The intracellular uptake and localization of a ยฏuorescently labeled Pluronic P-105 in HL-60 leukemia cells and in A2780 drug-sensitive and A2780/ADR MDR ovarian carcinoma cells were characterized by ยฏow cytometry and ยฏuorescence microscopy. Pluronic P-105 molecules were labeled with a pH-sensitive ยฏ
Studies on the uptake and intracellular localization of 3H actinomycin D in lens epithelial cells
โ Scribed by David Sonneborn; Howard Rothstein
- Publisher
- Elsevier Science
- Year
- 1967
- Tongue
- English
- Weight
- 182 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0303-2647
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Actinomycin D(AM), an inhibitor of DNA-dependent RNA synthesis, produces a reversible cessation of red blood cell production. This study examines the in vivo cellular uptake of 3H-AM in the hematological tissues and livers of B6D2FI mice. 3H-AM (sp. act. = 2.97 to 4.20 C/mmole) was given IV at a dos
## Abstract The rate of uptake of 2โdeoxyglucose in normal rat hepatic cells and chemically induced hepatoma cells in culture was studied. The hepatoma cells possessed a higher permeability to the sugar at all stages of culture. However, a decrease in the uptake of 2โdeoxyglucose at confluency was
## Abstract Cultured neural crest melanocytes from chick embryos were treated with actinomycin D or cycloheximide. The effects of these inhibitors upon melanogenesis was determined by monitoring the incorporation of ^3^HโDOPA into premelanosomes and melanosomes using high resolution autoradiography
## Abstract Chinese hamster cells of an established clone line grown in monolayers were incubated for up to two hours with either lucanthone (0.3โ30 mฬg/ ml) or actinomycin D (0.06โ0.10 mฬg/ml) and subjected to radioautographic investigations with ^3^Hโuridine during the period of treatment. At co