• Western blot analysis using XBP-1 monoclonal antibody against XBP1-hIgGFc transfected HEK293 cell lysate.

Anti-XBP1 antibody [1C4] (STJ98455)

SKU:
STJ98455

Current Stock:
Host: Mouse
Applications: WB/ELISA
Reactivity: Human
Note: STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Short Description: Mouse monoclonal antibody anti-X-box-binding protein 1 is suitable for use in Western Blot and ELISA research applications.
Clonality: Monoclonal
Clone ID: 1C4
Conjugation: Unconjugated
Isotype: IgG1
Formulation: Liquid in PBS containing 0.03% Sodium Azide, 0.5% BSA, 50% Glycerol.
Purification: Affinity purification
Dilution Range: WB 1:500-1:2000
ELISA 1:10000
Storage Instruction: Store at-20°C for up to 1 year from the date of receipt, and avoid repeat freeze-thaw cycles.
Gene Symbol: XBP1
Gene ID: 7494
Uniprot ID: XBP1_HUMAN
Specificity: XBP-1 Monoclonal Antibody detects endogenous levels of XBP-1 protein.
Immunogen: Purified recombinant fragment of human XBP-1 expressed in E. Coli.
Post Translational Modifications Isoform 2: Acetylated by EP300.acetylation positively regulates the transcriptional activity of XBP1 isoform 2. Isoform 2 is deacetylated by SIRT1.deacetylation negatively regulates the transcriptional activity of XBP1 isoform 2. Isoform 1: Ubiquitinated, leading to proteasome-mediated degradation in response to ER stress. X-box-binding protein 1, cytoplasmic form and luminal form are produced by intramembrane proteolytic cleavage of ER membrane-anchored isoform 1 triggered by HM13/SPP in a DERL1-RNF139-dependent and VCP/p97-independent manner. X-box-binding protein 1, luminal form is ubiquitinated leading to proteasomal degradation.
Function Functions as a transcription factor during endoplasmic reticulum (ER) stress by regulating the unfolded protein response (UPR). Required for cardiac myogenesis and hepatogenesis during embryonic development, and the development of secretory tissues such as exocrine pancreas and salivary gland. Involved in terminal differentiation of B lymphocytes to plasma cells and production of immunoglobulins. Modulates the cellular response to ER stress in a PIK3R-dependent manner. Binds to the cis-acting X box present in the promoter regions of major histocompatibility complex class II genes. Involved in VEGF-induced endothelial cell (EC) proliferation and retinal blood vessel formation during embryonic development but also for angiogenesis in adult tissues under ischemic conditions. Functions also as a major regulator of the UPR in obesity-induced insulin resistance and type 2 diabetes for the management of obesity and diabetes prevention. Isoform 1: Plays a role in the unconventional cytoplasmic splicing processing of its own mRNA triggered by the endoplasmic reticulum (ER) transmembrane endoribonuclease ERN1: upon ER stress, the emerging XBP1 polypeptide chain, as part of a mRNA-ribosome-nascent chain (R-RNC) complex, cotranslationally recruits its own unprocessed mRNA through transient docking to the ER membrane and translational pausing, therefore facilitating efficient IRE1-mediated XBP1 mRNA isoform 2 production. In endothelial cells (EC), associated with KDR, promotes IRE1-mediated XBP1 mRNA isoform 2 productions in a vascular endothelial growth factor (VEGF)-dependent manner, leading to EC proliferation and angiogenesis. Functions as a negative feed-back regulator of the potent transcription factor XBP1 isoform 2 protein levels through proteasome-mediated degradation, thus preventing the constitutive activation of the ER stress response signaling pathway. Inhibits the transactivation activity of XBP1 isoform 2 in myeloma cells. Acts as a weak transcriptional factor. Together with HDAC3, contributes to the activation of NFE2L2-mediated HMOX1 transcription factor gene expression in a PI(3)K/mTORC2/Akt-dependent signaling pathway leading to EC survival under disturbed flow/oxidative stress. Binds to the ER stress response element (ERSE) upon ER stress. Binds to the consensus 5'-GATGACGTGTGN(3)ATT-3' sequence related to cAMP responsive element (CRE)-like sequences. Binds the Tax-responsive element (TRE) present in the long terminal repeat (LTR) of T-cell leukemia virus type 1 (HTLV-I) and to the TPA response elements (TRE). Associates preferentially to the HDAC3 gene promoter region in a static flow-dependent manner. Binds to the