GoTaq DNA Polymerase from Promega

Product Specs
ItemGoTaq DNA Polymerase
CompanyPromega
Price Supplier Page View Company Product Page
Catalog NumberM3008
Quantity2,500u
Concentration5 U/µl

Add to Compare List

Promega

2800 Woods Hollow Rd

Madison, WI 53711

United States

Phone: Tel: +1 (608) 274-4330
Fax: +1 (608) 277-2516

Email: custserv@promega.com
techserv@promega.com

Company Profile

Website: http://www.promega.com

(1) HTLV-1 HBZ inhibits DHX9 to reprogram circRNA biogenesis in ATLLTumour Virus ResJuly 20, 2026Julien Ladet, Mateo Bazire, Nicolas Fontrodona, Anne Van den Broeke, Ambroise Marçais, Mariam Shallak, Greta Forlani, Roberto S. Accolla, Cyril F. Bourgeois, Franck Mortreux(7.5 ng) was used as a template for PCR amplification in a reaction tube containing GoTaq polymerase (M3008, Promega). PCR products were separated by agarose gel electrophoresis stained with ethidium bromide

(2) Elucidating the protein interaction network of one of the largest icosahedral capsids in the virosphereThe EMBO JournalApril 10, 2026Hela Safi, Alain Schmitt, Alwena Tollec, Lucid Belmudes, Agathe M G Colmant, Olivier Poirot, Sebastien Santini, Matthieu Legendre, Yohann Couté, Hugo Bisio, et al.,Thermo Fisher,F530L In Fusion Snap Assembly,Takara,638948 Terra PCR Direct RedDye Premix,Takara,639286 GoTaq,Promega,M3008 NotI-HF,New England Biolabs (NEB),R3189S EcoRI-HF,New England Biolabs (NEB),R0101S HindIII-HF,New England Biolabs

(3) Cranial neural crest shortage leads to extensive craniofacial anomalies in mice mutant for the NR2F1/2 nuclear receptorsDevelopmental BiologyFebruary 1, 2026David Paulding, Simon J. Y. Han, Jonathan Timmons, Michelle Caye, Alexa Riedel, Samantha A. Brugmann, Lindsey Barskeand migration (labeled as 4–5ss). PCR genotyping was carried out using GoTaq DNA Polymerase (Promega M3008) on ear or tail clippings from mouse pups and amnion and/or tail tissue from embryos, extracted using

(4) Three Staphylococcus Bacteriophages Isolated from Swine Farm Environment in Quebec, Canada, Infecting S. chromogenesVirusesJanuary 22, 2026Mousumi Sarker Chhanda, Rébecca E. St-Laurent, Valérie E. Paquet, Nicolas Deslauriers, Cynthia Gagné-Thivierge, Martine Denicourt, Marie-Ève Lambert, Antony T. Vincent, Steve J. Charetteprepared as previously described [29]. PCR amplification was carried out using GoTaq® DNA polymerase (PR M3008, Promega Corporation, Fitchburg, WI, USA) and the RAPD #18 primer (5′-GCCAGCAGG-3′) [30]. The thermal

(5) Usp21 Knockout Causes Abnormal Lipid Metabolism in Mouse and Its Polymorphism Correlates with Hypercholesterolemia in OutpatientsInt J Mol SciOctober 6, 2025Sailakshmi Iyer, Naoko Hattori, Hiroshi Okuda, Takeya Nakagawa, Satoshi Fujii, Takahiro Maeda, Haruhiko Koseki, Takashi ItoSNP are mentioned in Table S4. The PCR was performed using the GoTaq DNA polymerase (Promega Cat.No.M3008, Madison, WI, USA). The PCR master mix included 5xGoTaq buffer 2 μL, 2.5 mM dNTP 0.8 μL, 10μM forward

