PrimePCR™ Probe Assay: MMP2, Human

RT

Real-time PCR probe assay designed for gene expression analysis. Probe assays consist of unlabeled PCR primers and a dual labeled fluorescent probe.

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PrimePCR™ PreAmp for Probe Assay: MMP2, Human
Reaction:     400 reactions
Gene-specific PCR primers for the unbiased preamplification of small quantities of cDNA for subsequent use in downstream gene expression analysis.

PrimePCR™ Template for Probe Assay: MMP2, Human
Reaction:     200 x 20 µl reactions
Gene-specific synthetic DNA template designed to give a positive real-time PCR result when used with the corresponding probe assay.


Wet Lab Validated

Assay Information

Technology:   qPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   qHsaCEP0049822
Assay Design:   exonic
Chromosome Location:   16:55516872-55516983question
Amplicon Length:   82
Splice Variants Targeted:   ENST00000570308 ENST00000568715 ENST00000219070 ENST00000564864 ENST00000543485 ENST00000437642

Gene Information

Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes such as embryonic development reproduction and tissue remodeling as well as in disease processes such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. This gene encodes an enzyme which degrades type IV collagen the major structural component of basement membranes. The enzyme plays a role in endometrial menstrual breakdown regulation of vascularization and the inflammatory response. Mutations in this gene have been associated with Winchester syndrome and Nodulosis-Arthropathy-Osteolysis (NAO) syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq Jul 2008]

Gene Symbol:   MMP2
Gene Name:   matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase)
Aliases:   CLG4, CLG4A, MMP-II, MONA, TBE-1
RefSeq:   NC_000016.9 NT_010498.15 NG_008989.1
Ensembl:   ENSG00000087245
Entrez:   4313
Chromosome Mapping:   16q13-q21

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