Anti-SULT4A1 Polyclonal Antibody (CABT-BL5788) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use

Total Page：16

File Type：pdf, Size：1020Kb

Anti-SULT4A1 polyclonal antibody (CABT-BL5788) This product is for research use only and is not intended for diagnostic use. PRODUCT INFORMATION Product Overview Rabbit polyclonal antibody to Human SULT4A1. Antigen Description This gene encodes a member of the sulfotransferase family. The encoded protein is a brain- specific sulfotransferase believed to be involved in the metabolism of neurotransmitters. polymorphisms in this gene may be associated with susceptibility to schizophrenia. Immunogen A KLH conjugated synthetic peptide selected from the N-term of human SULT4A1 (region common to both isoforms a and b). Isotype IgG Source/Host Rabbit Species Reactivity Mouse, Human Purification Protein G purified Conjugate Unconjugated Cellular Localization Cytoplasmic Format Liquid Size 100 μg Buffer PBS Preservative 0.09% Sodium Azide Storage Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze/thaw cycles. BACKGROUND Introduction This gene encodes a member of the sulfotransferase family. The encoded protein is a brain- specific sulfotransferase believed to be involved in the metabolism of neurotransmitters. Polymorphisms in this gene may be associated with susceptibility to schizophrenia. [provided by RefSeq, Jul 2008] 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 GENE INFORMATION Entrez Gene ID 25830 Protein Refseq NP_055166 UniProt ID Q9BR01 Chromosome Location 22q13.2 Pathway Biological oxidations, organism-specific biosystem; Cytosolic sulfonation of small molecules, organism-specific biosystem; Metabolism, organism-specific biosystem; Phase II conjugation, organism-specific biosystem; Function sulfotransferase activity; transferase activity; 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.

Copy Link

Recommended publications

Identification of Potential Key Genes and Pathway Linked with Sporadic Creutzfeldt-Jakob Disease Based on Integrated Bioinformatics Analyses
medRxiv preprint doi: https://doi.org/10.1101/2020.12.21.20248688; this version posted December 24, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission. Identification of potential key genes and pathway linked with sporadic Creutzfeldt-Jakob disease based on integrated bioinformatics analyses Basavaraj Vastrad1, Chanabasayya Vastrad*2 , Iranna Kotturshetti 1. Department of Biochemistry, Basaveshwar College of Pharmacy, Gadag, Karnataka 582103, India. 2. Biostatistics and Bioinformatics, Chanabasava Nilaya, Bharthinagar, Dharwad 580001, Karanataka, India. 3. Department of Ayurveda, Rajiv Gandhi Education Society`s Ayurvedic Medical College, Ron, Karnataka 562209, India. * Chanabasayya Vastrad [email protected] Ph: +919480073398 Chanabasava Nilaya, Bharthinagar, Dharwad 580001 , Karanataka, India NOTE: This preprint reports new research that has not been certified by peer review and should not be used to guide clinical practice. medRxiv preprint doi: https://doi.org/10.1101/2020.12.21.20248688; this version posted December 24, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission. Abstract Sporadic Creutzfeldt-Jakob disease (sCJD) is neurodegenerative disease also called prion disease linked with poor prognosis. The aim of the current study was to illuminate the underlying molecular mechanisms of sCJD. The mRNA microarray dataset GSE124571 was downloaded from the Gene Expression Omnibus database. Differentially expressed genes (DEGs) were screened.
