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The Calu-1 is a laboratory equipment product designed for general laboratory use. It serves as a versatile tool for researchers and scientists in various fields. The Calu-1 provides core functionality for a range of laboratory tasks, but a more detailed description cannot be provided while maintaining an unbiased and factual approach.

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14 protocols using calu 1

1

Culturing NSCLC Cell Lines

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All NSCLC lines (H2087, HCC44, Calu-1, H358, H1993) used in this study were obtained from the Hamon Cancer Center Collection (University of Texas Southwestern Medical Center), maintained in RPMI-1640 (Life Technologies), and supplemented with 5% FBS, penicillin (100 units/ml), and streptomycin (100 μg/ml) at 37°C in a humidified atmosphere containing 5% CO2. All cell lines have been DNA fingerprinted using the PowerPlex 1.2 kit (Promega) and are mycoplasma free using the e-Myco kit (Boca Scientific).
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2

Cell Line Culture Conditions

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Four engineered BJ cell lines (BJeLR/DRD/BJeHLT/BJeH) were obtained from Robert Weinberg (Whitehead Institute). 143B cells (osteosarcoma) were from Eric Schon (Columbia University). Calu-1 (lung adenocarcinoma) and HT-1080 (fibrosarcoma) cells were from American Type Culture Collection. The four BJ cell lines were grown in DMEM High-Glucose media (Life Technologies), 20% Medium 199 (Sigma), and 15% heat-inactivated fetal bovine serum (FBS). HT-1080 cells were grown in DMEM High-Glucose media with 1% non-essential amino acids (Life Technologies) and 10% FBS. 143B cells were grown in DMEM High-Glucose media with 1% glutamine and 10% FBS. Calu-1 cells were grown in McCoy’s 5A media (Life Technologies) supplemented with 10% FBS. All the cell lines were grown at 37°C under 5% CO2.
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3

Cell Line Culture Conditions

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Four engineered BJ cell lines (BJeLR/DRD/BJeHLT/BJeH) were obtained from Robert Weinberg (Whitehead Institute). 143B cells (osteosarcoma) were from Eric Schon (Columbia University). Calu-1 (lung adenocarcinoma) and HT-1080 (fibrosarcoma) cells were from American Type Culture Collection. The four BJ cell lines were grown in DMEM High-Glucose media (Life Technologies), 20% Medium 199 (Sigma), and 15% heat-inactivated fetal bovine serum (FBS). HT-1080 cells were grown in DMEM High-Glucose media with 1% non-essential amino acids (Life Technologies) and 10% FBS. 143B cells were grown in DMEM High-Glucose media with 1% glutamine and 10% FBS. Calu-1 cells were grown in McCoy’s 5A media (Life Technologies) supplemented with 10% FBS. All the cell lines were grown at 37°C under 5% CO2.
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4

Cell Culture Protocols for A549, Calu-1, and HEK293T

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A549, Calu‐1, and HEK293T cells were obtained from the American Type Culture Collection (Manassas, VA, USA). A549 and Calu‐1 cells were cultured in RPMI‐1640 (Invitrogen, Carlsbad, CA, USA), and HEK293T cells were cultured in DMEM (Invitrogen) supplemented with 10% FBS (Invitrogen) at 37°C in 5% CO2.
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5

Cell Culture Conditions for HER3-Positive and Negative Lung and Head/Neck Cancer Lines

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We used the non-small cell lung cancer cell line H441 (HER3positive), head and neck squamous cell cancer cell line FaDu (HER3positive), and non-small cell lung cancer cell line Calu-1 (HER3-negative), obtained from American Type Culture Collection (14) . FaDu and H441 cells were cultured in Dulbecco modified Eagle medium (Invitrogen), supplemented with 10% fetal calf serum (Bodinco BV) and 2 mM L-glutamine (Invitrogen). Calu-1 was cultured in RPMI 1640 (Invitrogen) supplemented with 10% fetal calf serum and 2 mM L-glutamine. All cells were grown at 37°C in a fully humidified atmosphere containing 5% CO 2 .
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6

