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Recombinant Human MMP-2 Protein, CF

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Product Details

Summary
Reactivity HuSpecies Glossary
Applications Enzyme Activity
Format
Carrier-Free

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Recombinant Human MMP-2 Protein, CF Summary

Details of Functionality
Measured by its ability to cleave the fluorogenic peptide substrate, Mca-PLGL-Dpa-AR-NH2 (Catalog # ES001). The specific activity is >1,000 pmol/min/µg, as measured under the described conditions.
Source
Chinese Hamster Ovary cell line, CHO-derived human MMP-2 protein
Ile34-Cys660
Accession #
N-terminal Sequence
Ile34
Structure / Form
Pro form
Protein/Peptide Type
Recombinant Enzymes
Gene
MMP2
Purity
>90%, by SDS-PAGE under reducing conditions and visualized by silver stain
Endotoxin Note
<1.0 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Enzyme Activity
Theoretical MW
71 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
71 kDa, reducing conditions
Publications
Read Publications using
902-MP in the following applications:

Packaging, Storage & Formulations

Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 6 months from date of receipt, -20 to -70 °C as supplied.
  • 3 months, -20 to -70 °C under sterile conditions after opening.
Buffer
Supplied as a 0.2 μm filtered solution in Tris, CaCl2, NaCl and Brij-35.
Purity
>90%, by SDS-PAGE under reducing conditions and visualized by silver stain
Assay Procedure
  • Assay Buffer: 50 mM Tris, 10 mM CaCl2, 150 mM NaCl, 0.05% (w/v) Brij 35, pH 7.5 (TCNB)
  • Recombinant Human MMP-2 (rhMMP-2) (Catalog # 902-MP)
  • p-aminophenylmercuric acetate (APMA), (Sigma, Catalog # A-9563), 100 mM stock in DMSO
  • Fluorogenic Peptide Substrate I: MCA-Pro-Leu-Gly-Leu-DPA-Ala-Arg-NH2 (Catalog # ES001)
  • F16 Black Maxisorp Plate (Nunc, Catalog # 475515)
  • Fluorescent Plate Reader (Model: SpectraMax Gemini EM by Molecular Devices) or equivalent
  1. Dilute rhMMP-2 to 100 µg/mL in Assay Buffer.
  2. Activate rhMMP-2 by adding APMA to a final concentration of 1 mM.
  3. Incubate at 37 °C for 1 hour.
  4. Dilute activated rhMMP-2 to 0.2 ng/µL in Assay Buffer.
  5. Dilute Substrate to 20 µM in Assay Buffer.
  6. Load into a black well plate 50 µL of the 0.2 ng/µL rhMMP-2 and start the reaction by adding 50 µL of 20 µM Substrate. Include a Substrate Blank containing 50 µL Assay Buffer and 50 µL of 20 µM Substrate.
  7. Read at excitation and emission wavelengths of 320 nm and 405 nm, respectively, in kinetic mode for 5 minutes.
  8. Calculate specific activity:

     Specific Activity (pmol/min/µg) =

Adjusted Vmax* (RFU/min) x Conversion Factor** (pmol/RFU)
amount of enzyme (µg)

     *Adjusted for Substrate Blank

     **Derived using calibration standard MCA-Pro-Leu-OH (Bachem, Catalog # M-1975).

Per Well:
  • rhMMP-2: 0.010 µg
  • Substrate: 10 µM

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Human MMP-2 Protein, CF

  • 72 kDa gelatinase
  • CLG4
  • CLG4A72 kDa type IV collagenase
  • collagenase type IV-A
  • EC 3.4.24
  • EC 3.4.24.24
  • Gelatinase A
  • matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IVcollagenase)
  • matrix metalloproteinase 2 (gelatinase A, 72kD gelatinase, 72kD type IVcollagenase)
  • Matrix metalloproteinase-2
  • matrix metalloproteinase-II
  • MMP2
  • MMP-2
  • MMP-II
  • MONA
  • neutrophil gelatinase
  • TBE-1matrix metalloproteinase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IVcollagenase)

Background

Matrix metalloproteinases are a family of zinc and calcium dependent endopeptidases with the combined ability to degrade all the components of the extracellular matrix. MMP-2 (gelatinase A), a type IV collagenase, can degrade a broad range of substrates including type IV, V, VII and X collagens as well as elastin and fibronectin. It is believed to act synergistically with interstitial collagenase (MMP-1) in the degradation of fibrillar collagens as it degrades their denatured gelatin forms. MMP-2 has been shown to be associated with many connective tissue cells as well as neutrophils, macrophages and monocytes. Structurally, MMP-2 may be divided into several distinct domains: a pro-domain which is cleaved upon activation; a catalytic domain containing the zinc binding site; a fibronectin-like domain thought to play a role in substrate targeting; and a carboxyl terminal (hemopexin-like) domain containing 2 N-linked glycosylation sites.

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Publications for MMP-2 (902-MP)(29)

We have publications tested in 4 confirmed species: Human, Rat, Bovine, Equine.