[Show full text]
Integrated Mrnaseq and Micrornaseq Data Analysis for Grade III Gliomas
7468 MOLECULAR MEDICINE REPORTS 16: 7468-7478, 2017 Integrated mRNAseq and microRNAseq data analysis for grade III gliomas JUNQIANG DAI1*, ZHITONG BING2*, YINIAN ZHANG1, QIAO LI1, LIANG NIU1, WENTAO LIANG1, GUOQIANG YUAN3, LEI DUAN1, HANG YIN1 and YAWEN PAN1,3 1Department of Neurosurgery, Lanzhou University Second Hospital, Lanzhou, Gansu 730030; 2Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou, Gansu 730000; 3Institute of Neurology, Lanzhou University Second Hospital, Lanzhou, Gansu 730030, P.R. China Received August 10, 2016; Accepted July 6, 2017 DOI: 10.3892/mmr.2017.7545 Abstract. The World Health Organization classification distin- represent 10% of primary brain tumors (2), which can infil- guishes four grades for gliomas. Grade III gliomas, which trate the surrounding brain parenchyma. Using standard are brain malignant brain tumors with variable biological therapeutic protocols, patients with malignant glioma have behavior and propensity, have been not widely investigated. different pathological appearances and clinical outcomes. The objective of the present study was to identify specific gene Treatments include surgery, radiation therapy, and chemo- modules and valuable hubs associated with gliomagenesis and therapy, however, there is no specialized treatment available. molecular signatures to assist in determining grade III glioma There are insufficient molecular targets relevant in the choice prognosis. mRNAseq and micro (mi)RNAseq data were of therapy, and their role in clinical trials requires validation. used to construct a co-expression network of gliomas using Novel therapeutic methods based on the specific mechanism weight gene co-expression network analysis, and revealed of high grade glioma carcinogenesis are required to improve the prognostic molecular signature of grade III gliomas.
[Show full text]
Apriorigwas, a New Pattern Mining Strategy for Detecting Genetic Variants Associated with Disease Through Interaction Effects
AprioriGWAS, a New Pattern Mining Strategy for Detecting Genetic Variants Associated with Disease through Interaction Effects Qingrun Zhang1*, Quan Long1*, Jurg Ott2,3 1 Department of Genetics and Genomic Sciences, Institute of Genomics and Multi-scale Biology, Icahn School of Medicine at Mount Sinai, New York, New York, United States of America, 2 Institute of Psychology, Chinese Academy of Sciences, Chaoyang District, Beijing, PR China, 3 Laboratory of Statistical Genetics, The Rockefeller University, New York, New York, United States of America Abstract Identifying gene-gene interaction is a hot topic in genome wide association studies. Two fundamental challenges are: (1) how to smartly identify combinations of variants that may be associated with the trait from astronomical number of all possible combinations; and (2) how to test epistatic interaction when all potential combinations are available. We developed AprioriGWAS, which brings two innovations. (1) Based on Apriori, a successful method in field of Frequent Itemset Mining (FIM) in which a pattern growth strategy is leveraged to effectively and accurately reduce search space, AprioriGWAS can efficiently identify genetically associated genotype patterns. (2) To test the hypotheses of epistasis, we adopt a new conditional permutation procedure to obtain reliable statistical inference of Pearson’s chi-square test for the 2|f contingency table generated by associated variants. By applying AprioriGWAS to age-related macular degeneration (AMD) data, we found that: (1) angiopoietin 1 (ANGPT1) and four retinal genes interact with Complement Factor H (CFH). (2) GO term ‘‘glycosaminoglycan biosynthetic process’’ was enriched in AMD interacting genes. The epistatic interactions newly found by AprioriGWAS on AMD data are likely true interactions, since genes interacting with CFH are retinal genes, and GO term enrichment also verified that interaction between glycosaminoglycans (GAGs) and CFH plays an important role in disease pathology of AMD.
