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Chloroquine dihydrochloride

Manufactured by Merck Group
Sourced in Sao Tome and Principe

Chloroquine dihydrochloride is a synthetic chemical compound used as a laboratory reagent. It is a dichloride salt of the organic compound chloroquine, which is commonly used as an antimalarial drug. As a laboratory chemical, chloroquine dihydrochloride is primarily used for research and analysis purposes, but its specific applications may vary depending on the research context.

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2 protocols using chloroquine dihydrochloride

1

Packaging and Transducing Cell Lines

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Phoenix A (amphotropic) cells were plated at a density of 4 × 105 cells/well on a 6-well plate. On the following day, culture media was replaced with fresh media (Dulbecco’s modified Eagle medium, high glucose, 10% fetal bovine serum, pen-strep, L-glutamine). Chloroquine dihydrochloride (S764663; Sigma, St. Louis, MO) was added to Phoenix cells 5 minutes before transfection and 2 μg of plasmid DNA was transfected into cells using the Profection kit (E1200; Promega, Madison, WI). The media was changed 10 hours after transfection. Retroviral supernatant was collected the following day and 2 mL was added to GP+E86 cells, plated at 4 × 104 cells/well on a 6-well dish the previous day, after filtration (0.45 μm) and supplemented with protamine sulfate (5 μg/mL). GP+E86 cells were transduced again on the following day. Viral supernatant from GP+E86 cells was collected on the following 2 days and used to transduce C3H10T1/2 cells.
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2

Retroviral Transduction of C3H10T1/2 Cells

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Phoenix A (amphotropic) cells were plated at a density of 4 × 105 cells/well on a 6-well plate. On the following day, culture media was replaced with fresh media (Dulbecco's modified Eagle medium, high glucose, 10% fetal bovine serum, pen-strep, L-glutamine). Chloroquine dihydrochloride (S764663; Sigma, St. Louis, MO) was added to Phoenix cells 5 minutes before transfection and 2 μg of plasmid DNA was transfected into cells using the Profection kit (E1200; Promega, Madison, WI). The media was changed 10 hours after transfection. Retroviral supernatant was collected the following day and 2 mL was added to GP+E86 cells, plated at 4 × 104 cells/well on a 6-well dish the previous day, after filtration (0.45 μm) and supplemented with protamine sulfate (5 μg/mL). GP+E86 cells were transduced again on the following day. Viral supernatant from GP+E86 cells was collected on the following 2 days and used to transduce C3H10T1/2 cells.
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