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E600003

Manufactured by Sangon
Sourced in China

The E600003 is a laboratory equipment product. It is used for [core function]. The product specifications and technical details are not available for this response.

Automatically generated - may contain errors

3 protocols using e600003

1

Culturing Cervical Cell Lines

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Normal cervical cell line HcerEpic and human cervical cancer cell lines, including CaSki, C‐33A HeLa, HeLa‐229, ME‐180, MS751 and SiHa, were obtained from National Collection of Authenticated Cell Cultures of China. All cell lines were maintained in DMEM (E600003; Sangon Biotech) containing 10% foetal bovine serum (E510008; Sangon Biotech) in a 5% CO2 atmosphere at 37°C.
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2

Culturing Murine Tumor and Human Endothelial Cells

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The murine breast cancer 4T1 (Cell Bank of the Chinese Academy of Sciences, China) was cultured in the complete RPMI‐1640 medium (Sangon Biotech; E600028) including 10% fetal bovine serum (FBS; Excell Bio, Shanghai; FSP500) and 1% penicillin–streptomycin 100× (PS; Macgene, Beijing, CC004). The murine melanoma B16F10 (Cell Bank of the Chinese Academy of Sciences, China) was cultured in the complete DMEM medium (high glucose; Sangon Biotech; E600003) including 10% FBS and 1% penicillin–streptomycin 100×. The murine kidney cancer Renca was purchased from Procell (Wuhan; CL‐0568) and incubated with complete RPMI‐1640 (Procell, Wuhan; PM150110) with 10%FBS, 1% penicillin–streptomycin 100x, 1% MEM Nonessential Amino Acids Solution 100× (NEAA; Macgene; CC25025), 1 mM Sodium Pyruvate (Macgene; CC007), and 2 mM L‐glutamine (Macgene; CC009). The human normal endothelial cell line PUMC‐HUVEC‐T1 was cultured in the DMEM medium (high glucose) and added 1%NEAA and insulin (Macgene).
All the cells were incubated in their special medium and maintained in a carbon dioxide cell culture box (Thermo Fisher‐Forma 371) with 5% CO2 at 37°C.
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3

Transwell Assay for Invasion and Metastasis

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For the purpose of monitoring invasion and metastasis, Transwell migration chambers were utilized (24-well chambers, 354572 Corning, USA). Matrigel (356234 BD, Solarbio, China) was applied to the container inserts prior to cell invasion trials. In both tests, the upper chamber of each well was seeded with 2×105 cells in 300 µL of serum-free media. A mixture of 600–800 µL DMEM (E600003, Sangon Biotech) supplemented with 10% FBS (E510008, Sangon Biotech) was used to fill the lower chambers of the Transwell. Subsequently, the cells were incubated for 24 hours. The top chambers were then rinsed with phosphate-buffered saline (PBS, E607008, Sangon Biotech), fixed with 4% paraformaldehyde (PFA, E672002, Sangon Biotech) for 30–60 minutes, and dyed with 1% crystal violet (A600331, Sangon Biotech) to obtain the desired appearance. Photomicrographs of the cell layers were taken with an Olympus BX51 microscope.
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