GSTM2) Monoclonal Antibody(Clone: CPTC-Gstmu2-2

Total Page：16

File Type：pdf, Size：1020Kb

GSTM2) Monoclonal Antibody(Clone: CPTC-Gstmu2-2

9853 Pacific Heights Blvd. Suite D. San Diego, CA 92121, USA Tel: 858-263-4982 Email: [email protected] 36-2435: Anti-Glutathione S-Transferase Mu2 (GSTM2) Monoclonal Antibody(Clone: CPTC-GSTMu2-2) Clonality : Monoclonal Clone Name : CPTC-GSTMu2-2 Application : FACS, IHC Reactivity : Human Gene : GSTMu2 Gene ID : 2946 Uniprot ID : P28161 Glutathione S alkyltransferase M2; Glutathione S transferase 4; GST class mu 2; GST4; GST Alternative Name : muscle Isotype : Mouse IgG1, kappa Immunogen Information : Recombinant human full-length GSTMu2 protein Product Info Amount : 20 µg / 100 µg 200 µg/ml of Ab Purified from Bioreactor Concentrate by Protein A/G. Prepared in 10mM PBS with Content : 0.05% BSA & 0.05% azide. Also available WITHOUT BSA & azide at 1.0mg/ml. Antibody with azide - store at 2 to 8°C. Antibody without azide - store at -20 to -80°C. Antibody is Storage condition : stable for 24 months. Non-hazardous. Application Note Flow Cytometry (1-2Âµg/million cells); (Immunofluorescence (1-2Âµg/ml);Immunohistochemistry (Formalin-fixed) (0.5-1Âµg/ml for 30 min at RT)(Staining of formalin-fixed tissues requires boiling tissue sections in 10mM Citrate Buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 minutes)Optimal dilution for a specific application should be determined. Fig. 1: Formalin-fixed, paraffin-embedded human Breast Carcinoma stained with GSTMu2 Mouse Monoclonal Antibody (CPTC-GSTMu2-2). Fig. 2: Immunofluorescence Analysis of MeOH-fixed HeLa cells labeling GSTMu2 with GSTMu2 Mouse Monoclonal Antibody (CPTC-GSTMu2-2) followed by Goat anti-Mouse IgG-CF488 (Green). The nuclear counterstain is Reddot (Red). For Research Use Only. Not for use in diagnostic/therapeutics procedures. 9853 Pacific Heights Blvd. Suite D. San Diego, CA 92121, USA Tel: 858-263-4982 Email: [email protected] Fig. 3: Flow Cytometric Analysis of PFA-fixed HeLa cells using GSTMu2 Mouse Monoclonal Antibody (CPTC-GSTMu2-2) followed by Goat anti-Mouse IgG-CF488 (Blue); Isotype Control (Red). Fig. 4: SDS-PAGE Analysis Purified GSTMu2 Mouse Monoclonal Antibody (CPTC- GSTMu2-2). Confirmation of Purity and Integrity of Antibody. For Research Use Only. Not for use in diagnostic/therapeutics procedures..

