Antibodies for Unfolded Protein Response

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Novus-lu-2945 Antibodies for Unfolded rotein Response Unfolded roteins ER lumen GR78 IRE-1 GR78 ERK Cytosol GR78 TRAF2 ASK1 JNK Activator Intron RIDD elf2α Degraded mrna XB1 mrna Translation XB1-S (p50) XB1-S Nucleus Chaperones Learn more Lipid novusbio.com Synthesis Amino Acid Metabolism Redox Homeostasis Cha Lipid

INTRODUCTION The unfolded protein response (UR) is a signaling mechanism activated in eukaryotic cells in response to endoplasmic reticulum (ER) stress, an accumulation of unfolded proteins in the ER lumen. Conditions such as high protein demand, viral infection, mutant protein expression, hypoxia, energy deprivation, or exposure to excessive oxidative stress can trigger UR or ER stress. UR serves three major functions: (i) blocking protein translation to restore homeostasis; (ii) positive regulation of protein folding related molecular chaperones; and (iii) up-regulation of signaling pathways responsible for targeting mis-/un-folded proteins in ER for ubiquitination mediated degradation. When ER stress is not relieved, UR can induce apoptosis and cause cell death. A sustained over-activation of UR is known to be involved in many human diseases including cancer, hyperglycemia, autoimmune conditions, hepatic disorders, retinopathies, acute lung injury and neuro-degeneration. Accordingly, a complete mechanistic understanding of UR signaling is critical for the evaluation of its biological effects in normal and/or disease conditions, and for developing preventive as well as therapeutic measures against UR associated diseases. Learn more novusbio.com Learn more novusbio.com

Regulation of UR Signaling UR signaling is regulated via three major effector proteins which localize to the ER: inositol-requiring enzyme 1 (IRE1), activating transcription factor 6 (), and protein kinase RNA-like ER kinase (ERK). These proteins are maintained in their inactive/membrane bound state through binding to glucose response protein 78 (GR78/Bi). Upon interaction with unfolded proteins, GR78 is released from the UR effector proteins, which leads to their activation. UR is generally activated by an orchestrated interplay of all three arms of the ER stress signaling (see the pathway image). UR induction in mammalian cells Unfolded roteins ER lumen GR78 GR78 IRE-1 ERK GR78 (p90) Cytosol TRAF2 JNK Activator ASK1 Intron RIDD elf2α S1, S2 Degraded mrna Translation XB1 mrna XB1-S Golgi (p50) XB1-S Nucleus Chaperones Lipid Synthesis ERAD Amino Acid Metabolism Redox Homeostasis Apoptosis Chaperones Lipid Synthesis Learn more novusbio.com 1

Inositol-Requiring Enzyme 1 Alpha (IRE1 Alpha) IRE1 alpha, predicted mol. wt. 109.7 kda, is an ER resident protein which is expressed ubiquitously in all tissue types. It is a single-pass type I membrane protein which localizes to the ER lumen, and interacts with several other proteins, including GR78, DAB2I, TRAF2, and TAOK3. Upon UR activation, IRE1 alpha undergoes dimerization/auto-phosphorylation mediated activation (e.g. phospho-ser724 IRE1 alpha). The active form of IRE1 alpha then induces the splicing of mrna encoding the transcription factor, XB1. Removal of an intron from XB1 leads to the expression of an active form of XB1 (XB1-S, the spliced form) which positively regulates ER chaperones, as well as genes coding for the ER-associated protein degradation (ERAD) pathway and lipid metabolism. Through XB1-independent pathways, IRE1 binds to tumour necrosis factor (TNF) receptor-associated factor 2 (TRAF2) and induces JUN amino-terminal kinase (JNK) activation. This interaction is known to modulate autophagic and apoptotic cell death. IRE1 s endo-ribonuclease activity also induces Regulated IRE1-Dependent mrna Decay (RIDD) which is implicated in lipid anabolism and apoptosis. IRE1 alpha is also involved in the processes of cell cycle arrest, insulin metabolism, angiogenesis, and regulation of macroautophagy. pser724 IRE1 alpha Antibody [NB100-2323*] Western blot (WB) detection of pser724 IRE1 alpha Min6 cells treated with increasing concentrations of glucose for 3 hours prior to lysate preparation. IRE1 alpha Antibody (Total) [NB100-2324] WB detection of total IRE1 alpha protein in lysates from Min6 cells which were transfected with GF-siRNA or Ire1-siRNA. XB1 Antibody (S Isoform) [MAB4257] FLOW analysis of FA fixed and saponin permeabilized RMI 8226 human multiple myeloma cells using XB1S antibody (filled histogram) or isotype control (MAB002, open histogram) with ACconjugated secondary antibody (F0101B). TRAF2 Antibody (33A1293) [NB100-56715] IHC- analysis of a formalin-fixed tissue section of human transitional cell carcinoma of the urinary bladder. Signal was developed using HR-DAB method and the nuclei were counterstained using hematoxylin. *Most cited phospho-ire1 alpha antibody among offerings from all antibody companies. 2 Learn more novusbio.com

