Datasheet A03090 Anti-NOX5 Antibody

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Product datasheet Anti-NOX5 Antibody Catalog Number: A03090 BOSTER BIOLOGICAL TECHNOLOGY Special NO.1, International Enterprise Center, 2nd Guanshan Road, Wuhan, China Web: www.boster.com.cn Phone: +86 27 67845390 Fax: +86 27 67845390 Email: [email protected] Basic Information Product Name Anti-NOX5 Antibody Gene Name NOX5 Source Rabbit IgG Species Reactivity human Tested Application WB,FCM,Direct ELISA,ICC/IF Contents 500ug/ml antibody with PBS ，0.02% NaN3 , 1mg BSA and 50% glycerol. Immunogen E. coli-derived human NOX5 recombinant protein (Position: E13-F197). Purification Immunogen affinity purified. Observed MW 86KD Dilution Ratios Western blot: 1:500-2000 Flow Cytometry: 1-3μg/1x106 cells Direct ELISA： 1:100-1000 Immunocytochemistry/Immunofluorescence (ICC/IF): 1:50-400 Storage 12 months from date of receipt，-20℃ as supplied.6 months 2 to 8℃ after reconstitution. Avoid repeated freezing and thawing Background Information NOX5(Nadph Oxidase 5), also known as NOX5A or NOX5B, is a protein which in humans is encoded by the NOX5 gene. The International Radiation Hybrid Mapping Consortium mapped the NOX5 gene to chromosome 15. NOX5 is a novel NADPH oxidase that generates superoxide and functions as an H+ channel in a Ca2+-dependent manner. It is found that, when heterologously expressed, NOX5 was quiescent in unstimulated cells. However, in response to elevations of the cytosolic Ca2+ concentration, it generated large amounts of superoxide. Using RT- PCR and Southern and Western blot analyses, NOX5 was identified as a flavin-containing Ca2+-dependent oxidase present in hairy leukemic cells (HC), but not normal B cells. Reference Anti-NOX5 Antibody被引用在1文献中。 CRISPR-Cas9 Mediated NOX4 Knockout Inhibits Cell Proliferation and Invasion in HeLa Cells | Jafari N, Kim H, PubMed:28099519 Park R, Li L, Jang M, Morris AJ, Park J, Huang C. | PLoS One. 2017 Jan 18;12(1):e0170327. doi: 10.1371/journal.pone.0170327. eCollection 2017. FOR RESEARCH USE ONLY. NOT FOR DIAGNOSTIC AND CLINICAL USE. 1 Product datasheet Anti-NOX5 Antibody Catalog Number: A03090 BOSTER BIOLOGICAL TECHNOLOGY Special NO.1, International Enterprise Center, 2nd Guanshan Road, Wuhan, China Web: www.boster.com.cn Phone: +86 27 67845390 Fax: +86 27 67845390 Email: [email protected] Selected Validation Data Figure 1. Western blot analysis of NOX5 using anti-NOX5 antibody (A03090). The sample well of each lane was loaded with 50ug of sample under reducing conditions. Lane 1: human Hela whole cell lysate,Lane 2: human placenta tissue lysates,Lane 3: human SGC-7901 whole cell lysate,Lane 4: human Jurkat whole cell lysate,Lane 5: human THP-1 whole cell lysate. probed with a goat anti- rabbit IgG-HRP secondary antibody . The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) A specific band was detected for NOX5 at approximately 86KD. The expected band size for NOX5 is at 86KD. FOR RESEARCH USE ONLY. NOT FOR DIAGNOSTIC AND CLINICAL USE. 2 Powered by TCPDF (www.tcpdf.org).

