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J. Biol. Chem. 272, 12809-12815.. Characterization of retinoic acid-induced AP-1 activity in B16 mouse melanoma cells. 1997

Desai, S. H. , Niles, R. M.

Notes: In this paper, the pGL2 Basic Vector, the pSV-Beta Galactosidase Control Vector and the Luciferase Assay System were used to study gene expression in B16 mouse melanoma cells. (1271)

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Proc. Natl. Acad. Sci. USA 94, 9487-9492. Characterization of the α1B-adrenergic receptor gene promoter region and hypoxia regulatory elements in vascular smooth muscle. 1997

Eckhart, A.D. , Yang, N. , Xin, X. , Faber, J.E.

Notes: Luciferase studies were performed in aortic and vena caval smooth muscle cells. Transfections were normalized to β-galactosidase activity. Researchers report that pGL3 Promoter and pGL3 Control Vectors were 55-± 3-fold and 340±41-fold greater activity, respectively, than the pGL3 Basic Vector alone. The CREB consensus oligo was used in gel shifts of aortic and vena cava smooth muscle cell nuclear extracts. (1214)

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J. Biol. Chem. 272, 12692-12698.. Cloning and characterization of the promoter region of a gene encoding a 67-kDa glycoprotein. 1997

Chatterjee, N. , Zou, C. , Osterman, J. C. , Gupta, N. K.

Notes: Luciferase studies were performed in KRC-7 rat hepatoma cells using constructs prepared in the pGL3 Basic Vector. The luciferase constructs were cotransfected with the pSV-beta-galactosidase Vector. Luciferase activities determined with the Luciferase Assay System were normalized to readings from the Beta-Galactosidase Enzyme Assay System. (1364)

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J. Biol. Chem. 272, 22425-22431. Cloning and characterization of the Type I inositol 1,4,5-trisphosphate receptor gene promoter. regulation by 17β-estradiol in osteoblasts. 1997

Kirkwood, K.L., Homick, K., Dragon, M.B., Bradford, P.G.

Notes: CAT reporter studies were performed in G-292 osteosarcoma cells using constructs prepared in the pCAT®-Basic Vector. CAT activity was normalized to β-Galactosidase activity. (0903)

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J. Biol. Chem. 272, 5915-5920. Direct association of Csk homologous kinase (CHK) with the diphosphorylated site Tyr568/570 of the activated c-KIT in megakaryocytes. 1997

Price, D. J., Rivnay, B., Fu, Y., Jiang, S., Avraham, S., Avraham, H.

Notes: The pSV-β-Galactosidase Vector was used as transfection control. The protein of interest was detected by western blotting. The amount of protein loaded on the gel was normalized to β-galactosidase activity. (0547)

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Mol. Pharmacol. 51, 703-710.. Effect of transforming growth factor-beta1 on expression of aryl hydrocarbon receptor and genes of Ah gene battery: clues for independent down-regulation in A549 cells. 1997

Dohr, O. , Sinning, R. , Vogel, C. , Munzel, P. , Abel, J.

Notes: The Transfectam® Reagent was used to transiently transfect A549 human lung cancer cells. Many details of the transfection are provided. Luciferase activity was normalized to Beta Galactosidase activity. (1240)

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J. Biol. Chem. 272, 22905-22912. Glomerular Mesangial Cell-specific Transactivation of Matrix Metalloproteinase 2 Transcription Is Mediated by YB-1 1997

Mertens, P.R., Harendza, S., Pollock, A.S., Lovett, D.H.

Notes: Luciferase studies were performed in mesanglia cells and glomerular epithelial cells. The experimental constructs were made in the pGL2 Basic and pGL2 Promoter Vectors. Luciferase activity was normalized to β-Galactosidase activity via cotransfection with the pSV-β-Galactosidase Control Vector. (0683)

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J. Biol. Chem. 272, 22776-22780. Glucose Catabolism in Cancer Cells. The type ii hexokinase promoter contains functionally active response elements for the tumor suppressor p53. 1997

Mathupala, S.P., Heese, C., Pedersen, P.L.

