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anti-Human XBP1 Antibodies:
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Human Polyclonal XBP1 Primary Antibody for ChIP, IHC - ABIN256411
Bogaert, De Vos, Olievier, Peeters, Elewaut, Lambrecht, Pouliot, Laukens: Involvement of endoplasmic reticulum stress in inflammatory bowel disease: a different implication for colonic and ileal disease? in PLoS ONE 2011
Show all 4 Pubmed References
Human Monoclonal XBP1 Primary Antibody for ELISA, WB - ABIN969462
Martino, Olsen, Fulcher, Wolfgang, ONeal, Ribeiro: Airway epithelial inflammation-induced endoplasmic reticulum Ca2+ store expansion is mediated by X-box binding protein-1. in The Journal of biological chemistry 2009
Show all 3 Pubmed References
Human Monoclonal XBP1 Primary Antibody for ELISA, WB - ABIN967263
Jiang, Yang, Thorne, Zhu, Hersey, Zhang: Human melanoma cells under endoplasmic reticulum stress acquire resistance to microtubule-targeting drugs through XBP-1-mediated activation of Akt. in Neoplasia (New York, N.Y.) 2009
Show all 3 Pubmed References
Human Polyclonal XBP1 Primary Antibody for ICC, IF - ABIN4366342
Baek, Kim, Park, Jang, Kang, Lee, Moon, Chae, Chung: Involvement of endoplasmic reticulum stress in myofibroblastic differentiation of lung fibroblasts. in American journal of respiratory cell and molecular biology 2012
Show all 2 Pubmed References
Human Polyclonal XBP1 Primary Antibody for IF (p), IHC (p) - ABIN732728
Li, Han, Shi: IRE1?-XBP1 Pathway Is Activated Upon Induction of Single-Prolonged Stress in Rat Neurons of the Medial Prefrontal Cortex. in Journal of molecular neuroscience : MN 2015
Human Polyclonal XBP1 Primary Antibody for ELISA, ICC - ABIN4366344
Park, Shin, Lim, Lee, Kang: Purple perilla extracts allay ER stress in lipid-laden macrophages. in PLoS ONE 2014
Human Polyclonal XBP1 Primary Antibody for ICC, IF - ABIN4366347
Ciccia, Accardo-Palumbo, Rizzo, Guggino, Raimondo, Giardina, Cannizzaro, Colbert, Alessandro, Triolo: Evidence that autophagy, but not the unfolded protein response, regulates the expression of IL-23 in the gut of patients with ankylosing spondylitis and subclinical gut inflammation. in Annals of the rheumatic diseases 2014
Human Monoclonal XBP1 Primary Antibody for CyTOF, FACS - ABIN4899365
Hasegawa, Wendling, He, Trilisky, Stevenson, Franey, Kinderman, Li, Piedmonte, Osslund, Shen, Ketchem: In vivo crystallization of human IgG in the endoplasmic reticulum of engineered Chinese hamster ovary (CHO) cells. in The Journal of biological chemistry 2011
MiR (show MLXIP Antibodies)-665 induced apoptosis by inhibiting XBP1 and ORMDL3 (show ORMDL3 Antibodies).
IRE1alpha (show ERN1 Antibodies) was shown to cleave miR (show MLXIP Antibodies)-150 and thereby to release the suppressive effect that miR (show MLXIP Antibodies)-150 exerted on alphaSMA (show ACTA2 Antibodies) expression through c-Myb (show MYB Antibodies). Inhibition of IRE1alpha (show ERN1 Antibodies) was also demonstrated to block endoplasmic reticulum expansion through an XBP-1-dependent pathway.
mTORC2 (show CRTC2 Antibodies) responds to glutamine (show GFPT1 Antibodies) catabolite levels to modulate the hexosamine biosynthesis enzyme GFAT1 (show GFPT1 Antibodies), and is essential for proper expression and nuclear accumulation of the GFAT1 (show GFPT1 Antibodies) transcriptional regulator, Xbp1s.
we identify a positive feedback regulatory loop consisting of XBP1 and NCOA3 (show NCOA3 Antibodies) that maintains high levels of NCOA3 (show NCOA3 Antibodies) and XBP1 expression in breast cancer tissues.
The findings indicate that IRE1 (show ERN1 Antibodies)-XBP1 downregulation distinguishes germinal center B-cell-like diffuse large B-cell lymphoma (DLBCL) from other DLBCL subtypes and contributes to tumor growth.
XBP1 does not act as a direct activator of STAT3 phosphorylation. Hence, in regenerati (show DDR1 Antibodies)ng livers, XBP1 deficiency most likely affects STAT3 phosphorylation in an indirect manner, possibly related to unresolved ER stress.
reciprocal regulation of Pin1 (show PIN1 Antibodies) and XBP1s is associated with the activation of oncogenic pathways, and the relationship of PIN1 (show PIN1 Antibodies) and XBP1 may be an attractive target for novel therapy in cancers
Our data indicate that reduced response of IRE1alpha (show ERN1 Antibodies)/Xbp-1 signaling pathway to bortezomib may contribute to drug resistance in myeloma cells
XBP1 regulates VEGF-mediated cardiac angiogenesis.