[Show full text]
Transmission Disequilibrium Suggests a Role for the Sulfotransferase-4A1 Gene in Schizophrenia Mark D
American Journal of Medical Genetics Part B (Neuropsychiatric Genetics) 139B:69–72 (2005) Transmission Disequilibrium Suggests a Role for the Sulfotransferase-4A1 Gene in Schizophrenia Mark D. Brennan1,2* and Jodi Condra1 1Department of Biochemistry and Molecular Biology, Center for Genetics and Molecular Medicine, University of Louisville School of Medicine, Louisville, Kentucky 2SureGene, LLC, Louisville, Kentucky Previous studies suggest a role for chromosome be limited to Chinese lineages [Liu et al., 2002; Shifman et al., 22q13 in schizophrenia. This segment of chromo- 2002; Williams et al., 2003; Li et al., 2004]. Likewise, for more some 22 contains the sulfotransferase-4A1 (Sult4A1) distally located genes and polymorphisms, family-based gene, which encodes an enzyme thought to be transmission studies have given somewhat modest or even involved in neurotransmitter metabolism in the contradictory results [Vallada et al., 1995; Stober et al., 2000; central nervous system. To evaluate this candi- Meyer et al., 2001; Georgieva et al., 2003; Takahashi et al., date, we developed a microsatellite marker tar- 2003; Kaganovich et al., 2004]. geting a polymorphism in its 50 nontranslated The sulfotransferase-4A1 gene (Sult4A1) is located in 22q13 region (D22s1749E). Using samples obtained from and encodes a brain-speciﬁc sulfotransferase believed to be the National Institutes of Mental Health Schizo- involved in metabolism of neurotransmitters [Falany et al., phrenia Genetics Initiative, we evaluated 27 2000; Sakakibara et al., 2002; Liyou et al., 2003]. Here we families having multiple siblings with schizophre- described a new microsatellite polymorphism in the 50 end of nia and schizophrenia-spectrum disorders for this gene and evaluated this gene as a candidate for sus- transmission disequilibrium (TDT) of this marker ceptibility to schizophrenia by family-based transmission along with three single nucleotide polymorph- disequilibrium (TDT) analysis of 27 families from the NIMH isms (SNPs) spanning a 37 kb segment containing Schizophrenia Genetics Initiative.
[Show full text]
SULTA4A1 Modulates Synaptic Development and Function by Promoting the Formation of PSD-95/NMDAR Complex
bioRxiv preprint doi: https://doi.org/10.1101/583419; this version posted March 21, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. SULTA4A1 modulates synaptic development and function by promoting the formation of PSD-95/NMDAR complex 1 Lorenza Culotta1, Benedetta Terragni2, Ersilia Vinci1, Alessandro Sessa3, Vania Broccoli1, Massimo 2 Mantegazza5 and Chiara Verpelli1 3 4 1CNR Neuroscience Insitute, Milan, Milano; 5 2U.O. of Neurophysiopathology and Diagnostic Epileptology, Foundation Istituto di Ricerca e Cura 6 a Carattere Scientifico (IRCCS) Neurological Institute Carlo Besta, Milan; 7 3Stem Cell and Neurogenesis Unit, Division of Neuroscience, San Raffaele Scientific Institute, 8 20132 Milan, Italy 9 4Institute of Molecular and Cellular Pharmacology (IPMC), Laboratory of Excellence Ion Channel 10 Science and Therapeutics (LabEx ICST), CNRS UMR7275 and University of Nice-Sophia 11 Antipolis, Valbonne 12 13 Corresponding author: 14 Chiara Verpelli 15 CNR Neuroscience Institute 16 Via Vanvitelli 32 17 20129 Milano 18 Email: [email protected] 19 20 21 22 23 bioRxiv preprint doi: https://doi.org/10.1101/583419; this version posted March 21, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 24 Abstract 25 Sulfotransferase 4A1 (SULT4A1) is a cytosolic sulfotransferase, that is highly conserved across 26 species and extensively expressed in the brain.
