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Promega Corporation

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Proc. Natl. Acad. Sci. USA 94, 6916-6921. Efficient photoreceptor-targeted gene expression in vivo by recombinant adeno-associated virus. 1997

Flannery, J., Zolotukhin, S., Vaquero, M., LaVail, M., Muzyczka, N., Hauswirth, W.

Notes: Tth DNAPolymerase was used to perform RT-PCR with a two-buffer protocol. (1935)

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J. Biochem. (Tokyo) 272, 1842-1848. Molecular Cloning, Characterization, and Regulation of the Human Mitochondrial Serine Hydroxymethyltransferase Gene. 1997

Stover, P., Chen, L., Suh, J., Stover, D., Keyomarsi, K., Shane, B.

Notes: Tth DNA Polymerase was used to perform RT-PCR with a two-buffer protocol. (1936)

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J. Biol. Chem. 272, 17112-17117. Structure of the m1 muscarinic acetylcholine receptor gene and its promoter 1997

Pepitoni, S., Wood, I.C. Buckley, N.J.

Notes: The Dual-Luciferase® Reporter Assay System was used to study transfections of IMR32 and NIH3T3 cells with firefly luciferase vector (pGL3 Basic) constructs. Transfections were controlled with co-transfected pRL-CMV Vector. Tth DNA Polymerase was used as a high temperature reverse transcriptase. SP6 RNA Polymerase was used to produce probes for RNase protection assays. (0558)

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J. Biochem. (Tokyo) 271, 27802-27809. A Cytosolic Granzyme B Inhibitor Related to the Viral Apoptotic Regulator Cytokine Response Modifier A Is Present in Cytotoxic Lymphocytes. 1996

Sun.J., Bird.C., Sutton.V., McDonald.L., Coughlin.P., DeJong.T., Trapani.J., Bird.P.

Notes: Tth DNA Polymerase was used to amplify some cDNA. (1950)

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J. Clin. Invest. 98(1), 43-49. Acute regulation by insulin of phosphatidylinositol-3-kinase, Rad, Glut 4, and lipoprotein lipase mRNA levels in human muscle. 1996

Laville, M., Auboeuf, D., Khalfallah, Y., Vega, N., Riou, J.P. and Vidal H.

Notes: Promega's Tth DNA Polymerase, pGEM®-T Vector System and Riboprobe® System were used in this study. (2002)

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J. Clin. Microbiol. 33, 2643-2646. Inhibition of PCR by aqueous and vitreous fluids. 1995

Wiedbrauk, D. L., Werner, J. C., Drevon, A. M.

Notes: The inhibition of PCR amplification by aqueous and vitreous fluids from the eyes was studied using Taq, Tth and Tfl DNA polymerase from Promega and AmpliTaq DNA polymerase from Perkin-Elmer Cetus. The inhibition can be removed by dilution of the specimen, by chloroform extraction or by using Tth or Tfl DNA polymerase. (0185)

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