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Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix for both normal physiological processes, such as embryonic development, reproduction and tissue remodeling, and disease processes, such as asthma and metastasis. Zusätzlich bieten wir Ihnen MMP28 Kits (24) und MMP28 Proteine (5) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 80 products:
Human Polyclonal MMP28 Primary Antibody für ELISA, IHC - ABIN4335121
Singh, Kindelberger, Nagymanyoki, Ng, Quick, Elias, Yamamoto, Fichorova, Fulop, Berkowitz: Matrix metalloproteinases and their inhibitors and inducer in gestational trophoblastic diseases and normal placenta. in Gynecologic oncology 2011
Circulating MMP-28 was elevated in atrial fibrillation
Results suggest a crucial role of MMP9 (zeige MMP9 Antikörper) at the early stage of carcinogenesis in the large intestine. The increase in MMP9 (zeige MMP9 Antikörper) and TIMP1 (zeige TIMP1 Antikörper) mRNA concentration and the decrease in MMP28 in the large intestinal tissue may be a confirmation of cancer.
These results proved for the first time that epilysin expression was significantly elevated in glioblastoma
A decreased level of IL-33 (zeige IL33 Antikörper) and an elevated concentration of MMP-28 were found in coronary heart disease patients and correlated with disease severity.
MMP28 mRNA expression is highest in healthy tissues when compared to diseased periodontal tissues.
Data established a seven-gene (AR, ESR2 (zeige ESR2 Antikörper), GATA3 (zeige GATA3 Antikörper), GBX2 (zeige GBX2 Antikörper), KRT16 (zeige KRT16 Antikörper), MMP28 and WNT11 (zeige WNT11 Antikörper)) prognostic signature to define a subset of triple-negative breast cancer (TNBC).
Inhibition of BCMO1 (zeige BCMO1 Antikörper) expression is associated with increased invasiveness of colon cancer cells and increased expression of MMP7 (zeige MMP7 Antikörper) and MMP28. beta-Carotene can upregulate BCMO1 (zeige BCMO1 Antikörper) and reverse these effects.
Over-expression of MMP28 provides protection against apoptosis induced by either serum-deprivation or treatment with a protein kinase inhibitor.
Gene expression of MMP28 in the intervertebral disk is not regulated by inflammatory mechanisms, is donor-dependent and cannot be positively or negatively linked to the grade of degeneration and only weakly to the occurrence of trauma.
basal expression of MMP-2 (zeige MMP2 Antikörper), MMP-9 (zeige MMP9 Antikörper), MMP-28, and Filaggrin (zeige FLG Antikörper) was evaluated in oral keratinocytes to collect information about ability of cigarette smoke to modify basal expression pattern of these key enzymes in the absence of clinical signs in oral epithelium
results demonstrate that Ranbp2 controls nucleocytoplasmic, chemokine and metalloproteinase 28 signaling, and proteostasis of substrates that are crucial to motoneuronal homeostasis and whose impairments by loss of Ranbp2 drive ALS-like syndromes
MMP28 promotes macrophage polarization toward M2 cells and augments pulmonary fibrosis.
MMP-28 deletion aggravated MI-induced LV dysfunction and rupture as a result of defective inflammatory response and scar formation by suppressing M2 macrophage activation.
Epilysin is alternatively spliced and processed by a furin (zeige FURIN Antikörper)-like proprotein convertase.
These results suggest that MMP-28 plays an evolutionarily conserved role in neural development and is likely to modulate the axonal-glial extracellular microenvironment.
Epilysin serves as a negative regulator of early macrophage recruitment, a novel function that may have evolved as a mechanism to restrain unnecessary and untimely inflammation.
Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix for both normal physiological processes, such as embryonic development, reproduction and tissue remodeling, and disease processes, such as asthma and metastasis. This gene encodes a secreted enzyme that degrades casein. Its expression pattern suggests that it plays a role in tissue homeostasis and in wound repair. Transcript variants encoding different isoforms have been described.
matrix metalloproteinase-28 b
, matrix metallopeptidase 28 b
, matrix metallopeptidase 28
, matrix metalloproteinase 28
, matrix metalloproteinase-28
, matrix metallopeptidase 28 (epilysin)
, matrix metalloproteinase 28 (epilysin)