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CASP5 encodes a member of the cysteine-aspartic acid protease (caspase) family. Zusätzlich bieten wir Ihnen CASP5 Proteine (12) und CASP5 Kits (11) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 93 products:
Human Polyclonal CASP5 Primary Antibody für ELISA, ICC - ABIN4287993
Bian, Pelegrino, Pflugfelder, Volpe, Li, de Paiva: Desiccating Stress-Induced MMP Production and Activity Worsens Wound Healing in Alkali-Burned Corneas. in Investigative ophthalmology & visual science 2015
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Cow (Bovine) Polyclonal CASP5 Primary Antibody für WB - ABIN222884
Bian, Elner, Khanna, Murga-Zamalloa, Patil, Elner: Expression and functional roles of caspase-5 in inflammatory responses of human retinal pigment epithelial cells. in Investigative ophthalmology & visual science 2011
Human Polyclonal CASP5 Primary Antibody für WB - ABIN2477916
Munday, Vaillancourt, Ali, Casano, Miller, Molineaux, Yamin, Yu, Nicholson: Molecular cloning and pro-apoptotic activity of ICErelII and ICErelIII, members of the ICE/CED-3 family of cysteine proteases. in The Journal of biological chemistry 1995
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Study shows that CASP5 was positively correlated with inflammation in rheumatoid arthritis (RA), and provides evidence that certain CASP5 SNPs were associated with an increased risk of RA.
Th17 micro-milieu via IL-17A (zeige IL17A Antikörper) regulates NLRP1 (zeige NLRP1 Antikörper)-dependent CASP5 activity in psoriatic skin autoinflammation.
CASP5 gene overexpression significantly promoted angiogenesis ability of HMEC-1 cells, which was probably achieved by inhibiting angpt-1/Tie2 and promoting VEGF-1 signal pathway.
Caspase-4 (zeige CASP4 Antikörper) and caspase-5 mediate IL-1alpha and IL-1beta (zeige IL1B Antikörper) release from human monocytes after lipopolysaccharides stimulation.
The distribution of the other genotypes; rs507879, rs518604 and rs523104 of caspase-5) was not significantly different between patients with psoriasis vulgaris and the healthy controls.
both caspase-4 (zeige CASP4 Antikörper) and caspase-5 are functionally important for appropriate responses to intracellular Gram-negative bacteria.
Data show that exposure of hepatocytes to direct hypoxia resulted in acid sphingomyelinase (zeige SMPD1 Antikörper) activation and ceramide elevation associated with activation of caspase 5 and the subsequent cleavage of HuR (zeige ELAVL1 Antikörper) and apoptotic cell death.
Data suggest a positive association of caspase-3 (zeige CASP3 Antikörper) and diplotype analysis of caspase-5 to be associated with prostate cancer risk.
Mutual activation between caspase-5 and -1 suggests caspase-5 may work predominantly in concert with caspase-1 (zeige CASP1 Antikörper) in modulating retinal pigment epithelium inflammatory responses.
Association of death receptor 4, Caspase 3 (zeige CASP3 Antikörper) and 5 gene (zeige GPD1 Antikörper) polymorphism with increased risk to bladder cancer in North Indians.
This gene encodes a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes which undergo proteolytic processing at conserved aspartic residues to produce two subunits, large and small, that dimerize to form the active enzyme. Overexpression of the active form of this enzyme induces apoptosis in fibroblasts. Max, a central component of the Myc\\/Max\\/Mad transcription regulation network important for cell growth, differentiation, and apoptosis, is cleaved by this protein\\\\; this process requires Fas-mediated dephosphorylation of Max. The expression of this gene is regulated by interferon-gamma and lipopolysaccharide. Alternatively spliced transcript variants have been identified for this gene.
, TY protease
, caspase 5, apoptosis-related cysteine protease
, protease ICH-3
, protease TY
, caspase 5
, caspase 5, apoptosis-related cysteine peptidase