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MMP 9 Kit ELISA

MMP9 Reactivité: Humain Colorimetric Sandwich ELISA 0.15 ng/mL - 10 ng/mL Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
N° du produit ABIN3163616
  • Antigène Voir toutes MMP 9 (MMP9) Kits ELISA
    MMP 9 (MMP9) (Matrix Metallopeptidase 9 (Gelatinase B, 92kDa Gelatinase, 92kDa Type IV Collagenase) (MMP9))
    Reactivité
    • 12
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain
    Méthode de détection
    Colorimetric
    Type de méthode
    Sandwich ELISA
    Gamme de detection
    0.15 ng/mL - 10 ng/mL
    Seuil minimal de détection
    0.15 ng/mL
    Application
    ELISA
    Fonction
    The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of MMP9 in human 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 Matrix Metalloproteinase 9 (MMP9).
    No significant cross-reactivity or interference between Matrix Metalloproteinase 9 (MMP9) and analogues was observed.

    Réactivité croisée (Details)
    No significant cross-reactivity or interference between Matrix Metalloproteinase 9 (MMP9) and analogues was observed.
    Sensibilité
    0.055 ng/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
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  • Indications d'application
    • Limited by the current condition and scientific technology, we cannot completely conduct the comprehensive identification and analysis on the raw material provided by suppliers. So there might be some qualitative and technical risks to use the kit.
    • The final experimental results will be closely related to validity of the products, operation skills of the end users and the experimental environments. Please make sure that sufficient samples are available.
    • Kits from different batches may be a little different in detection range, sensitivity and color developing time.
    • Do not mix or substitute reagents from one kit lot to another. Use only the reagents supplied by manufacturer.
    • Protect all reagents from strong light during storage and incubation. All the bottle caps of reagents should be covered tightly to prevent the evaporation and contamination of microorganism.
    • There may be some foggy substance in the wells when the plate is opened at the first time. It will not have any effect on the final assay results. Do not remove microtiter plate from the storage bag until needed.
    • Wrong operations during the reagents preparation and loading, as well as incorrect parameter setting for the plate reader may lead to incorrect results. A microplate plate reader with a bandwidth of 10nm or less and an optical density range of 0-3 O.D. or greater at 450 ± 10nm wavelength is acceptable for use in absorbance measurement. Please read the instruction carefully and adjust the instrument prior to the experiment.
    • Even the same operator might get different results in two separate experiments. In order to get better reproducible results, the operation of every step in the assay should be controlled. Furthermore, a preliminary experiment before assay for each batch is recommended.
    • Each kit has been strictly passed Q.C test. However, results from end users might be inconsistent with our in-house data due to some unexpected transportation conditions or different lab equipments. Intra-assay variance among kits from different batches might arise from above factors, too.
    • Kits from different manufacturers for the same item might produce different results, since we have not compared our products with other manufacturers.
    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
    100 μL
    Durée du test
    3 h
    Plaque
    Pre-coated
    Protocole
    The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Matrix Metalloproteinase 9 (MMP9). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Matrix Metalloproteinase 9 (MMP9). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Matrix Metalloproteinase 9 (MMP9), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Matrix Metalloproteinase 9 (MMP9) in the samples is then determined by comparing the O.D. of the samples to the standard curve.
    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 1.0 mL of Standard Diluent, keep for 10 minutes at room temperature, shake gently (not to foam). The concentration of the standard in the stock solution is 20 ng/mL. Firstly dilute the stock solution to 10 ng/mL and the diluted standard serves as the highest standard (10 ng/mL). Then prepare 7 tubes containing 0.5 mL Standard Diluent and use the diluted standard to produce a double dilution series. Mix each tube thoroughly before the next transfer. Set up 7 points of diluted standard such as 10 ng/mL, 5 ng/mL, 2.5 ng/mL, 1.25 ng/mL, 0.625 ng/mL, 0.312 ng/mL, 0.156 ng/mL, and the last microcentrifuge tube with Standard Diluent is the blank as 0 ng/mL.
    3. Detection Reagent A and Detection Reagent B - If lyophilized reconstitute the Detection Reagent A with 150μL of Reagent Diluent, keep 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 standards within 15 minutes before assay. Please do not dissolve the reagents at 37 °C directly.
    3. 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.
    4. The reconstituted Standards, Detection Reagent A and Detection Reagent B can be used only once.
    5. If crystals have formed in the Wash Solution concentrate (30x), warm to room temperature and mix gently until the crystals are completely dissolved.
    6. Contaminated water or container for reagent preparation will influence the detection result.
    Précision du teste

    Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Matrix Metalloproteinase 9 (MMP9) were tested 20 times on one plate, respectively.
    Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Matrix Metalloproteinase 9 (MMP9) 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
  • Validation #029794 (ELISA)
    'Independent Validation' signe
    by
    Alamo Laboratories
    No.
    #029794
    Date
    21.08.2014
    Antigène
    Numéro du lot
    L140624541
    Application validée
    ELISA
    Contrôle positif
    Human serum - expression is ~305 ng/mL
    Contrôle négative
    Chicken serum (non-reactive species)
    Conclusion
    Target protein was detected in the positive control sample and not in the negative control sample as expected.
    'Independent Validation' signe
    Validation Images
    Protocole
    Anticorps primaire
    Anticorps secondaire
    Full Protocol
    • 1. All reagents in the ELISA kit were brought up to room temperature (RT) before use.
    • 2. 100 μL of standard or sample were added to wells in ELISA plate pre-coated with capture antibody.
    • 3. All samples and standards were assayed in triplicate.
    • 4. The plate was covered with sealer (provided in kit) and incubated for 2 hours at 37°C. Unbound material was aspirated but the wells were NOT washed.
    • 5. 100 μL of Detection Reagent-A Working Solution was added to each well. Plate was covered with sealer (provided in kit) and incubated for 1 hour at 37°C. Unbound material was removed from each well and plate was washed three times with 350 μL of 1x Wash Solution (provided in the kit). After the last wash the plate was inverted and blotted against clean absorbent paper to remove any remaining liquid.
    • 6. 100 μL of Detection Reagent-B Working Solution was added to each well. Plate was covered with sealer (provided in kit) and incubated for 30 minutes at 37°C.
    • 7. Unbound material was removed by washing five times with 350 μL of 1x Wash Solution (provided in the kit). After the last wash the plate was inverted and blotted against clean absorbent paper to remove any remaining liquid.
    • 8. 90 μL of Substrate Solution was added to wells and the plate was covered with a new plate sealer. The plate was gently tapped to ensure mixing and incubated for 25 minutes at 37°C in the dark.
    • 9. After 25 minutes, when an apparent gradient appeared in the standard wells, the reaction was terminated by adding 50 μL of Stop Solution to each well.
    • 10. The optical density (OD value) of each well was read using a microplate reader set to 450 nm.
    • 11. The triplicate readings for each sample were averaged and the average zero standard optical density subtracted to yield ‘corrected absorbance at 450 nm’. A standard curve was generated by plotting the mean OD value for each standard on the X-axis against the concentration on the Y-axis using Excel. Standard curve was generated by regression analysis with four-parameter logistic.
    • 12. An equation (y = -0.3106x^4 + 1.5995x^3 - 0.3488x^2 + 3.1612x - 0.0138) was derived from the standard curve and used to calculate MMP9 concentrations in samples based on their Average Absorbance values.
    Notes
    No experimental challenges noted.
  • 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.
    Conseil sur la manipulation
    The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5 % within the expiration date under appropriate storage condition.
    To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
    Stock
    4 °C
    Stockage commentaire
    • For unopened kit: All the reagents should be kept according to the labels on vials. The Standard, Detection Reagent A, Detection Reagent B and the 96-well strip plate should be stored at -20°C upon receipt while the others should be at 4°C.
    • For opened kit: When the kit is opened, the remaining reagents still 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 reseal along entire edge of zip-seal.
      Note: It is highly recommended to use the remaining reagents within 1 month provided this is within the expiration date of the kit.
    • For ELISA kit, 1 day storage at 37°C can be considered as 2 months at 4°C, which means 3 days at 37°C equaling 6 months at 4°C.
    Date de péremption
    6 months
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    Raimondi, De Luca, Fontana, Amodio, Costa, Carina, Bellavia, Raimondo, Siragusa, Monteleone, Alessandro, Fini, Giavaresi: "Multiple Myeloma-Derived Extracellular Vesicles Induce Osteoclastogenesis through the Activation of the XBP1/IRE1α Axis." dans: Cancers, Vol. 12, Issue 8, (2020) (PubMed).

    Ramirez-Tortosa, Sanchez, Perez-Ramirez, Quiles, Robles-Almazan, Pulido-Moran, Sanchez-Rovira, Ramirez-Tortosa: "Hydroxytyrosol Supplementation Modifies Plasma Levels of Tissue Inhibitor of Metallopeptidase 1 in Women with Breast Cancer." dans: Antioxidants (Basel, Switzerland), Vol. 8, Issue 9, (2019) (PubMed).

    Zhu, Li, Li, Jiang: "MicroRNA-30a functions as tumor suppressor and inhibits the proliferation and invasion of prostate cancer cells by down-regulation of SIX1." dans: Human cell, Vol. 30, Issue 4, pp. 290-299, (2018) (PubMed).

    Bai, Wang, Wang, Li, Zhao, Wu, Yang, Deng, Zhang: "The MiR-495/Annexin A3/P53 Axis Inhibits the Invasion and EMT of Colorectal Cancer Cells." dans: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, Vol. 44, Issue 5, pp. 1882-1895, (2018) (PubMed).

