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Read our guarantee »Products:Cardiovascular >> Angiogenesis >> Adhesion / ECM >> Matrix Metalloproteinases >> MMP
Anti-MMP7 antibody - Middle of active MMP-7
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Rabbit polyclonal to MMP7 - Middle of active MMP-7
Ab38997 recognizes a site midway between the aminoterminal end and the zinc site (active site) of MMP7. It does not cross react with the other MMP family members.
Reacts with
Human, Pig
Synthetic peptide corresponding to a site midway between the aminoterminal end and the zinc site of human MMP7.
(Peptide available as ab41057.)
WB: Human MMP7 and cell media from pig kidney, epithelial morphology (treated with IL1 alpha).
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze / thaw cycles.
Preservative: 0.05% Sodium Azide
Constituents: 50% Glycerol, PBS
Concentration information loading...
Immunogen affinity purified
Polyclonal
IgG
Cancer >> Tumor biomarkers >> Enzymes >> MMPs
Cell Biology >> Proteolysis / Ubiquitin >> Proteolytic enzymes >> Metalloprotease >> MMPs
Cancer >> Invasion/microenvironment >> ECM >> Extracellular matrix >> 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 ab38997 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: Use at an assay dependent dilution. Predicted molecular weight: 29 kDa.(A recommended starting concentration for Western blots is 1/1000 when using colorimetric substrates such as BCIP/NBT and 1/5000 for chemiluminescent substrates. Note: MMP7 does not appear to be produced by most normal quiescent cells, but treatment of many cell types with the phorbol ester TPA stimulates its production. Due to the low protein levels produced (pg/mL) concentration of cell culture media is often required to visualize the bands.)
Degrades casein, gelatins of types I, III, IV, and V, and fibronectin. Activates procollagenase.
Belongs to the peptidase M10A family.
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 accessionP09237
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - MMP7 antibody (ab38997)
All lanes : Anti-MMP7 antibody - Middle of active MMP-7 (ab38997) at 1/1000 dilution
Lane 1 : Human MMP-7
Lane 2 : Cell media from Pig kidney (treated with IL1 alpha)
Predicted band size : 29 kDa
Observed band size : 28 kDa (why is the actual band size different from the predicted?)
Additional bands at : 45 kDa (possible dimer).
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)-MMP7 antibody - Middle of active MMP-7(ab38997)

Ab38997 staining human normal placenta tissue. Staining is localised to extracellular space.
Left panel: with primary antibody at 1 ug/ml. Right panel: isotype control.
Sections were stained using an automated system DAKO Autostainer Plus , at room temperature. Sections were rehydrated and antigen retrieved with the Dako 3-in-1 AR buffer EDTA pH 9.0 in a DAKO PT Link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 minutes. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 minutes and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that for manual staining we recommend to optimize the primary antibody concentration and incubation time (overnight incubation), and amplification may be required.
ab38997 has not yet been referenced specifically in any publications.
Publishing research using ab38997? Please let us know so that we can cite the reference in this datasheet
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All lanes : Anti-MMP7 antibody - Middle of active MMP-7 (ab38997) at 1/1000 dilution
Lane 1 : Human MMP-7
Lane 2 : Cell media from Pig kidney (treated with IL1 alpha)
Predicted band size : 29 kDa
Observed band size : 28 kDa (why is the actual band size different from the predicted?)
Additional bands at : 45 kDa (possible dimer).

Ab38997 staining human normal placenta tissue. Staining is localised to extracellular space.
Left panel: with primary antibody at 1 ug/ml. Right panel: isotype control.
Sections were stained using an automated system DAKO Autostainer Plus , at room temperature. Sections were rehydrated and antigen retrieved with the Dako 3-in-1 AR buffer EDTA pH 9.0 in a DAKO PT Link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 minutes. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 minutes and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that for manual staining we recommend to optimize the primary antibody concentration and incubation time (overnight incubation), and amplification may be required.
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