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Chicken Monoclonal HSP90 Primary Antibody for AA, ELISA - ABIN361717
Loo, Jensen, Cui, Hou, Chang, Riordan: Perturbation of Hsp90 interaction with nascent CFTR prevents its maturation and accelerates its degradation by the proteasome. in The EMBO journal 1999
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Chicken Monoclonal HSP90 Primary Antibody for IF, IP - ABIN967957
Brouet, Sonveaux, Dessy, Balligand, Feron: Hsp90 ensures the transition from the early Ca2+-dependent to the late phosphorylation-dependent activation of the endothelial nitric-oxide synthase in vascular endothelial growth factor-exposed endothelial cells. in The Journal of biological chemistry 2001
Show all 6 Pubmed References
Chicken Monoclonal HSP90 Primary Antibody for IF, IP - ABIN967958
Miyamoto, Nakayama, Imaki, Hirose, Jiang, Abe, Tsukiyama, Nagahama, Ohno, Hatakeyama, Nakayama: Increased proliferation of B cells and auto-immunity in mice lacking protein kinase Cdelta. in Nature 2002
Show all 6 Pubmed References
Human Monoclonal HSP90 Primary Antibody for WB - ABIN1882255
Yamazaki, Akaogi, Miwa, Imai, Soeda, Yokoyama: Nucleotide sequence of a full-length cDNA for 90 kDa heat-shock protein from human peripheral blood lymphocytes. in Nucleic acids research 1989
Show all 5 Pubmed References
Human Polyclonal HSP90 Primary Antibody for ICC, IF - ABIN361823
Arlander, Eapen, Vroman, McDonald, Toft, Karnitz: Hsp90 inhibition depletes Chk1 and sensitizes tumor cells to replication stress. in The Journal of biological chemistry 2003
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Human Monoclonal HSP90 Primary Antibody for WB - ABIN3043076
Jiang, Wang, Li, Shi, Li, Ma, Li, Luo, Yang, Xu: Heat shock protein 90-mediated inactivation of nuclear factor-?B switches autophagy to apoptosis through becn1 transcriptional inhibition in selenite-induced NB4 cells. in Molecular biology of the cell 2011
Show all 2 Pubmed References
Human Monoclonal HSP90 Primary Antibody for ICC, IF - ABIN361731
Dalman, Bresnick, Patel, Perdew, Watson, Pratt: Direct evidence that the glucocorticoid receptor binds to hsp90 at or near the termination of receptor translation in vitro. in The Journal of biological chemistry 1989
Show all 12 Pubmed References
Cow (Bovine) Monoclonal HSP90 Primary Antibody for IF, IP - ABIN222933
Lange, Kistler, Jutzi, Bazhin, Klemke, Schadendorf, Eichmueller: Detergent fractionation with subsequent subtractive suppression hybridization as a tool for identifying genes coding for plasma membrane proteins. in Experimental dermatology 2009
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Human Polyclonal HSP90 Primary Antibody for BP, Neut - ABIN266753
Liu, Zhang, Shi, Quinn, Bradner, Beyer, Chen, Zhang: Rab11a and HSP90 regulate recycling of extracellular alpha-synuclein. in The Journal of neuroscience : the official journal of the Society for Neuroscience 2009
Show all 2 Pubmed References
Fish Polyclonal HSP90 Primary Antibody for WB - ABIN361873
Barent, Nair, Carr, Ruan, Rimerman, Fulton, Zhang, Smith: Analysis of FKBP51/FKBP52 chimeras and mutants for Hsp90 binding and association with progesterone receptor complexes. in Molecular endocrinology (Baltimore, Md.) 1998
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Escargot and Scratch regulate neural commitment by antagonizing Notch (show NOTCH1 Antibodies) activity in Drosophila sensory organs
Nup358 (show RANBP2 Antibodies) facilitates JH-induced Met nuclear transport in a manner dependent on importin beta (show KPNB1 Antibodies) and Hsp83.
