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anti-Human XBP1 Antikörper:
anti-Mouse (Murine) XBP1 Antikörper:
anti-Rat (Rattus) XBP1 Antikörper:
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Human Polyclonal XBP1 Primary Antibody für 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
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Human Monoclonal XBP1 Primary Antibody für 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
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Human Monoclonal XBP1 Primary Antibody für 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
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Human Polyclonal XBP1 Primary Antibody für 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
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Human Polyclonal XBP1 Primary Antibody für 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 für 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 für 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 für 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 (zeige MLXIP Antikörper)-665 induced apoptosis by inhibiting XBP1 and ORMDL3 (zeige ORMDL3 Antikörper).
IRE1alpha (zeige ERN1 Antikörper) was shown to cleave miR (zeige MLXIP Antikörper)-150 and thereby to release the suppressive effect that miR (zeige MLXIP Antikörper)-150 exerted on alphaSMA (zeige ACTA2 Antikörper) expression through c-Myb (zeige MYB Antikörper). Inhibition of IRE1alpha (zeige ERN1 Antikörper) was also demonstrated to block endoplasmic reticulum expansion through an XBP-1-dependent pathway.
mTORC2 (zeige CRTC2 Antikörper) responds to glutamine (zeige GFPT1 Antikörper) catabolite levels to modulate the hexosamine biosynthesis enzyme GFAT1 (zeige GFPT1 Antikörper), and is essential for proper expression and nuclear accumulation of the GFAT1 (zeige GFPT1 Antikörper) transcriptional regulator, Xbp1s.
we identify a positive feedback regulatory loop consisting of XBP1 and NCOA3 (zeige NCOA3 Antikörper) that maintains high levels of NCOA3 (zeige NCOA3 Antikörper) and XBP1 expression in breast cancer tissues.
The findings indicate that IRE1 (zeige ERN1 Antikörper)-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 (zeige DDR1 Antikörper)ng livers, XBP1 deficiency most likely affects STAT3 phosphorylation in an indirect manner, possibly related to unresolved ER stress.
reciprocal regulation of Pin1 (zeige PIN1 Antikörper) and XBP1s is associated with the activation of oncogenic pathways, and the relationship of PIN1 (zeige PIN1 Antikörper) and XBP1 may be an attractive target for novel therapy in cancers
Our data indicate that reduced response of IRE1alpha (zeige ERN1 Antikörper)/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 (zeige TNFSF11 Antikörper) 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 (zeige FOXO4 Antikörper).
Data show that LPS (zeige TLR4 Antikörper) induces endoplasmic reticulum (ER) stress and P300 (zeige NOTCH1 Antikörper) activity via the XBP1/IRE1 (zeige ERN1 Antikörper) pathway.
Data suggest that activation of GRP78 (zeige HSPA5 Antikörper)/Ire1 (zeige ERN1 Antikörper)/Xbp1 pathway of ER stress-unfolded protein response is involved in mouse decidualization.
insulin (zeige INS Antikörper) and aPC (zeige APC Antikörper) 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 (zeige CYP7A1 Antikörper) expression, serum C4 levels increased significantly up to levels similar to chow-fed Xbp1(fl/fl (zeige FLT3LG Antikörper)) mice and the total bile acid pool normalized. In conclusion, loss of hepatic XBP1 decreased the bile acid pool and CYP7A1 (zeige CYP7A1 Antikörper) synthetic activity.
However, depletion of XBP1 and ATF6 (zeige ATF6 Antikörper), 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 (zeige DDR1 Antikörper) in hepatocytes. In regenerating livers, XBP1 deficiency leads to endoplasmic reticulum stress and DNA damage.
Ire1alpha (zeige ERN1 Antikörper)-Xbp1s and associated molecular targets link ER stress in arcuate Pomc (zeige POMC Antikörper) 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 (zeige VEGFA Antikörper), high glucose, or hydrogen peroxide up-regulated the XBP1/IRE1 alpha (zeige ERN1 Antikörper) and ATF6 (zeige ATF6 Antikörper) arms of the unfolded protein response compared with untreated cells.
Expression of xbp1 is significantly upregulated in the liver of Cdipt (zeige CDIPT Antikörper)-deficient zebrafish due to persistent endoplasmic reticulum stress. Cdipt (zeige CDIPT Antikörper)-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 (zeige IGF1 Antikörper)/Akt (zeige AKT1 Antikörper) 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