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MMP3 Antibody / Matrix Metalloproteinase 3

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-3, MMP-10 and MMP-11 (also designated stromelysin-1, 2 and 3, respectively) activate procollagenase. MMP-3 activation of procollagenase can occur via two pathways. Direct activation by MMP-3 is slow and activation by MMP-3 in conjunction with tissue or plasma proteinases is rapid. MMP-10 is expressed in small intestine, and at lower levels in lung and heart. MMP-11 is specifically expressed in stromal cells of breast carcinomas and contributes to epithelial cell malignancies.

Product Specifications

CAS Number

9007-83-4

Specifications

ELISA (order BSA-free format for coating), Immunohistochemistry (FFPE) : 1-2 µg/mL

UniProt

P08254

Host

Mouse

Reactivity

Human

Immunogen

A recombinant full length human protein was used as the immunogen for this MMP3 antibody.

Clonality

Monoclonal

Isotype

IgG2c κ

Clone

MMP3/2806

Applications

ELISA, IHC-P

Purity

Protein G affinity chromatography

Format

Purified

Buffer

1 mg/ml in 1X PBS; BSA free, sodium azide free

Reconstitution

Store the MMP3 antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).

Limitations

This MMP3 antibody is available for research use only.

Storage Conditions

Store the MMP3 antibody at 2-8°C (with azide) or aliquot and store at -20°C or colder (without azide) .

Formulation

1 mg/mL in 1X PBS; BSA free, sodium azide free

Applications Notes

Optimal dilution of the MMP3 antibody should be determined by the researcher.

Location

Cytoplasmic, secreted

Image Legend

IHC staining of FFPE human placenta with MMP3 antibody. HIER: boil tissue sections in pH 9 10mM Tris with 1mM EDTA for 20 min and allow to cool before testing. Negative control inset: PBS used instead of primary antibody to control for secondary Ab binding.
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