[Show full text]
Generation and Characterization of SULT4A1 Mutant Mouse Models S
Supplemental material to this article can be found at: http://dmd.aspetjournals.org/content/suppl/2017/11/06/dmd.117.077560.DC1 1521-009X/46/1/41–45$25.00 https://doi.org/10.1124/dmd.117.077560 DRUG METABOLISM AND DISPOSITION Drug Metab Dispos 46:41–45, January 2018 Copyright ª 2017 by The American Society for Pharmacology and Experimental Therapeutics Short Communication Generation and Characterization of SULT4A1 Mutant Mouse Models s Received July 14, 2017; accepted November 2, 2017 ABSTRACT Sulfotransferase 4A1 (SULT4A1) belongs to the cytosolic sulfo- and progressive neurologic symptoms, including tremor, absence transferase (SULT) superfamily of enzymes that catalyze sulfona- seizures, abnormal gait, ataxia, decreased weight gain compared tion reactions with a variety of endogenous and exogenous with littermates, and death around postnatal days 21–25. SULT4A1 substrates. Of the SULTs, SULT4A1 was shown to have the highest immunostaining was decreased in brains of heterozygous pups Downloaded from sequence homology between vertebrate species, yet no known and not detectable in homozygous pups of both SULT4A1 mutants. function or enzymatic activity has been identified for this orphan SULT4A1 localization in subcellular fractions of mouse brain SULT. To better understand SULT4A1 function in mammalian brain, showed SULT4A1 associated with mitochondrial, cytosolic, and two mutant SULT4A1 mouse strains were generated utilizing microsomal fractions, a novel localization pattern for SULTs. clustered regulatory interspaced short palindromic repeats Finally, primary cortical neurons derived from embryonic (E15) – (CRISPR) content-addressable storage (Cas) 9 technology. The CD-1 mice expressed high levels of SULT4A1 throughout the cell dmd.aspetjournals.org first strain possessed a 28-base pair (bp) deletion (D28) in exon except in nuclei.
[Show full text]
Genetic Findings As the Potential Basis of Personalized Pharmacotherapy in Phelan-Mcdermid Syndrome
G C A T T A C G G C A T genes Review Genetic Findings as the Potential Basis of Personalized Pharmacotherapy in Phelan-McDermid Syndrome Brianna Dyar 1, Erika Meaddough 1, Sara M. Sarasua 1, Curtis Rogers 2, Katy Phelan 3 and Luigi Boccuto 1,* 1 Healthcare Genetics Program, School of Nursing, Clemson University, Clemson, SC 29634, USA; [email protected] (B.D.); [email protected] (E.M.); [email protected] (S.M.S.) 2 Greenwood Genetic Center, Greenwood, SC 29649, USA; [email protected] 3 Florida Cancer Specialists & Research Institute, Fort Myers, FL 33905, USA; kphelan@ﬂcancer.com * Correspondence: [email protected] Abstract: Phelan-McDermid syndrome (PMS) is a genetic disorder often characterized by autism or autistic-like behavior. Most cases are associated with haploinsufﬁciency of the SHANK3 gene resulting from deletion of the gene at 22q13.3 or from a pathogenic variant in the gene. Treatment of PMS often targets SHANK3, yet deletion size varies from <50 kb to >9 Mb, potentially encompassing dozens of genes and disrupting regulatory elements altering gene expression, inferring the potential for multiple therapeutic targets. Repurposed drugs have been used in clinical trials investigating therapies for PMS: insulin-like growth factor 1 (IGF-1) for its effect on social and aberrant behaviors, intranasal insulin for improvements in cognitive and social ability, and lithium for reversing regression and stabilizing behavior. The pharmacogenomics of PMS is complicated by the CYP2D6 enzyme which metabolizes antidepressants and antipsychotics often used for treatment. The gene coding for Citation: Dyar, B.; Meaddough, E.; CYP2D6 maps to 22q13.2 and is lost in individuals with deletions larger than 8 Mb.
[Show full text]
Lorenza Culotta Phd Thesis
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by AIR Universita degli studi di Milano UNIVERSITÀ DEGLI STUDI DI MILANO Ph.D. Course in Experimental and Clinical Pharmacological Sciences XXX CYCLE Deciphering the role of Sulfotransferase 4A1 in brain development and neuronal functioning Ph.D. Thesis of: Lorenza Culotta R10999 Tutor: Prof. Monica Di Luca Co-Tutor: Dr. Chiara Verpelli Coordinator: Prof. Alberico L. Catapano Academic Year 2016/2017 Table of contents ABSTRACT ............................................................................................................. 3 INTRODUCTION ..................................................................................................... 8 1. Sulfotransferases ............................................................................................. 9 1.1. Cytosolic Sulfotransferases ....................................................................... 9 2. Sulfotransferase 4A1 ..................................................................................... 10 2.1. Tissue distribution ................................................................................... 12 2.2. Pharmacogenetics and possible relevance to disease ........................... 13 2.2.1. Schizophrenia ................................................................................ 13 2.2.2. Phelan-McDermid Syndrome ........................................................ 14 2.2.3. Other Pathologies .........................................................................
