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The protein encoded by NEU1 is a lysosomal enzyme that cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids. Zusätzlich bieten wir Ihnen NEU1 Antikörper (56) und viele weitere Produktgruppen zu diesem Protein an.
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Neu1 (zeige NEURL Proteine) inhibits lipolysis induced by beta-adrenergic stimulation in adipocytes via interactions with Plin1 (zeige PLIN1 Proteine) on lipid drops.
Neu1 (zeige NEURL Proteine) is the only lysosomal multienzyme complex gene underexpressed in mucopolysaccharidosis type I mice.
Neu1 (zeige NEURL Proteine) desialylation is a mechanism of Fc-independent platelet clearance in immune thrombocytopenia.
Data indicate a role for neuraminidase 1 (Neu1) in regulating Siglec E protein-toll-like receptor 4 (TLR4 (zeige TLR4 Proteine)) interaction and endotoxemia.
elastin (zeige ELN Proteine)-derived peptides as an enhancer of atherogenesis and defines the Neuraminidase 1/PI3Kgamma (zeige PIK3CG Proteine) signalling pathway as a key mediator
significant increases in Col1a1 (zeige COL1A1 Proteine), serine/threonine-protein kinase 1, Ctnnb1 (zeige CTNNB1 Proteine), CSRNP1 (zeige CSRNP1 Proteine), Ddit4 (zeige DDIT4 Proteine), Cyp2e1 (zeige CYP2E1 Proteine), and Krit1 (zeige KRIT1 Proteine) expressions and great decreases inreceptor D2, Neu1 (zeige NEURL Proteine), and Dhcr7 (zeige DHCR7 Proteine) expressions following long-term exposure to TiO2 NPs (zeige NPS Proteine)
NEU1 (zeige NEURL Proteine) deficiency has a role in determining amyloid precursor protein (zeige APP Proteine) levels and amyloid-beta secretion via deregulated lysosomal exocytosis
Neu1 (zeige NEURL Proteine) sialidase and matrix metalloproteinase-9 (zeige MMP9 Proteine) cross-talk regulates nucleic acid-induced endosomal TOLL-like receptor-7 (zeige TLR7 Proteine) and -9 activation, cellular signaling and pro-inflammatory responses.
The activity of NEU1 (zeige NEURL Proteine) was preferentially higher in epididymal fat and lower in the livers of two strains of obese and diabetic mice.
these studies identify Neu1 (zeige NEURL Proteine) as a novel component of the signaling pathways of energy metabolism and glucose uptake.
EGFR (zeige EGFR Proteine) protein, human is predictive of adjuvant chemo response. Also, It is a prognostic factor.
Data suggest that mutations c.90delC (p.Tyr30Ter) and c.572A>T (p.Asp191Val) of the NFU1 (zeige NFU1 Proteine) gene probably underlie the pathogenesis of multiple mitochondrial dysfunction syndrome (MMDS).
Elevated NEU1 expression alters functional activities of distinct lung cell types in vitro and recapitulates lymphocytic infiltration and collagen accumulation in vivo, consistent with mechanisms implicated in lung fibrosis.
initial treatment with an EGFR (zeige EGFR Proteine)-TKI is a reasonable option for patients presenting with EGFR (zeige EGFR Proteine) mutation-positive NSCLC and a CM.
miR (zeige MLXIP Proteine)-125b functions as an oncogene (zeige RAB1A Proteine) in gastric cancer and represents a new potential therapeutic target for gastric cancer.
NEU1 siRNA can effectively inhibit proliferation, apoptosis, and invasion of human ovarian cancer cells by targeting lysosome and oxidative phosphorylation signaling, which can serve as a new target ovarian cancer treatment
How the point mutations of the neuraminidase (zeige NEU Proteine) sequences affected the susceptibility of H9N2 virus to oseltamivir is still to be determined and deserve further investigations
Basal Neu-1 catalytic activity is strongly increased in aged cells.
Neu1 desialylation is a mechanism of Fc-independent platelet clearance in immune thrombocytopenia.
Flagellin (zeige FliC Proteine) drives NEU1 to desialylate MUC1 (zeige MUC1 Proteine), thereby increasing its adhesiveness for Pseudomonas aeruginosa and its shedding
NEU1 gene is not responsible for the lysosomal storage disease of Japanese Black cattle.
The protein encoded by this gene is a lysosomal enzyme that cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids. In the lysosome, this enzyme is part of a heterotrimeric complex together with beta-galactosidase and cathepsin A (the latter is also referred to as 'protective protein'). Mutations in this gene can lead to sialidosis, a lysosomal storage disease that can be type 1 (cherry red spot-myoclonus syndrome or normosomatic type), which is late-onset, or type 2 (the dysmorphic type), which occurs at an earlier age with increased severity.
, N-acetyl-alpha-neuraminidase 1
, acetylneuraminyl hydrolase
, lysosomal sialidase
, sialidase 1 (lysosomal sialidase)
, Isotocin-neurophysin IT 1
, neuraminidase 1
, HLA-B-associated transcript 7
, sialidase 1