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Read our guarantee »Products:Cardiovascular >> Angiogenesis >> Adhesion / ECM >> Matrix Metalloproteinases >> MMP
Anti-MMP12 antibody [EP1261Y] - Carboxyterminal end
See all MMP12 products (12) ...
Rabbit monoclonal [EP1261Y] to MMP12 - Carboxyterminal end
WB, IP, Flow Cyt, IHC-P, ICC/IFmore details
Reacts with
Mouse, Rat, Human
Synthetic peptide corresponding to residues on the C-terminus of human MMP12.
Human breast carcinoma tissue or HeLa cells.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.01% Sodium Azide
Constituents: 40% Glycerol, 0.05% BSA, Tissue culture supernatant, 0.15M Sodium chloride, 50mM Tris glycine, pH 7.4
Tissue culture supernatant
Monoclonal
EP1261Y
IgG
Cardiovascular >> Atherosclerosis >> Thrombosis >> Other
Cancer >> Tumor biomarkers >> Enzymes >> MMPs
Cancer >> Invasion/microenvironment >> Angiogenesis >> ECM enzymes >> MMPs
Signal Transduction >> Cytoskeleton / ECM >> Extracellular Matrix >> ECM Enzymes >> MMP
Cardiovascular >> Angiogenesis >> Adhesion / ECM >> Matrix Metalloproteinases >> MMP
Our Abpromise guarantee covers the use of ab52897 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: 1/2000Detects a band of approximately 54 kDa (predicted molecular weight: 54 kDa).
IP: 1/30
Flow Cyt: 1/100
IHC-P: 1/100 - 1/250.(We strongly recommend that customers perform an antigen retrieval step.)
ICC/IF: 1/100 - 1/250.
May be involved in tissue injury and remodeling. Has significant elastolytic activity. Can accept large and small amino acids at the P1' site, but has a preference for leucine. Aromatic or hydrophobic residues are preferred at the P1 site, with small hydrophobic residues (preferably alanine) occupying P3.
Found in alveolar macrophages but not in peripheral blood monocytes.
Belongs to the peptidase M10A family.
Contains 4 hemopexin-like domains.
The conserved cysteine present in the cysteine-switch motif binds the catalytic zinc ion, thus inhibiting the enzyme. The dissociation of the cysteine from the zinc ion upon the activation-peptide release activates the enzyme.
Secreted > extracellular space > extracellular matrix.
Target information above from: UniProt accessionP39900
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - MMP12 antibody [EP1261Y] - Carboxyterminal end (ab52897)
![Western blot - MMP12 antibody [EP1261Y] - Carboxyterminal end (ab52897)](/ps/datasheet/images/52/ab52897/MMP12-Primary-antibodies-ab52897-1.jpg)
Predicted band size : 54 kDa
Based on Western blot, ab52897 recognizes both pro and active MMP. The propeptide is 54 kDa, and 45 kDa and 22 kDa are active forms. The primary was used at 1:100 to detect recombinant MMP12 protein, but can be diluted more to decrease the intensity of the bands.
Immunohistochemistry (Paraffin-embedded sections) - MMP12 antibody [EP1261Y] (ab52897)
![Immunohistochemistry (Paraffin-embedded sections) - MMP12 antibody [EP1261Y] (ab52897)](/ps/datasheet/Images/52/ab52897/ab52897_2.jpg)
Ab52897 (1:100) staining human MMP12 in human breast carcinoma tissue by immunohistochemistry using paraffin embedded tissue.
Immunocytochemistry/ Immunofluorescence - MMP12 antibody [EP1261Y] (ab52897)
![Immunocytochemistry/ Immunofluorescence - MMP12 antibody [EP1261Y] (ab52897)](/ps/datasheet/Images/52/ab52897/ab52897_3.jpg)
Immunofluorescent staining of HeLa cells using ab52897 (1:100).
Flow Cytometry - MMP12 antibody [EP1261Y] - Carboxyterminal end (ab52897)
![Flow Cytometry - MMP12 antibody [EP1261Y] - Carboxyterminal end (ab52897)](/ps/datasheet/images/52/ab52897/MMP12-Primary-antibodies-ab52897-2.jpg)
Overlay histogram showing A549 cells stained with ab52897 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab52897, 1/100 dilution) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (ab96899) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was rabbit IgG (monoclonal) (1µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in A549 cells fixed with 4% paraformaldehyde (10 min)/permeabilized in 0.1% PBS-Tween used under the same conditions.
This product has been referenced in:
See all 6 publications for this product
Publishing research using ab52897? Please let us know so that we can cite the reference in this datasheet
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![Western blot - MMP12 antibody [EP1261Y] - Carboxyterminal end (ab52897)](/ps/datasheet/images/52/ab52897/MMP12-Primary-antibodies-ab52897-1.jpg)
Predicted band size : 54 kDa
Based on Western blot, ab52897 recognizes both pro and active MMP. The propeptide is 54 kDa, and 45 kDa and 22 kDa are active forms. The primary was used at 1:100 to detect recombinant MMP12 protein, but can be diluted more to decrease the intensity of the bands.
![Immunohistochemistry (Paraffin-embedded sections) - MMP12 antibody [EP1261Y] (ab52897)](/ps/datasheet/Images/52/ab52897/ab52897_2.jpg)
Ab52897 (1:100) staining human MMP12 in human breast carcinoma tissue by immunohistochemistry using paraffin embedded tissue.
![Immunocytochemistry/ Immunofluorescence - MMP12 antibody [EP1261Y] (ab52897)](/ps/datasheet/Images/52/ab52897/ab52897_3.jpg)
Immunofluorescent staining of HeLa cells using ab52897 (1:100).
![Flow Cytometry - MMP12 antibody [EP1261Y] - Carboxyterminal end (ab52897)](/ps/datasheet/images/52/ab52897/MMP12-Primary-antibodies-ab52897-2.jpg)
Overlay histogram showing A549 cells stained with ab52897 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab52897, 1/100 dilution) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (
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