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Znso4

Manufactured by Nacalai Tesque
Sourced in Japan

Zinc sulfate (ZnSO4) is a chemical compound that is commonly used in laboratory settings. It is a white, crystalline solid that is soluble in water. Zinc sulfate serves as a source of the zinc ion (Zn2+) and the sulfate ion (SO4^2-) in various chemical reactions and applications.

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2 protocols using znso4

1

SK-MEL-2 Luciferase Cell Culture

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SK-MEL-2 cells containing the Luc gene (JCRB cell bank) were maintained at 37 °C in a humidified 5% CO2 incubator using RPMI1640 culture medium (FUJIFILM Wako Pure Chemical) containing 10% heat-inactivated fetal calf serum (Sigma–Aldrich), 100 U/ml penicillin, and 100 μl/ml streptomycin (Nacalai Tesque) in 10 cm dish (Thermo Fisher Scientific). Dulbecco’s modified Eagle’s medium (FUJIFILM Wako Pure Chemical) or Iscove’s modified Dulbecco’s medium (Nacalai Tesque) was used to maintain A549 or HAP1 cells as previously described (16 (link), 25 (link)). Zinc-supplementation experiments involved adding the indicated concentrations of ZnSO4 (Nacalai Tesque) to the cell culture medium.
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2

Zinc Pretreatment Protects Against Carbon Tetrachloride-Induced Liver Toxicity in Mice

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Mice were divided into two groups of ten or eleven mice each. At -72, -48, and -24 hr, animals of the group-1 were administered at 24-hr intervals by s.c. injection with 50 mg/kg ZnSO 4 (Nacalai Tesque, Kyoto, Japan). Twentyfour hours after the final ZnSO 4 injection, both group-1 and group-2 (not treated with ZnSO 4 ) were injected i.p. with 4 g/kg (at 5 mL/kg) CCl 4 . At 6 hr after the CCl 4 injection, three randomly selected mice from each group were euthanized and bled for plasma. The resulting plasma samples were stored at -80°C (pending alanine aminotransferase (ALT) assays). Livers were harvested from each of these animals, and separate samples from each liver were stored at -80°C (pending quantitative reverse transcription (RT)-PCR assay) or fixed in 15% neutral buffered formalin (pH 7.2) (pending processing for histological evaluation). The remaining seven or eight mice of each group were monitored every 3 hr until 24 hr after CCl 4 administration to determine acute mortality; the surviving animals were weighed and then terminated. Using equivalent protocols, protection from CCl 4 lethal toxicity was assessed using single pre-CCl 4 injections with 50 mg/kg ZnSO 4 or with 3 mg/kg CdCl 2 · 2.5H 2 O (Wako Chemical) administered s.c..
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