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MMP3 ELISA Kit

MMP3 Reactivity: Human AA 18-477 Colorimetric Sandwich ELISA 156-10000 pg/mL Cell Culture Supernatant, Plasma (heparin), Serum
Catalog No. ABIN411330
  • Target See all MMP3 ELISA Kits
    MMP3 (Matrix Metallopeptidase 3 (Stromelysin 1, Progelatinase) (MMP3))
    Binding Specificity
    AA 18-477
    Reactivity
    • 15
    • 9
    • 7
    • 5
    • 5
    • 5
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Detection Method
    Colorimetric
    Method Type
    Sandwich ELISA
    Detection Range
    156-10000 pg/mL
    Minimum Detection Limit
    156 pg/mL
    Application
    ELISA
    Purpose
    Sandwich High Sensitivity ELISA kit for Quantitative Detection of Human MMP-3
    Brand
    PicoKine™
    Sample Type
    Cell Culture Supernatant, Serum, Plasma (heparin)
    Analytical Method
    Quantitative
    Specificity
    Expression system for standard: NSO
    Immunogen sequence: Y18-C477
    Cross-Reactivity (Details)
    There is cross-reactivity with MMP-10 approximately 2 % , and no detectable cross-reactivity with other MMPs.
    Sensitivity
    <10pg/mL
    Material not included
    Microplate reader in standard size. Automated plate washer. Adjustable pipettes and pipette tips. Multichannel pipettes are recommended in the condition of large amount of samples in the detection. Clean tubes and Eppendorf tubes. Washing buffer (neutral PBS or TBS). Preparation of 0.01M TBS: Add 1.2g Tris, 8.5g Nacl
    Immunogen
    Expression system for standard: NSO
    Immunogen sequence: Y18-C477
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  • Application Notes
    Before using Kit, spin tubes and bring down all components to bottom of tube. Duplicate well assay was recommended for both standard and sample testing.
    Comment

    Sequence similarities: Belongs to the peptidase M10A family.

    Plate
    Pre-coated
    Protocol
    human MMP-3 ELISA Kit was based on standard sandwich enzyme-linked immune-sorbent assay technology. A monoclonal antibody from mouse specific for MMP-3 has been precoated onto 96-well plates. Standards(NSO, Y18-C477) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for MMP-3 is added subsequently and then followed by washing with PBS or TBS buffer. Avidin-Biotin-Peroxidase Complex was added and unbound conjugates were washed away with PBS or TBS buffer. HRP substrate TMB was used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the human MMP-3 amount of sample captured in plate.
    Assay Procedure

    Aliquot 0.1 mL per well of the 10000pg/mL, 5000pg/mL, 2500pg/mL, 1250pg/mL, 625pg/mL, 312pg/mL, 156pg/mL human MMP-3 standard solutions into the precoated 96-well plate. Add 0.1 mL of the sample diluent buffer into the control well (Zero well). Add 0.1 mL of each properly diluted sample of human cell culture supernates, serum or plasma( heparin) to each empty well. See "Sample Dilution Guideline" above for details. It is recommended that each human MMP-3 standard solution and each sample be measured in duplicate.

    Assay Precision
    • Sample 1: n=16, Mean(pg/ml): 983, Standard deviation: 45.2, CV(%): 4.6
    • Sample 2: n=16, Mean(pg/ml): 3544, Standard deviation: 194.92, CV(%): 5.5
    • Sample 3: n=16, Mean(pg/ml): 5954, Standard deviation: 351.3, CV(%): 5.9,
    • Sample 1: n=24, Mean(pg/ml): 1247, Standard deviation: 72.3, CV(%): 5.8
    • Sample 2: n=24, Mean(pg/ml): 3721, Standard deviation: 230.7, CV(%): 6.2
    • Sample 3: n=24, Mean(pg/ml): 6125, Standard deviation: 453.25, CV(%): 7.4
    Restrictions
    For Research Use only
  • Handling Advice
    Avoid multiple freeze-thaw cycles.
    Storage
    -20 °C,4 °C
    Storage Comment
    Store at 4°C for 6 months, at -20°C for 12 months. Avoid multiple freeze-thaw cycles
    Expiry Date
    12 months
  • Lin, Qiu, Xie, Liu, Sun: "Nimbolide suppresses non-small cell lung cancer cell invasion and migration via manipulation of DUSP4 expression and ERK1/2 signaling." in: Biomedicine & pharmacotherapy, Vol. 92, pp. 340-346, (2017) (PubMed).

    Nosratzehi, Alijani, Moodi: "Salivary MMP-1, MMP-2, MMP-3 and MMP-13 Levels in Patients with Oral Lichen Planus and Squamous Cell Carcinoma" in: Asian Pacific journal of cancer prevention : APJCP, Vol. 18, Issue 7, pp. 1947-1951, (2017) (PubMed).

    Ozcamdalli, Misir, Kizkapan, Uzun, Duygulu, Yazici, Kafadar: "Comparison of Intra-articular Injection of Hyaluronic Acid and N-Acetyl Cysteine in the Treatment of Knee Osteoarthritis: A Pilot Study." in: Cartilage, Vol. 8, Issue 4, pp. 384-390, (2017) (PubMed).

