Standard Taq (No Magnesium) Reaction Buffer

• Description:

  Standard Taq (No Magnesium) Reaction Buffer _x000D_ Catalog number: B2019390_x000D_ Lot number: Batch Dependent_x000D_ Expiration Date: Batch dependent_x000D_ Amount: 6 mL_x000D_ Molecular Weight or Concentration: N/A_x000D_ Supplied as: Solution_x000D_ Applications: a molecular tool for various biochemical applications_x000D_ Storage: -20°C_x000D_ Keywords: Standard Taq (No Magnesium) Reaction Buffer_x000D_ Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ References:_x000D_ 1: Markoulatos P, Siafakas N, Moncany M. Multiplex polymerase chain reaction: a practical approach J Clin Lab Anal. 2002;16(1):47-51._x000D_ 2: Markoulatos P, Siafakas N, Moncany M. Multiplex polymerase chain reaction: a practical approach J Clin Lab Anal. 2002;16(1):47-51._x000D_ 3: Cerda A, Rivera M, Armijo G, Ibarra-Henriquez C, Reyes J, Blázquez-Sánchez P, Avilés J, Arce A, Seguel A, Brown AJ, Vásquez Y, Cortez-San Martín M, Cubillos FA, García P, Ferres M, Ramírez-Sarmiento CA, Federici F, Gutiérrez RA. An Open One-Step RT-qPCR for SARS-CoV-2 detection medRxiv [Preprint]. 2023 May 26:2021.11.29.21267000._x000D_ 4: Cerda A, Rivera M, Armijo G, Ibarra-Henriquez C, Reyes J, Blázquez-Sánchez P, Avilés J, Arce A, Seguel A, Brown AJ, Vásquez Y, Cortez-San Martín M, Cubillos FA, García P, Ferres M, Ramírez-Sarmiento CA, Federici F, Gutiérrez RA. An Open One-Step RT-qPCR for SARS-CoV-2 detection PLoS One. 2024 Jan 25;19(1):e0297081._x000D_ 5: Miura M, Tanigawa C, Fujii Y, Kaneko S. Comparison of six commercially-available DNA polymerases for direct PCR Rev Inst Med Trop Sao Paulo. 2013 Nov-Dec;55(6):401-6._x000D_ 6: Mortarino M, Franceschi A, Mancianti F, Bazzocchi C, Genchi C, Bandi C. [Quantitative PCR in the diagnosis of Leishmania] Parassitologia. 2004 Jun;46(1-2):163-7._x000D_ 7: Casareale D, Pottathil R, Diaco R. Improved blood sample processing for PCR PCR Methods Appl. 1992 Nov;2(2):149-53._x000D_ 8: Hanaki K, Nakatake H, Yamamoto K, Odawara T, Yoshikura H. DNase I activity retained after heat inactivation in standard buffer Biotechniques. 2000 Jul;29(1):38-40, 42._x000D_ 9: Lopata A, Jójárt B, Surányi ÉV, Takács E, Bezúr L, Leveles I, Bendes ÁÁ, Viskolcz B, Vértessy BG, Tóth J. Beyond Chelation: EDTA Tightly Binds Taq DNA Polymerase, MutT and dUTPase and Directly Inhibits dNTPase Activity Biomolecules. 2019 Oct 17;9(10):621._x000D_ 10: Eskandarion M, Najafi M, Akbari Eidgahi M, Alipour Tabrizi A, Golmohamadi T. Optimization of short tandem repeats (STR) typing method and allele frequency of 8 STR markers in referring to forensic medicine of Semnan Province J Med Life. 2015;8(Spec Iss 4):180-185._x000D_ _x000D_ Products Related to Standard Taq (No Magnesium) Reaction Buffer can be found at Chemicals

• Short Description:

  Catalog Number: B2019390 (6 mL)_x000D_ Standard Taq (No Magnesium) Reaction Buffer is a PCR buffer designed for use with Taq DNA polymerase. It contains essential components like Tris-HCl and KCl but lacks magnesium ions. Magnesium is added separately for optimal enzyme activity, allowing precise control over its concentration in the reaction. This product has been used as a molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request._x000D_ _x000D_

• Weight:

  0.8

• Length:

  2

• Width:

  0.9

• Height :

  0.9