Copy Link

Recommended publications

Chuanxiong Rhizoma Compound on HIF-VEGF Pathway and Cerebral Ischemia-Reperfusion Injury’S Biological Network Based on Systematic Pharmacology
ORIGINAL RESEARCH published: 25 June 2021 doi: 10.3389/fphar.2021.601846 Exploring the Regulatory Mechanism of Hedysarum Multijugum Maxim.-Chuanxiong Rhizoma Compound on HIF-VEGF Pathway and Cerebral Ischemia-Reperfusion Injury’s Biological Network Based on Systematic Pharmacology Kailin Yang 1†, Liuting Zeng 1†, Anqi Ge 2†, Yi Chen 1†, Shanshan Wang 1†, Xiaofei Zhu 1,3† and Jinwen Ge 1,4* Edited by: 1 Takashi Sato, Key Laboratory of Hunan Province for Integrated Traditional Chinese and Western Medicine on Prevention and Treatment of 2 Tokyo University of Pharmacy and Life Cardio-Cerebral Diseases, Hunan University of Chinese Medicine, Changsha, China, Galactophore Department, The First 3 Sciences, Japan Hospital of Hunan University of Chinese Medicine, Changsha, China, School of Graduate, Central South University, Changsha, China, 4Shaoyang University, Shaoyang, China Reviewed by: Hui Zhao, Capital Medical University, China Background: Clinical research found that Hedysarum Multijugum Maxim.-Chuanxiong Maria Luisa Del Moral, ﬁ University of Jaén, Spain Rhizoma Compound (HCC) has de nite curative effect on cerebral ischemic diseases, *Correspondence: such as ischemic stroke and cerebral ischemia-reperfusion injury (CIR). However, its Jinwen Ge mechanism for treating cerebral ischemia is still not fully explained. [email protected] †These authors share ﬁrst authorship Methods: The traditional Chinese medicine related database were utilized to obtain the components of HCC. The Pharmmapper were used to predict HCC’s potential targets. Specialty section: The CIR genes were obtained from Genecards and OMIM and the protein-protein This article was submitted to interaction (PPI) data of HCC’s targets and IS genes were obtained from String Ethnopharmacology, a section of the journal database.
[Show full text]
GSTM2 Monoclonal Antibody (M03), Clone 1E10
GSTM2 monoclonal antibody (M03), clone 1E10 Catalog # : H00002946-M03 規格 : [ 100 ug ] List All Specification Application Image Product Mouse monoclonal antibody raised against a partial recombinant Western Blot (Cell lysate) Description: GSTM2. Immunogen: GSTM2 (NP_000839, 90 a.a. ~ 189 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. Sequence: SEKEQIREDILENQFMDSRMQLAKLCYDPDFEKLKPEYLQALPEMLKLYS QFLGKQPWFLGDKITFVDFIAYDVLERNQVFEPSCLDAFPNLKDFISRFE enlarge Western Blot (Recombinant Host: Mouse protein) Reactivity: Human, Mouse Immunohistochemistry (Formalin/PFA-fixed paraffin- Isotype: IgG1 Kappa embedded sections) Quality Control Antibody Reactive Against Recombinant Protein. Testing: enlarge Immunofluorescence enlarge Western Blot detection against Immunogen (36.74 KDa) . Sandwich ELISA (Recombinant Storage Buffer: In 1x PBS, pH 7.4 protein) Storage Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing. Instruction: MSDS: Download enlarge Datasheet: Download ELISA Publication Reference 1. A DNA hypermethylation profile reveals new potential biomarkers for prostate cancer diagnosis and prognosis. Ashour N, Angulo JC, Andres G, Alelu R, Gonzalez-Corpas A, Toledo MV, Rodriguez- Barbero JM, Lopez JI, Sanchez-Chapado M, Ropero SProstate. 2014 Sep;74(12):1171- 82. doi: 10.1002/pros.22833. Epub 2014 Jun 24. Applications Western Blot (Cell lysate) Page 1 of 3 2016/5/21 GSTM2 monoclonal antibody (M03), clone 1E10. Western Blot analysis of GSTM2 expression in NIH/3T3 ( Cat # L018V1 ). Protocol Download Western Blot (Recombinant protein) Protocol Download Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) enlarge this image Immunoperoxidase of monoclonal antibody to GSTM2 on formalin-fixed paraffin-embedded human breast cancer. [antibody concentration 3 ug/ml] Protocol Download Immunofluorescence enlarge this image Immunofluorescence of monoclonal antibody to GSTM2 on HeLa cell .
