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Wallac wizard 3 1480 automatic gamma counter

Manufactured by PerkinElmer
Sourced in United States

The Wallac Wizard 3'' 1480 Automatic Gamma Counter is a laboratory equipment designed for the measurement and analysis of gamma radiation. It features automatic sample handling and data processing capabilities.

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2 protocols using wallac wizard 3 1480 automatic gamma counter

1

Uptake Assays for Radiolabeled Probes

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Uptake assays were performed as previously described [15 ]. Briefly, U87 cells were plated 1 day prior at 50 % confluency in 15-cm tissue culture-treated plates. On the day of the experiment, media was replaced with 15 ml of media conditioned to 37 °C and 5 % CO2, supplemented with 185 kBq/ml F-18 labeled probe, 0.37 kBq/ml [14C]FMAU, or 37 kBq/ml [124I]FIAU and placed in a cell incubator at 37 °C and 5 % CO2 for 2 h. Cells were collected by scraping and centrifugation, and washed twice with ice-cold PBS. For F-18 and I-124 labeled assays, cell pellets and corresponding supernatant samples were counted on a Wallac Wizard 3″ 1480 Automatic Gamma Counter (PerkinElmer). For [14C]FMAU, cell pellets and supernatant samples were resuspended in Insta-Fluor scintillation liquid (Perkin Elmer), vortexed and counted on a TriCarb 2910 Scintillation Counter (PerkinElmer). Cell pellets were normalized to their respective masses.
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2

Cytotoxicity Assay for Effector T Cells

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The cytotoxicity of effector T cells was measured by a standard 4-h 51Cr-release assay that used T24 cells, K562 cells, or tumor antigen-pulsed DCs as targets. Effector cells were incubated with 51Cr-labeled target cells (5 × 103) for 4 h at 37 °C in 200 µL of RPMI 1640 medium containing 10% FCS in round-bottomed 96-well cell culture plates. After incubation, the plates were centrifuged for 10 min at 330×g, and 100 µL of cell-free supernatant was collected to measure radioactivity with a Wallac Wizard 3 (1480 Automatic Gamma Counter; Perkin Elmer, Waltham, MA, USA). Maximum release was determined from the supernatant of cells that had been lysed by the addition of 5% Triton X-100, and spontaneous release was determined from target cells incubated without added effector cells. The percent specific lysis was calculated as follows: 100 × (experimental release − spontaneous release)/(maximum release − spontaneous release).
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