Taq 2X PCR MasterMix

Cat. No.
G888
Unit
400 rxn (10.0 ml)
Price
$62.00

PCR buffet

Cat. No. G888
Name Taq 2X PCR MasterMix
Unit 400 rxn (10.0 ml)
Category PCR Polymerase
Description

Your cost-effective choice for routine amplification!

Taq 2X PCR MasterMix is a ready-to-use MasterMix containing Taq DNA Polymerase (Cat. No. G009) in a uniquely-formulated buffer with gel loading dye. Taq is a highly thermostable enzyme that catalyzes the 5’-3’ synthesis of DNA and features 5’-3’ exonuclease activity, producing 3’-dA-tailed amplicons that are ideal for TA cloning vectors. While it lacks proofreading activity due to the absence of 3'-5' activity, Taq Polymerase is known for its robust performance and reliability in generating DNA products quickly and efficiently. Its ability to perform well at high temperatures makes it an excellent choice for routine PCR applications across various research needs.

Product Features:

  • Consistent results over a wide range of DNA templates
  • Excellent yield and sensitivity
  • Contains gel loading dye for direct loading of PCR products onto an agarose gel
  • Ideal for TA cloning vectors
  • Included in abm's PCR Buffet Program
Product Component Quantity
Taq 2X PCR MasterMix 400 rxn (10.0 ml)

1 MasterMix contains 1.5 mM Mg2+

ISO 13485:2016 MDSAP Certified

ISO 13485:2016 MDSAP Certified
Our PCR Products are manufactured under a Quality Management System conforming with ISO 13485:2016 as certified by Intertek (a MDSAP recognized auditing organization).

Storage Condition

Store at -20°C.

Material Citation If use of this material results in a scientific publication, please cite the material in the following manner: Applied Biological Materials Inc, Cat. No. G888
Datasheet
  • Bharamappanavara, M., Siddaiah, A.M., Ponnuvel, S. et al. Mapping QTL hotspots associated with weed competitive traits in backcross population derived from Oryza sativa L. and O. glaberrima Steud.. Sci Rep 10, 22103 (2020). https://doi.org/10.1038/s41598-020-78675-7

    Cocci, P., Roncarati, A., Capriotti, M., Mosconi, G., & Palermo, F. A. (2020). Transcriptional alteration of gene biomarkers in hemocytes of wild Ostrea edulis with molecular evidence of infections with Bonamia spp. and/or Marteilia refringens parasites. Pathogens, 9(5), 323. https://doi.org/10.3390/pathogens9050323

    Dally, M., Lalzar, M., Belausov, E., Gottlieb, Y., Coll, M., & Zchori-Fein, E. (2020). Cellular localization of two Rickettsia symbionts in the digestive system and within the ovaries of the mirid bug, Macrolophous pygmaeus. Insects, 11(8), 530. https://doi.org/10.3390/insects11080530

    Finetti, L., Leyria, J., Orchard, I., & Lange, A. B. (2023). Tyraminergic control of vitellogenin production and release in the blood-feeding insect, Rhodnius prolixus. Insect Biochemistry and Molecular Biology, 156, 103948. https://doi.org/10.1016/j.ibmb.2023.103948

    Liu, Q., Guo, X., Xun, G., Li, Z., Chong, Y., Yang, L., ... & Feng, Y. (2021). Argonaute integrated single-tube PCR system enables supersensitive detection of rare mutations. Nucleic acids research, 49(13), e75-e75. https://doi.org/10.1093/nar/gkab274

    Salcedo-Porras, N., Guarneri, A., Oliveira, P. L., & Lowenberger, C. (2019). Rhodnius prolixus: Identification of missing components of the IMD immune signaling pathway and functional characterization of its role in eliminating bacteria. PLoS One, 14(4), e0214794. https://doi.org/10.1371/journal.pone.0214794

    SÁNCHEZ NEIRA, Y. A. L. I. N. E., FERREBUZ CARDOZO, A. J., GONZÁLEZ TORRES, F. J., & URBANO CÁCERES, E. X. (2020). Genes de resistencia en cepas bacterianas asociadas a infecciones en una institución prestadora de servicios de salud del departamento de Boyacá. Revista Salud Uninorte, 36(2), 394-411. http://dx.doi.org/10.14482/sun.36.2.614.57

    Wang, Q., Wang, P., & Yang, Q. (2018). Occurrence and diversity of antibiotic resistance in untreated hospital wastewater. Science of the Total Environment, 621, 990-999. https://doi.org/10.1016/j.scitotenv.2017.10.128

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