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2020.05.13.092460V1.Full.Pdf
bioRxiv preprint doi: https://doi.org/10.1101/2020.05.13.092460; this version posted May 15, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. An adaptive pre-DNA-damage-response protects genome integrity Sandrine Ragu1,2, Gabriel Matos-Rodrigues1,2, Nathalie Droin3, Aurélia Barascu1, Sylvain Caillat4, Gabriella Zarkovic5, Capucine Siberchicot6, Elodie Dardillac1,2, Camille Gelot1, Juan Pablo Radicella6, Alexander A. Ishchenko5, Jean-Luc Ravanat4, Eric Solary3 and Bernard S. Lopez1,2 * 1Institut Cochin, INSERM U1016, UMR 8104 CNRS, Université de Paris, Paris-Descartes, Equipe Labellisée Ligue Contre le Cancer 24 rue du Faubourg St Jacques, 75014 Paris, France 2CNRS UMR 8200, Institut de Cancérologie Gustave-Roussy, Université Paris Saclay, 114 Rue Edouard Vaillant, 94805 Villejuif, France. 3Institut de Cancérologie Gustave-Roussy, INSERM U1170, Université Paris Saclay, Equipe Labellisée Ligue Contre le Cancer 114 Rue Edouard Vaillant, 94805 Villejuif, France. 4CEA, INAC-SCIB-LAN, Université Grenoble Alpes, F-38000 Grenoble. 5 Groupe «Réparation de l'ADN», Equipe Labellisée par la Ligue Nationale contre le Cancer, CNRS UMR 8200, Gustave Roussy, Université Paris Saclay, F-94805 Villejuif, France 6Institute of Cellular and Molecular Radiobiology, Inst. de Biologie François Jacob, CEA, Université de Paris, Université Paris-Saclay, F-92260 Fontenay aux Roses, France *Correspondence to: Bernard S. Lopez. [email protected] Running title: Adapt cell response to stress severity 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.05.13.092460; this version posted May 15, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder.
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Identifizierung Und Charakterisierung Von T-Zell-Definierten Antigenen
Identifizierung und Charakterisierung von Zielantigenen alloreaktiver zytotoxischer T-Zellen mittels cDNA-Bank-Expressionsklonierung in akuten myeloischen Leukämien Dissertation zur Erlangung des Grades Doktor der Naturwissenschaften am Fachbereich Biologie der Johannes Gutenberg-Universität Mainz Sabine Domning Mainz, 2012 Fachbereich Biologie der Johannes Gutenberg-Universität Mainz Dekan: 1.Berichterstatter: 2.Berichterstatter: Tag der mündlichen Prüfung: ZUSAMMENFASSUNG Zusammenfassung Allogene hämatopoetische Stammzelltransplantationen (HSZTs) werden insbesondere zur Behandlung von Patienten mit Hochrisiko-Leukämien durchgeführt. Dabei bewirken T- Zellreaktionen gegen Minorhistokompatibilitätsantigene (mHAgs) sowohl den therapeutisch erwünschten graft-versus-leukemia (GvL)-Effekt als auch die schädigende graft-versus-host (GvH)- Erkrankung. Für die Identifizierung neuer mHAgs mittels des T-Zell-basierten cDNA- Expressionsscreenings waren leukämiereaktive T-Zellpopulationen durch Stimulation naïver CD8+- T-Lymphozyten gesunder HLA-Klasse I-identischer Buffy Coat-Spender mit Leukämiezellen von Patienten mit akuter myeloischer Leukämie (AML) generiert worden (Albrecht et al., Cancer Immunol. Immunother. 60:235, 2011). Im Rahmen der vorliegenden Arbeit wurde mit diesen im AML-Modell des Patienten MZ529 das mHAg CYBA-72Y identifiziert. Es resultiert aus einem bekannten Einzelnukleotidpolymorphismus (rs4673: CYBA-242T/C) des Gens CYBA (kodierend für Cytochrom b-245 α-Polypeptid; syn.: p22phox), der zu einem Austausch von Tyrosin (Y) zu Histidin (H) an Aminosäureposition 72 führt. Das mHAg wurde von T-Lymphozyten sowohl in Assoziation mit HLA-B*15:01 als auch mit HLA-B*15:07 erkannt. Eine allogene T-Zellantwort gegen CYBA-72Y wurde in einem weiteren AML-Modell (MZ987) beobachtet, die ebenso wie in dem AML-Modell MZ529 polyklonal war. Insgesamt konnte bei drei von fünf getesteten HLA-B*15:01-positiven Buffy Coat-Spendern, die homozygot für CYBA-72H (H/H) waren, eine CYBA-72Y-spezifische T- Zellantwort generiert werden.
