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Cal 148

Manufactured by Leibniz Institute DSMZ
Sourced in Germany, Australia

The CAL-148 is a laboratory instrument used for the analysis and characterization of biological samples. It is designed to provide accurate and reliable measurements of various parameters, including cell count, viability, and cell size distribution. The CAL-148 utilizes advanced technology to deliver consistent and reproducible results, making it a valuable tool for researchers and scientists in the field of life sciences.

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5 protocols using cal 148

1

Breast Cancer Cell Line Cultivation Protocol

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Human TNBC cell lines MDA-MB-231, MDA-MB-436, MDA-MB-157, HCC1806, HCC1937, Hs578T, HCC38, BT549, HCC1187, and HCC1395 were obtained from American Type Culture Collection (ATCC, Manassas, VA). CAL-51, CAL-85-1, CAL-120, CAL-148 and HDQ-P1 were obtained from the Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ, Braunschweig, Germany). MDA-MB-468, BT20, and HCC70 were obtained from the University of Colorado Cancer Center (UCCC) Tissue Culture Core laboratory. The MCF-10A cell line was obtained as a kind gift from Traci Lyons, PhD and used as a control. All breast cancer cells were cultured in DMEM supplemented with 10% FBS, 1% penicillin–streptomycin, 1% MEM nonessential amino acids and 1% normocin. All cells were grown in an incubator at 37°C containing 5% CO2. Cell lines were routinely authenticated by the Barbara Davis Center for Childhood Diabetes Core and screened for mycoplasma every 3 months.
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2

Breast Cancer Cell Line Cultures

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The BT549, BT20, DU4475, HCC38, HCC70, HCC1500, HCC1569, HCC1954, HCC1806, HCC1143, HCC1937, HS578T, MDA-MB-157, MDA-MB-436, MDA-MB-453, MDA-MB-231, and MDA-MB-468 cell lines were purchased from the American Type Culture Collection; CAL51, CAL148, and CAL851 cells were obtained from Deutsche Sammlung von Mikroorganismen und Zellkulturen; SUM185PE and SUM149PT cells were purchased from Asterand Bioscience; MFM223 cells were purchased from Sigma-Aldrich; and CAL120 cells were a gift from Professor Elgene Lim from the Garvan Institute of Medical Research, Darlinghurst, NSW, Australia. All the above cell lines were cultured in RPMI supplemented with 10% FBS and 0.023 IU/ml (or 10 µg/ml) insulin. MDA-MB231(LM2) cells (a kind gift from Dr. Joan Massague, Sloan-Kettering Memorial Institute, New York, NY; Minn et al., 2005 (link)) were cultured in DMEM supplemented with 10% FBS.
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3

Comprehensive Breast Cancer Cell Line Panel

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The BT549, BT20, DU4475, HCC38, HCC70, HCC1500, HCC1569, HCC1954, HCC1806, HCC1143, HCC1937, HS578T, MDA-MB-157, MDA-MB-436, MDA-MB-453, MDA-MB-231 and MDA-MB-468 cell lines were purchased from the American Type Culture Collection (ATCC; Manassas, VA, USA). CAL51, CAL148 and CAL851 cells were obtained from Deutsche Sammlung von Mikroorganismen und Zellkulturen (DSMZ) and CAL120 cells were a gift from Professor Elgene Lim from the Garvan Institute of Medical Research, Darlinghurst, NSW 2010, Australia. MFM223 cells were purchased from Sigma Aldrich. SUM185PE and SUM149PT cells were purchased from Asterand Bioscience. Cells were cultured in RPMI 1640 (Gibco) supplemented with 10% (v/v) FBS, 10 μg/mL insulin and 20 mM HEPES.
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4

Comprehensive TNBC Cell Line Characterization

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Nine of the 12 TNBC cell lines, as well as the non-transformed, immortalized control breast cell line MCF10A were obtained from the American Type Culture Collection (ATCC, Manassas, VA 20110, USA). Excluding BT-20 and MDA-MB-231, which were received in 2012, the cell lines were received in 2011. MDA-MB-468, BT-474, and ZR-75-1 were obtained by the Cell Culture Facility at Fox Chase Cancer Center from ATCC as part of the NCI-60 panel. The NCI-60 panel was obtained in 2003. The two additional TNBC cell lines, CAL-148 and MFM-223, were purchased from the Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (Braunschweig, Germany) in 2011. The suppliers routinely authenticate the cell lines by short tandem repeat profiling though the cell lines were not authenticated by our laboratory. All cell lines were amplified and frozen within 2 months of receipt. Cell lines are periodically tested for Mycoplasma contamination using DAPI (4′,6-diamidino-2-phenylindole) to stain DNA. Two different primary human mammary epithelial cell (HMEC) isolates were obtained from GIBCO (Details A10565) and Lonza (CC-2551), respectively, in 2012. Culture media for the cell lines can be found in Supplementary Table S1.
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5

Cultivation of Human Cell Lines

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MDA-MB-453, T-47D, 22Rv1, VCaP, ZR75–1, MDA-MB-231, MCF7 and HEK293T/17 cells were obtained from the American Type Culture Collection (Manassas, VA, USA). MFM-223, Cal-51 and Cal-148 cells were obtained from the Leibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures (Braunschweig, Germany). LNCaP-95 cells were a kind gift from Dr. Alan K. Meeker (Johns Hopkins University). MDA-MB-453, T-47D, ZR75–1 and 22Rv1 cells were maintained in RPMI-1640 medium containing 10% fetal bovine serum (FBS); VCaP cells were maintained in Dulbecco's Modified Eagle's Medium (DMEM) containing 10% FBS, 1% sodium pyruvate, 1% MEM non-essential amino acids and 0.1 nM 5α-dihydrotestosterone (DHT; Sigma, St. Louis, MO, USA); MDA-MB-231 cells were maintained in RPMI-1640 medium containing 5% FBS; MCF7 cells were maintained in Eagle's Minimum Essential Medium (EMEM) containing 10% FBS, 2 mM L-glutamine, sodium pyruvate and 0.2 U/mL insulin; MFM-223 cells were maintained in EMEM containing 10% FBS, 2 mM L-glutamine, and insulin-transferrin-sodium selenite (ITS) supplement; Cal-51 cells were maintained in DMEM containing 10% FBS; Cal-148 cells were maintained in DMEM containing 10%FBS, 2 mM L-Glutamine and EGF (1ug/100mL); HEK293T/17 cells were maintained in DMEM containing 10% FBS and 20 mM HEPES.
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