XBP1s expression in mouse and human fibroblasts is critical for TiAl6 V4 particle-induced RANKL (show TNFSF11 Antibodies) expression and osteolysis
XBP1 deficiency in smooth muscle cells caused VSMC dedifferentiation and aggravated aortic aneurysms. XBP1u directly associated with the N terminus of FoxO4 (show FOXO4 Antibodies).
Data show that LPS (show TLR4 Antibodies) induces endoplasmic reticulum (ER) stress and P300 (show NOTCH1 Antibodies) activity via the XBP1/IRE1 (show ERN1 Antibodies) pathway.
Data suggest that activation of GRP78 (show HSPA5 Antibodies)/Ire1 (show ERN1 Antibodies)/Xbp1 pathway of ER stress-unfolded protein response is involved in mouse decidualization.
insulin (show INS Antibodies) and aPC (show APC Antibodies) converge on a common spliced-X-box binding protein-1 (sXBP1) signaling pathway to maintain endoplasmic reticulum (ER) homeostasis.
although feeding LS-Xbp1(-/-) mice cholesterol did not increase CYP7A1 (show CYP7A1 Antibodies) expression, serum C4 levels increased significantly up to levels similar to chow-fed Xbp1(fl/fl (show FLT3LG Antibodies)) mice and the total bile acid pool normalized. In conclusion, loss of hepatic XBP1 decreased the bile acid pool and CYP7A1 (show CYP7A1 Antibodies) synthetic activity.
However, depletion of XBP1 and ATF6 (show ATF6 Antibodies), alone or in combination, prevented autophagy induction and significantly enhanced Japanese encephalitis virus-induced cell death.
XBP1 expression regulates the unfolded protein response, acute-phase response, and DDR (show DDR1 Antibodies) in hepatocytes. In regenerating livers, XBP1 deficiency leads to endoplasmic reticulum stress and DNA damage.
Ire1alpha (show ERN1 Antibodies)-Xbp1s and associated molecular targets link ER stress in arcuate Pomc (show POMC Antibodies) neurons to aspects of normal energy and glucose homeostasis.
analyzed XBP1 level and location to explore the effect of ER stress on oocyte maturation and developmental competency of porcine embryos in an in vitro culture system
Knock-down of XBP1 enhanced endoplasmic reticulum stress-mediated cell death in porcine embryonic fibroblasts.
Exposure of endothelial cells to VEGF (show VEGFA Antibodies), high glucose, or hydrogen peroxide up-regulated the XBP1/IRE1 alpha (show ERN1 Antibodies) and ATF6 (show ATF6 Antibodies) arms of the unfolded protein response compared with untreated cells.
Expression of xbp1 is significantly upregulated in the liver of Cdipt (show CDIPT Antibodies)-deficient zebrafish due to persistent endoplasmic reticulum stress. Cdipt (show CDIPT Antibodies)-deficient zebrafish exhibits hepatic lipid accumulation.
zebrafish XBP-1 spliced form not only activates genes responsible for protein folding, transporting, glycosylation and Endoplasmic Reticulum associated degradation but also activates anti-apoptosis signal via IGF1 (show IGF1 Antibodies)/Akt (show AKT1 Antibodies) pathway in unfolded protein
XBP1 might function as an inhibitor of mesodermal and neural tissue formation by acting either as transcriptional activator or as repressor.
This gene encodes a transcription factor that regulates MHC class II genes by binding to a promoter element referred to as an X box. This gene product is a bZIP protein, which was also identified as a cellular transcription factor that binds to an enhancer in the promoter of the T cell leukemia virus type 1 promoter. It may increase expression of viral proteins by acting as the DNA binding partner of a viral transactivator. It has been found that upon accumulation of unfolded proteins in the endoplasmic reticulum (ER), the mRNA of this gene is processed to an active form by an unconventional splicing mechanism that is mediated by the endonuclease inositol-requiring enzyme 1 (IRE1). The resulting loss of 26 nt from the spliced mRNA causes a frame-shift and an isoform XBP1(S), which is the functionally active transcription factor. The isoform encoded by the unspliced mRNA, XBP1(U), is constitutively expressed, and thought to function as a negative feedback regulator of XBP1(S), which shuts off transcription of target genes during the recovery phase of ER stress. A pseudogene of XBP1 has been identified and localized to chromosome 5.
X-box binding protein 1 pseudogene 1
, X-box binding protein pseudogene 1
, X-box binding protein 1
, X-box-binding protein 1
, tax-responsive element-binding protein 5
, tax-responsive element-binding protein 5 homolog
, hepatocarcinogenesis-related transcription factor
, X-box binding protein 1B