Activating Transcription Factor 6 () is a transmembrane glycoprotein and transcription activator, which functions to initiate the UR during ER stress. The predicted molecular weight of the canonical form of is 74.5 kda. However, may be detected at approximately 90 kda in Western blot, as the protein often undergoes glycosylation, forming the p90 version of. Upon sensing of ER stress, p90 is transported to the Golgi apparatus, where it is processed through site 1 protease (S1) and S2 protease, releasing the N-terminal processed cam-dependent ATF-6 alpha form (cytosolic/cleaved-, p50). The cleaved p50 form of then translocates to the nucleus of the cell, where it binds DNA on the ER stress response element (ERSE) for regulation of ER-associated protein degradation (ERAD) and UR genes. In addition to mediating the stress response through ERSE and ERAD, p50 also regulates transcription of the XB1 protein, as well as the induction of apoptosis, regulation of transcription from RNA polymerase II promoter, occular tissue development and visual perception. Antibody (70B1413.1) [NB1-40256] WB analysis of HEK293 cells transfected with full-length, or with partial protein (AA 1-373), and the non-transfected control cells. Antibody [NB1-75478] ICC/IF analysis of HeLa cells using antibody with detection employing FITC conjugated secondary (green). Nuclei were counterstained with DAI (blue). GR78/HSA5 Antibody [NB100-56411] WB analysis of lysates from HeLa cells (A), human liver (B), mouse liver (C), and rat liver (D) tissues using GR78 antibody with detection employing HR labelled secondary and icotect ECL substrate. ERp72 Antibody [NB2-16371] IHC analysis of a formalin fixed and paraffinembedded tissue section of breast cancer using ERp72 antibody with HR-DAB detection. Nuclei were counterstained using hematoxylin. Learn more novusbio.com 3

rotein kinase RNA-like ER Kinase (ERK) ERK, predicted molecular weight 125.2 kda, is a transmembrane protein kinase belonging to the EK family of proteins, and is best known for its role in insulin processing. During ER stress responses and activation of the UR, ERK functions to inhibit translation of new proteins. Specifically, ER stress causes oligomerization of the ER luminal domain (N-terminal) of ERK, which facilitates the trans-autophosphorylation of ERK s cytoplasmic kinase domain (C-terminal) at Thr-982. Thus, the phosphorylated form of ERK at the Thr 982 site is often assessed as a measure of ER stress. Activated ERK phosphorylates eukaryotic translation initiation factor 2 alpha (eif2 alpha), which inhibits translation of proteins to maintain homeostasis. hospho-eif2 alpha does not impact the translation of, however. Upon accumulation, translocates to the nucleus, where it induces the expression of ER chaperones, autophagy/apoptosis genes (especially CHO), oxidative response genes, and activates amino acid metabolism signaling pathways. ERK facilitates cell cycle exit during UR, and is involved in the regulation of mitochondrial morphology as well as function. ERK Antibody [NB1-78017] WB analysis of lysates from ERK over-expressing 293T cells (lanes 1 & 2), Wild type MEFs (Lanes 3 & 4), and ERK knock-out MEFs (lanes 5 & 6). The MEFs were treated with vehicle (-) or Tunicamycin (+) for induction of ER stress. eif2a Antibody (3A7B11) [NB2-26296] ICC/IF analysis of HeLa cells using eif2a antibody with Dylight 488 (green) conjugated secondary antibody. Nuclei were counterstained with DAI (blue). Alpha-tubulin was labelled using anti-tubulin with Dylight 550 (red) conjugated secondary antibody. Antibody (739441) [MAB7218] ICC/IF analysis of Jurkat human acute T-cell leukemia cells using mab with NorthernLights 557- conjugated secondary antibody (red; Catalog # NL007). Specific staining was localized to nuclei and cytoplasm. GADD153/CHO Antibody (9C8) [NB600-1335] Simple Western lane view shows a specific band for CHO/GADD153 in 1.0 mg/ml of HeLa lysate. This experiment was performed under reducing conditions using the 12-230 kda separation system. 4 Learn more novusbio.com 2

ER Stress / UR Antibody Sampler ack This pack contains sample size antibodies against the top six UR markers: GR78, pire1 alpha (Ser724), total IRE1 alpha, XB1,, and CHO. See catalog number: NB2-52746 Related ublications Western Blot Handbook Organelle Markers Flyer Apoptosis oster Request print copies of these publications at www.novusbio.com/mailing-list Laverne more than a research assistant Laverne can help you with her unbiased review of proteins, pathways, diseases and post-translational modifications related to your target of interest. See ERN1 s related proteins below and visit www.novusbio.com/explorer to learn more about Laverne! HSA5 JNK TRAF2 ERK ERN1 CHO XB1S XB1 Learn more novusbio.com 5

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