Rabbit Recombinant Monoclonal MMP1 antibody. Carrier free. Suitable for ICC/IF, IP, WB and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: PBS
ICC/IF | Flow Cyt (Intra) | IP | Flow Cyt | WB | IHC-P | |
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Human | Tested | Not recommended | Tested | Not recommended | Tested | Not recommended |
Mouse | Not recommended | Not recommended | Not recommended | Not recommended | Not recommended | Not recommended |
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Species Human | Dilution info - | Notes - |
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Species Human, Mouse | Dilution info - | Notes - |
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Species Mouse | Dilution info - | Notes - |
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Species Human, Mouse | Dilution info - | Notes - |
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Species Human | Dilution info - | Notes - |
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Cleaves collagens of types I, II, and III at one site in the helical domain. Also cleaves collagens of types VII and X (PubMed:1645757, PubMed:2153297, PubMed:2557822). In case of HIV infection, interacts and cleaves the secreted viral Tat protein, leading to a decrease in neuronal Tat's mediated neurotoxicity (PubMed:16807369).
CLG, MMP1, Interstitial collagenase, Fibroblast collagenase, Matrix metalloproteinase-1, MMP-1
Rabbit Recombinant Monoclonal MMP1 antibody. Carrier free. Suitable for ICC/IF, IP, WB and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: PBS
ab240086 is the carrier-free version of Anti-MMP1 antibody [EP1249Y] ab134184.
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species. Please contact us for more information.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
MMP1 also known as collagenase-1 is an enzyme belonging to the matrix metalloproteinase (MMP) family. It is responsible for the degradation of type I II and III collagens making it an important player in collagen turnover. MMP1 has a molecular weight of approximately 54 kDa. This enzyme is expressed in various tissues including skin lung and reproductive organs primarily during tissue remodeling and repair. Scientists often use MMP1 ELISA kits and MMP1 inhibitors to study its expression and activity levels.
MMP1 plays a significant role in the modulation of the extracellular matrix. It facilitates cellular processes by breaking down structural proteins and allowing for cell migration proliferation and differentiation. Although it acts independently MMP1 works in harmony with other MMP family members to maintain extracellular matrix homeostasis and is often linked to tissue remodeling complexes. This makes the MMP1 a valuable target for researchers interested in tissue repair and fibrosis.
Studies show MMP1 involvement in critical processes such as the inflammatory response and wound healing. In the inflammatory pathway MMP1 expression is regulated by cytokines that respond to tissue injury. Within the wound healing pathway this enzyme interacts with proteins like transforming growth factor-beta (TGF-beta) to coordinate the repair process by remodeling extracellular matrix components. This illustrates the interconnected nature of MMP1 with significant regulatory proteins.
MMP1 has significant associations with osteoarthritis and cancer metastasis. MMP1 contributes to the breakdown of cartilage in osteoarthritis highlighting its role in disease progression and joint degradation. In the context of cancer elevated MMP1 expression correlates with the metastatic potential where it assists tumor invasion by degrading the surrounding matrix. MMP1's involvement with other MMPs including MMP2 and MMP9 highlights its importance in these pathological conditions making it a therapeutic target in related research.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
This data was developed using Anti-MMP1 antibody [EP1249Y] ab134184, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST
All lanes: Western blot - Anti-MMP1 antibody [EP1249Y] (Anti-MMP1 antibody [EP1249Y] ab134184) at 1/500 dilution
Lane 1: MDA-MB-231 (human breast adenocarcinoma epithelial) whole cell lysate at 10 µg
Lane 2: Lysate from HeLa cells untreated with TPA at 10 µg
Lane 3: HeLa treated with 100 ng/mL TPA for 10 hours cell lysate at 10 µg
Lane 4: Human colon cancer tissue lysate at 10 µg
Lane 5: Human breast cancer tissue lysate at 10 µg
All lanes: Goat Anti-Rabbit IgG H&L (HRP) at 1/1000 dilution
Predicted band size: 54 kDa
Observed band size: 54 kDa
Exposure time: 30s
This data was developed using Anti-MMP1 antibody [EP1249Y] ab134184, the same antibody clone in a different buffer formulation.
All lanes: Western blot - Anti-MMP1 antibody [EP1249Y] (Anti-MMP1 antibody [EP1249Y] ab134184) at 1/1000 dilution
All lanes: A431 cell lysate at 10 µg
All lanes: HRP labelled goat anti-rabbit at 1/2000 dilution
Predicted band size: 54 kDa
This data was developed using Anti-MMP1 antibody [EP1249Y] ab134184, the same antibody clone in a different buffer formulation.MMP1 was immunoprecipitated from 0.35 mg MDA-MB-231 (Human breast adenocarcinoma epithelial cell) whole cell lysate 10 µg with Anti-MMP1 antibody [EP1249Y] ab134184 at 1/50 dilution (2µg). VeriBlot for IP Detection Reagent (HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: MDA-MB-231 (Human breast adenocarcinoma epithelial cell) whole cell lysate 10 µg
Lane 2: abab134184 IP in MDA-MB-231 whole cell lysate
Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-MMP1 antibody [EP1249Y] ab134184 in MDA-MB-231 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
All lanes: Immunoprecipitation - Anti-MMP1 antibody [EP1249Y] (Anti-MMP1 antibody [EP1249Y] ab134184)
Predicted band size: 54 kDa
Observed band size: 54 kDa
This data was developed using Anti-MMP1 antibody [EP1249Y] ab134184, the same antibody clone in a different buffer formulation.
Immunocytochemistry/ Immunofluorescence analyis of HUVEC (human umbilical vein endothelial cell) labeling MMP1 with at Anti-MMP1 antibody [EP1249Y] ab134184 at 1/100 followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 at 1/1000 dilution as the secondary antibody. Alexa Fluor® 594 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker ab195889 at 1/200 was used as counterstain. Cells were fixed with 4% Paraformaldehyde and permeabilised with 0.1% TritonX-100. Nuclear counterstain was DAPI (blue).
Confocal image showing cytoplasmic staining in HUVEC cell line (shown in green). The counterstain was observed in magenta. Nuclear DNA was labeled with DAPI (shown in blue).
Low expression: A549.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
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