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J. Biomol. Scr. 13, 968–974. Mouse thymus targeted peptide isolated by in vivo phage display can inhibit bioactivity of thymus output in vivo. 2008

Yu, Y., Wang, Z. and Du, T.

Notes: In this study, in vivo selection of a phage display random peptide library was performed in mice, isolating specific peptides that homed to mouse thymus. A thymus-homing and kidney-recovered peptide were injected into BALB/c mice, and peripheral blood removed at intervals of 15 minutes, 1 hour, 3 hours, 6 hours and 24 hours. DNA was extracted using the ReadyAmp™ Genomic DNA Purification System. Thymus activity was assessed by using real-time PCR. (4020)

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Int. Congr. Ser. 1239, 207–12. Population data on Powerplex 2.1 (FGA, vWA, TPOX, THO1, Penta E, D18S51, D21S11, D3S1358, D8S1179) and Gammastar (D16S539, D7S820, D13S317, D5S818) in a sample of Caucasian-Mestizos from Colombia. 2008

Yunis, J.J., García, O., Moreno, S., Pineda, C., Rodriguez, C., Uriarte, I. and Yunis, E.J.

Notes: The authors generated population data for unrelated Caucasian-Mestizos from Columbia using the PowerPlex® 2.1 System and the GammaSTR® Multiplex. DNA was isolated from whole blood using the Wizard® Genomic DNA Purification Kit or ReadyAmp™ Genomic DNA Purification System, then amplified per the manufacturer's recommendations. Amplified fragments were detected using a Hitachi FMBIO® II fluorescence imaging system. (3856)

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J. Forensic Sci. 51, 274–281. A proposal for standardization in forensic canine DNA typing: allele nomenclature of six canine-specific STR loci. 2006

Hellmann, A.P., Rohleder, U., Eichmann, C., Pfeiffer, I., Parson, W. and Schleenbecker, U.

Notes: Saliva samples from a total of 142 dogs (36 different pure breeds and several cross breeds) were collected on cotton swabs. Genomic DNA was isolated using the ReadyAmp™ Genomic DNA Purification System. Single amplifications of six canine STR loci were performed using 1–5µl of saliva DNA extract. (3424)

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Reproduction 127, 201–205. Quantitative analysis of mitochondrial DNAs in macaque embryos reprogrammed by rabbit oocytes. 2004

Yang, C.X., Kou, Z.H., Wang, K., Jiang, Y., Mao, W.W., Sun, Q.Y., Sheng, H.Z. and Chen, D.Y.

Notes: Nuclear transfer (NT) embryos (macaque fibroblasts introduced into matured metaphase II stage rabbit oocytes) were placed into PCR tubes containing 10µl of lysis solution, ReadyAmp™ Genomic DNA Purification System resin and 200µg/ml proteinase K. To break open the cells and access the genomic DNA, the embryos were incubated for 30 minutes at 55°C, boiled for 10 minutes, centrifuged for 1 minute then used for PCR. The amplified DNA was then cloned into the pGEM®-T Easy Vector and sequenced to determine if the product was macaque or rabbit. (3423)

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Am. J. Physiol. Regul. Integr. Comp. Physiol. 287, R298–R305. Role for CD14, TLR2, and TLR4 in bacterial product-induced anorexia. 2004

von Meyenburg, C., Hrupka, B.H., Arsenijevic, D., Schwartz, G.J., Landmann, R. and Langhans, W.

Notes: Genomic DNA was isolated from murine plasma samples using the ReadyAmp™ Genomic DNA Purification System. The purified genomic DNA was then used for PCR genotype analysis of the CD14 and TLR2-KO loci. (3422)

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J. Clin. Microbiol. 37, 127-131. Detection of Pneumocystis carinii DNA in blood specimens from human immunodeficiency virus-infected patients by nested PCR. 1999

Rabodonirina, M., Cotte, L., Boibieux, A., Kaiser, K., Mayçon, M., Raffenot, D., Trepo, C., Peyramond, D, Picot, S.

Notes: The ReadyAmp™ Genomic DNA Purification System was used to isolate genomic DNA from 200µl of whole blood. The PCR-quality DNA was used for nested PCR amplification. (0527)

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