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Figure S1. HAEC ROS Production and ML090 NOX5-Inhibition
Figure S1. HAEC ROS production and ML090 NOX5-inhibition. (a) Extracellular H2O2 production in HAEC treated with ML090 at different concentrations and 24 h after being infected with GFP and NOX5-β adenoviruses (MOI 100). **p< 0.01, and ****p< 0.0001 vs control NOX5-β-infected cells (ML090, 0 nM). Results expressed as mean ± SEM. Fold increase vs GFP-infected cells with 0 nM of ML090. n= 6. (b) NOX5-β overexpression and DHE oxidation in HAEC. Representative images from three experiments are shown. Intracellular superoxide anion production of HAEC 24 h after infection with GFP and NOX5-β adenoviruses at different MOIs treated or not with ML090 (10 nM). MOI: Multiplicity of infection. Figure S2. Ontology analysis of HAEC infected with NOX5-β. Ontology analysis shows that the response to unfolded protein is the most relevant. Figure S3. UPR mRNA expression in heart of infarcted transgenic mice. n= 12-13. Results expressed as mean ± SEM. Table S1: Altered gene expression due to NOX5-β expression at 12 h (bold, highlighted in yellow). N12hvsG12h N18hvsG18h N24hvsG24h GeneName GeneDescription TranscriptID logFC p-value logFC p-value logFC p-value family with sequence similarity NM_052966 1.45 1.20E-17 2.44 3.27E-19 2.96 6.24E-21 FAM129A 129. member A DnaJ (Hsp40) homolog. NM_001130182 2.19 9.83E-20 2.94 2.90E-19 3.01 1.68E-19 DNAJA4 subfamily A. member 4 phorbol-12-myristate-13-acetate- NM_021127 0.93 1.84E-12 2.41 1.32E-17 2.69 1.43E-18 PMAIP1 induced protein 1 E2F7 E2F transcription factor 7 NM_203394 0.71 8.35E-11 2.20 2.21E-17 2.48 1.84E-18 DnaJ (Hsp40) homolog.
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THE ROLE of NADPH OXIDASE in NEURITE OUTGROWTH and ZEBRAFISH NEURODEVELOPMENT Cory J
Purdue University Purdue e-Pubs Open Access Dissertations Theses and Dissertations January 2016 THE ROLE OF NADPH OXIDASE IN NEURITE OUTGROWTH AND ZEBRAFISH NEURODEVELOPMENT Cory J. Weaver Purdue University Follow this and additional works at: https://docs.lib.purdue.edu/open_access_dissertations Recommended Citation Weaver, Cory J., "THE ROLE OF NADPH OXIDASE IN NEURITE OUTGROWTH AND ZEBRAFISH NEURODEVELOPMENT" (2016). Open Access Dissertations. 1476. https://docs.lib.purdue.edu/open_access_dissertations/1476 This document has been made available through Purdue e-Pubs, a service of the Purdue University Libraries. Please contact [email protected] for additional information. Graduate School Form 30 Updated 12/26/2015 PURDUE UNIVERSITY GRADUATE SCHOOL Thesis/Dissertation Acceptance This is to certify that the thesis/dissertation prepared By Cory J. Weaver Entitled THE ROLE OF NADPH OXIDASES IN NEURITE OUTGROWTH AND ZEBRAFISH NEURODEVELOPMENT For the degree of Doctor of Philosophy Is approved by the final examining committee: Daniel M. Suter Chair Yuk Fai Leung Christopher J. Staiger Joseph P. Ogas To the best of my knowledge and as understood by the student in the Thesis/Dissertation Agreement, Publication Delay, and Certification Disclaimer (Graduate School Form 32), this thesis/dissertation adheres to the provisions of Purdue University’s “Policy of Integrity in Research” and the use of copyright material. Approved by Major Professor(s): Daniel M. Suter Daoguo Zhou 5/14/2016 Approved by: Head of the Departmental Graduate Program Date i
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Integration of Text Mining with Systems Biology Provides New Insight Into the Pathogenesis of Diabetic Neuropathy
INTEGRATION OF TEXT MINING WITH SYSTEMS BIOLOGY PROVIDES NEW INSIGHT INTO THE PATHOGENESIS OF DIABETIC NEUROPATHY by Junguk Hur A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy (Bioinformatics) in The University of Michigan 2010 Doctoral Committee: Professor Eva L. Feldman, Co-Chair Professor Hosagrahar V. Jagadish, Co-Chair Professor Matthias Kretzler Research Assistant Professor Maureen Sartor Professor David J. States, University of Texas Junguk Hur © 2010 All Rights Reserved DEDICATION To my family ii ACKNOWLEDGMENTS Over the past few years, I have been tremendously fortunate to have the company and mentorship of the most wonderful and smartest scientists I know. My advisor, Prof. Eva Feldman, guided me through my graduate studies with constant support, encouragement, enthusiasm and infinite patience. I would like to thank her for being a mom in my academic life and raising me to become a better scientist. I would also like to thank my co-advisors Prof. H. V. Jagadish and Prof. David States. They provided sound advice and inspiration that have been instrumental in my Ph.D. study. I am also very grateful to Prof. Matthias Kretzler and Prof. Maureen Sartor for being an active part of my committee as well as for their continuous encouragement and guidance of my work. I would also like to thank Prof. Daniel Burns, Prof. Margit Burmeister, Prof. Gil Omenn and Prof. Brain Athey from the Bioinformatics Program, who have been very generous with their support and advice about academic life. I am also very grateful to Sherry, Julia and Judy, who helped me through the various administrative processes with cheerful and encouraging dispositions.