    Qiu, Li, Zhang, Liu, Tian, Fang: "P2X7 mediates ATP-driven invasiveness in prostate cancer cells." in: PLoS ONE, Vol. 9, Issue 12, pp. e114371, (2015) (PubMed).

    Capsoni, Ongari, Lonati, Accetta, Gatti, Catania: "?-Melanocyte-stimulating-hormone (?-MSH) modulates human chondrocyte activation induced by proinflammatory cytokines." in: BMC musculoskeletal disorders, Vol. 16, pp. 154, (2015) (PubMed).

    Zhu, Liu, Li, Zhang: "Eotaxin-1 promotes prostate cancer cell invasion via activation of the CCR3-ERK pathway and upregulation of MMP-3 expression." in: Oncology reports, Vol. 31, Issue 5, pp. 2049-54, (2014) (PubMed).

    Ågren, Schnabel, Christensen, Mirastschijski: "Tumor necrosis factor-?-accelerated degradation of type I collagen in human skin is associated with elevated matrix metalloproteinase (MMP)-1 and MMP-3 ex vivo." in: European journal of cell biology, Vol. 94, Issue 1, pp. 12-21, (2014) (PubMed).

    Bellei, Pitisci, Ottaviani, Ludovici, Cota, Luzi, DellAnna, Picardo: "Vitiligo: a possible model of degenerative diseases." in: PLoS ONE, Vol. 8, Issue 3, pp. e59782, (2014) (PubMed).

    Zhao, Fan, Zhang, Sun, Li, Xiong, Zhang, Fan: "Chitosan-plasmid DNA nanoparticles encoding small hairpin RNA targeting MMP-3 and -13 to inhibit the expression of dedifferentiation related genes in expanded chondrocytes." in: Journal of biomedical materials research. Part A, Vol. 102, Issue 2, pp. 373-80, (2013) (PubMed).

    An, Wu, Lin: "Detection and comparison of matrix metalloproteinase in primary and recurrent pterygium fibroblasts." in: International journal of ophthalmology, Vol. 4, Issue 4, pp. 353-6, (2012) (PubMed).

  • Target See all MMP3 ELISA Kits
    MMP3 (Matrix Metallopeptidase 3 (Stromelysin 1, Progelatinase) (MMP3))
    Alternative Name
    MMP3 (MMP3 Products)
    Synonyms
    CHDS6 ELISA Kit, MMP-3 ELISA Kit, SL-1 ELISA Kit, STMY ELISA Kit, STMY1 ELISA Kit, STR1 ELISA Kit, SLN-1 ELISA Kit, SLN1 ELISA Kit, STR-1 ELISA Kit, Stmy1 ELISA Kit, Str1 ELISA Kit, MMP10 ELISA Kit, chds6 ELISA Kit, mmp-3 ELISA Kit, mmp13 ELISA Kit, mmp3 ELISA Kit, sl-1 ELISA Kit, stmy ELISA Kit, stmy1 ELISA Kit, str1 ELISA Kit, matrix metallopeptidase 3 ELISA Kit, matrix metallopeptidase 3 (stromelysin 1, progelatinase) ELISA Kit, matrix metallopeptidase 3 L homeolog ELISA Kit, MMP3 ELISA Kit, Mmp3 ELISA Kit, mmp3.L ELISA Kit
    Background

    Protein Function: Can degrade fibronectin, laminin, gelatins of type I, III, IV, and V, collagens III, IV, X, and IX, and cartilage proteoglycans. Activates procollagenase.

    Background: Matrix metalloproteinase-3(MMP-3) also called stromelysin or transin, is a proteoglycanase closely related to collagenase(MMP1) with a wide range of substrate specificities. The complete primary structure for human MMP-3, which has 477 residues including a 17-residue signal peptide. MMP-3 and collagenase are 54 % identical in sequence, suggesting a common origin for the evolution of the two proteinases. MMP-3 and collagenase expression are coordinately modulated in synovial fibroblast cultures. MMP-3 is a secreted metalloprotease produced predominantly by connective tissue cells. Together with other metalloproteases, it can synergistically degrade the major components of the extracellular matrix. It is capable of degrading proteoglycan, fibronectin, laminin, and type IV collagen, but not interstitial type I collagen. MMP-3 genotype may be an important determinant of vascular remodeling and age-related arterial stiffening, with the heterozygote having the optimal balance between matrix accumulation and deposition. The standard product used in this kit is recombinant human MMP-3, consisting of 460 amino acids with the molecular mass of 52KDa. The detected MMP-3 includes zymogen and active enzyme.

    Synonyms: Stromelysin-1,SL-1,3.4.24.17,Matrix metalloproteinase-3,MMP-3,Transin-1,MMP3,STMY1,

    Full Gene Name: Stromelysin-1

    Cellular Localisation: Secreted, extracellular space, extracellular matrix.
    Gene ID
    4314
    UniProt
    P08254
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