MMP13 Antibody (YA6284)
(Synonyms: MMP13; Collagenase 3; Matrix metalloproteinase-13; MMP-13)Based on 1 Customer Validation
MMP13 Antibody (YA6284) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to MMP13.
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Host:
Rabbit
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Isotype:
IgG
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Application:
WB, IHC-P, ICC/IF, ELISA
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Reactivity :
Human
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Formulation:
Supplied in PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
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Conjugation:
Non-conjugated
Applications
| Application |
IHC-P
IHC-P: Immunohistochemistry-Paraffin
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WB
WB: Western Blot
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ICC/IF
ICC/IF: Immunocytochemistry/
Immunofluorescence |
ELISA
ELISA: Enzyme Linked Immunosorbent Assay
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|---|---|---|---|---|
| Dilution Ratio | 1:100-500 | 1:500-2000 | 1:200-1000 | 1:5000-20000 |
Product Details
MMP13 Antibody (YA6284) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to MMP13.
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Host Rabbit
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Clonality Monoclonal
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Species ReactivityHuman
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Observed Molecular WeightObserved band size: 60 kDaNote: Due to possible protein modifications or aggregation, the molecular weight should be confirmed by actual measurement, and the predicted value is for reference only.
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Calculated Molecular Weight Predicted band size: 54 kDa
Protein A
Non-conjugated
Unmodified
IgG
Product Properties
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Appearance
Solution
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Formulation
Supplied in PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
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Concentration
Batch-dependent, Please check the COA for the concentration of each lot. Check Lot Concentration
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Storage & Stability
Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.
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Shipping
Shipping with blue ice.
Background
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Function
MMP-13 (matrix metalloproteinase-13), also known as collagenase-3, is a zinc-dependent extracellular matrix protease that plays a central role in collagen turnover and tissue remodeling, with particularly high activity toward type II collagen, the major structural collagen of articular cartilage[1][2]. Mechanistically, MMP-13 participates in extracellular matrix degradation by cleaving fibrillar collagens and other matrix components, thereby regulating cartilage homeostasis, skeletal development, endochondral ossification, and matrix remodeling processes[1][3]. In disease settings, dysregulated MMP-13 expression is strongly associated with osteoarthritis (OA), where enhanced type II collagen degradation contributes directly to cartilage destruction and progressive joint pathology[1][2][4]. Experimental studies have demonstrated that cartilage-specific overexpression of active MMP-13 induces osteoarthritis-like changes characterized by collagen cleavage, proteoglycan loss, and articular cartilage degeneration, supporting a causal role in disease progression[2]. MMP-13 expression is regulated by inflammatory and signaling pathways, including IL-1, TNF-α, Wnt/β-catenin, TGF-β-related signaling, and other transcriptional networks that influence chondrocyte catabolism and matrix breakdown[3][5]. Compared with related collagenases such as MMP-1 and MMP-8, MMP-13 exhibits particularly efficient cleavage of type II collagen and is considered the predominant collagenase driving cartilage degradation in OA tissues[1][3][5]. Because of its substrate preference and disease-specific upregulation, MMP-13 has become an important therapeutic target, and selective MMP-13 inhibitors are widely used in experimental studies investigating cartilage protection and disease-modifying strategies for osteoarthritis[3][6].
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Subcellular Localization
Secreted, extracellular space, extracellular matrix; Secreted
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Expression
Tissue_specificity:It was detected in chondrocytes of fetal cartilage and skull, hypertrophic vertebral cartilage, osteoblasts and periosteal cells beneath the periosteum of ossifying ribs, and in other chondrocytes. It was also detected in chondrocytes of articular cartilage treated with TNF and IL-1β, but not in untreated chondrocytes. It was also detected in T lymphocytes and breast cancer tissue.
Induction:Up-regulated by TNF and IL1B -
Subunit
Monomer. Interacts with TIMP1, TIMP2 and TIMP3. Binds (via the C-terminal region) to collagen
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SwissProt ID
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Synonyms
MMP13; Collagenase 3; Matrix metalloproteinase-13; MMP-13
Documentation
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Data Sheet (262 KB)
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SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 KB)
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User Guide for Antibodies (1077 KB)
[1]. Dlugosz P, et al. Disabled 1 Is Part of a Signaling Pathway Activated by Epidermal Growth Factor Receptor. Int J Mol Sci. 2021 Feb 9;22(4):1745. [Content Brief]
[2]. Neuhold LA, et al. Postnatal expression in hyaline cartilage of constitutively active human collagenase-3 (MMP-13) induces osteoarthritis in mice. J Clin Invest. 2001 Jan;107(1):35-44. [Content Brief]
[3]. Huang Y, et al. The adjuvant treatment role of ω-3 fatty acids by regulating gut microbiota positively in the acne vulgaris. J Dermatolog Treat. 2024 Dec;35(1):2299107. [Content Brief]
[4]. Moore BA, et al. Induction of collagenase-3 (MMP-13) in rheumatoid arthritis synovial fibroblasts. Biochim Biophys Acta. 2000 Oct 18;1502(2):307-18. [Content Brief]
[5]. Vincenti MP, et al. Transcriptional regulation of collagenase (MMP-1, MMP-13) genes in arthritis: integration of complex signaling pathways for the recruitment of gene-specific transcription factors. Arthritis Res. 2002;4(3):157-64. [Content Brief]
[6]. Spicer TP, et al. Characterization of selective exosite-binding inhibitors of matrix metalloproteinase 13 that prevent articular cartilage degradation in vitro. J Med Chem. 2014 Nov 26;57(22):9598-611. [Content Brief]