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J. Immunol. 160, 2297-2307. Characterization of the interactions between MHC class I subunits: a systematic approach for the engineering of higher affinity variants of beta 2-microglobulin. 1998

Shields, M. J., Assefi, N., Hodgson, W., Kim, E. J., Ribaudo, R.K.

Notes: The authors co-translated mRNAs for beta 2 microglobulin and MHC class I proteins in Flexi® Rabbit Reticulocyte Lysate System with Canine Pancreatic Microsomal Membranes (CMMs). They generated mRNAs using RiboMAX™ T7 Large Scale RNA Production System. Treated transcription reactions with RQ1 RNase-Free DNase I after transcription to remove template DNA. (0393)

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Am. J. Respir. Cell Mol. Biol. 19, 316-323. Egr-1 and Sp1 interact functionally with the 5-lipoxygenase promoter and its naturally occurring mutants. 1998

Silverman, E. S., Du, J., De Sanctis, G. T., Radmark, O., Samuelsson, B., Drazen, J. M., Collins, T.

Notes: The authors used the pCAT® Basic Vector in their promoter studies and RQ1 RNase-free DNase and rhSP1 in their footprinting studies with Drosophila SL2 cells. Promega's pCAT Vectors have now been replaced by the next generation pCAT® 3 Reporter Vectors. (0407)

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J. Bacteriol. 180, 2043-2049. ntn genes determining the early steps in the divergent catabolism of 4-nitrotoluene and toluene in Pseudomonas sp. Strain TW3. 1998

James, K.D., Williams, P.A.

Notes: The Access RT-PCR System was used to study expression of three ntn genes from TW3 cells grown in either 4-nitrotoluene, toluene or succinate. The pET-5a Vector (discontinued) was used to express the ntnC protein in E. coli strain BL21(DE3) pLysS. (0968)

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J. Biol. Chem. 273, 5607-5614. Transcriptional activation of the UDP-glucuronosyltransferase 1A7 gene in rat liver by aryl hydrocarbon receptor ligands and oltipraz. 1998

Metz, R.P. and Ritter, J.K

Notes: The RNasin Ribonuclease Inhibitor was used to protect RNA transcripts during primer extension analysis and in vitro transcription of RNA probes. The resultant RNA probes were used for RNase protection assays. (1639)

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J. Biol. Chem. 272, 16364-16373.. Expression of mixed lineage kinase-1 in pancreatic beta-cell lines at different stages of maturation and during embryonic pancreas development 1997

DeAizpurua, H. J. , Cram, D. S. , Naselli, G. , Devereux, L. , Dorow, D. S.

Notes: Poly(A)+ RNA was isolated from RIN rat insulinoma cell total RNA with PolyATtract® mRNA Isolation System III. (1264)

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J. Biol. Chem. 272(26), 16364-16373. Expression of mixed lineage kinase-1 in pancreatic beta-cell lines at different stages of maturation and during embryonic pancreas development. 1997

DeAixpurua, H.J., Cram, D.S., Naselli, G., Devereux, L. and Dorow, D.S.

Notes: Poly(A+) RNA was isolated from RIN rat insulinoma cell total RNA and was used for Northern blots. The authors used Promega's PolyATtract® mRNA Isolation System and AMV Reverse Transcriptase in this study. (2107)

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J. Biol. Chem. 272, 8618-8627. Gene structure of the rat kainate receptor subunit KA2 and characterization of an intronic negative regulatory region. 1997

Huang, F., Gallo, V.

Notes: Reporter studies were performed in the neural cell lines, CG-4 and PC-12, and the non-neural cell lines, HeLa and NIH3T3, using constructs prepared in the pCAT®-Basic Vector. The pCAT® Vectors have been replaced with the next generation pCAT®3 Vectors. (1027)

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J. Biol. Chem. 272(26), 16637-16643. Novel progesterone target genes identified by an improved differential display technique suggest that progestin-induced growth inhibition of breast cancer cells coincides with enhancement of differentiation. 1997

Kester, H.A., van der Leede, B.M., van der Saag, P.T. and van der Burg, B.

