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MFAP4 encodes a protein with similarity to a bovine microfibril-associated protein. Zusätzlich bieten wir Ihnen Microfibrillar-Associated Protein 4 Kits (14) und Microfibrillar-Associated Protein 4 Proteine (13) und viele weitere Produktgruppen zu diesem Protein an.
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Human Polyclonal MFAP4 Primary Antibody für FACS, IHC (p) - ABIN651133
Edelman, Girirajan, Finucane, Patel, Lupski, Smith, Elsea: Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 cases. in Clinical genetics 2007
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plasma MFAP4 was significantly increased among patients with a previous diagnosis of liver disease or congestive heart failure compared to patients with other diagnoses.
Data suggest that MFAP4 specifically binds tropoelastin (zeige ELN Antikörper) and fibrillin-1 (zeige FBN1 Antikörper)/-2, as well as elastin (zeige ELN Antikörper) cross-linking amino acid desmosine; MFAP4 co-localizes with fibrillin-1 (zeige FBN1 Antikörper)-positive fibers; MFAP4 actively promotes tropoelastin (zeige ELN Antikörper) self-assembly.
MFAP4 regulates integrin alphaVbeta3 (zeige ITGAV Antikörper)-induced VSMC proliferation and migration, as well as monocyte chemotaxis, and accelerates neointimal hyperplasia after vascular injury.
Serum MFAP4 varies in groups of patients with different cardiovascular conditions.
The findings support the biomarker potential of systemic MFAP4, with elevated levels in the serum reflecting pathological processes involving ECM (zeige MMRN1 Antikörper) remodeling and degradation.
skin with enhanced MFAP-4 expression was protected from UVB-induced photodamage/photoaging accompanied by the prevention of ECM (zeige MMRN1 Antikörper) degradation and aggravated elasticity
Microfibrillar associated protein 4 binds pulmonary surfactant protein A (zeige GPR153 Antikörper) (SP-A) and colocalizes with SP-A in the extracellular matrix of the lung.
MFAP4 promoted the development of asthmatic airway disease in vivo and pro-asthmatic functions of bronchial smooth muscle cells in vitro
Mfap4 knockout mice develop a spontaneous loss of lung function.
This gene encodes a protein with similarity to a bovine microfibril-associated protein. The protein has binding specificities for both collagen and carbohydrate. It is thought to be an extracellular matrix protein which is involved in cell adhesion or intercellular interactions. The gene is located within the Smith-Magenis syndrome region. Two transcript variants encoding different isoforms have been found for this gene.
microfibril-associated glycoprotein 4
, microfibrillar-associated protein 4
, Microfibril-associated glycoprotein 4
, 36 kDa MAP
, 36 kDa microfibril-associated glycoprotein
, angiopoietin-like 7