MMP-7 polyclonal, anti-human, mouse, rat
€388.00
In stock
SKU
BS6059
Background:
The matrix metalloproteinases (MMP) are a family of peptidase enzymes responsible for the degradation of extracellular matrix components, including collagen, gelatin, fibronectin, laminin and proteoglycan. Transcription of MMP genes is differentially activated by phorbol ester, lipopolysaccharide (LPS) or staphylococcal enterotoxin B (SEB). MMP catalysis requires both calcium and zinc. MMP-7 (also designated Pump-1, matrilysin or uterine metalloproteinase) degrades casein, fibronectin and gelatin types I, III, IV and V. MMP-7 mRNA is produced exclusively by epithelial cells in mouse and expression is restricted to specific organs, suggesting that in addition to matrix degradation and remodeling, MMP-7 may be involved in the differentiated function of these organs.
Alternative Name:
Matrilysin, Matrilysin uterine, Matrin, Matrix Metalloproteinase 7, Matrix metalloproteinase-7, MMP 7, MMP-7, MMP7, MMP7, MPSL1, PUMP 1, Pump 1 protease, Pump-1 protease, PUMP1, Uterine Matrilysin, Uterine metalloproteinase,
Application Dilution: WB: 1:500~1:2000, IHC: 1:50~1:200
Specificity: MMP7 polyclonal antibody detects endogenous levels of MMP7 protein.
Immunogen:
Recombinant full length Human MMP-7.
MW: ~ 30 kDa
Swis Prot.: P09237
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
The matrix metalloproteinases (MMP) are a family of peptidase enzymes responsible for the degradation of extracellular matrix components, including collagen, gelatin, fibronectin, laminin and proteoglycan. Transcription of MMP genes is differentially activated by phorbol ester, lipopolysaccharide (LPS) or staphylococcal enterotoxin B (SEB). MMP catalysis requires both calcium and zinc. MMP-7 (also designated Pump-1, matrilysin or uterine metalloproteinase) degrades casein, fibronectin and gelatin types I, III, IV and V. MMP-7 mRNA is produced exclusively by epithelial cells in mouse and expression is restricted to specific organs, suggesting that in addition to matrix degradation and remodeling, MMP-7 may be involved in the differentiated function of these organs.
Alternative Name:
Matrilysin, Matrilysin uterine, Matrin, Matrix Metalloproteinase 7, Matrix metalloproteinase-7, MMP 7, MMP-7, MMP7, MMP7, MPSL1, PUMP 1, Pump 1 protease, Pump-1 protease, PUMP1, Uterine Matrilysin, Uterine metalloproteinase,
Application Dilution: WB: 1:500~1:2000, IHC: 1:50~1:200
Specificity: MMP7 polyclonal antibody detects endogenous levels of MMP7 protein.
Immunogen:
Recombinant full length Human MMP-7.
MW: ~ 30 kDa
Swis Prot.: P09237
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
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