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Human Polyclonal HSP90B1 Primary Antibody for IHC (f), ICC - ABIN966318
Green: The illusion of common ground and mythical pluralism. in The International journal of psycho-analysis 2005
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GRP94 is tightly associated with the cell surface of parietal cells from rabbit gastric mucosa, where it exhibits high-affinity binding for the adenosine receptor agonist NECA and specific inhibitor radicicol.
These data demonstrate the essential role of the gp96-TLR interaction in priming T cell immunity and provide further molecular basis for the coupling of gp96-mediated innate with adaptive immunity.
Heat-shock protein gp96 enhances T cell responses and protective potential to BCG (显示 SLC11A1 抗体) vaccine.
binding of PCSK9 (显示 PCSK9 抗体) to GRP94 protects LDLR (显示 LDLR 抗体) from degradation likely by preventing early binding of PCSK9 (显示 PCSK9 抗体) to LDLR (显示 LDLR 抗体)
These data indicate that macrophage gp96 is essential for protective immunity during Gram-negative pneumonia
gp96 participates in the generation of natural Treg cells, which might be involved in the control of liver regeneration in the periphery
These studies imply GRP78 (显示 HSPA5 抗体), but not GRP94, is required for mammary gland development.
GRP94 deficiency in the liver led to injury, LPC (显示 PCSK7 抗体) expansion, increased proliferation, activation of oncogenic signaling, progressive repopulation of GRP94-positive hepatocytes and HCC (显示 FAM126A 抗体) development in aged mice.
GP96 serves as an essential chaperone for the cell-surface protein (显示 CD28 抗体) glycoprotein A repetitions predominant (GARP (显示 LRRC32 抗体)), which is a docking receptor for latent membrane-associated TGF-beta (显示 TGFB1 抗体) (mLTGF-beta).
this work uncovered the essential role of gp96 in regulating melanogenesis.
Deletion of CD24 (显示 CD24 抗体) impairs development of heat shock protein gp96-driven autoimmune disease through expansion of myeloid-derived suppressor cells.
Immuno-stimulating peptide derived from HMGB1 (显示 HMGB1 抗体) is more effective than the N-terminal domain of Gp96 as an endogenous adjuvant for improvement of protein vaccines.
mutations in GRP94 that affect its IGF chaperone activity represent a novel causal genetic mechanism that limits IGF biosynthesis, quite a distinct mechanism from the known genes in the GH/IGF signaling network.
In this instance, the ATP5B (显示 ATP5B 抗体)/CALR (显示 CALR 抗体)/HSP90B1/HSPB1 (显示 HSPB1 抗体)/HSPD1 (显示 HSPD1 抗体)-signaling network was revealed as the predominant target which was associated with the majority of the observed protein-protein interactions. As a result, the identified targets may be useful in explaining the anticancer mechanisms of ursolic acid and as potential targets for colorectal cancer therapy.
High HSP90B1 expression is associated with non-small-cell lung cancer.
data suggest that the GRP94/CCT8 (显示 CCT8 抗体)/c-Jun (显示 JUN 抗体)/EMT (显示 ITK 抗体) signaling cascade might be a new therapeutic target for HCC (显示 FAM126A 抗体)
We filtered four OSCC genes including SERPINB9 (显示 SERPINB9 抗体), SERPINE2 (显示 SERPINE2 抗体), GAK (显示 GAK 抗体), and HSP90B1 through the gene global prioritization score (P < 0.005).
Our results demonstrated that GRP94 is a key molecule in Hepatocellular carcinoma (HCC (显示 FAM126A 抗体)) progression that modulates the AKT (显示 AKT1 抗体) pathway and eNOS (显示 NOS3 抗体) levels
Results indicate that FN14 (显示 TNFRSF12A 抗体) and GRP94 are prediction/prognosis markers which open up new possibilities for preventing/treating brain metastasis in breast cancer patients.
This study clarifies a Grp94-mediated ERAD pathway for GABAA (显示 GABRg1 抗体) receptors, which provides a novel way to finely tune their function in physiological and pathophysiological conditions.
structural maturation of the client protein substrate, rather than ATP binding or hydrolysis, serves as the primary signal for dissociation of GRP94-client protein complexes [GRP94]
These results identify a compact, intertwined quaternary conformation of native GRP94
This study showed that ubiquitinated ALK5 (显示 TGFBR1 抗体) and phosphorylated heat shock protein 27 specifically accumulate in the cytoskeleton fraction, and ALK1 (显示 ACVRL1 抗体) and ALK5 (显示 TGFBR1 抗体) interact with heat shock protein 90(HSP90 (显示 HSP90 抗体)).
In Xenopus, gp96 can prime CD8(+) T-cell effectors that are not MHC restricted.
This gene encodes a member of a family of adenosine triphosphate(ATP)-metabolizing molecular chaperones with roles in stabilizing and folding other proteins. The encoded protein is localized to melanosomes and the endoplasmic reticulum. Expression of this protein is associated with a variety of pathogenic states, including tumor formation. There is a microRNA gene located within the 5' exon of this gene. There are pseudogenes for this gene on chromosomes 1 and 15.
tumor rejection antigen (gp96) 1
, 94 kD glucose-regulated protein
, endoplasmin-like protein
, 94 kDa glucose-regulated protein
, endoplasmic reticulum resident protein 99
, heat shock protein 90 kDa beta member 1
, polymorphic tumor rejection antigen 1
, transforming growth factor alpha regulated gene 2
, tumor rejection antigen gp96
, heat shock protein 90kDa beta (grp94), member 1
, heat shock protein 90kDa beta (Grp94), member 1
, endothelial cell (HBMEC) glycoprotein
, stress-inducible tumor rejection antigen gp96
, tumor rejection antigen 1
, 98 kDa protein kinase
, PPK 98
, gp96 homolog
, heat shock protein 90kDa beta, member 1
, heat shock protein gp96
, HSP 108
, heat shock 108 kDa protein
, heat shock protein 108
, transferrin-binding protein