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Human Polyclonal HSP90AB1 Primary Antibody pour WB - ABIN2801931
Wiemann, Weil, Wellenreuther, Gassenhuber, Glassl, Ansorge, Böcher, Blöcker, Bauersachs, Blum, Lauber, Düsterhöft, Beyer, Köhrer, Strack, Mewes, Ottenwälder, Obermaier, Tampe, Heubner, Wambutt, Korn et al.: Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs. ... dans Genome research 2001
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Human Polyclonal HSP90AB1 Primary Antibody pour ICC, IF - ABIN361850
Wagatsuma, Shiozuka, Kotake, Takayuki, Yusuke, Mabuchi, Matsuda, Yamada: Pharmacological inhibition of HSP90 activity negatively modulates myogenic differentiation and cell survival in C2C12 cells. dans Molecular and cellular biochemistry 2011
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Human Polyclonal HSP90AB1 Primary Antibody pour FACS, IF (p) - ABIN725495
Ding, Wu, Su, Zhou, Zhao, Deng, Zhang, Liu, Wang, Liu: Expression of heat shock protein 90 genes during early development and infection in Megalobrama amblycephala and evidence for adaptive evolution in teleost. dans Developmental and comparative immunology 2013
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Human Monoclonal HSP90AB1 Primary Antibody pour FACS, IF - ABIN966320
Zhang, Li, Yu, Zou, Jiang, Sun: Characterization of celastrol to inhibit hsp90 and cdc37 interaction. dans The Journal of biological chemistry 2009
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Human Polyclonal HSP90AB1 Primary Antibody pour IHC - ABIN966322
Zhao, Houry: Molecular interaction network of the Hsp90 chaperone system. dans Advances in experimental medicine and biology 2007
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Human Monoclonal HSP90AB1 Primary Antibody pour IHC, ELISA - ABIN966319
McDowell, Bryan Sutton, Obermann: Expression of Hsp90 chaperone [corrected] proteins in human tumor tissue. dans International journal of biological macromolecules 2009
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Human Monoclonal HSP90AB1 Primary Antibody pour IHC, ELISA - ABIN361720
Arlander, Eapen, Vroman, McDonald, Toft, Karnitz: Hsp90 inhibition depletes Chk1 and sensitizes tumor cells to replication stress. dans The Journal of biological chemistry 2003
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Human Polyclonal HSP90AB1 Primary Antibody pour FACS, IHC (p) - ABIN392346
Wu, Huang, Liu, Liu: Heat shock protein 90-? over-expression is associated with poor survival in stage I lung adenocarcinoma patients. dans International journal of clinical and experimental pathology 2015
the expressions of HSP90AB1 can predict prognosis in astrocytic tumors
We found that the nutrient value of the culturing medium and the length of induction had significant effect on Hsp90 (Montrer HSP90 Anticorps) production in Escherichia coli. Our fast, single-day purification protocol resulted in a stable, well-folded and pure sample that was resistant to degradation in a reproducible manner.
Data show that C allele of rs2282151 was associated with increased expression level of heat shock protein 90 alpha (Montrer HSP90AA1 Anticorps) family class B member 1 (HSP90AB1).
Hsp90beta induced endothelial cell-dependent tumor angiogenesis by activating VEGFRs transcription.
The authors find that the interaction between sB-Raf (Montrer RAF1 Anticorps) and the Hsp90 chaperone (Montrer HSP90 Anticorps) system is based on contacts with the M domain of Hsp90 (Montrer HSP90 Anticorps), which contributes in forming the ternary complex with Cdc37 (Montrer CDC37 Anticorps) as long as the kinase is not stabilized by nucleotide.
High HSP90B expression is associated with laryngeal carcinoma.
The expression level of Hsp90AB1 in lung cancer tissues was significantly higher than that in normal lung tissue and was associated with lung cancer pathological type and overall survival in lung adenocarcinoma patients.
We revealed that Hsp90A (Montrer HSP90AA1 Anticorps) and Hsp90B are partly colocalized with heparan sulfate proteoglycans (HSPGs) on the cell surface and that this colocalization was sensitive to heparin.
Apart from these distinct Cdc37/Hsp90 interfaces, binding of the B-Raf protein kinase to the cochaperone is conserved between mammals and nematodes.
HSP90AB1: Helping the good and the bad
The results demonstrate that in renal cells, NHE1 (Montrer SLC9A1 Anticorps) is associated with several regulatory proteins including Hsp90 (Montrer HSP90 Anticorps), and that Hsp90 (Montrer HSP90 Anticorps) affects its function possibly through altered phosphorylation of the protein via the AKT (Montrer AKT1 Anticorps) kinase.
Extracellular Hsp70 (Montrer HSP70 Anticorps) and Hsp90 (Montrer HSP90 Anticorps), either in soluble form or secreted as part of exosomes from tumor cells, are responsible for tumor induction of cachexia.
a surface population of Hsp90 (Montrer HSP90 Anticorps) extracellularly binds TGFbetaRI and this complex behaves as an active participant in collagen production in TGFbeta (Montrer TGFB1 Anticorps)-activated fibroblasts.