(6) Use of HSALR female mice as a model for the study of myotonic dystrophy type ILab Anim (NY)April 1, 2025Marc Carrascosa-Sàez, Anna Colom-Rodrigo, Irene González-Martínez, Raquel Pérez-Gómez, Andrea García-Rey, Diego Piqueras-Losilla, Ana Ballestar, Beatriz Llamusí, Estefanía Cerro-Herreros, Ruben Arterosplicing was assayed by standard PCR, using 20 ng of cDNA as template, GoTaq polymerase (Promega, cat. no. M3008) and specific primers for Atp2a1, Nfix, Clcn1, Mbnl1, Bin1 and Cacna1s alternative splicing events,

(7) Multiple Immune and Genetic Mechanisms Contribute to Cmv5s-Driven Susceptibility and Tissue Damage during Acute Murine Cytomegalovirus InfectionThe Journal of ImmunologyMarch 1, 2024Jessica L. Annis, John Benjamin W. Duncan, Helen O. Billcheck, Anna G. Kuzma, Rowena B. Crittenden, Michael G. Brownisolated from toe and/or tail clips from pre-weanling pups. PCR was run using the Promega GoTaq® kit (Cat. M3008) reagents, dNTPs purchased from Genesee Scientific (Cat. 42–410), EvaGreen® dye purchased from Biotium

(8) Recombinant Attenuated Edwardsiella piscicida Vaccine Displaying Regulated Lysis to Confer Biological Containment and Protect Catfish against EdwardsiellosisVaccines (Basel)September 9, 2023Banikalyan Swain, Vanessa A. Campodonico, Roy Curtisswere used to carry out cloning. To perform all PCR reactions, GoTaq DNA polymerase (Promega, catalog# M3008) was used. To perform plasmid DNA isolation and the purification of gel fragments and PCR products,

(9) High density SNP array and reanalysis of genome sequencing uncovers CNVs associated with neurodevelopmental disorders in KOLF2.1J iPSCsbioRxivJuly 27, 2023Carolina Gracia-Diaz, Jonathan E. Perdomo, Munir E. Khan, Brianna Disanza, Gregory G. Cajka, Sunyimeng Lei, Alyssa Gagne, Jean Ann Maguire, Thomas Roule, Ophir Shalem, et al.(Invitrogen, #18427013), 0.5 µM forward and 0.5 µM reverse primers, GoTaq DNA Polymerase (Promega, #M3008) and 1µL of template gDNA. To prepare PCR products for Sanger Sequencing we enzymatically purified the

(10) Large-scale F0 CRISPR screens in vivo using MIC-DropNature ProtocolsJune 1, 2023Saba Parvez, Zachary J. Brandt, Randall T. PetersonSetup)Uracil-DNA glycosylase (UDG) (New England Biolabs, cat. no. M0280S)GoTaq DNA polymerase (Promega, cat. no. M3008)Exonuclease I (New England Biolabs, cat. no. M0293)Shrimp alkaline phosphatase (New England Biolabs,

(11) Construction and Evaluation of Recombinant Attenuated Edwardsiella piscicida Vaccine (RAEV) Vector System Encoding Ichthyophthirius multifiliis (Ich) Antigen IAG52BFrontiers in ImmunologyJanuary 25, 2022Banikalyan Swain, Cole T. Powell, Roy Curtissand T4 ligase were used for cloning. For all PCR reactions, GoTaq DNA polymerase (Promega, catalog# M3008) was used. For plasmid DNA isolation and purification of gel fragments and PCR products, Qiagen products

(12) A simple one-step PCR assay for SNP detectionMicroPubl BiolJune 11, 2021Jian Chen, Tim Schedlsystems. Methods All primers designed to have Tm between 58 °C to 61 °C. GoTaq DNA Polymerase (Promega, cat#M3008) was used in all PCR reactions described, following the manufacturer’s instructions. The single worm

(13) A Salmonella Typhi RNA thermosensor regulates virulence factors and innate immune evasion in response to host temperaturePLoS pathogensMarch 1, 2021Brewer SM, Twittenhoff C, Kortmann J, Brubaker SW, Honeycutt J, Massis LM, Pham THM, Narberhaus F, Monack DM.10 minutes before being used as the DNA template in PCR reactions using GoTaq polymerase (Promega #M3008) and primers oSMB64/65 and oSMB75/76 (see S3 Table). PCR products were run on a 0.9% agarose TAE gel