We have publications tested in 7 applications: Bioassay, Control, ELISA (Standard), Enzyme Assay, Gelatin Zymography Control, Western Blot, Zymography.


Filter By Application
Bioassay
(14)
Control
(1)
ELISA (Standard)
(1)
Enzyme Assay
(8)
Gelatin Zymography Control
(1)
Western Blot
(1)
Zymography
(3)
All Applications
Filter By Species
Human
(18)
Rat
(1)
Bovine
(1)
Equine
(1)
All Species
Showing Publications 1 - 10 of 29. Show All 29 Publications.
Publications using 902-MP Applications Species
AA Welter, WJ Wu, R Maurer, TG O'Quinn, MD Chao, DL Boyle, ER Geisbrecht, SD Hartson, BC Bowker, H Zhuang An Investigation of the Altered Textural Property in Woody Breast Myopathy Using an Integrative Omics Approach Frontiers in Physiology, 2022-03-17;13(0):860868. 2022-03-17 [PMID: 35370787] (Bioassay, Human) Bioassay Human
S Spiller, T Wippold, K Bellmann-S, S Franz, A Saalbach, U Anderegg, AG Beck-Sicki Protease-Triggered Release of Stabilized CXCL12 from Coated Scaffolds in an Ex Vivo Wound Model Pharmaceutics, 2021-10-01;13(10):. 2021-10-01 [PMID: 34683890] (Enzyme Assay, Human) Enzyme Assay Human
B Howng, MB Winter, C LePage, I Popova, M Krimm, O Vasiljeva Novel Ex Vivo Zymography Approach for Assessment of Protease Activity in Tissues with Activatable Antibodies Pharmaceutics, 2021-09-02;13(9):. 2021-09-02 [PMID: 34575469] (Bioassay, Human) Bioassay Human
F Uliana, M Vizovišek, L Acquasalie, R Ciuffa, A Fossati, F Frommelt, S Goetze, B Wollscheid, M Gstaiger, V De Filippi, U Auf dem Ke, R Aebersold Mapping specificity, cleavage entropy, allosteric changes and substrates of blood proteases in a high-throughput screen Nature Communications, 2021-03-16;12(1):1693. 2021-03-16 [PMID: 33727531] (Bioassay, Human) Bioassay Human
M Kareskoski, J Vakkamäki, K Laukkanen, M Palviainen, A Johannisso, T Katila Matrix metalloproteinase (MMP)-2, MMP-9, semen quality and sperm longevity in fractionated stallion semen Theriogenology, 2021-02-02;164(0):93-99. 2021-02-02 [PMID: 33571920] (Gelatin Zymography Control, Equine) Gelatin Zymography Control Equine
K Falkowski, E Bielecka, IB Thøgersen, O Boche?ska, K P?aza, M Kali?ska, L S?siadek, M Magoch, A P?cak, M Wi?niewska, N Gruba, M Wysocka, A Wojtysiak, M Brzezi?ska, K Sychowska, A Pejkovska, M Rehders, G Butler, CM Overall, K Brix, G Dubin, A Lesner, A Kozik, JJ Enghild, J Potempa, T Kantyka Kallikrein-Related Peptidase 14 Activates Zymogens of Membrane Type Matrix Metalloproteinases (MT-MMPs)-A CleavEx Based Analysis Int J Mol Sci, 2020-06-19;21(12):. 2020-06-19 [PMID: 32575583] (Bioassay, Human) Bioassay Human
L Devel, G Almer, C Cabella, F Beau, M Bernes, P Oliva, F Navarro, R Prassl, H Mangge, I Texier Biodistribution of Nanostructured Lipid Carriers in Mice Atherosclerotic Model Molecules, 2019-09-26;24(19):. 2019-09-26 [PMID: 31561608] (Bioassay, Human) Bioassay Human
D Huo, J Zhu, G Chen, Q Chen, C Zhang, X Luo, W Jiang, X Jiang, Z Gu, Y Hu Eradication of unresectable liver metastasis through induction of tumour specific energy depletion Nat Commun, 2019-07-11;10(1):3051. 2019-07-11 [PMID: 31296864] (Bioassay, Human) Bioassay Human
G Ruiz-Gómez, S Vogel, S Möller, MT Pisabarro, U Hempel Glycosaminoglycans influence enzyme activity of MMP2 and MMP2/TIMP3 complex formation - Insights at cellular and molecular level Sci Rep, 2019-03-20;9(1):4905. 2019-03-20 [PMID: 30894640] (Enzyme Assay, Human) Enzyme Assay Human
G Pintus, R Giordo, Y Wang, W Zhu, SH Kim, L Zhang, L Ni, J Zhang, R Telljohann, KR McGraw, RE Monticone, C Ferris, L Liu, M Wang, EG Lakatta Reduced vasorin enhances angiotensin II signaling within the aging arterial wall Oncotarget, 2018-06-05;9(43):27117-27132. 2018-06-05 [PMID: 29930755] (Enzyme Assay, Rat) Enzyme Assay Rat
Show All 29 Publications.

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Bioinformatics

Gene Symbol MMP2
Uniprot