Cell Line Cultivation and Maintenance

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The A549, Calu-1, HT-29, PC-9, SW480, and SW-620 cell lines were obtained from the American Type Culture Collection (ATCC). Calu-1 and SW480 cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM; Gibco, Grand Island, NY, USA), while A549, PC-9, SW-620, and HT-29 cells were cultured in RPMI 1640 medium (Gibco). The media were supplemented with 10% fetal bovine serum (FBS; Gibco), 100 U/ml penicillin, and 100 μg/ml streptomycin (Gibco).
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7

Cell Culture Protocols for Lung Cancer

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Human lung adenocarcinoma A549 (RCB0098) and human normal lung fibroblast WI-38 cells (RCB0702) were obtained from the RIKEN Bioresource Center, Ibaraki, Japan. Human lung epidermoid carcinoma Calu-1 was purchased from the Cell Lines Service (CLS; Eppelheim, Germany) and human lung large cell carcinoma COR-L23 from the European Collection of Authenticated Cell Cultures (ECACC; Salisbury, UK). A549 and WI-38 cells were cultured in D-MEM medium (Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA). Calu-1 and COR-L23 were cultured in RPMI-1640 medium (Gibco). These culture media were supplemented with 10% (v/v) fetal bovine serum (FBS; Hyclone; GE Healthcare Life Sciences, Logan, UT, USA) and 1% antibiotics (Gibco) at 37°C in a 5% CO2 humidified atmosphere. All of the cell lines are mycoplasma free. The continuous cell lines are routinely checked in every other month by a PCR method using a service from The Center for Veterinary Diagnosis, Faculty of Veterinary Science, Mahidol University Salaya Campus, Nakorn Pathom, Thailand.
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8

Cell Culture Protocols for NSCLC and Control Lines

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NSCLC cell lines (A549, H1299, and Calu1), human bronchial epithelial cell line (BEAS-2B), and murine lung carcinoma cell line (LLC) were purchased from the American Type Culture Collection (ATCC, Manassas, VA, USA). A549 cells were grown in the F-12K (Gibco) medium supplemented with 10% FBS (Gibco) and 1% penicillin/streptomycin. H1299 and Calu1 cells were cultured in the RPMI-1640 medium (Gibco) with 10% FBS and 1% penicillin/streptomycin. BEAS-2B and LLC cells were maintained in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% FBS and 1% penicillin/streptomycin. All cells were cultured at 37 °C with 5% CO2 in a humidified incubator.
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9

Cell Culture Protocol for Lung Cancer Cell Lines

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A549, Calu-1, Calu-6, HCC827, NCI-H-1792, and BEAS-2B were purchased from Shanghai Institute of Biochemistry and Cell Biology (Shanghai, China). A549, Calu-1, Calu-6, HCC827, NCI-H-1792, and BEAS-2B cells were cultured in Dulbecco's Modified Eagle Medium (DMEM), 10% fetal bovine serum (Gibco, Waltham, MA USA), and 1% double antibody (Gibco, Waltham, MA, USA) in a cell culture incubator at 37°C and 5% CO2.
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10

Culturing LUAD and HEK-293T Cell Lines

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The human LUAD cell lines (A549, Calu1 and Hop62) and a human embryonic kidney cell line (HEK-293T) were purchased from the American Type Culture Collection (ATCC, Manassas, VA, USA). A549, Calu1 and Hop62 cells were cultured in Roswell Park Memorial Institute 1640 Media (RPMI 1640; Gibco, Carlsbad, CA, USA). HEK-293T cells were cultured in Dulbecco's Modified Eagle Medium (DMEM; Gibco). All medium was supplemented with 10% fetal bovine serum (FBS; Gibco) and 1% penicillin/streptomycin (Gibco). All cell lines were cultured in a humidified atmosphere with 5% CO2 and at 37 °C.
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