Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
Weitere Synonyme anzeigen
Wählen Sie die gewünschte Spezies
Human HSPB1 Protein expressed in Wheat germ - ABIN1307214
Iizuka, Okamoto, Matsushita, Kimura, Nagai, Arito, Kurokawa, Masuko, Suematsu, Hirohata, Kato: Identification of autoantigens specific for systemic lupus erythematosus with central nervous system involvement. in Lupus 2010
Show all 2 Pubmed References
Human HSPB1 Protein expressed in Escherichia coli (E. coli) - ABIN1686676
Van Montfort, Slingsby, Vierling: Structure and function of the small heat shock protein/alpha-crystallin family of molecular chaperones. in Advances in protein chemistry 2002
Show all 3 Pubmed References
Human HSPB1 Protein expressed in Escherichia coli (E. coli) - ABIN2002650
Bruey, Paul, Fromentin, Hilpert, Arrigo, Solary, Garrido: Differential regulation of HSP27 oligomerization in tumor cells grown in vitro and in vivo. in Oncogene 2000
Show all 6 Pubmed References
Hsp27 may up-regulate the expression of ABCA1 and promotes cholesterol efflux through activation of the PI3K/PKCzeta/Sp1 signal pathway in THP-1 macrophage-derived foam cells
These findings indicate that activation of HSF1 (zeige HSF1 Proteine) at Ser326 residue and transcription of HSP27 is related to the maintenance of gynecological CSCs/CICs.
This study reports solution-state nuclear magnetic resonance spectroscopy investigations of the conformation and dynamics of the disordered and flexible C-terminal region of human HSP27. These data indicate a potential role for cis (zeige CISH Proteine)-trans proline isomerization in regulating the oligomerization.
Overexpression of both HSPB5 and Hsp27 significantly reduced the intracellular aggregation of alpha-synuclein.
HspB1 structural organization displays dynamic and complex rearrangements in response to changes in the cellular environment or when the cell physiology is modified. [review]
Glutathione-S-transferase (zeige GSTa2 Proteine) - HspB1 fusion protein prevents more aggregation of malate dehydrogenase (zeige ME1 Proteine) compared to glutathione-S-transferase (zeige GSTa2 Proteine) -HspB5 (zeige CRYAB Proteine) fusion protein and wild type HspB1.
The data suggest that oncogene (zeige RAB1A Proteine)-addicted cells require the small heat-shock protein of 27 kDa (HSP27) for survival and that HSP27 might interfere with the effectiveness of targeted agents.
Data indocate six cytostatic drugs which inhibit heat shock 27 kDa protein (HSP27) and tackle drug resistance by computational drug repositioning approach.
Different from C-M-T phenotype in hereditary neuropathies caused by mutations in the HSPB1 gene.
found knock down of HSPB1 further increased the proportion of apoptotic cells in hyperthermic treated melanoma cells when compared with either single agent alone, and both agents leaded to cell cycle arrest at G0/G1 or G2/M phases
HspB1 is recruited to sites of increased traction force in cells geometrically constrained on micropatterned substrates. Findings elucidate a molecular pathway by which a mechanical signal is transduced via activation of p38 MAPK (zeige MAPK14 Proteine) to influence actin remodeling and cell migration via a zyxin (zeige ZYX Proteine)-independent process.
Study report a novel interaction between mutant HSPB1-P182L and the RNA binding protein PCBP1 (zeige PCBP1 Proteine), leading to a reduction in its translational repression activity. Identifying PCBP1 (zeige PCBP1 Proteine) mRNA targets revealed a marked prevalence for an RNA recognition motif, preferably seen in their 5' and 3'UTRs. Findings further support a role for mutant HSPB1 in neurodegenerative diseases.
Expression of a phosphomimetic HSPB1 mutant in astrocytes reduced toxicity to motor neurons.
AMPK (zeige PRKAA1 Proteine)-mediated HSPB1 expression enhanced insulin (zeige INS Proteine) sensitivity in the skeletal muscle.
e confirmed the modulatory effect of Hspb1 on Purkinje cell degeneration (zeige AGTPBP1 Proteine) in vivo, as knockdown by Hspb1 shRNA significantly enhanced neuron loss. These results suggest that strategies to promote HSPB1 activity may slow the rate of cerebellar degeneration in NPC (zeige NPC1 Proteine) disease and highlight the use of bioinformatics tools to uncover pathways leading to neuronal protection in neurodegenerative disorders
Dp71Delta78-79 dystrophin (zeige DMD Proteine) mutant stimulates neurite outgrowth in cultured neuronal cells via upregulation and phosphorylation of HspB1.