Notes: Luciferase studies were performed in the AS-30D hepatoma cell line using constructs made in the pGL2 Basic Vector. The effect of p53 on the hexokinase promoter was assayed in vivo by expression of the p53 from the pCI-neo Mammalian Expression Vector and promoter activity was reported with luciferase. All transfections were normalized to β-Galactosidase activity supplied by the pSV-β-Galactosidase Control Vector. (0700)

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J. Biol. Chem. 272, 8013-8018. Hyaluronan fragments induce nitric-oxide synthase in murine macrophages through a nuclear factor kappaB-dependent mechanism. 1997

McKee, C.M., Lowenstein, C.J., Horton, M.R., Wu, J., Bao, C., Chin, B.Y., Choi, A.M., Noble, P.W.

Notes: Reporter studies were performed in the mouse macrophage-like cell line RAW 264.7. Promoter constructs were prepared in the pGL2 Basic Vector and luciferase activity monitored with the Luciferase Assay System. Transfections were normalized by co-transfecting the pSV-β-Galactosidase Control Vector. The β-gal activity was assayed with the β-Galactosidase Assay System. (0713)

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J. Biol. Chem. 272, 29821-29828. Interaction between the amino- and carboxyl-terminal regions of the rat androgen receptor modulates transcriptional activity and is influenced by nuclear receptor coactivators. 1997

Ikonen, T., Palvimo, J.J., Janne, O.A.

Notes: The authors used the Promega pSV-β-Galactosidase Control Vector, pGL3-Control and pGL3-Basic Vectors, Luciferase Assay Reagent, TNT® Coupled Wheat Germ Extract Systems and TNT® Coupled Reticulocyte Lysate Systems in their studies NF-κB. (0994)

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J. Biol. Chem. 272, 15003-15010. Isolation and characterization of the human gp130 promoter. Regulation by STATS. 1997

O'Brien, C. A. , Manolagas, S. C.

Notes: Luciferase studies performed in HepG2 cells using constructs prepared in the pGL3 Basic Vector. The luciferase constructs were cotransfected with the pSV-beta-Galactosidase Control Vector to normalize for transfection efficiency. Luciferase activities were measured with the Luciferase Assay System. (0629)

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Mol. Pharmacol. 51, 620-629. Promoter analysis of the rat β1-adrenergic receptor gene identifies sequences involved in basal expression. 1997

Bahouth, S.W., Cui, X., Beauchamp, M.J., Shimomura, H., George, S.T. and Park, E.A.

Notes: Reporter studies were performed in primary rat ventricular myocytes, HepG2 cells and SK-N-MC cells using the pGL3 Basic Vector. All luciferase values were normalized to β-galactosidase activity provided by the pSV-β-Galactosidase Control Vector. PCR-generated deletion mutants of promoter constructs were subcloned into the pGEM®-T Vector and sequenced. (1491)

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J. Biol. Chem. 272, 26620-26626. Regulation of clusterin gene expression by transforming growth factor β. 1997

Jin, G., Howe, P.H.

Notes: Luciferase reporter studies performed in CCL64 (Mv1Lu) mink lung cells using constructs prepared in the pGL2-Basic Vector and were normalized to β-galactosidase activity. Studies performed in 10T1/2, 3Tp, HeLa cells and primary bovine aortic endothelial cells were normalized to the Renilla luciferase. A five to one (w/w) ratio of experimental to control vector was used with pRL-CMV Control Vector. A two to one (w/w) ratio of experimental to control vector was used with pSV-β-Galactosidase Control Vector. (0981)

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Proc. Natl. Acad. Sci. USA 94, 3296-3301. Resistance to apoptosis in CTLL-2 cells constitutively expressing c-Myb is associated with induction of BCL-2 expression and Myb-dependent regulation of bcl-2 promoter activity. 1997

Salomoni, P., Perrotti, D., Martinez, R., Franceschi, C., Calabretta, B.

