MMP2 Antibody (Center) Blocking peptide
€363.00
In stock
SKU
AC-BP13693c
Background:
Proteins of the matrix metalloproteinase (MMP) family areinvolved in the breakdown of extracellular matrix in normalphysiological processes, such as embryonic development,reproduction, and tissue remodeling, as well as in diseaseprocesses, such as arthritis and metastasis. Most MMP's aresecreted as inactive proproteins which are activated when cleavedby extracellular proteinases. This gene encodes an enzyme whichdegrades type IV collagen, the major structural component ofbasement membranes. The enzyme plays a role in endometrialmenstrual breakdown, regulation of vascularization and theinflammatory response. Mutations in this gene have been associatedwith Winchester syndrome and Nodulosis-Arthropathy-Osteolysis (NAO)syndrome. Two transcript variants encoding different isoforms havebeen found for this gene.
Other Names:
72 kDa type IV collagenase, 72 kDa gelatinase, Gelatinase A, Matrix metalloproteinase-2, MMP-2, TBE-1, PEX, MMP2, CLG4A
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP13693c was selected from the Center region of MMP2. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: MMP2
Gene ID: 4313
Primary Accession: P08253
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
Proteins of the matrix metalloproteinase (MMP) family areinvolved in the breakdown of extracellular matrix in normalphysiological processes, such as embryonic development,reproduction, and tissue remodeling, as well as in diseaseprocesses, such as arthritis and metastasis. Most MMP's aresecreted as inactive proproteins which are activated when cleavedby extracellular proteinases. This gene encodes an enzyme whichdegrades type IV collagen, the major structural component ofbasement membranes. The enzyme plays a role in endometrialmenstrual breakdown, regulation of vascularization and theinflammatory response. Mutations in this gene have been associatedwith Winchester syndrome and Nodulosis-Arthropathy-Osteolysis (NAO)syndrome. Two transcript variants encoding different isoforms havebeen found for this gene.
Other Names:
72 kDa type IV collagenase, 72 kDa gelatinase, Gelatinase A, Matrix metalloproteinase-2, MMP-2, TBE-1, PEX, MMP2, CLG4A
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP13693c was selected from the Center region of MMP2. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: MMP2
Gene ID: 4313
Primary Accession: P08253
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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