HSPB1 depletion in a mouse model of lung tumorigenesis induced the endothelial-to-mesenchymal transition
Overexpression of HSP27-S135F protein causes peripheral neuropathy. The mouse model can be applied to future development of therapeutic strategies forhereditary motor neuropathy (dHMN) and Charcot-Marie-Tooth disease type 2 F.
cardiac HMGB1 (zeige HMGB1 Proteine) increases HSPB1 expression and attenuates cardiomyocyte apoptosis associated with doxorubicin-induced cardiomyopathy.
These results suggest that Sox2 (zeige SOX2 Proteine)-Hspb1 signaling is a possible pathway responsible to tumor progression of QRsP-11
Loss of HspB1 specifically reduces myofibril size in embryonic craniofacial muscles.
Results show the sequence, expression, regulation, and function of a zebrafish protein (zfHsp27) and define zebrafish as a new model for the study of Hsp27 function.
initial upregulation of hsp27 expression occurs during early gastrulation
hspb1 is expressed during development
Hsp27 is dispensable for zebrafish morphogenesis but could play a role in long-term maintenance of heart and muscle tissues.
The data support a mechanism of Hsp27 function where interactions with the titin (zeige TTN Proteine) filament system protect myofibrils from stress-induced degradation.
Xenopus HSP27, like HSP30, is a developmentally-regulated heat-inducible molecular chaperone (zeige HSP90AA1 Proteine).
It indicated that Hsp27 was required for porcine circovirus type 2 replication in PK-15 cells culture.
HSP27 expression is gut (zeige GUSB Proteine) region- and cell type-specific in response to dietary components, microbes, and microbial metabolites to which the mucosa surface is exposed.
These results indicate that Hsp27 expression in the porcine gut (zeige GUSB Proteine) could be associated with specific dietary fiber components but not the overall microbiota diversity.
Data suggest that targeting HSP27 might offer a useful strategy in cancer treatment.
Data show that the expression of HSP27 and CLIC1 (zeige CLIC1 Proteine) was strongly positive in 61 (59.2%) and 49 cases (47.6%), respectively.
Data suggest that HSP27 enhanced the metastatic property of NPC (zeige NPC1 Proteine) cells probably via the NF-kappaB (zeige NFKB1 Proteine)-mediated activation of MMPs.
Hsp27 expression and its direct chaperoning interaction increase Akt (zeige AKT1 Proteine) stability and p21 (zeige CDKN1A Proteine) phosphorylation and nuclear-to-cytoplasm translocation, both essential effects for the survival of ultraviolet-induced DNA-damaged cells.
HSP27 could be a good candidate involved in migration and/or function of neutrophils within the porcine endmetrium.
HSP27 and HSP70 (zeige HSP70 Proteine) may be used as differential markers to distinguish conventional and low grade central osteosarcoma.
HSP-27 and HSP-70 (zeige HSP70 Proteine) contribute to modulation of K(+) channel (zeige KCNC4 Proteine)-induced pial artery dilation
These findings suggest that HSPB1 mediates androgen signaling by binding directly to androgen receptor (zeige AR Proteine) and then enhancing androgen-mediated myogenesis in myogenic cells.
HSPB1 could have an important role during testosterone-related myogenesis.
CaMKII (zeige CAMK2G Proteine) is required for redox-sensitive activation of p38 MAPK (zeige MAPK14 Proteine)/heat shock protein 27 pathway and ERK1/2
The protein encoded by this gene is induced by environmental stress and developmental changes. The encoded protein is involved in stress resistance and actin organization and translocates from the cytoplasm to the nucleus upon stress induction. Defects in this gene are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN).
28 kDa heat shock protein
, HSP 27
, estrogen-regulated 24 kDa protein
, heat shock 27 kDa protein
, heat shock 27kD protein 1
, heat shock protein beta-1
, stress-responsive protein 27
, HSP 25
, growth-related 25 kDa protein
, heat shock 25 kDa protein
, heat shock 27kDa protein 1
, heat shock protein, 25 kDa
, truncated hsp25
, heat shock 27 kDa protein 1
, 25 kDa heat shock protein
, 25 kDa IAP
, actin polymerization inhibitor
, inhibitor of actin polymerization
, heat-shock protein
, heat shock protein 27