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Proc. Natl. Acad. Sci. USA 94, 5131-5136. Cooperative functions of the reaper and head involution defective genes in the programmed cell death of Drosophila central nervous system midline cells. 1997

Zhou, L.,, Schnitzler, A., Agapite, J., Schwartz, L.M., Steller, H. and Nambu, J.R.

Notes: The antibody was used in immunohistochemical localization of beta-galactosidase protein in Drosphila embryos. (1551)

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EMBO J. 16, 515-522. D-mef2 is a target for Tinman activation during Drosophila heart development. 1997

Gajewski, K. , Kim, Y. , Lee, Y. M. , Olson, E. N. , Schulz, R. A.

Notes: The Anti-β-Galactosidase mAb was used for immunohistochemical localization of lacZ fusion proteins in whole mount Drosophila embryos. (1135)

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J. Biol. Chem. 272(18), 11979-11985. Defining a region of the human keratin 6a gene that confers inducible expression in stratified epithelia of transgenic mice. 1997

Takahashi, K. and Coulombe, P.A.

Notes: The Anti-β-Galactosidase Purified Monoclonal Antibody was used to immunohistochemically stain paraffin-embedded transgenic mouse skin epithelial tissue sections. Induced β-Galactosidase expression was detected by immunohistochemically staining 5μm tissue sections fixed in Bouin’s fixative and embedded in paraffin. Staining was visualized using a peroxidase labeled secondary antibody and a colorimetric peroxidase substrate.  (3028)

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J. Biol. Chem. 272, 22191-22198. SV40 large tumor antigen nuclear import is regulated by the double- stranded DNA-dependent protein kinase site (Serine 120) flanking the nuclear localization sequence 1997

Xiao, C. Y. , Hubner, S. , Jans, D. A.

Notes: Promega's Casein Kinase II and DNA-Dependent Protein Kinase were used for in vitro phosphorylation of the SV40 large T antigen expressed either from Rabbit Reticulocyte Lysate or a large Tantigen-β-Gal fusion protein expressed in a rat hepatoma cell line. Lysates and cell extracts were assayed for DNA-dependent protein kinase activity with a peptide substrate. The ability of β-Gal-T antigen fusions (± phosphorylation) to bind to murine importin subunits was assessed by an ELISA system using the Anti-β-Galactosidase mAb. (0120)

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J. Neurosci. 17, 676-696. Temporal and spatial expression patterns of transgenes containing increasing amounts of the Drosophila clock gene period and a lacZ reporter: Mapping elements of the PER protein involved in circadian cycling. 1997

Stanewsky, R., Frisch, B., Brandes, C., Hamblen-Coyle, M.J., Rosbash, M. and Hall, J.C.

Notes: The Anti-β-Galactosidase mAb was used to localize β-galactosidase in adult fly brains. The antibody was also used to probe immunoblots of fly brain extracts. (1543)

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EMBO J. 16, 5509-5519. The ubiquitin-like protein Smt3p is activated for conjugation to other proteins by an Aos1p/Uba2p heterodimer. 1997

Johnson, E.S., Schwienhorst, I., Dohmen, R.J., Blobel, G.

Notes: The Anti-β-Galactosidase mAb was used to detect β-Galactosidase fusion proteins in S. cerevisiae extract by immunoblotting. (0940)

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Cell 86, 411-422. Hedgehog, transmitted along retinal axons, triggers neurogenesis in the developing visual centers of the Drosophila brain. 1996

Huang, Z. and Kunes, S.

Notes: The antibody is used to localize beta-galactosidase protein by immunohistochemistry of Drosophila tissues. (1579)

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Cell 87, 651-660. Reiterative use of the EGF receptor triggers differentiation of all cell types in the Drosophila eye. 1996

Freeman, M.

Notes: The antibody was used to localize beta-galactosidase by immunohistochemistry of Drosophila eyes. (1571)

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Proc. Natl. Acad. Sci. USA 93, 13250-13255. The 3´-untranslated region of CaMKII alpha is a cis-acting signal for the localization and translation of mRNA in dendrites. 1996

Mayford, M., Baranes, D., Podsypanina, K. and Kandel, E.R.

Notes: The antibody is used to localize β-galactosidase protein by immunocytochemistry of neuronal cultures of mouse hippocampi. (1587)

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Development 121, 2681-2693. Analysis of function and expression of the chick GPA receptor (GPAR α) suggests multiple roles in neuronal development. 1995

Heller, S., Finn, T.P., Huber, J., Nishi, R., Geissen, M., Puschel, A.W., Rohrer, H.

Notes: The authors used the CellTiter 96® Non-Radioactive Cell Proliferation Assay (MTT) and Anti-β-Galactosidase mAb in a TF-1 cell line. (1034)

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