[Show full text]
Identification of 22Q13 Genes Most Likely to Contribute to Phelan
European Journal of Human Genetics (2018) 26:293–302 https://doi.org/10.1038/s41431-017-0042-x REVIEW ARTICLE Identification of 22q13 genes most likely to contribute to Phelan McDermid syndrome 1 2 3,4 2 5 Andrew R. Mitz ● Travis J. Philyaw ● Luigi Boccuto ● Aleksandr Shcheglovitov ● Sara M. Sarasua ● 3,4,6,7 8 Walter E. Kaufmann ● Audrey Thurm Received: 1 June 2017 / Revised: 4 September 2017 / Accepted: 31 October 2017 / Published online: 22 January 2018 © The Author(s) 2018. This article is published with open access Abstract Chromosome 22q13.3 deletion (Phelan McDermid) syndrome (PMS) is a rare genetic neurodevelopmental disorder resulting from deletions or other genetic variants on distal 22q. Pathological variants of the SHANK3 gene have been identified, but terminal chromosomal deletions including SHANK3 are most common. Terminal deletions disrupt up to 108 protein-coding genes. The impact of these losses is highly variable and includes both significantly impairing neurodevelopmental and somatic manifestations. The current review combines two metrics, prevalence of gene loss and predicted loss pathogenicity, to identify likely contributors to phenotypic expression. These genes are grouped according to function as follows: molecular 1234567890 signaling at glutamate synapses, phenotypes involving neuropsychiatric disorders, involvement in multicellular organization, cerebellar development and functioning, and mitochondrial. The likely most impactful genes are reviewed to provide information for future clinical and translational investigations. Introduction neurodevelopmental disorder-associated syndrome caused by heterozygous contiguous gene deletions at 22q13.3 deletion syndrome, also called Phelan–McDermid chromosome 22q13 or by pathological variants of SHANK3 syndrome (PMS or PHMDS, OMIM 606232) is a [1].
[Show full text]
SULT4A1 Modulates Synaptic Development and Function By
SULT4A1 Modulates Synaptic Development and Function by Promoting the Formation of PSD-95/NMDAR Complex Lorenza Culotta, Paolo Scalmani, Ersilia Vinci, Benedetta Terragni, Alessandro Sessa, Vania Broccoli, Massimo Mantegazza, Chiara Verpelli To cite this version: Lorenza Culotta, Paolo Scalmani, Ersilia Vinci, Benedetta Terragni, Alessandro Sessa, et al.. SULT4A1 Modulates Synaptic Development and Function by Promoting the Formation of PSD- 95/NMDAR Complex. Journal of Neuroscience, Society for Neuroscience, 2020, 40 (37), pp.7013-7026. 10.1523/JNEUROSCI.2194-19.2020. hal-03011735 HAL Id: hal-03011735 https://hal.archives-ouvertes.fr/hal-03011735 Submitted on 18 Nov 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. The Journal of Neuroscience https://jneurosci.msubmit.net JN-RM-2194-19R2 SULT4A1 modulates synaptic development and function by promoting the formation of PSD-95/NMDAR complex Chiara Verpelli, CNR, Neuroscience Institute Lorenza Culotta, CNR, Institute of Neuroscience Paolo Scalmani, Fondazione IRCCS Istituto Neurologico Carlo Besta
[Show full text]
Generation and Characterization of SULT4A1 Mutant Mouse Models S