We show that while Hsp70 or Hsp83 expression under normal or stress conditions was not affected by AR feeding, Hsp27 levels were elevated in AR-fed wild-type control as well as heat-shocked larvae
The results revealed that the high-fat diet augmented the rate of lipid peroxidation and SOD (show SOD2 Antibodies) and CAT activity and induced a higher expression of HSP83 and MPK2 (show MAPK1 Antibodies) mRNA.
Hsp83 facilitates methoprene-tolerant nuclear import to modulate juvenile hormone signaling.
Interaction of Spag with both Hsp70 and Hsp90 suggests a model whereby R2TP would accompany clients from Hsp70 to Hsp90 to facilitate their assembly into macromolecular complexes.
Our results reveal that Hsp83 plays a heretofore unappreciated role in promoting APC (show APC Antibodies)/C function during cell cycle exit and suggest a mechanism by which Hsp90 inhibition could promote genomic instability and carcinogenesis
Using computational and biochemical analyses, study find that Hsp90 maintains and optimizes RNA polymerase II pausing via stabilization of the negative elongation factor (show RDBP Antibodies) complex.
Data suggest that that an Sgt1 (show SUGT1 Antibodies)/Hsp90-LKB1 (show STK11 Antibodies)-AMPK (show GRK4 Antibodies) pathway acts redundantly with a microtubule-induced polarity pathway to generate neuroblast cortical polarity, and the absence of neuroblast cortical polarity can produce neuroblast tumors.
Piwi (show PIWIL1 Antibodies) functions in Hsp90-mediated suppression of phenotypic variation
Fusion of human SGT1 (show SUGT1 Antibodies) (hSGT1 (show ECD Antibodies)) to NOD1 (show NOD1 Antibodies) LRR significantly enhanced the solubility, and the fusion protein was stabilized by coexpression of mouse Hsp90alpha (show HSP90AA2 Antibodies).
The major capsid protein of the mouse polyomavirus VP1 binds microtubules, HSP90, promotes their acetylation and blocks the host cell cycle.
Artificially maintaining Hsp90alpha (show HSP90AA2 Antibodies) or knocking down Aarsd1L expression interferes with the differentiation of C2C12 myotubes.
Immune-mediated destruction of ovarian follicles associated with the presence of HSP90 antibodies.
identify that Hsp90alpha (show HSP90AA2 Antibodies) at the transition neck region represents a signalling platform on which IRS-1 (show IRS1 Antibodies) interacts with intracellular downstream signalling molecules involved in IGF-1 (show IGF1 Antibodies) receptor signalling.
The study demonstrated that HSP90alpha plays an important role in the biogenesis of fetal PIWI-interacting RNAs (piRNA), which act against the transposon activities, in mouse male germ cells.
Data show that the heat shock protein 90 (HSP90) isoforms HSP90AA1 (show HSP90AA1 Antibodies) and HSP90AB1 (show HSP90AB1 Antibodies) are responsible for maintaining proper cellular levels of BMAL1 (show ARNTL Antibodies) protein.
deficiency does not affect immunoglobulin gene hypermutation and class switch but causes enhanced MHC class II antigen presentation
study identified the essential role of Hsp90 in iNOS (show NOS2 Antibodies) gene transactivation
Hsp90alpha (show HSP90AA2 Antibodies) may be required to maintain and to activate these regulators and/or to disassemble the synaptonemal complex that holds homologous chromosomes together
FKBP51 (show FKBP4 Antibodies) is primarily localized in mitochondria and hTERT is totally nuclear, upon the onset of oxidative stress, FKBP51 (show FKBP4 Antibodies) (but not FKBP52 (show FKBP4 Antibodies)) becomes mostly nuclear colocalizing with hTERT, and longer exposure times to peroxide favors hTERT export to mitochondria.
High HSP90 expression is associated with Colorectal Cancers.
High HSP90 expression is associated with prostate cancer.
