MMP12 Kit ELISA
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- MMP12 (Matrix Metallopeptidase 12 (Macrophage Elastase) (MMP12))
- Épitope
- AA 18-462
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Reactivité
- Souris
- Méthode de détection
- Colorimetric
- Type de méthode
- Sandwich ELISA
- Gamme de detection
- 62.5-4000 pg/mL
- Seuil minimal de détection
- 62.5 pg/mL
- Application
- ELISA
- Fonction
- Sandwich High Sensitivity ELISA kit for Quantitative Detection of Mouse MMP-12
- Marque
- PicoKine™
- Type d'échantillon
- Cell Culture Supernatant, Serum, Plasma (heparin)
- Analytical Method
- Quantitative
- Specificité
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Expression system for standard: NSO
Immunogen sequence: A18-C462 - Réactivité croisée (Details)
- There is no detectable cross-reactivity with other relevant proteins.
- Sensibilité
- <10pg/mL
- Matériel non inclus
- 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
- Immunogène
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Expression system for standard: NSO
Immunogen sequence: A18-C462 - Featured
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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.
- Commentaires
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Sequence similarities: Belongs to the peptidase M10A family.
- Plaque
- Pre-coated
- Protocole
- mouse MMP-12 ELISA Kit was based on standard sandwich enzyme-linked immune-sorbent assay technology. A monoclonal antibody from rat specific for MMP-12 has been precoated onto 96-well plates. Standards(NSO, A18-C462) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for MMP-12 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 mouse MMP-12 amount of sample captured in plate.
- Procédure de l'essai
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Aliquot 0.1 mL per well of the 4000pg/mL, 2000pg/mL,1000pg/mL, 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/mL mouse MMP-12 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 mouse cell culture supernates, serum or plasma(heparin) to each empty well. See "Sample Dilution Guideline" above for details. It is recommended that each mouse MMP-12 standard solution and each sample be measured in duplicate.
- Précision du teste
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- Sample 1: n=16, Mean(pg/ml): 337, Standard deviation: 18.2, CV(%): 5.4
- Sample 2: n=16, Mean(pg/ml): 1472, Standard deviation: 92.74, CV(%): 6.3
- Sample 3: n=16, Mean(pg/ml): 2522, Standard deviation: 121.1, CV(%): 4.8,
- Sample 1: n=24, Mean(pg/ml): 426, Standard deviation: 27.69, CV(%): 6.5
- Sample 2: n=24, Mean(pg/ml): 1538, Standard deviation: 109.2, CV(%): 7.1
- Sample 3: n=24, Mean(pg/ml): 2768, Standard deviation: 157.8, CV(%): 5.7
- Restrictions
- For Research Use only
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- Conseil sur la manipulation
- Avoid multiple freeze-thaw cycles.
- Stock
- -20 °C,4 °C
- Stockage commentaire
- Store at 4°C for 6 months, at -20°C for 12 months. Avoid multiple freeze-thaw cycles
- Date de péremption
- 12 months
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Acute exacerbations of COPD are associated with significant activation of matrix metalloproteinase 9 irrespectively of airway obstruction, emphysema and infection." dans: Respiratory research, Vol. 16, pp. 78, (2016) (PubMed).
: "Pulmonary C Fibers Modulate MMP-12 Production via PAR2 and Are Involved in the Long-Term Airway Inflammation and Airway Hyperresponsiveness Induced by Respiratory Syncytial Virus Infection." dans: Journal of virology, Vol. 90, Issue 5, pp. 2536-43, (2016) (PubMed).
: "Myeloid-specific Fos-related antigen-1 regulates cigarette smoke-induced lung inflammation, not emphysema, in mice." dans: American journal of respiratory cell and molecular biology, Vol. 53, Issue 1, pp. 125-34, (2015) (PubMed).
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Acute exacerbations of COPD are associated with significant activation of matrix metalloproteinase 9 irrespectively of airway obstruction, emphysema and infection." dans: Respiratory research, Vol. 16, pp. 78, (2016) (PubMed).
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- Antigène Voir toutes MMP12 Kits ELISA
- MMP12 (Matrix Metallopeptidase 12 (Macrophage Elastase) (MMP12))
- Autre désignation
- MMP12 (MMP12 Produits)
- Synonymes
- MMP12 Kit ELISA, AV378681 Kit ELISA, Mmel Kit ELISA, Mme Kit ELISA, HME Kit ELISA, ME Kit ELISA, MME Kit ELISA, MMP-12 Kit ELISA, matrix metallopeptidase 12 Kit ELISA, MMP12 Kit ELISA, Mmp12 Kit ELISA
- Sujet
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Protein Function: May be involved in tissue injury and remodeling. Has significant elastolytic activity. Can accept large and small amino acids at the P1' site, but has a preference for leucine. Aromatic or hydrophobic residues are preferred at the P1 site, with small hydrophobic residues (preferably alanine) occupying P3 (By similarity). .
Background: Matrix metalloproteinase-12(MMP12), also known as MME or ME, is an enzyme that in humans is encoded by the MMP12 gene. The gene is part of a cluster of MMP genes which localize to chromosome 11q22.2. It is thought that the protein encoded by this gene is cleaved at both ends to yield the active enzyme, but this processing has not been fully described. The enzyme degrades soluble and insoluble elastin. It may play a role in aneurysm formation and studies in mice suggest a role in the development of emphysema. This gene may involved in tissue injury and remodeling.
Synonyms: Macrophage metalloelastase,MME,3.4.24.65,Matrix metalloproteinase-12,MMP-12,Mmp12,Mme, Mmel,
Full Gene Name: Macrophage metalloelastase
Cellular Localisation: Secreted, extracellular space, extracellular matrix. - ID gène
- 17381
- UniProt
- P34960
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