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And ROS-Related Targets Junguk Hur1,2, Kelli a Sullivan2, Adam D Schuyler4, Yu Hong2, Manjusha Pande2,3, David J States5, H V Jagadish1,3, Eva L Feldman1,2,3*
Hur et al. BMC Medical Genomics 2010, 3:49 http://www.biomedcentral.com/1755-8794/3/49 RESEARCH ARTICLE Open Access Literature-based discovery of diabetes- and ROS-related targets Junguk Hur1,2, Kelli A Sullivan2, Adam D Schuyler4, Yu Hong2, Manjusha Pande2,3, David J States5, H V Jagadish1,3, Eva L Feldman1,2,3* Abstract Background: Reactive oxygen species (ROS) are known mediators of cellular damage in multiple diseases including diabetic complications. Despite its importance, no comprehensive database is currently available for the genes associated with ROS. Methods: We present ROS- and diabetes-related targets (genes/proteins) collected from the biomedical literature through a text mining technology. A web-based literature mining tool, SciMiner, was applied to 1,154 biomedical papers indexed with diabetes and ROS by PubMed to identify relevant targets. Over-represented targets in the ROS-diabetes literature were obtained through comparisons against randomly selected literature. The expression levels of nine genes, selected from the top ranked ROS-diabetes set, were measured in the dorsal root ganglia (DRG) of diabetic and non-diabetic DBA/2J mice in order to evaluate the biological relevance of literature-derived targets in the pathogenesis of diabetic neuropathy. Results: SciMiner identified 1,026 ROS- and diabetes-related targets from the 1,154 biomedical papers (http://jdrf. neurology.med.umich.edu/ROSDiabetes/). Fifty-three targets were significantly over-represented in the ROS-diabetes literature compared to randomly selected literature. These over-represented targets included well-known members of the oxidative stress response including catalase, the NADPH oxidase family, and the superoxide dismutase family of proteins.
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Effects of Curcumin on Canine Semen Parameters and Expression of NOX5 Gene in Cryopreserved Spermatozoa
Archive of SID ORIGINAL Veterinary Research Forum. 2019; 10 (3) 221 – 226 Veterinary ARTICLE doi: 10.30466/vrf.2019.76137.2015 Research Forum Journal Homepage: vrf.iranjournals.ir Effects of curcumin on canine semen parameters and expression of NOX5 gene in cryopreserved spermatozoa Parisa Aparnak1, Adel Saberivand2* 1 PhD Candidate, Department of Clinical Sciences, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran; 2 Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Tabriz, Tabriz, Iran. Article Info Abstract Article history: Canine seminal plasma contains antioxidant enzymes to protect sperm against internally generated ROS. These enzymes are removed from seminal plasma during the process of Received: 02 December 2017 cryopreservation. The freezing/thawing process can cause some morphological and Accepted: 21 February 2018 functional changes via ice crystallization and osmolality imbalance. The present study was Available online: 15 September 2019 conducted to evaluate the effects of curcumin supplementation on sperm total count, motility, progressive motility, viability, morphology, total antioxidant capacity (TAC), DNA Key words: integrity and NOX5 gene expression of dog frozen semen. The pooled semen was allocated to fresh (Group 1) and frozen (Group 2) controls, curcumin (2.50 mM) (Group 3) and curcumin Cryopreservation (5.00 mM), (Group 4). Sperm parameters including total sperm count, morphology, motility, Curcumin progressive motility, sperm concentration and DNA integrity in addition to TAC were Dog evaluated in fresh and frozen-thawed semen samples. Real-time RT-PCR was used to NOX5 investigate NOX5 and GADPH (reference gene) genes expressions. Curcumin at 2.50 mM Total antioxidant capacity provided a greater protective effect on the DNA integrity compared to 5.00 mM and control groups.