    Yan, Zhu, Zhang, Li, Li, Wang, Leng: "HMGB1-RAGE signaling pathway in pPROM." dans: Taiwanese journal of obstetrics & gynecology, Vol. 57, Issue 2, pp. 211-216, (2018) (PubMed).

    Ji, Zhang, Zhao: "Liver X receptor α (LXRα) promoted invasion and EMT of gastric cancer cells by regulation of NF-κB activity." dans: Human cell, Vol. 30, Issue 2, pp. 124-132, (2017) (PubMed).

    Ying, Jiang, He, Yu, Chen, Chen, Ru, Chen, Chen, Zhu, Li, Zhang, Guo, Yin, Zhang, Lou: "Serum HMGB1 as a Potential Biomarker for Patients with Asbestos-Related Diseases." dans: Disease markers, Vol. 2017, pp. 5756102, (2017) (PubMed).

    Deiner, Luo, Lin, Sessler, Saager, Sieber, Lee, Sano, Jankowski, Bergese, Candiotti, Flaherty, Arora, Shander, Rock et al.: "Intraoperative Infusion of Dexmedetomidine for Prevention of Postoperative Delirium and Cognitive Dysfunction in Elderly Patients Undergoing Major Elective Noncardiac Surgery: A Randomized Clinical ..." dans: JAMA surgery, Vol. 152, Issue 8, pp. e171505, (2017) (PubMed).

    Corrado, Saieva, Raimondo, Santoro, De Leo, Alessandro: "Chronic myelogenous leukaemia exosomes modulate bone marrow microenvironment through activation of epidermal growth factor receptor." dans: Journal of cellular and molecular medicine, Vol. 20, Issue 10, pp. 1829-39, (2016) (PubMed).

    Serra, Gallelli, Butrico, Buffone, Caliò, De Caridi, Massara, Barbetta, Amato, Labonia, Mimmi, Iaccino, de Franciscis: "From varices to venous ulceration: the story of chronic venous disease described by metalloproteinases." dans: International wound journal, (2016) (PubMed).

    Jiang, Wang, Tang, Yao, Zhou: "Regulation of Viral Infection-induced Airway Remodeling Cytokine Production by the TLR3-EGFR Signaling Pathway in Human Bronchial Epithelial Cells." dans: COPD, pp. 1-6, (2016) (PubMed).

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    Strazic-Geljic, Guberovic, Didak, Schmid-Antomarchi, Schmid-Alliana, Boukhechba, Bouler, Scimeca, Verron: "Gallium, a promising candidate to disrupt the vicious cycle driving osteolytic metastases." dans: Biochemical pharmacology, Vol. 116, pp. 11-21, (2016) (PubMed).

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  • Antigène Voir toutes MMP 9 (MMP9) Kits ELISA
    MMP 9 (MMP9) (Matrix Metallopeptidase 9 (Gelatinase B, 92kDa Gelatinase, 92kDa Type IV Collagenase) (MMP9))
    Autre désignation
    MMP9 (MMP9 Produits)
    Synonymes
    CLG4B Kit ELISA, GELB Kit ELISA, MANDP2 Kit ELISA, MMP-9 Kit ELISA, AW743869 Kit ELISA, B/MMP9 Kit ELISA, Clg4b Kit ELISA, pro-MMP-9 Kit ELISA, mmp-9 Kit ELISA, fgMMP-9 Kit ELISA, mmp9 Kit ELISA, ZFMMP-9 Kit ELISA, wu:fb02g06 Kit ELISA, wu:fb07b05 Kit ELISA, wu:fi98c09 Kit ELISA, wu:fj05a08 Kit ELISA, zgc:64165 Kit ELISA, clg4b Kit ELISA, gelb Kit ELISA, mandp2 Kit ELISA, matrix metallopeptidase 9 Kit ELISA, collagenase Kit ELISA, matrix metalloproteinase 9 Kit ELISA, matrix metallopeptidase 9 S homeolog Kit ELISA, MMP9 Kit ELISA, RB3913 Kit ELISA, BPSS0666 Kit ELISA, Sbal_3732 Kit ELISA, Bcer98_0486 Kit ELISA, Shew185_0630 Kit ELISA, Shal_3056 Kit ELISA, Sbal195_0657 Kit ELISA, Lbys_3550 Kit ELISA, Palpr_2084 Kit ELISA, Mmp9 Kit ELISA, mmp9 Kit ELISA, mmp9.S Kit ELISA
    UniProt
    P14780
    Pathways
    Cellular Response to Molecule of Bacterial Origin, Positive Regulation of Immune Effector Process, CXCR4-mediated Signaling Events
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