[Show full text]
32-2407: GSTM2 Recombinant Protein Description Product Info
ABGENEX Pvt. Ltd., E-5, Infocity, KIIT Post Office, Tel : +91-674-2720712, +91-9437550560 Email : [email protected] Bhubaneswar, Odisha - 751024, INDIA 32-2407: GSTM2 Recombinant Protein Alternative Name : Glutathione S-transferase Mu 2,GST class-mu 2,GSTM2-2,GSTM2,GST4,GSTM,GTHMUS,MGC117303. Description Source : Escherichia Coli. GSTM2 Human Recombinant fused with a 20 amino acid His tag at N-terminus produced in E.Coli is a single, non-glycosylated, polypeptide chain containing 238 amino acids (1-218 a.a.) and having a molecular mass of 27.9kDa. The GSTM2 is purified by proprietary chromatographic techniques. Glutathione S-transferase Mu 2 (GSTM2) belongs to the glutathione s-transferase (GST) family of proteins. GSTM2 is a glutathione S-transferase that belongs to the mu class. There are 8 families of GST proteins, specifically: alpha, kappa, mu, omega, pi, sigma, theta and zeta, each of which is composed of proteins that have various functions throughout the cell. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are structured in a gene cluster on chromosome 1p13.3 and are proven to be highly polymorphic. These genetic variants can change an individual''s susceptibility to carcinogens and toxins as well as have an effect on the toxicity and efficacy of several drugs. Product Info Amount : 20 µg Purification : Greater than 95.0% as determined by SDS-PAGE. The GSTM2 solution (0.5 mg/ml) contains 20mM Tris-HCl buffer (pH8.0), 10% glycerol,0.1M NaCl Content : and 1mM DTT.
[Show full text]
Copy Number Profiles of Prostate Cancer in Men of Middle Eastern
cancers Article Copy Number Proﬁles of Prostate Cancer in Men of Middle Eastern Ancestry Alia Albawardi 1,2,†, Julie Livingstone 3,4,5,† , Saeeda Almarzooqi 1,2 , Nallasivam Palanisamy 6 , Kathleen E. Houlahan 3,4,5,7, Aktham Adnan Ahmad Awwad 1, Ramy A. Abdelsalam 8,9, Paul C. Boutros 3,4,5,10,11 and Tarek A. Bismar 8,12,13,14,* 1 Tawam Hospital, Abu Dhabi P.O. Box 15258, United Arab Emirates; [email protected] (A.A.); [email protected] (S.A.); [email protected] (A.A.A.A.) 2 Pathology College of Medicine & Health Sciences, United Arab Emirates University, Al Ain, Abu Dhabi P.O. Box 15551, United Arab Emirates 3 Departments of Human Genetics, University of California, Los Angeles, CA 94607, USA; [email protected] (J.L.); [email protected] (K.E.H.); [email protected] (P.C.B.) 4 Jonsson Comprehensive Cancer Centre, University of California, Los Angeles, CA 94607, USA 5 Institute for Precision Health, University of California, Los Angeles, CA 94607, USA 6 Department of Urology, Vattikuti Urology Institute, Henry Ford Health System Detroit, Detroit, MI 48202, USA; [email protected] 7 Department of Medical Biophysics, University of Toronto, Toronto, ON M5G 1L7, Canada 8 Department of Pathology and Laboratory Medicine, University of Calgary-Cumming School of Medicine and Alberta Precision Labs, Calgary, AB T2N 4N1, Canada; [email protected] 9 Department of Pathology, Mansoura University, Mansoura 35516, Egypt 10 Department of Pharmacology & Toxicology, University of Toronto, Toronto,
[Show full text]
Exploration of Non-Hierarchical Classification Methods Combined