Data suggest HSP90AA1-dependent regulation of ATM-NBN-CHK2 and ATR-CHK1 axes influences cells capability to repair double-stranded DNA damage; mechanisms include phosphorylation, polyubiquitination, and proteasomal degradation/proteolysis. (HSP90AA1 = heat shock protein 90kDa alpha; ATM = ataxia telangiectasia mutated protein; NBN = nibrin; CHK = checkpoint kinase; ATR = ataxia telangiectasia and Rad3 related kinase)
We found that the nutrient value of the culturing medium and the length of induction had significant effect on Hsp90 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 (show HSP90AA1 Antibodies) family class B member 1 (HSP90AB1 (show HSP90AB1 Antibodies)).
Data show that pyruvate kinase M2 (PKM2) directly interacted with mutant growth factor receptor (show RYK Antibodies) (EGFR (show EGFR Antibodies)) and heat-shock protein 90 (HSP90), and thus stabilized EGFR (show EGFR Antibodies) by maintaining its binding with HSP90 and co-chaperones.
Binding of FM807 to the N-terminus of Hsp90 disrupted Hsp90/client complexes, resulting in degradation of the Hsp90 client protein EGFR (show EGFR Antibodies) and inhibition of the downstream pathway.
Conventional as well as scaled molecular dynamics simulations further demonstrate that citrullination of selected Arg residues leads to progressive disruption of HSP90 tertiary structure, promoting exposure of R502/R510 to PAD modification and subsequent autoantibody binding.
SYK (show SYK Antibodies) is an HSP90 client protein, and B-cell receptor signaling-dependent phosphorylation of HSP90 on Y197 is required for this interaction. HSP90 promotes Burkitt lymphoma cell survival by maintaining tonic B-cell receptor signaling.
Feed intake remains low whereas respiratory frequency and body temperature remain higher and expression of HSP90, CAT1 (show SLC7A1 Antibodies), SGLT1 (show SLC5A1 Antibodies) and GLUT4 (show SLC2A4 Antibodies) increases in some tissues in pigs under chronic heat stress conditions.
HSP90AA1 (show HSP90AA1 Antibodies) sperm content and the prediction of the boar ejaculate freezability.
Hsp90 is a modulator of eNOS (show NOS3 Antibodies) activity and vascular reactivity in the newborn piglet pulmonary circulation
Apo (show C9orf3 Antibodies)-Hsp90 is in a conformational equilibrium between two open states that have never been described previously.
Findings indicate an essential role for Hsp90 in nongenomic estrogen signaling in coronary artery smooth muscle cells.
Data from Xenopus laevis embryo suggest hsp90alpha (show HSP90AA2 Antibodies) and hsp90Beta (show HSP90AB1 Antibodies) genes are conserved among vertebrates, and are differentially regulated in a tissue, stress, and development stage-specific manner. Hspalpha may play a role in myogenesis.
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 protein Hsp90
, heat shock protein 90
, Heat Shock Protein 90
, heat shock protein 83
, enhancer of sevenless 3A
, enhancer of seven in absentia 2
, HSP 86
, heat shock 86 kDa
, heat shock protein 1, alpha
, heat shock protein 90kDa alpha (cytosolic), class A member 1
, heat shock protein HSP 90-alpha
, heat shock protein, 1
, heat shock protein, 86 kDa 1
, heat shock protein, 89 kDa
, tumor-specific transplantation 86 kDa antigen
, heat shock protein 86
, epididymis luminal secretory protein 52
, heat shock 90kD protein 1, alpha
, heat shock 90kD protein 1, alpha-like 4
, heat shock 90kD protein, alpha-like 4
, heat shock 90kDa protein 1, alpha
, renal carcinoma antigen NY-REN-38
, 90-kDa heat shock protein
, hsp90 alpha
, heat shock 84 kDa
, heat shock 90kD protein 1, beta
, heat shock protein HSP 90-beta