Anti-MMP8 antibody
4
(7 Reviews)
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(19 Publications)
Rabbit Polyclonal MMP8 antibody. Suitable for WB, IHC-P, ICC/IF and reacts with Mouse, Human samples. Cited in 19 publications. Immunogen corresponding to Synthetic Peptide within Human MMP8.
View Alternative Names
CLG1, MMP8, Neutrophil collagenase, Matrix metalloproteinase-8, PMNL collagenase, MMP-8, PMNL-CL
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-MMP8 antibody (AB53017)
ICC/IF image of ab63017 stained HeLa cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab53017, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MMP8 antibody (AB53017)
Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue using MMP8 antibody at 1/50 dilution. Left hand image; untreated tissue, Right hand image; tissue treated with the immunising peptide.
- WB
Unknown
Western blot - Anti-MMP8 antibody (AB53017)
All lanes:
Western blot - Anti-MMP8 antibody (ab53017) at 1/500 dilution
Lane 1:
Extracts from NIH/3T3 cells with no immunizing peptide
Lane 2:
Extracts from NIH/3T3 cells with immunizing peptide
Predicted band size: 53 kDa
Observed band size: 53 kDa
false
Reactivity data
Properties and storage information
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Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
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Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
MMP-8 participates in the degradation of collagen types I II and III contributing to extracellular matrix remodeling. It acts independently rather than being part of a larger enzyme complex. Its activity is tightly regulated by tissue inhibitors of metalloproteinases (TIMPs) to prevent excessive tissue damage. By modulating the extracellular matrix MMP-8 influences processes like wound healing cell migration and angiogenesis indicating its essential role in maintaining tissue homeostasis.
Pathways
MMP-8 plays a role in the inflammatory response and wound healing pathways. It interacts with and processes other proteins like pro-inflammatory cytokines and growth factors which are important for regulating these pathways. MMP-8 collaborates with matrix metalloproteinase-9 (MMP-9) in the inflammatory pathway to facilitate leukocyte migration and rapid tissue remodeling during acute inflammatory responses. Its regulation involves complex interactions among proteolytic enzymes emphasizing its function in balancing matrix degradation and formation.
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Publications (19)
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Current research in toxicology 7:100184 PubMed39285937
2024
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Frontiers in immunology 15:1366319 PubMed38799464
2024
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EBioMedicine 95:104739 PubMed37544202
2023
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Journal of the American Heart Association 12:e028215 PubMed36565196
2022
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Cells 11: PubMed36291087
2022
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Hernia : the journal of hernias and abdominal wall surgery 26:1695-1705 PubMed36048398
2022
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Frontiers in physiology 13:953977 PubMed36105291
2022
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Journal of inflammation research 15:4693-4708 PubMed35996686
2022
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Frontiers in cell and developmental biology 10:883266 PubMed35531096
2022
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Journal of periodontology 93:1540-1552 PubMed35184279
2022
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Product promise
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