BMC Proceedings BioMed Central Proceedings Open Access Exploration of non-hierarchical classification methods combined with linkage analysis to identify loci influencing clusters of co-regulated transcripts Alka Malhotra*1,2, Helen C Looker2 and Robert L Hanson2 Address: 1Genetic Basis of Human Disease Division, Translational Genomics Research Institute, 445 North Fifth Street, Phoenix, Arizona 85004, USA and 2Diabetes Epidemiology and Clinical Research Section, National Institute of Diabetes & Digestive & Kidney Diseases, 1550 East Indian School Road, Phoenix, Arizona 85014, USA Email: Alka Malhotra* - [email protected]; Helen C Looker - [email protected]; Robert L Hanson - [email protected] * Corresponding author from Genetic Analysis Workshop 15 St. Pete Beach, Florida, USA. 11–15 November 2006 Published: 18 December 2007 BMC Proceedings 2007, 1(Suppl 1):S48 <supplement>Marsha A Wilcox, <title> John <p>Genetic S Witte, Qiong Analysis Yang, Workshop Andreas Ziegler,15: Gene Laura Expression Almasy Analysisand Jean andW MacCluer</editor>Approaches to Detecting <note>Proceedings</note> Multiple Functional Loci</p> <url>http://www.biomedcentral.com/content/pdf/1753-6561-1-S1-info.pdf</url> </title> <editor>Heather J Cordell, Mariza de Andrade, Marie-Claude Babron, </supplement> Christopher W Bartlett, Joseph Beyene, Heike Bickeböller, Robert Culverhouse, Adrienne Cupples, E Warwick Daw, Josée Dupuis, Catherine T Falk, Saurabh Ghosh, Katrina A Goddard, Ellen L Goode, Elizabeth R Hauser, Lisa J Martin, Maria Martinez, Kari E North, Nancy L Saccone, Silke Schmidt, William Tapper, Duncan Thomas, David Tritchler, Veronica J Vieland, Ellen M Wijsman, This article is available from: http://www.biomedcentral.com/1753-6561/1/S1/S48 © 2007 Malhotra et al; licensee BioMed Central Ltd.
[Show full text]
Stimulation of Both Estrogen and Androgen Receptors Maintains Skeletal Muscle Mass in Gonadectomized Male Mice but Mainly Via Different Pathways
45 Stimulation of both estrogen and androgen receptors maintains skeletal muscle mass in gonadectomized male mice but mainly via different pathways Johan Svensson, Soﬁa Move´rare-Skrtic, Sara Windahl, Charlotte Swanson and Klara Sjo¨ gren Division of Endocrinology, Department of Internal Medicine, Institute of Medicine, Sahlgrenska University Hospital, SE-41345 Go¨teborg, Sweden (Correspondence should be addressed to K Sjo¨gren; Email: [email protected]) Abstract Testosterone is a major regulator of muscle mass. Little is known whether this is due to a direct stimulation of the androgen receptor (AR) or mediated by aromatization of testosterone to estradiol (E2), the ligand for the estrogen receptors (ERs), in peripheral tissues. In this study, we differentiated between the effects mediated by AR and ER by treating orchidectomized (orx) male mice for 5 weeks with E2 or the non-aromatizable androgen dihydrotestosterone (DHT). Both E2 and DHT increased muscle weight and lean mass, although the effect was less marked after E2 treatment. Studies of underlying mechanisms were performed using gene transcript proﬁling (microarray and real-time PCR) in skeletal muscle, and they demonstrated that E2 regulated 51 genes and DHT regulated 187 genes, with 13 genes (Z25% of E2-regulated genes) being regulated by both treatments. Both E2 and DHT altered the expression of Fbxo32, a gene involved in skeletal muscle atrophy, affected the IGF1 system, and regulated genes involved in angiogenesis and the glutathione metabolic process. Only E2 affected genes that regulate intermediary glucose and lipid metabolism, and only DHT increased the expression of genes involved in synaptic transmission and heme and polyamine biosynthesis.
