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The protein encoded by HSPB8 belongs to the superfamily of small heat-shock proteins containing a conservative alpha-crystallin domain at the C-terminal part of the molecule. Zusätzlich bieten wir Ihnen Heat Shock 22kDa Protein 8 Proteine (23) und Heat Shock 22kDa Protein 8 Kits (15) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 169 products:
Human Polyclonal HSPB8 Primary Antibody für ELISA, WB - ABIN249692
Benndorf, Sun, Gilmont, Biederman, Molloy, Goodmurphy, Cheng, Andrews, Welsh: HSP22, a new member of the small heat shock protein superfamily, interacts with mimic of phosphorylated HSP27 ((3D)HSP27). in The Journal of biological chemistry 2001
Human Polyclonal HSPB8 Primary Antibody für ICC, IF - ABIN4320602
Stadler, Rexhepaj, Singan, Murphy, Pepperkok, Uhlén, Simpson, Lundberg: Immunofluorescence and fluorescent-protein tagging show high correlation for protein localization in mammalian cells. in Nature methods 2013
HSPB8 is involved in regulating the cell cycle and cell migration in MCF-7 cells.
suggest that HSPB8 may act as an intracellular factor against hepatitis C virus replication and that DNAJC5B has the same function, with more relevant results for genotype 3
It has been demonstrated that HSPB8-BAG3 (zeige BAG3 Antikörper)-HSP70 (zeige HSP70 Antikörper) ensures the functionality of stress granules and restores proteostasis by targeting defective ribosomal products for degradation.
We report that overexpression of HSPB8 in immortalized motor neurones decreased the accumulation of TDP-25 and TDP-35 and that protection against mislocalized/truncated TDP-43 (zeige TARDBP Antikörper) was observed for HSPB8 in Drosophila melanogaster Overexpression of HSP67Bc, the functional ortholog of human HSPB8, suppressed the eye degeneration caused by the cytoplasmic accumulation of a TDP-43 (zeige TARDBP Antikörper) variant
HSPB8 counteracts accumulation of aberrantly localized misfolded forms of TDP-43 (zeige TARDBP Antikörper) and its 25 KDa fragment involved in most sporadic cases of Amyotrophic Lateral Sclerosis and of Fronto Lateral Temporal Dementia.
expands the understanding of disease mechanisms, tissue involvement, and phenotypic outcome of HSPB8 mutations
our findings suggest the existence of a so-far unrecognized quality control mechanism involving BAG3 (zeige BAG3 Antikörper), HSPB8 and p62/SQSTM1 (zeige SQSTM1 Antikörper) for accurate remodelling of actin-based mitotic structures that guide spindle orientation.
This study demonstreated that expression of HSPB8 was restricted to GFAP (zeige GFAP Antikörper)+ astrocytes in patient with multiple sclerosis.
Pangenomic profiling of velcade-sensitive and resistant cells showed that the small heat shock protein HSPB8 was overexpressed in multiple myeloma resistant cells.
HSP22 acts as a positive regulator in TGF-alpha (zeige TGFA Antikörper)-induced migration of ovarian cancer cells, subsequently directing ovarian cancer toward progression.
GA genotype of SNP g.507G>A of HSPB8 gene has a probable role in heat tolerance in Sahiwal cattle.
HSP22 functions as a negative regulator in the TGF-beta (zeige TGFB1 Antikörper)-stimulated migration of osteoblasts.
Results revealed that the apoptosis-suppressing effect of heat shock protein B8 was mediated by the PI3K/Akt (zeige AKT1 Antikörper) pathway in an in vitro model of ischemia.
Increased Hsp20 (zeige HSPB6 Antikörper) expression protects against OGDR-induced Golgi fragmentation and apoptosis, likely through interaction with Bax (zeige BAX Antikörper) and subsequent amelioration of the OGDR-induced elevation in p115 (zeige ARHGAP4 Antikörper) cleavage via the Fas (zeige FAS Antikörper)/FasL (zeige FASL Antikörper) signaling pathway.
Translocation of both Hsp22 and iNOS to the mitochondria is necessary for Hsp22-mediated stimulation of oxidative phosphorylation
analysis of the phenotype of cardiomyopathy in cardiac-specific heat shock protein B8 K141N transgenic mouse
The results of this study strongly suggested that Hspb8 and its alpha-crystallin domain might act as pleiotropic prosurvival factor in the adult hippocampus.
Hspb8 mRNA is constitutively expressed in specific brain structures across ontogeny; eventually these structures could be affected by the malfunction or deregulation of the Hspb8 molecule.
Hsp22 represents a previously undescribed activator of both nuclear and mitochondrial functions of STAT3 (zeige STAT3 Antikörper), and its deletion in the context of pressure overload in vivo accelerates the transition into heart failure and increases mortality.
HspB8 increases misfolded SOD1 (zeige SOD1 Antikörper) clearance via autophagy.
Findings show that despite the ubiquitous presence of HSPB8, only motor neurons appear to be affected by the K141N and K141E mutations.
The protein encoded by this gene belongs to the superfamily of small heat-shock proteins containing a conservative alpha-crystallin domain at the C-terminal part of the molecule. The expression of this gene in induced by estrogen in estrogen receptor-positive breast cancer cells, and this protein also functions as a chaperone in association with Bag3, a stimulator of macroautophagy. Thus, this gene appears to be involved in regulation of cell proliferation, apoptosis, and carcinogenesis, and mutations in this gene have been associated with different neuromuscular diseases, including Charcot-Marie-Tooth disease.
heat shock 22kDa protein 8
, heat shock 27kDa protein 8
, heat shock protein beta-8
, E2-induced gene 1 protein
, alpha-crystallin C chain
, protein kinase H11
, small stress protein-like protein HSP22
, H11 kinase
, crystallin, alpha C
, heat shock protein 20-like protein
, heat shock protein 8