MMP3 Kit ELISA
Aperçu rapide pour MMP3 Kit ELISA (ABIN921069)
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Reactivité
Méthode de détection
Type de méthode
Gamme de detection
Application
Type d'échantillon
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Seuil minimal de détection
- 156 pg/mL
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Fonction
- Sandwich Mouse MMP-3 ELISA Kit to quantitate Mouse Mmp3 in cell culture supernatants, serum and plasma (heparin).
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Analytical Method
- Quantitative
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Specificité
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Expression system for standard: NS0
Immunogen sequence: Y18-C477Capture antibody and Detection antibody: monoclonal antibody from rat, polyclonal antibody from goat
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Réactivité croisée (Details)
- There is cross-reactivity with MMP-10 approximately 2 % and no detectable cross-reactivity with other MMPs.
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Sensibilité
- < 10 pg/mL
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Ingrédients
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- Pre-coated 96-well strip microplate
- Standard
- Biotinylated antibody (100x)
- Avidin-Biotin-Peroxidase Complex (100x)
- Sample Diluent
- Antibody Diluent
- Avidin-Biotin-Peroxidase Diluent
- Color Developing Reagent (TMB)
- Stop Solution
- Wash Buffer (25x)
- Adhesive plate sealers
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Matériel non inclus
- Microplate Reader capable of reading absorbance at 450nm. Incubator. Automated plate washer (optional). Pipettes and pipette tips capable of precisely dispensing 0.5 μL through 1 mL volumes of aqueous solutions. Multichannel pipettes are recommended for large amount of samples. Deionized or distilled water. 500 mL graduated cylinders. Test tubes for dilution.
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Indications d'application
- 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.
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Volume d'échantillon
- 100 μL
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Plaque
- Pre-coated
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Protocole
- ELISA Kit is based on standard sandwich enzyme-linked immune-sorbent assay technology. An antibody has been precoated onto 96-well plates. Standards and test samples are added to the wells, a biotinylated detection antibody specific for target 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 target amount in sample captured in plate.
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Précision du teste
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Intra-Assay Precision (CV%): 6.1%, 4.8%, 5.2%
Inter-Assay Precision (CV%): 7%, 6.7%, 6% -
Restrictions
- For Research Use only
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Conseil sur la manipulation
- Avoid multiple freeze-thaw cycles.
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Stock
- -20 °C,4 °C
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Stockage commentaire
- Store at 4°C for 6 months, at -20°C for 12 months. Avoid multiple freeze-thaw cycles (Ships with gel ice, can store for up to 3 days in room temperature. Freeze upon receiving.)
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Date de péremption
- 12 months
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: "Olfactory Ensheathing Cells Inhibit Gliosis in Retinal Degeneration by Downregulation of the Müller Cell Notch Signaling Pathway." dans: Cell transplantation, Vol. 26, Issue 6, pp. 967-982, (2018) (PubMed).
: "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." dans: European journal of cell biology, Vol. 94, Issue 1, pp. 12-21, (2014) (PubMed).
: "Chitosan-plasmid DNA nanoparticles encoding small hairpin RNA targeting MMP-3 and -13 to inhibit the expression of dedifferentiation related genes in expanded chondrocytes." dans: Journal of biomedical materials research. Part A, Vol. 102, Issue 2, pp. 373-80, (2013) (PubMed).
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- MMP3 (Matrix Metallopeptidase 3 (Stromelysin 1, Progelatinase) (MMP3))
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Autre désignation
- MMP3
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Sujet
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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.
Gene Full Name: matrix metallopeptidase 3
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ID gène
- 17392
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UniProt
- P28862
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