[Show full text]
Itraq-Based Quantitative Proteomic Analysis Reveals Important
www.nature.com/scientificreports OPEN iTRAQ-based quantitative proteomic analysis reveals important metabolic pathways for Received: 22 September 2017 Accepted: 31 January 2018 arsenic-induced liver fbrosis in rats Published: xx xx xxxx Shunhua Wu 1, Jing Li1 & Xiang Jin1,2 Long-term consumption of sodium arsenite contaminated water can cause endemic arsenic disease. The proteome profle changes of liver fbrosis after exposure to arsenite containing water remain unclear. In this study, Sprague-Dawley (SD) male rats were treated with sodium arsenite (iAs3+), using a daily dose of 1.36 mg/kg body weight (medium dose group, M), 2.73 mg/kg body weight (high dose group, H) or deionized water (control group, C). Isobaric tags for relative and absolute quantitation (iTRAQ) were used to identify the diferent abundant proteins (DAPs) after arsenic-induced liver fbrosis. A total of 2987 high-quality proteins were detected (95% confdent peptides ≥ 2), 608 of which were diferentially expressed (fold change > 2 and p < 0.05) in M group and 475 in H group. Moreover, 431 DAPs were found in both M and H groups and used in subsequent bioinformatic analyses. Gene ontology (GO) analysis revealed 4,709 GO terms could be mapped, among which purine binding, actin flament binding and protein kinase binding were the most enriched terms for molecular function category. In addition, protein-protein interaction analysis showed six clusters of interaction networks. Our data provided new insights into the proteome changes after arsenic-induced liver fbrosis in model rats. In nature, trivalent arsenite [As (III)] is the most common oxidation states for soluble arsenic1.
[Show full text]
GSTM2 (NM 000848) Human Tagged ORF Clone – RC210718 | Origene
OriGene Technologies, Inc. 9620 Medical Center Drive, Ste 200 Rockville, MD 20850, US Phone: +1-888-267-4436 [email protected] EU: [email protected] CN: [email protected] Product datasheet for RC210718 GSTM2 (NM_000848) Human Tagged ORF Clone Product data: Product Type: Expression Plasmids Product Name: GSTM2 (NM_000848) Human Tagged ORF Clone Tag: Myc-DDK Symbol: GSTM2 Synonyms: GST4; GSTM; GSTM2-2; GTHMUS Vector: pCMV6-Entry (PS100001) E. coli Selection: Kanamycin (25 ug/mL) Cell Selection: Neomycin ORF Nucleotide >RC210718 ORF sequence Sequence: Red=Cloning site Blue=ORF Green=Tags(s) TTTTGTAATACGACTCACTATAGGGCGGCCGGGAATTCGTCGACTGGATCCGGTACCGAGGAGATCTGCC GCCGCGATCGCC ATGCCCATGACACTGGGGTACTGGAACATCCGCGGGCTGGCCCATTCCATCCGCCTGCTCCTGGAATACA CAGACTCAAGCTACGAGGAAAAGAAGTACACGATGGGGGACGCTCCTGATTATGACAGAAGCCAGTGGCT GAATGAAAAATTCAAGCTGGGCCTGGACTTTCCCAATCTGCCCTACTTGATTGATGGGACTCACAAGATC ACCCAGAGCAACGCCATCCTGCGGTACATTGCCCGCAAGCACAACCTGTGCGGGGAATCAGAAAAGGAGC AGATTCGCGAAGACATTTTGGAGAACCAGTTTATGGACAGCCGTATGCAGCTGGCCAAACTCTGCTATGA CCCAGATTTTGAGAAACTGAAACCAGAATACCTGCAGGCACTCCCTGAAATGCTGAAGCTCTACTCACAG TTTCTGGGGAAGCAGCCATGGTCTCTTGGGGACAAGATCACCTTTGTGGATTTCATCGCTTATGATGTCC TTGAGAGAAACCAAGTATTTGAGCCCAGCTGCCTGGATGCCTTCCCAAACCTGAAGGACTTCATCTCCCG ATTTGAGGGCTTGGAGAAGATCTCTGCCTACATGAAGTCCAGCCGCTTCCTCCCAAGACCTGTGTTCACA AAGATGGCTGTCTGGGGCAACAAG ACGCGTACGCGGCCGCTCGAGCAGAAACTCATCTCAGAAGAGGATCTGGCAGCAAATGATATCCTGGATT ACAAGGATGACGACGATAAGGTTTAA This product is to be used for laboratory only. Not for diagnostic or therapeutic use. View online » ©2021
[Show full text]
A Six-Gene Prognostic Model Predicts Overall Survival in Bladder Cancer