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Anti-NOX5 (Internal Region) Polyclonal Antibody (DPAB-DC3268) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
Anti-NOX5 (internal region) polyclonal antibody (DPAB-DC3268) This product is for research use only and is not intended for diagnostic use. PRODUCT INFORMATION Antigen Description This gene is predominantly expressed in the testis and lymphocyte-rich areas of spleen and lymph nodes. It encodes a calcium-dependen NADPH oxidase that generates superoxide, and functions as a calcium-dependent proton channel that may regulate redox-dependent processes in lymphocytes and spermatozoa. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. Specificity This antibody is expected to recognize all reported isoforms (NP_078781.3; NP_001171708.1; NP_001171709.1). Immunogen A synthetic peptide corresponding to amino acids at internal region of human NOX5. The sequence is C-EWHPFTISSAPEQKD Source/Host Goat Species Reactivity Human Purification Antigen affinity purification Conjugate Unconjugated Applications WB (Tissue lysate), ELISA, Format Liquid Concentration 0.5 mg/mL Size 100 μg Buffer In 0.5 mg/mL in Tris saline, pH7.3 (0.5% BSA, 0.02% sodium azide) Preservative 0.02% Sodium Azide Storage Store at -20°C.Aliquot to avoid repeated freezing and thawing. GENE INFORMATION Gene Name NOX5 NADPH oxidase, EF-hand calcium binding domain 5 [ Homo sapiens (human) ] 45-1 Ramsey Road, Shirley, NY 11967, USA Email: [email protected] Tel: 1-631-624-4882 Fax: 1-631-938-8221 1 © Creative Diagnostics All Rights Reserved Official Symbol NOX5 Synonyms NOX5; NADPH oxidase, EF-hand calcium binding domain 5; NADPH oxidase 5; Entrez Gene ID 79400 Protein Refseq NP_001171708 UniProt ID A3QRJ0 Chromosome Location 15q23 Function NADP binding; calcium ion binding; flavin adenine dinucleotide binding; heme binding 45-1 Ramsey Road, Shirley, NY 11967, USA Email: [email protected] Tel: 1-631-624-4882 Fax: 1-631-938-8221 2 © Creative Diagnostics All Rights Reserved.
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NADPH Oxidases in Parkinson's Disease
Belarbi et al. Molecular Neurodegeneration (2017) 12:84 DOI 10.1186/s13024-017-0225-5 REVIEW Open Access NADPH oxidases in Parkinson’s disease: a systematic review Karim Belarbi1, Elodie Cuvelier1, Alain Destée1, Bernard Gressier1 and Marie-Christine Chartier-Harlin1,2* Abstract Parkinson’s disease (PD) is a progressive movement neurodegenerative disease associated with a loss of dopaminergic neurons in the substantia nigra of the brain. Oxidative stress, a condition that occurs due to imbalance in oxidant and antioxidant status, is thought to play an important role in dopaminergic neurotoxicity. Nicotinamide adenine dinucleotide phosphate (NADPH) oxidases are multi-subunit enzymatic complexes that generate reactive oxygen species as their primary function. Increased immunoreactivities for the NADPH oxidases catalytic subunits Nox1, Nox2 and Nox4 have been reported in the brain of PD patients. Furthermore, knockout or genetic inactivation of NADPH oxidases exert a neuroprotective effect and reduce detrimental aspects of pathology in experimental models of the disease. However, the connections between NADPH oxidases and the biological processes believed to contribute to neuronal death are not well known. This review provides a comprehensive summary of our current understanding about expression and physiological function of NADPH oxidases in neurons, microglia and astrocytes and their pathophysiological roles in PD. It summarizes the findings supporting the role of both microglial and neuronal NADPH oxidases in cellular disturbances associated with PD such as neuroinflammation, alpha-synuclein accumulation, mitochondrial and synaptic dysfunction or disruption of the autophagy-lysosome system. Furthermore, this review highlights different steps that are essential for NADPH oxidases enzymatic activity and pinpoints major obstacles to overcome for the development of effective NADPH oxidases inhibitors for PD.
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Program Book
The Genetics Society of America Conferences 15th International Xenopus Conference August 24-28, 2014 • Pacific Grove, CA PROGRAM GUIDE LEGEND Information/Guest Check-In Disabled Parking E EV Charging Station V Beverage Vending Machine N S Ice Machine Julia Morgan Historic Building W Roadway Pedestrian Pathway Outdoor Group Activity Area Program and Abstracts Meeting Organizers Carole LaBonne, Northwestern University John Wallingford, University of Texas at Austin Organizing Committee: Julie Baker, Stanford Univ Chris Field, Harvard Medical School Carmen Domingo, San Francisco State Univ Anna Philpott, Univ of Cambridge 9650 Rockville Pike, Bethesda, Maryland 20814-3998 Telephone: (301) 634-7300 • Fax: (301) 634-7079 E-mail: [email protected] • Web site: genetics-gsa.org Thank You to the Following Companies for their Generous Support Platinum Sponsor Gold Sponsors Additional Support Provided by: Carl Zeiss Microscopy, LLC Monterey Convention & Gene Tools, LLC Visitors Bureau Leica Microsystems Xenopus Express 2 Table of Contents General Information ........................................................................................................................... 5 Schedule of Events ............................................................................................................................. 6 Exhibitors ........................................................................................................................................... 8 Opening Session and Plenary/Platform Sessions ............................................................................