CDH5/VE-cadherin gene promoter region. Isoform 2: Functions as a stress-inducible potent transcriptional activator during endoplasmic reticulum (ER) stress by inducing unfolded protein response (UPR) target genes via binding to the UPR element (UPRE). Up-regulates target genes encoding ER chaperones and ER-associated degradation (ERAD) components to enhance the capacity of productive folding and degradation mechanism, respectively, in order to maintain the homeostasis of the ER under ER stress. Plays a role in the production of immunoglobulins and interleukin-6 in the presence of stimuli required for plasma cell differentiation. Induces phospholipid biosynthesis and ER expansion. Contributes to the VEGF-induced endothelial cell (EC) growth and proliferation in a Akt/GSK-dependent and/or -independent signaling pathway, respectively, leading to beta-catenin nuclear translocation and E2F2 gene expression. Promotes umbilical vein EC apoptosis and atherosclerotisis development in a caspase-dependent signaling pathway, and contributes to VEGF-induced EC proliferation and angiogenesis in adult tissues under ischemic conditions. Involved in the regulation of endostatin-induced autophagy in EC through BECN1 transcriptional activation. Plays a role as an oncogene by promoting tumor progression: stimulates zinc finger protein SNAI1 transcription to induce epithelial-to-mesenchymal (EMT) transition, cell migration and invasion of breast cancer cells. Involved in adipocyte differentiation by regulating lipogenic gene expression during lactation. Plays a role in the survival of both dopaminergic neurons of the substantia nigra pars compacta (SNpc), by maintaining protein homeostasis and of myeloma cells. Increases insulin sensitivity in the liver as a response to a high carbohydrate diet, resulting in improved glucose tolerance. Improves also glucose homeostasis in an ER stress- and/or insulin-independent manner through both binding and proteasome-induced degradation of the transcription factor FOXO1, hence resulting in suppression of gluconeogenic genes expression and in a reduction of blood glucose levels. Controls the induction of de novo fatty acid synthesis in hepatocytes by regulating the expression of a subset of lipogenic genes in an ER stress- and UPR-independent manner. Associates preferentially to the HDAC3 gene promoter region in a disturbed flow-dependent manner. Binds to the BECN1 gene promoter region. Binds to the CDH5/VE-cadherin gene promoter region. Binds to the ER stress response element (ERSE) upon ER stress. Binds to the 5'-CCACG-3' motif in the PPARG promoter.
Protein Name X-Box-Binding Protein 1
Xbp-1
Tax-Responsive Element-Binding Protein 5
Treb-5 Cleaved Into - X-Box-Binding Protein 1 - Cytoplasmic Form - X-Box-Binding Protein 1 - Luminal Form
Database Links Reactome: R-HSA-381038 P17861-2
Reactome: R-HSA-381070 P17861-2
Reactome: R-HSA-381183 P17861-2
Cellular Localisation Endoplasmic Reticulum
Colocalizes With Ern1 And Kdr In The Endoplasmic Reticulum In Endothelial Cells In A Vascular Endothelial Growth Factor (Vegf)-Dependent Manner
Isoform 1: Nucleus
Cytoplasm
Endoplasmic Reticulum Membrane
Single-Pass Type Ii Membrane Protein
Peripheral Membrane Protein
Membrane
Shows No Preferential Localization To Either The Nucleus Or The Cytoplasm
Shuttles Between The Nucleus And The Cytoplasm In A Crm1-Dependent Manner
Localizes Predominantly At The Endoplasmic Reticulum Membrane As A Membrane-Spanning Protein
Whereas May Be Only Marginally Localized On The Cytosolic Side Of The Er Membrane As A Peripheral Membrane
Isoform 2: Nucleus
Localizes Predominantly In The Nucleus
Colocalizes In The Nucleus With Sirt1
Translocates Into The Nucleus In A Pik3r-
Er Stress-Induced- And/Or Insulin-Dependent Manner
X-Box-Binding Protein 1
Cytoplasmic Form: Cytoplasm
Nucleus
Localizes In The Cytoplasm And Nucleus After Hm13/Spp-Mediated Intramembranaire Proteolytic Cleavage Of Isoform 1
Alternative Antibody Names Anti-X-Box-Binding Protein 1 antibody
Anti-Xbp-1 antibody
Anti-Tax-Responsive Element-Binding Protein 5 antibody
Anti-Treb-5 Cleaved Into - X-Box-Binding Protein 1 - Cytoplasmic Form - X-Box-Binding Protein 1 - Luminal Form antibody
Anti-XBP1 antibody
Anti-TREB5 antibody
Anti-XBP2 antibody

Information sourced from Uniprot.org

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