MMP11 Antibody (C-term)
Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application ![]()
| WB, E |
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Primary Accession | P24347 |
Other Accession | NP_005931 |
Reactivity | Human, Mouse |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 54590 Da |
Antigen Region | 398-426 aa |
Gene ID | 4320 |
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Other Names | Stromelysin-3, SL-3, ST3, 3424-, Matrix metalloproteinase-11, MMP-11, MMP11, STMY3 |
Target/Specificity | This MMP11 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 398-426 amino acids from the C-terminal region of human MMP11. |
Dilution | WB~~1:1000 |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | MMP11 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | MMP11 |
---|---|
Synonyms | STMY3 |
Function | May play an important role in the progression of epithelial malignancies. |
Cellular Location | Secreted, extracellular space, extracellular matrix |
Tissue Location | Specifically expressed in stromal cells of breast carcinomas |

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Provided below are standard protocols that you may find useful for product applications.
Background
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 MMPs are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. MMP11 may play an important role in the progression of epithelial malignancies. It is specifically expressed in stromal cells of breast carcinomas.
References
Anglard, P., et al., J. Biol. Chem. 270(35):20337-20344 (1995).
Basset, P., et al., Nature 348(6303):699-704 (1990).

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