Supplemental material to this article can be found at: http://dmd.aspetjournals.org/content/suppl/2017/11/06/dmd.117.077560.DC1 1521-009X/46/1/41–45$25.00 https://doi.org/10.1124/dmd.117.077560 DRUG METABOLISM AND DISPOSITION Drug Metab Dispos 46:41–45, January 2018 Copyright ª 2017 by The American Society for Pharmacology and Experimental Therapeutics Short Communication Generation and Characterization of SULT4A1 Mutant Mouse Models s Received July 14, 2017; accepted November 2, 2017 ABSTRACT Sulfotransferase 4A1 (SULT4A1) belongs to the cytosolic sulfo- and progressive neurologic symptoms, including tremor, absence transferase (SULT) superfamily of enzymes that catalyze sulfona- seizures, abnormal gait, ataxia, decreased weight gain compared tion reactions with a variety of endogenous and exogenous with littermates, and death around postnatal days 21–25. SULT4A1 substrates. Of the SULTs, SULT4A1 was shown to have the highest immunostaining was decreased in brains of heterozygous pups sequence homology between vertebrate species, yet no known and not detectable in homozygous pups of both SULT4A1 mutants. Downloaded from function or enzymatic activity has been identified for this orphan SULT4A1 localization in subcellular fractions of mouse brain SULT. To better understand SULT4A1 function in mammalian brain, showed SULT4A1 associated with mitochondrial, cytosolic, and two mutant SULT4A1 mouse strains were generated utilizing microsomal fractions, a novel localization pattern for SULTs. clustered regulatory interspaced short palindromic repeats Finally, primary cortical neurons derived from embryonic (E15) (CRISPR)–content-addressable storage (Cas) 9 technology. The CD-1 mice expressed high levels of SULT4A1 throughout the cell first strain possessed a 28-base pair (bp) deletion (D28) in exon except in nuclei.
[Show full text]
Sulfotransferase 1A3 (SULT1A3)
A Dissertation entitled Functional Genomic Studies On The Genetic Polymorphisms Of The Human Cytosolic Sulfotransferase 1A3 (SULT1A3) by Ahsan Falah Hasan Bairam Submitted to the Graduate Faculty as partial fulfillment of the requirements for the Doctor of Philosophy Degree in Experimental Therapeutics ________________________________________ Dr. Ming-Cheh Liu, Committee Chair ________________________________________ Dr. Ezdihar Hassoun, Committee Member ________________________________________ Dr. Zahoor Shah, Committee Member ________________________________________ Dr. Caren Steinmiller, Committee Member ________________________________________ Dr. Amanda Bryant-Friedrich, Dean College of Graduate Studies The University of Toledo May 2018 Copyright 2018, Ahsan Falah Hasan Bairam This document is copyrighted material. Under copyright law, no parts of this document may be reproduced without the expressed permission of the author. An Abstract of Functional Genomic Studies On The Genetic Polymorphisms Of The Human Cytosolic Sulfotransferase 1A3 (SULT1A3) by Ahsan Falah Hasan Bairam Submitted to the Graduate Faculty as partial fulfillment of the requirements for the Doctor of Philosophy Degree in Experimental Therapeutics (Pharmacology/Toxicology) The University of Toledo May 2018 Abstract Previous studies have demonstrated the involvement of sulfoconjugation in the metabolism of catecholamines and serotonin (5-HT), as well as a wide range of xenobiotics including drugs. The study presented in this dissertation aimed to clarify the effects of coding single nucleotide polymorphisms (cSNPs) of the human SULT1A3 and SULT1A4 genes on the enzymatic characteristics of the sulfation of catecholamines, 5- HT, and selected drugs by SULT1A3 allozymes. Following a comprehensive search of different SULT1A3 and SULT1A4 genotypes, thirteen non-synonymous (missense) cSNPs of SULT1A3/SULT1A4 were identified. cDNAs encoding the corresponding SULT1A3 allozymes, packaged in pGEX-2T vector were generated by site-directed mutagenesis.
[Show full text]