(14) Bone Morphogenic Proteins Are Immunoregulatory Cytokines Controlling FOXP3⁺ T_reg CellsCell reportsOctober 6, 2020Browning LM, Miller C, Kuczma M, Pietrzak M, Jing Y, Rempala G, Muranski P, Ignatowicz L, Kraj P.SuperScript IV First-Strand Synthesis System,Thermo Fisher Scientific,Cat# 18091050 GoTaq DNA polymerse with buffer,Promega,Cat# M3008 ,, Deposited Data,, ,, RNA-seq,This paper,GEO: GSE103124 ,, Experimental Models: Organisms/Strains,Experimental Models

(15) A Rapid, SuperSelective Method for Detection of Single Nucleotide Variants in Caenorhabditis elegansGeneticsOctober 1, 2020Denis Touroutine, Jessica E. Tanisshown). Gradient PCR was performed by aliquoting a master mix containing GoTaq DNA Polymerase (Promega Cat. No. M3008), 500 nM of each primer, and 5 ng of clean gDNA into 15 µl reactions. Instead of 1 µl clean gDNA, 1

(16) TIAM2S Mediates Serotonin Homeostasis and Provokes a Pro-Inflammatory Immune Microenvironment Permissive for Colorectal TumorigenesisCancersJuly 8, 2020Chan YL, Lai WC, Chen JS, Tseng JT, Chuang PC, Jou J, Lee CT, Sun HS.expression of TIAM2S transcripts was examined by PCR to amplify 352-bp amplicons using GoTaq DNA polymerase (M3008, Promega, Madison, WI, USA) with its buffer and dNTP (forward primer 5′-CTTCTGCCCCATTAAACGAA-3′, reverse

(17) Pancreatic cancer organoids recapitulate disease and allow personalized drug screeningProceedings of the National Academy of Sciences of the United States of AmericaDecember 26, 2019Driehuis E, van Hoeck A, Moore K, Kolders S, Francies HE, Gulersonmez MC, Stigter ECA, Burgering B, Geurts V, Gracanin A, et al.5′-ACACGTCTGCAGTCAACTGG-3′ and reverse primer 5′- TAACTTGAAACCCAAGGTAC-3′, with GoTaq DNA Polymerase (Promega; M3008) according to protocol at an annealing temperature of 58 °C. A 1% Agarose gel was used to purify the

(18) Does the widely distributed rodent Calomys tener (Cricetidae: Sigmodontinae) constitute a single evolutionary unit?ZoologiaMay 28, 2019Raul E. Gonzalez-Ittig, Narayan P. Kandel, Cibele R. Bonvicino, Jorge Salazar-Bravomixtures were set at 25μL total volume with 1 μL of DNA (20–30 ng/μL), 0.13 μL of Promega Taq (Cat# M3008, 5U/μL), 0.8 μL of dNTPs mix (Cat#U151B, 10mM), 2 μL of MgCL2 (25 mM), 2.5 μL of 5 × Go Taq Green buffer,

(19) Cas4-Dependent Prespacer Processing Ensures High-Fidelity Programming of CRISPR ArraysMolecular CellApril 1, 2018Hayun Lee, Yi Zhou, David W. Taylor, Dipali G. Sashital,New England Biolabs,#R3101L T4 Polynucleotide Kinase,New England Biolabs,#M0201L GoTaq DNA polymerase,Promega,#M3008 DpnI,New England Biolabs,#R0176L Agar,AMRESCO,#J637-1kg Carbenicillin disodium salt,RPI,#C46000-25.0 Kanamycin monosulfate

(20) Human cardiomyocytes for drug discoveryVigilância Sanitária em DebateFebruary 28, 2018Diogo Gonçalves Biagi et al.samples were diluted for 10 ng/mL. For the endpoint PCR were used Promega’s GoTaq DNA Polimerase # m3008 and for quantitative PCR was used Power SyBer Green Master Mix PCR #4367659. Primers sequences are available

Be the First to Write a Review!