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Datasheet A03119 Anti-NOX5 Antibody
Product datasheet Anti-NOX5 Antibody Catalog Number: A03119 BOSTER BIOLOGICAL TECHNOLOGY Special NO.1, International Enterprise Center, 2nd Guanshan Road, Wuhan, China Web: www.boster.com.cn Phone: +86 27 67845390 Fax: +86 27 67845390 Email: [email protected] Basic Information Product Name Anti-NOX5 Antibody Gene Name NOX5 Source Rabbit IgG Species Reactivity human Tested Application WB,IHC-P,FCM,Direct ELISA Contents 500ug/ml antibody with PBS ，0.02% NaN3 , 1mg BSA and 50% glycerol. Immunogen E.coli-derived human NOX5 recombinant protein (Position: A21-F765). Purification Immunogen affinity purified. Observed MW 86KD Dilution Ratios Western blot: 1:500-2000 Immunohistochemistry in paraffin section IHC-(P)： 1:50-400 Flow cytometry (FCM)： 1-3μg/1x106 cells Direct ELISA： 1:100-1000 Storage 12 months from date of receipt，-20℃ as supplied.6 months 2 to 8℃ after reconstitution. Avoid repeated freezing and thawing Background Information NOX5(Nadph Oxidase 5), also known as NOX5A or NOX5B, is a protein which in humans is encoded by the NOX5 gene. The International Radiation Hybrid Mapping Consortium mapped the NOX5 gene to chromosome 15. NOX5 is a novel NADPH oxidase that generates superoxide and functions as an H+ channel in a Ca2+-dependent manner. It is found that, when heterologously expressed, NOX5 was quiescent in unstimulated cells. However, in response to elevations of the cytosolic Ca2+ concentration, it generated large amounts of superoxide. Using RT- PCR and Southern and Western blot analyses, NOX5 was identified as a flavin-containing Ca2+-dependent oxidase present in hairy leukemic cells (HC), but not normal B cells.
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NOX5 Antibody (RQ4593)
NOX5 Antibody (RQ4593) Catalog No. Formulation Size RQ4593 0.5mg/ml if reconstituted with 0.2ml sterile DI water 100 ug Bulk quote request Availability 1-3 business days Species Reactivity Human Format Antigen affinity purified Clonality Polyclonal (rabbit origin) Isotype Rabbit IgG Purity Antigen affinity purified Buffer Lyophilized from 1X PBS with 2% Trehalose and 0.025% sodium azide UniProt Q96PH1 Applications Western blot : 0.5-1ug/ml Immunofluorescence : 2-4ug/ml Direct ELISA : 0.1-0.5ug/ml (human recombinant protein) Western blot testing of human 1) HeLa, 2) placenta, 3) SCG-7901, 4) Jurkat and 5) THP-1 lysate with NOX5 antibody at 0.5ug/ml. Predicted molecular weight: ~86 kDa. Immunofluorescent staining of FFPE human HeLa cells with NOX5 antibody (green) at 2ug/ml and DAPI nuclear stain (blue). HIER: steam section in pH6 citrate buffer for 20 min. Description NOX5 (Nadph Oxidase 5) is a protein which in humans is encoded by the NOX5 gene. The International Radiation Hybrid Mapping Consortium mapped the NOX5 gene to chromosome 15. NOX5 is a novel NADPH oxidase that generates superoxide and functions as an H+ channel in a Ca2+-dependent manner. It is found that, when heterologously expressed, NOX5 was quiescent in unstimulated cells. However, in response to elevations of the cytosolic Ca2+ concentration, it generated large amounts of superoxide. Using RT-PCR and Southern and Western blot analyses, NOX5 was identified as a flavin-containing Ca2+-dependent oxidase present in hairy leukemic cells (HC), but not normal B cells. Application Notes Optimal dilution of the NOX5 antibody should be determined by the researcher.
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