détection
    Colorimetric
    Type de méthode
    Sandwich ELISA
    Gamme de detection
    0.31 ng/mL - 20 ng/mL
    Seuil minimal de détection
    0.31 ng/mL
    Application
    ELISA
    Fonction
    The kit is a sandwich enzyme immunoassay technique for the in vitro quantitative measurement in various sample types.
    Type d'échantillon
    Cell Culture Supernatant, Plasma, Serum
    Analytical Method
    Quantitative
    Specificité
    This kit recognizes Rat CASP3 in samples. No Significant cross-reactivity or interference between Rat CASP3 and analogues was observed.
    Sensibilité
    0.19 ng/mL
    Ingrédients
    • Pre-coated, ready to use 96-well strip plate, flat buttom
    • Plate sealer for 96 wells
    • Reference Standard
    • Reference Standard & Sample Diluent
    • Biotinylated Detection Antibody (100 x concentrate)
    • HRP Conjugate (100 x concentrate)
    • Biotinylated Detection Antibody Diluent
    • HRP Conjugate Diluent
    • Substrate Reagent
    • Stop Solution
    • Wash Buffer (25 x concentrate)
    • Instruction manual
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  • Volume d'échantillon
    100 μL
    Durée du test
    3.5 h
    Plaque
    Pre-coated
    Protocole
    1. Add 100 µL standard or sample to each well. Incubate for 90 min at 37 °C.
    2. Remove the liquid. Add 100 µL Biotinylated Detection Antibody. Incubate for 1 hour at 37 °C.
    3. Aspirate and wash 3 times.
    4. Add 100 µL HRP Conjugate. Incubate for 30 min at 37 °C.
    5. Aspirate and wash 5 times.
    6. Add 90 µL Substrate Reagent. Incubate for 15 min at 37 °C.
    7. Add 50 µL Stop Solution. Read at 450 nm immediately.
    8. Calculation of results.
    Préparation des réactifs
    1. Bring all reagents to room temperature (18~25 °C) before use. Follow the Microplate reader manual for set-up and preheat it for 15 min before OD measurement.
    2. Wash Buffer: Dilute 30 mL of Concentrated Wash Buffer with 720 mL of deionized or distilled water to prepare 750 mL of Wash Buffer.Note: if crystals have formed in the concentrate, warm it in a 40 °C water bath and mix it gently until the crystals have completely dissolved
    3. Standard working solution: Centrifuge the standard at 10,000xg for 1 min. Add 1.0 mL of Reference Standard &Sample Diluent, let it stand for 10 min and invert it gently several times. After it dissolves fully, mix it thoroughly with a pipette. This reconstitution produces a working solution of 20 ng/mL. Then make serial dilutions as needed. The recommended dilution gradient is as follows: 20, 10, 5, 2.5, 1.25, 0.63, 0.31, 0 ng/mL. Dilution method: Take 7 EP tubes, add 500 μLof Reference Standard & Sample Diluent to each tube. Pipette 500 μLof the 20 ng/mL working solution to the first tube and mix up to produce a 10 ng/mL working solution. Pipette 500 μLof the solution from the former tube into the latter one according to these steps. The illustration below is for reference. Note: the last tube is regarded as a blank. Don't pipette solution into it from the former tube.
    4. Biotinylated Detection Antibody working solution: Calculate the required amount before the experiment (100 μL/well). In preparation, slightly more than calculated should be prepared. Centrifuge the stock tube before use, dilute the 100x Concentrated Biotinylated Detection Antibody to 1xworking solution with Biotinylated Detection Antibody Diluent.
    5. Concentrated HRP Conjugate working solution: Calculate the required amount before the experiment (100 μL/well). In preparation, slightly more than calculated should be prepared. Dilute the 100x Concentrated HRP Conjugate to 1x working solution with Concentrated HRP Conjugate Diluent.
    Préparation de l'échantillon
    • It is recommended to use fresh samples without long storage, otherwise protein degradation and denaturation may occur in these samples, leading to false results. Samples should therefore be stored for a short period at 2 - 8 °C or aliquoted at -20 °C (≤1 month) or -80 °C (≤ 3 months). Repeated freeze-thaw cycles should be avoided. Prior to assay, the frozen samples should be slowly thawed and centrifuged to remove precipitates.
    • If the sample type is not specified in the instructions, a preliminary test is necessary to determine compatibility with the kit.
    • If a lysis buffer is used to prepare tissue homogenates or cell culture supernatant, there is a possibility of 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 the range of the standard curve, the optimal sample dilution for the particular experiment has to be determined.
    Précision du teste
    Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level Rat CASP3 were tested 20 times on one plate, respectively.
    Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level Rat CASP3 were tested on 3 different plates, 20 replicates in each plate.
    Both intra-CV and inter-CV are < 10 %.
    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, so they are stable up to 12 months after receipt of the kit. The Reference Standard, Biotinylated Detection Antibody, HRP Conjugate and the 96-well stripe plate should be stored at -20 °C upon receipt while the other reagents should be stored at 4 °C.
    2. For used kit: When the kit is used, the remaining reagents need to be stored according to the above storage condition. Besides, please return the unused wells to the foil pouch containing the desiccant pack, and zip-seal the foil pouch.
    Date de péremption
    12 months
  • Caputo, Piccialli, Ciccone, de Caprariis, Massa, De Feo, Pannaccione: "Lavender and coriander essential oils and their main component linalool exert a protective effect against amyloid-β neurotoxicity." dans: Phytotherapy research : PTR, Vol. 35, Issue 1, pp. 486-493, (2021) (PubMed).

