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The DLD-1 is a laboratory equipment designed for DNA extraction and purification. It utilizes a combination of chemical and mechanical processes to isolate DNA from biological samples. The core function of the DLD-1 is to provide a reliable and efficient method for extracting high-quality DNA for use in various research and analytical applications.

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4 protocols using dld 1

1

Culturing Human Cancer Cell Lines

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The human CRC cell lines, CCK-81 and DLD-1, and the gastric cancer cell line, MKN45, were obtained from the Health Science Research Resources Bank (Osaka, Japan). The human gastric cancer cell lines, HGC-27 and NUGC-4, and the human cholangiocellular cancer cell line, HuH-28, were obtained from the RIKEN Bio Resource Center (Ibaraki, Japan). The human CRC cell line, M7609, was kindly provided by Dr. S Machida (Hirosaki University, Hirosaki, Japan). Adult human dermal fibroblasts (HDFa), as a primary normal adult human dermal fibroblast cell line from skin, were purchased from Thermo Fisher Scientific Inc. (Wilmington, DE). Each cell line was cultured in the recommended medium containing 10% fetal calf serum at 37 °C with 5% CO2.
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2

Cell Lines for Colon Cancer Research

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The Balb/c mouse colon cancer cell line CT26 was obtained from the American Type Culture Collection (Manassas, VA, USA). The human colon cancer cell lines DLD1, SW480, HCT116, KM12C, Lovo, HT29, WiDr, and Caco2 were obtained from the Health Science Research Resources Bank (Osaka, Japan), and KM12SM was kindly gifted by Dr. Isaiah J. Fidler (University of Texas, Austin, TX, USA). Balb/c mouse-derived mesenchymal stem cells (MSCs) were obtained from Cyagen Biosciences Inc. (Tokyo, Japan).
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3

Cell Line Authentication and Mycoplasma Screening

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The human embryonic kidney cell line HEK293 and the human colorectal cancer cell line DLD-1 were obtained from the Health Science Research Resources Bank (Osaka, Japan) and maintained in DMEM (Thermo Fisher Scientific) and RPMI (Thermo Fisher Scientific) supplemented with 10% fetal calf serum (Thermo Fisher Scientific), respectively. The human colorectal cancer cell line HCT116 was purchased from the American Type Culture Collection and cultured in RPMI supplemented with 10% fetal calf serum. These cell lines are not listed in the International Cell Line Authentication Committee database of cross-contaminated or misidentified cell lines. Absence of mycoplasma contamination was routinely confirmed using the e-Myco VALiD Mycoplasma PCR Detection Kit (iNtRon Biotechnology). All cell lines were authenticated by short tandem repeat profiling.
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4

Colorectal Cancer Cell Line Cultivation

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The CRC cell lines DLD‐1, COLO320DM, HT‐29, LIM1215, and M7609 were used. DLD‐1 and COLO320DM cell lines were obtained from Health Science Research Resources Bank. HT‐29 and LIM1215 cell lines were purchased from ATCC and European Collection of Cell Cultures, respectively. The M7609 cell line was kindly provided by Dr R. Machida (Hirosaki University). COLO320DM cells were maintained in DMEM supplemented with 10% FBS, 50 U/mL penicillin, and 50 U/mL streptomycin. HT‐29 cells were maintained in McCoy's 5a medium supplemented with 10% FBS. The other cell lines were cultured in RPMI‐1640 medium supplemented with 10% FBS, 50 U/mL penicillin, and 50 U/mL streptomycin. All cells were cultured at 37°C with 5% CO2.
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