Notes: Promega's pCAT® Basic and pSV Beta-Galactosidase Vectors were used in this study. Beta-galactosidase activity was assayed with the Beta-Galactosidase Enzyme Assay System with Reporter Lysis Buffer. Promega's pCAT Vectors have now been replaced by the next generation pCAT® 3 Reporter Vectors. (0434)

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J. Biol. Chem. 272, 2969-2976. Selective reporter expression in mast cells using a chymase promoter. 1997

Liao, Y., Yi, T., Hoit, B.D., Walsh, R.A., Karnik, S.S., Husain, A.

Notes: The β-Galactosidase gene was excised from the pSV-β-Galactosidase Control Vector and used to make a construct for the production of a transgenic mouse line. The expressed β-Galactosidase protein was detected in mouse tissues by a enzymatic histochemical method. The mRNA of the enzyme was also measured in various tissues and normalized to GAPDH. Promoter activity was studied in COS cells. (0804)

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J. Mol. Neurosci. 8, 63-73. Sequences in the proximal 5´ flanking region of the rat neuron-specific enolase (NSE) gene are sufficient for cell type-specific reporter gene expression. 1997

Twyman, R.M. and Jones, E.A.

Notes: In this study, regulation of the rat neuron-specific enolase gene was examined. The pCAT®-Basic and pCAT®-Control Vectors, and the pSV-β-Galactosidase Control Vector were used. Studies were performed in LTK-, Neuro2A, HeLa, and PC12 cells. The pCAT® Vectors have now been replaced with the improved pCAT®-3 Vector series. (1546)

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J. Biol. Chem. 272, 1188-1196. The mitogen-activated protein kinase and JAK-STAT signaling pathways are required for an oncostatin M-responsive element-mediated activation of matrix metalloproteinase 1 gene expression. 1997

Korzus, E., Nagase, H., Rydell, R., Travis, J.

Notes: Luciferase studies were performed in normal human dermal fibroblasts and primary human astrocytes. The experimental constructs were prepared in the pGL2-Basic and pGL2-Promoter Vectors. All luciferase activities (determined with the Luciferase Assay System) were normalized to β-Galactosidase activity. (0884)

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J. Biol. Chem. 272, 13426-13431. The polymyositis-scleroderma autoantigen interacts with the helix-loop-helix proteins E12 and E47. 1997

Kho, C.J., Huggins, G.S., Endege, W.O., Patterson, C., Jain, M.K., Lee, M.E., Haber, E.

Notes: Luciferase reporter studies were performed in NIH3T3 cells. The researchers created sort of a two-hybrid pGL2 Vector to demonstrate that two cotransfected proteins can interact and bind an enhancer element, thus increasing luc activity. Researchers expressed one protein as a GST fusion and the other as a 35S-met protein in the TNT® Coupled Reticulocyte Lysate System and showed that the 35S-protein could be pulled out of the lysate. (0937)

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J. Biol. Chem. 272, 19253-19260. Transactivation and inhibitory domains of hypoxia-inducible factor 1α. Modulation of transcriptional activity by oxygen tension. 1997

Jiang, B.H., Zheng, J.Z., Leung, S.W., Roe, R., Semenza, G.L.

Notes: The pSV-β-Galactosidase Control Vector was used to control transfections into Hep3B cells. (0976)

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J. Biol. Chem. 272, 19575-19581. Transcriptional regulation of N-acetylglucosaminyltransferase V by the src oncogene. 1997

Buckhaults, P., Chen, L., Fregien, N., Pierce, M.

Notes: Luciferase studies were performed in HepG2 cells using the Luciferase Assay System. Experimental constructs were prepared in the pGL2-Basic Vector. Transfection efficiency was standardized using the β-Galactosidase Assay System with Reporter Lysis Buffer. (2245)

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J. Biol. Chem. 272(6), 3430-3436. Transcriptional regulation of the human PAX6 gene promoter. 1997

Xu, Z.P. and Saunders, G.F.

Notes: PolyA+ RNA was isolated from U87, K562, 293, HepB3, HeLa, NIH3T3 and lymphoblastiod total RNA using the PolyATtract® mRNA Isolation System. The isolated RNA was used for Northern analysis. Expression of CAT reporter constructs, derived from the pCAT® Basic Vector, was studied in the U87, K562 and HeLa cells and normalized to control beta-galactosidase. (1698)

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