    Adedara, Fabunmi, Ayenitaju, Atanda, Adebowale, Ajayi, Owoeye, Rocha, Farombi: "Neuroprotective mechanisms of selenium against arsenic-induced behavioral impairments in rats." dans: Neurotoxicology, Vol. 76, pp. 99-110, (2021) (PubMed).

    Owumi, Adedara, Farombi, Oyelere: "Protocatechuic acid modulates reproductive dysfunction linked to furan exposure in rats." dans: Toxicology, Vol. 442, pp. 152556, (2021) (PubMed).

    Chuang, Chen, Hsiao, Chou, Kuo, Feng, Ho, Chen, Chuang, Lee: "Alteration in angiotensin-converting enzyme 2 by PM1 during the development of emphysema in rats." dans: ERJ open research, Vol. 6, Issue 4, (2020) (PubMed).

    Çakır, Tekin, Okan, Çakan, Doğanyiğit: "The ameliorating effect of cannabinoid type 2 receptor activation on brain, lung, liver and heart damage in cecal ligation and puncture-induced sepsis model in rats." dans: International immunopharmacology, Vol. 78, pp. 105978, (2020) (PubMed).

    Delkhosh-Kasmaie, Farshid, Tamaddonfard, Imani et al.: "The effects of safranal, a constitute of saffron, and metformin on spatial learning and memory impairments in type-1 diabetic rats: behavioral and hippocampal histopathological and biochemical ..." dans: Biomedicine & pharmacotherapy, Vol. 107, pp. 203-211, (2019) (PubMed).

    Mahmoudi, Farshid, Tamaddonfard, Imani, Noroozinia: "Behavioral, histopathological, and biochemical evaluations on the effects of cinnamaldehyde, naloxone, and their combination in morphine-induced cerebellar toxicity." dans: Drug and chemical toxicology, pp. 1-12, (2019) (PubMed).

    Adedara, Adebowale, Atanda, Fabunmi, Ayenitaju, Rocha, Farombi: "Selenium abates reproductive dysfunction via attenuation of biometal accumulation, oxido-inflammatory stress and caspase-3 activation in male rats exposed to arsenic." dans: Environmental pollution (Barking, Essex : 1987), Vol. 254, Issue Pt B, pp. 113079, (2019) (PubMed).

    Lu, Wang: "SIRT1 exerts neuroprotective effects by attenuating cerebral ischemia/reperfusion-induced injury via targeting p53/microRNA-22." dans: International journal of molecular medicine, Vol. 39, Issue 1, pp. 208-216, (2017) (PubMed).

  • Antigène Voir toutes Caspase 3 (CASP3) Kits ELISA
    Caspase 3 (CASP3)
    Autre désignation
    Caspase 3 (CASP3 Produits)
    Synonymes
    CPP32 Kit ELISA, CPP32B Kit ELISA, SCA-1 Kit ELISA, A830040C14Rik Kit ELISA, AC-3 Kit ELISA, Apopain Kit ELISA, CC3 Kit ELISA, Caspase-3 Kit ELISA, Lice Kit ELISA, Yama Kit ELISA, mldy Kit ELISA, xcpp32 Kit ELISA, casp3 Kit ELISA, zgc:100890 Kit ELISA, CASP-3 Kit ELISA, caspase-3 Kit ELISA, caspase 3 Kit ELISA, caspase 3 S homeolog Kit ELISA, caspase 3, apoptosis-related cysteine peptidase a Kit ELISA, caspase 3, apoptosis-related cysteine peptidase Kit ELISA, CASP3 Kit ELISA, Casp3 Kit ELISA, casp3.S Kit ELISA, casp3a Kit ELISA
    Sujet
    CPP32, CPP32B, SCA-1, Apoptain, Yama
    Pathways
    Apoptose, Caspase Cascade in Apoptosis, Sensory Perception of Sound, ER-Nucleus Signaling, Positive Regulation of Endopeptidase Activity, Activated T Cell Proliferation
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