R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.
MMP-13 (E3Q4Y) Rabbit mAb #67329
Filter:
- WB
Supporting Data
| REACTIVITY | M |
| SENSITIVITY | Endogenous |
| MW (kDa) | 60 |
| Source/Isotype | Rabbit IgG |
Application Key:
- WB-Western Blotting
Species Cross-Reactivity Key:
- M-Mouse
Product Information
Product Usage Information
| Application | Dilution |
|---|---|
| Western Blotting | 1:1000 |
Storage
Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/mL BSA, 50% glycerol, and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.
Protocol
Specificity / Sensitivity
MMP-13 (E3Q4Y) Rabbit mAb recognizes endogenous levels of total MMP-13 protein. This antibody detects a band of unknown origin at 28 kDa by western blot.
Species Reactivity:
Mouse
Source / Purification
Monoclonal antibody is produced by immunizing animals with recombinant protein specific to the amino terminus of mouse MMP-13 protein.
Background
MMP-13 (collagenase 3) belongs to the matrix metalloproteinase (MMP) superfamily of enzymes that targets many extracellular proteins, including other proteases, growth factors, cell surface receptors, and adhesion molecules (1,2). MMP-13 is a member of a subgroup of collagenases (including MMP-1, MMP-8, and MMP-18) that play an even more important function targeting fibrillar collagen. MMP-13 is synthesized as a latent proenzyme, and proteolytic removal of the inhibitory propeptide domain is required for enzyme activation. MMP-13 protein levels are regulated at the transcriptional level via specific transcription factors and promoter DNA methylation (3,4). MMP-13 preferentially cleaves Type II collagen, and research studies have shown that aberrant upregulation of MMP-13 activity can lead to cartilage loss and osteoarthritis (5,6). In addition, MMP-13 has been shown to promote cancer development, in part through enhancing tumor angiogenesis and metastases (7-9), suggesting that collagenase activity may serve as a useful marker of tumor progression (10).
- McCawley, L.J. and Matrisian, L.M. (2001) Curr Opin Cell Biol 13, 534-40.
- Cathcart, J. et al. (2015) Genes Dis 2, 26-34.
- Chan, C.M. et al. (2017) J Biol Chem 292, 1625-36.
- Hashimoto, K. et al. (2013) J Biol Chem 288, 10061-72.
- Elayyan, J. et al. (2017) FASEB J 31, 3116-25.
- Wang, M. et al. (2011) Ann N Y Acad Sci 1240, 61-9.
- Mendonsa, A.M. et al. (2015) Mol Cancer 14, 49.
- Wang, C. et al. (2015) Oncotarget 6, 2903-16.
- Kudo, Y. et al. (2012) J Biol Chem 287, 38716-28.
- Brinckerhoff, C.E. et al. (2000) Clin Cancer Res 6, 4823-30.
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For Research Use Only. Not For Use In Diagnostic Procedures.
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