Wang et al. Cancer Cell Int (2019) 19:229 https://doi.org/10.1186/s12935-019-0950-7 Cancer Cell International PRIMARY RESEARCH Open Access A six-gene prognostic model predicts overall survival in bladder cancer patients Liwei Wang1,2, Jiazhong Shi3, Yaqin Huang3, Sha Liu3, Jingqi Zhang1, Hua Ding1, Jin Yang3* and Zhiwen Chen1* Abstract Background: The fatality and recurrence rates of bladder cancer (BC) have progressively increased. DNA methylation is an infuential regulator associated with gene transcription in the pathogenesis of BC. We describe a comprehensive epigenetic study performed to analyse DNA methylation-driven genes in BC. Methods: Data related to DNA methylation, the gene transcriptome and survival in BC were downloaded from The Cancer Genome Atlas (TCGA). MethylMix was used to detect BC-specifc hyper-/hypo-methylated genes. Metascape was used to carry out gene ontology (GO) enrichment and Kyoto Encyclopedia of Genes and Genomes (KEGG) path- way analyses. A least absolute shrinkage and selection operator (LASSO)-penalized Cox regression was conducted to identify the characteristic dimension decrease and distinguish prognosis-related methylation-driven genes. Subse- quently, we developed a six-gene risk evaluation model and a novel prognosis-related nomogram to predict overall survival (OS). A survival analysis was carried out to explore the individual prognostic signifcance of the six genes. Results: In total, 167 methylation-driven genes were identifed. Based on the LASSO Cox regression, six genes, i.e., ARHGDIB, LINC00526, IDH2, ARL14, GSTM2, and LURAP1, were selected for the development of a risk evalu- ation model. The Kaplan–Meier curve indicated that patients in the low-risk group had considerably better OS (P 1.679e 05).
[Show full text]
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Table S1. 103 ferroptosis-related genes retrieved from the GeneCards. Gene Symbol Description Category GPX4 Glutathione Peroxidase 4 Protein Coding AIFM2 Apoptosis Inducing Factor Mitochondria Associated 2 Protein Coding TP53 Tumor Protein P53 Protein Coding ACSL4 Acyl-CoA Synthetase Long Chain Family Member 4 Protein Coding SLC7A11 Solute Carrier Family 7 Member 11 Protein Coding VDAC2 Voltage Dependent Anion Channel 2 Protein Coding VDAC3 Voltage Dependent Anion Channel 3 Protein Coding ATG5 Autophagy Related 5 Protein Coding ATG7 Autophagy Related 7 Protein Coding NCOA4 Nuclear Receptor Coactivator 4 Protein Coding HMOX1 Heme Oxygenase 1 Protein Coding SLC3A2 Solute Carrier Family 3 Member 2 Protein Coding ALOX15 Arachidonate 15-Lipoxygenase Protein Coding BECN1 Beclin 1 Protein Coding PRKAA1 Protein Kinase AMP-Activated Catalytic Subunit Alpha 1 Protein Coding SAT1 Spermidine/Spermine N1-Acetyltransferase 1 Protein Coding NF2 Neurofibromin 2 Protein Coding YAP1 Yes1 Associated Transcriptional Regulator Protein Coding FTH1 Ferritin Heavy Chain 1 Protein Coding TF Transferrin Protein Coding TFRC Transferrin Receptor Protein Coding FTL Ferritin Light Chain Protein Coding CYBB Cytochrome B-245 Beta Chain Protein Coding GSS Glutathione Synthetase Protein Coding CP Ceruloplasmin Protein Coding PRNP Prion Protein Protein Coding SLC11A2 Solute Carrier Family 11 Member 2 Protein Coding SLC40A1 Solute Carrier Family 40 Member 1 Protein Coding STEAP3 STEAP3 Metalloreductase Protein Coding ACSL1 Acyl-CoA Synthetase Long Chain Family Member 1 Protein
[Show full text]
Functional Compensation of Glutathione S-Transferase M1