Hsp90 (Montrer HSP90 Anticorps) is highly expressed on the cell surface of melanoma cells, and synthetic agents that target Hsp90 (Montrer HSP90 Anticorps) are promising cancer therapeutic drugs
These findings identify the Ezh2 (Montrer EZH2 Anticorps)-Hsp90 (Montrer HSP90 Anticorps) interaction as a previously unrecognized mechanism essential for T-cell responses and an effective target for controlling graft-versus-host disease.
Data show that docetaxel, rapamycin and tanespimycin multi-drug loaded micelles targeted against HSP90 (Montrer HSP90 Anticorps) and the PI3K/AKT (Montrer AKT1 Anticorps)/mTOR (Montrer FRAP1 Anticorps) pathway in prostate cancer.
genes respond to HSP90 (Montrer HSP90 Anticorps) inhibition in a manner dependent on their genomic location with regard to strain-specific endogenous retroviruses-insertion sites.
PABPN1 (Montrer PABPN1 Anticorps) interacts with and is stabilized by heat shock protein 90 (Montrer HSP90 Anticorps).
Hyperacetylation of Hsp90 (Montrer HSP90 Anticorps) is a predictor and causal molecular determinant of stress resilience in mice. Brain-penetrant histone deacetylase 6 (Montrer HDAC6 Anticorps) inhibitors increase Hsp90 (Montrer HSP90 Anticorps) acetylation and modulate GR chaperone dynamics.
These findings demonstrate a critical role of Hsp90 (Montrer HSP90 Anticorps) in lipopolysaccharide (LPS (Montrer TLR4 Anticorps)) signaling, and a potential involvement of the heat shock response in LPS (Montrer TLR4 Anticorps)-induced preconditioning.
Data from Xenopus laevis embryo suggest hsp90alpha (Montrer HSP90AA2 Anticorps) and hsp90Beta genes are conserved among vertebrates, and are differentially regulated in a tissue, stress, and development stage-specific manner.
Heat tolerance was assessed in Boran and Nguni cows. Protein levels of HSP90AB1, skin thickness, rectal and skin temperature were higher in the Boran cows than Nguni cows. Breed, age and coat colour did not influence HSP90AB1 concentration.
Studied the nucleotide polymorphism within the HSP90AB1 gene (SNP g.4338T>C) in Indian breeds of dairy cattle.
Association analysis revealed that the T allele at SNP g.4338T>C of the HSP90AB1 gene improved heat tolerance in cattle. Allele T was 100% in White Lamphun animals, 84% in Mountain cattle, and 18% in Holstein Friesian heifers.
This study showed that ubiquitinated ALK5 (Montrer TGFBR1 Anticorps) and phosphorylated heat shock protein 27 (Montrer HSP27 Anticorps) specifically accumulate in the cytoskeleton fraction, and ALK1 (Montrer ACVRL1 Anticorps) and ALK5 (Montrer TGFBR1 Anticorps) interact with heat shock protein 90(HSP90 (Montrer HSP90 Anticorps)).
the protective effect exerted by HSP90 on eNOS degradation mediated by calpain represents a novel and critical mechanism that assures the reversibility of the intracellular trafficking and activation of the synthase
Data demonstrate that Hsp90alpha (Montrer HSP90AA2 Anticorps) and Hsp90beta exhibit similar interactions with co-chaperones, but significantly different behaviors with respect to substrate interactions under stress conditions.
Mapped six genes (EIF4G3 (Montrer EIF4G3 Anticorps), HSP90, RBBP6 (Montrer RBBP6 Anticorps), IL8 (Montrer IL8 Anticorps), TERT (Montrer TERT Anticorps), and TERC) on the chromosomes of Equus caballus, Equus asinus, Equus grevyi, and Equus burchelli by fluorescence in situ hybridization.
Hsp90 is involved in opposing signaling pathways of cartilage homeostasis and catabolic responses are more sensitive to Hsp90 inhibition than are anabolic responses.
This gene encodes a member of the heat shock protein 90 family\; these proteins are involved in signal transduction, protein folding and degradation and morphological evolution. This gene encodes the constitutive form of the cytosolic 90 kDa heat-shock protein and is thought to play a role in gastric apoptosis and inflammation. Alternative splicing results in multiple transcript variants. Pseudogenes have been identified on multiple chromosomes.
, heat shock 84 kDa
, heat shock 90kD protein 1, beta
, heat shock protein HSP 90-beta
, 94 kDa glucose-regulated protein
, heat shock protein 90 kDa beta member 1
, tumor rejection antigen (gp96) 1
, tumor rejection antigen 1
, Heat Shock Protein 90, endoplasmic reticulum
, heat shock protein 90B
, heat shock protein hsp90 beta
, hsp90 beta
, HSP 84
, heat shock 90kDa protein 1, beta
, heat shock protein 1, beta
, heat shock protein 90kDa alpha (cytosolic), class B member 1
, heat shock protein, 84 kDa 1
, retinal degeneration slow protein
, tumor-specific transplantation 84 kDa antigen
, heat shock cognate protein HSP 90-beta
, heat shock protein 90 beta
, heat shock 90kDa protein beta
, heat shock protein 90-beta
, heat shock protein 90kDa alpha, class B member 1
, Heat shock protein HSP 90-beta-like protein
, heat shock protein 90
, Heat shock protein HSP 90-beta