Notes: Poly(A+) RNA was isolated from total RNA extracted from T47D mammary carcinoma cell line using the PolyATtract® mRNA Isolation System. The RNA was used for northern blots. RQ1 was used to digest genomic DNA away from total RNA. The pGEM®-T Vector was used to subclone PCR products generated by differential display. (1673)

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EMBO J. 16, 4361-4373. Remodeling of regulatory nucleoprotein complexes on the Xenopus hsp70 promoter during meiotic maturation of the Xenopus oocyte. 1997

Landsberger, N. and Wolffe, A.P.

Notes: The inhibitor was used to protect transcripts during a run-on transcription assay. (1638)

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J. Neurosci. 17, 6504-6511. Targeted transduction of CNS neurons with adenoviral vectors carrying neurotrophic factor genes confers neuroprotection that exceeds the transduced population. 1997

Baumgartner, B.J. and Shine, H.D.

Notes: The GDNF Emax ImmunoAssay System was used to quantify the level of GDNF in the conditioned media of HeLa cells transduced with a recombinant adenovirus expressing GDNF. The RQ1 DNase was used to treat RNA sample to remove genomic DNA and the AMV reverse transcriptase was used for first strand cDNA synthesis. (1605)

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J. Neurosci. 17, 6105-6113. The role of CED-3-related cysteine proteases in apoptosis of cerebellar granule cells. 1997

Eldadah, B.A. , Yakovlev, A.G. , Faden, A.I.

Notes: The Wizard® Plus Minipreps DNA Purification Resin was used to isolate apoptotic DNA from primary cultures of cerebellar granule cells. The cells were lysed with 7M Guanidine HCl, mixed with 1ml of resin, spun down, resuspended in wash solution, collected in a minicolumn, washed and eluted in water. The DNA was treated with RNase A and treated with the nucleic acid stain, SYBR Green, for quantitation versus a DNA standard. Two hundred nanograms of the isolated DNA were analyzed by agarose gel electrophoresis and ethidium bromide staining. The RQ1 RNase-Free DNase was used to treated total RNA samples prior to RT-PCR. (1217)

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Development 122, 121-129. Apoptosis in the developing tooth: Association with an embryonic signaling center and suppression by EGF and FGF-4. 1996

Vaahtokari, A., Åberg, T., Thesleff, I.

Notes: Paraffin-embedded tissues were deparaffinized and treated with proteinase K. The sections were fixed in paraformaldehyde and labeled with digoxigenin-labeled dUTP. Histochemical detection was accomplished with an AP-conjugated antibody and BCIP/NBT staining. As a positive control, a section was treated with RQ1 RNase-Free DNase prior to labeling with Promega's TdT and the labeled-dUTP. (0211)

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J. Clin. Invest. 98(12), 2894-2902. Particle-mediated gene transfer with Transforming Growth Factor β1 cDNAs enhances wound repair in rat skin. 1996

Benn, S., Whitsitt, J., Broadley, K., Nanney, L., Perkins, D., Patel, L., Morgan, J., Swain, W., Davidson, J.

Notes: pGL2 Vector, Beetle Luciferin, Wizard® Plus Maxipreps DNA Purification System, RNasin® Ribonuclease Inhibitor, RQ1 RNase-Free DNase, AMV Reverse Transcriptase and Taq DNA Polymerase were used in this paper. (1963)

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J. Clin. Invest. 98(8), 1851-1859. Prevention of adoptively transferred diabetes in nonobese diabetic mice with IL-10-transduced islet-specific Th1 lymphocytes: A gene therapy model for autoimmune diabetes. 1996

Moritani, M., Yoshimoto, K., Ii, S., Kondo, M., Iwahana, H., Yamaoka, T., Sano, T., Nakano, N., Kikutani, H. and Itakura, M.

Notes: Promega's RQ1 RNase-Free DNase, M-MLV Reverse Transcriptase and RNasin® Ribonuclease Inhibitor were used in this study. (2020)

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