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HeLa cell lines are a type of immortalized human cervical cancer cells. They are widely used in scientific research as a model system for various studies, including cell biology, virology, and cancer research. The HeLa cell lines are characterized by their ability to proliferate indefinitely in cell culture, making them a valuable resource for researchers.

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2 protocols using hela cell lines

1

Protocol for Synthesizing Gold and Palladium Nanoparticles

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Deionized water (resistivity: 18.2 MΩ cm−1), which was obtained from a Milli-Q water purification system, was utilized for the preparation of all aqueous solutions. Hydrogen tetrachloroaurate(III) tetrahydrate (HAuCl4·4H2O, Nacalai Tesque), trisodium citrate dihydrate (Kanto Chemical, Japan), L-ascorbic acid (Fujifilm Wako Pure Chemical, Japan), palladium(II) chloride (PdCl2, Fujifilm Wako Pure Chemical, Japan), hydrochloric acid (HCl, Fujifilm Wako Pure Chemical, Japan), hydroxypropyl cellulose (Sigma-Aldrich, USA), 2-propanol (Kishida Chemical, Japan), ammonium aqueous solution (28 wt%, Kishida Chemical, Japan), titanium diisopropoxide bis(acetylacetonate) (TDAA, Sigma-Aldrich, USA), and 8-ArmPEG-Amine (20,000 Da, Biopharma PEG Scientific, USA) were used as received. Dulbecco's Modified Eagle's Medium (D-MEM, low glucose) with L-glutamine and phenol red and PBS(-) were obtained from Fujifilm Wako Pure Chemical, Japan. Penicillin streptomycin, trypsin–EDTA (0.25%), and fetal bovine serum (FBS) were obtained from Gibco, USA. HeLa cell lines were purchased from JCRB Cell Bank, Japan.
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2

Silencing ADAR1 in HPV Cell Lines

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HeLa cell lines were obtained from the Japanese Collection of Research Bioresources (JCRB) Cell Bank. SiHa cells were obtained from the American Type Culture Collection (ATCC). The HPV16-type SiHa, HPV18-type HeLa, and non-HPV-type Yumoto cell lines were maintained in Dulbecco’s Modified Eagle’s Medium (Life Technologies, CA, USA), supplemented with 10% fetal bovine serum. Cell lines were maintained in a humidified incubator containing 5% CO2 at 37 °C. Cells were used for functional experiments within 3 months of passaging post-receipt. The SiHa, HeLa, and Yumoto cell lines were trypsinized and plated in culture dishes. At ~ 50% confluency, the cell lines were transfected with an annealed ADAR1 siRNA (siADAR1, sc-37657; Santa Cruz Biotechnology, TX, USA), control siRNA (siControl, sc-37007; Santa Cruz Biotechnology, TX, USA), or an empty vector (mock) for gene silencing (final concentration, 100 nmol/L) using an siRNA transfection reagent (sc-29528; Santa Cruz Biotechnology, TX, USA).
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