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Cm0451

Manufactured by Procell
Sourced in China

The CM0451 is a laboratory equipment that functions as a centrifuge. It is designed to separate components of a liquid mixture based on their density differences through the application of centrifugal force. The specific technical details and intended uses are not provided.

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3 protocols using cm0451

1

siRNA-Mediated Knockdown of ESM1 in Human ACC

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The siRNA treatment was conducted as previously described (42 (link)). The human SW13 cell, one of the human ACC cell lines, was transfected with 50 nmol of ESM1 siRNA (siESM1) or negative control siRNA (siNC) in a special medium (CM0451, Procell, Wuhan, China) for 48 h. SW13 cells were then lysed by TRIzol reagent (Invitrogen, Waltham, MA, USA) for total RNA isolation. The cDNA was obtained by oligo-dT primers and reverse transcriptase kit (Invitrogen, USA). Quantitative real-time PCR (qRT-PCR) was performed by SYBR Green PCR Master Mix (Qiagen, Hilden, Germany) and specific primers in an ABI Prism 7500 analyzer (Applied Biosystems, Waltham, MA, USA). GAPDH was an endogenous reference gene. Three replicates were set for all reactions. The 2−ΔΔCt method was applied to calculate the relative expression of ESM1 in ACC samples. The related primers are listed in Supplementary Table S4.
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2

siRNA Knockdown of CENPF and CDK1 in ACC

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The siRNA transfections were performed according to the manufacturer’s instructions. As one of the human ACC cell lines, SW13 cells were transfected with 50 nmol of CENPF siRNA (siCENPF), CDK1 siRNA (siCDK1), or negative control siRNA (siNC) in a special medium (CM0451, Procell, China) for 48 h. Then, SW13 cells were lysed by TRIzol reagent (Invitrogen, USA) for total RNA isolation. The cDNA was obtained by reverse transcriptase kit (Invitrogen, USA). SYBR Green PCR Mixture (Qiagen, Germany) and specific primers were performed in ABI Prism 7500 analyzer (Applied Biosystems, USA). GAPDH was an endogenous reference gene. Three replicates were set for all reactions. The 2−ΔΔCt method was applied to calculate the relative expression of CENPF or CDK1 in ACC samples. The details of primers were listed in Additional file 4: Table S4.
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3

Culturing Human Adrenal Carcinoma Cells

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The human ACC cell lines, NCI-H295R and SW-13, were acquired from Procell Life Science &Technology (Wuhan, China). SW-13 cells were maintained in Leibovitz's L-15, with 10% FBS and 1% P/S (Procell, CM-0451). NCI-H295R cells were maintained in DMEM/F12, with 6.25 μg/mL insulin, 6.25 ng/mL selenium, 6.25 μg/mL transferrin, 5.35 μg/mL linoleic acid, 10% FBS and 1% P/S (Procell, CM-0399).
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