OPEN Functional compensation of glutathione SUBJECT AREAS: S-transferase M1 (GSTM1) null by FUNCTIONAL GENOMICS another GST superfamily member, GENE EXPRESSION PROFILING RNAI GSTM2 GENETICS Pritha Bhattacharjee1*, Somnath Paul1, Mayukh Banerjee1, Deblina Patra1, Priyam Banerjee2, Nanda Ghoshal3, Arun Bandyopadhyay2 & Ashok K. Giri1 Received 8 January 2013 1Molecular and Human Genetics Division, 2Cell Biology and Physiology Division, 3Structural Biology and Bio-Informatics Division, Accepted CSIR-Indian Institute of Chemical Biology, Kolkata – 700 032, India. 6 August 2013 Published The gene for glutathione-S-transferase (GST) M1 (GSTM1), a member of the GST-superfamily, is widely 19 September 2013 studied in cancer risk with regard to the homozygous deletion of the gene (GSTM1 null), leading to a lack of corresponding enzymatic activity. Many of these studies have reported inconsistent findings regarding its association with cancer risk. Therefore, we employed in silico, in vitro, and in vivo approaches to investigate Correspondence and whether the absence of a functional GSTM1 enzyme in a null variant can be compensated for by other family requests for materials members. Through the in silico approach, we identified maximum structural homology between GSTM1 and GSTM2. Total plasma GST enzymatic activity was similar in recruited individuals, irrespective of their should be addressed to GSTM1 genotype (positive/null). Furthermore, expression profiling using real-time PCR, western blotting, A.K.G. (akgiri15@ and GSTM2 overexpression following transient knockdown of GSTM1 in HeLa cells confirmed that the yahoo.com; akgiri@ absence of GSTM1 activity can be compensated for by the overexpression of GSTM2. iicb.res.in) lutathione-S-transferases (GSTs) belong to a superfamily of ubiquitous, multifunctional dimeric cyto- * Current address: solic enzymes that play a very important role in the Phase II detoxification (or biotransformation) 1,2 Department of pathway in humans and confer protection against a wide array of toxic insults .
[Show full text]
32-2407: GSTM2 Recombinant Protein Description Product Info
9853 Pacific Heights Blvd. Suite D. San Diego, CA 92121, USA Tel: 858-263-4982 Email: [email protected] 32-2407: GSTM2 Recombinant Protein Alternative Name : Glutathione S-transferase Mu 2,GST class-mu 2,GSTM2-2,GSTM2,GST4,GSTM,GTHMUS,MGC117303. Description Source : Escherichia Coli. GSTM2 Human Recombinant fused with a 20 amino acid His tag at N-terminus produced in E.Coli is a single, non-glycosylated, polypeptide chain containing 238 amino acids (1-218 a.a.) and having a molecular mass of 27.9kDa. The GSTM2 is purified by proprietary chromatographic techniques. Glutathione S-transferase Mu 2 (GSTM2) belongs to the glutathione s-transferase (GST) family of proteins. GSTM2 is a glutathione S-transferase that belongs to the mu class. There are 8 families of GST proteins, specifically: alpha, kappa, mu, omega, pi, sigma, theta and zeta, each of which is composed of proteins that have various functions throughout the cell. The mu class of enzymes functions in the detoxification of electrophilic compounds, including carcinogens, therapeutic drugs, environmental toxins and products of oxidative stress, by conjugation with glutathione. The genes encoding the mu class of enzymes are structured in a gene cluster on chromosome 1p13.3 and are proven to be highly polymorphic. These genetic variants can change an individual''s susceptibility to carcinogens and toxins as well as have an effect on the toxicity and efficacy of several drugs. Product Info Amount : 20 µg Purification : Greater than 95.0% as determined by SDS-PAGE. The GSTM2 solution (0.5 mg/ml) contains 20mM Tris-HCl buffer (pH8.0), 10% glycerol,0.1M NaCl Content : and 1mM DTT.
[Show full text]