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The SW1990 is a laboratory equipment designed for cell culture applications. It is a water bath that provides a controlled temperature environment for incubating and maintaining cell cultures. The device features precise temperature regulation and uniform heat distribution to ensure consistent and reliable conditions for cell growth and experimentation.

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366 protocols using sw1990

1

Culturing Pancreatic Cancer Cell Lines

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The five human pancreatic cancer cell lines Panc1, MIA PaCa-2, BxPC-3, AsPC-1 and SW1990 were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA). Panc1 cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM, ATCC) supplemented with 10% (v/v) fetal bovine serum (FBS) and 1% (v/v) penicillin/streptomycin (pen/strep). MIAPaCa-2 cells were kept in DMEM (ATCC) supplemented with 10% (v/v) FBS, 2.5% (v/v) horse serum, and 1% (v/v) pen/strep. BxPC-3, AsPC-1 and SW1990 were maintained in RPMI 1640 medium (ATCC) containing 10% (v/v) FBS and 1% (v/v) pen/strep. The additional three primary pancreatic cancer cell lines PaCaDD135, PaCaDD159 and PaCaDD185 were kindly provided by Dr. Felix Rueckert (Surgical Clinic Mannheim, University of Heidelberg, Mannheim, Germany). Culture medium for primary pancreatic cancer cells lines was assembled by mixing two parts of DMEM medium supplemented with 20% (v/v) FBS with one part of Keratinocyte-SFM. All cell lines were incubated at 37 °C in 5% CO2.
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2

Culturing Pancreatic Cancer Cell Lines

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The human pancreatic cancer cell lines PANC-1 and SW1990 were obtained from American Type Culture Collection (ATCC, Manassas, USA). The cells were cultured according to the standard protocols that were provided by the supplier. In brief, the PANC-1 cells were cultured in Dulbecco’s Modified Eagle’s Medium (DMEM; Invitrogen, Carlsbad, USA), containing foetal bovine serum (FBS; Invitrogen) at a final concentration of 10%. SW1990 cells were maintained in ATCC-formulated Leibovitz’s L-15 medium (ATCC) supplemented with FBS at a final concentration of 10%. Pancreatic cancer-associated fibroblasts (CAFs) were kindly provided by Dr. Chao Qu from Shanghai Cancer Center (Shanghai, China).
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3

Pancreatic Cell Line Cultivation

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All of the cell lines used in this study were purchased from the American Type Culture Collection (ATCC; Manassas, VA, USA), including the cancerous AsPC-1, CFPAC-1, Capan-1, SW1990, PANC-1, SW1990, BxPC-3, and MIA-PaCa-2 cell lines and the non-cancerous HPDE6C7 cell line. All of the above-mentioned cells were cultured in 5% CO2 at 37 °C in 100% humidity in Dulbecco’s modified Eagle’s medium (DMEM) containing 10% fetal bovine serum (FBS) and 1% antibiotic/antifungal solution (Biowest, Nuaillé, France).
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4

Culturing PC Cell Lines

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The human PC cell lines AsPC-1, CFPAC-1, Capan-1, SW1990, PANC-1, SW1990, BxPC-3, and MIA-PaCa-2 and the non-cancerous HPDE6C7 cell line were purchased from the American Type Culture Collection (ATCC; Manassas, VA, USA). Cells were cultured in Dulbecco's modi ed Eagle's medium (DMEM) supplemented with 10% fetal bovine serum (FBS) and 1% antibiotic/antifungal solution (Biowest, Nuaillé, France) in 5% CO 2 at 37°C in a humidi ed atmosphere.
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5

Culturing Human Pancreatic Cell Lines

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The human PC cell lines AsPC-1, CFPAC-1, Capan-1, SW1990, PANC-1, SW1990, BxPC-3, and MIA-PaCa-2 and the non-cancerous HPDE6C7 cell line were purchased from the American Type Culture Collection (ATCC; Manassas, VA, USA). Cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% fetal bovine serum (FBS) and 1% antibiotic/antifungal solution (Biowest, Nuaillé, France) in 5% CO2 at 37 °C in a humidified atmosphere.
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6

Culturing Human Pancreatic Cell Lines

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All of the cell lines used in this study were purchased from the American Type Culture Collection (ATCC; Manassas, VA, USA), including the cancerous AsPC-1, CFPAC-1, Capan-1, SW1990, PANC-1, SW1990, BxPC-3, and MIA-PaCa-2 cell lines and the non-cancerous HPDE6C7 cell line. All of the above-mentioned cells were cultured in 5% CO 2 at 37°C in 100% humidity in Dulbecco's modi ed Eagle's medium (DMEM) containing 10% fetal bovine serum (FBS) and 1% antibiotic/antifungal solution (Biowest, Nuaillé, France).
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7

Culturing Pancreatic Cancer Cell Lines

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HPDE6-C7, Capan-2, AsPC-1, SW1990, PANC-1, and SW1990 cells were purchased from the American Type Culture Collection (ATCC, VA., USA) and cultured in Dulbecco's Modified Eagle Medium (DMEM; Hyclone, UT., USA) supplemented with 10% fetal bovine serum (FBS, Gibco, NY., USA), 100 μg/ml streptomycin, and 100 IU/ml penicillin. The culture medium was kept in an incubator (Liuyi, Beijing, China) with 5% CO2 at 37°C.
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8

Pancreatic Cancer Cell Lines Protocol

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PDAC cell line: SW1990, PANC04.03 and PANC1 were obtained from ATCC. The human pancreatic ductal epithelial (HPDE) cell line was a gift from Dr. Ming-Sound Tsao (University Health Network, Ontario Cancer Institute and Princess Margaret Hospital Site, Toronto, Canada). All cell lines were cultured under the condition as described previously [11 (link)].
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9

Pancreatic Cancer Cell Line Maintenance

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The pancreatic cancer cell lines, Panc10.05, Panc02.03, Panc03.27, Capan1, SW1990, HPAF, MiaPaCa, CFPAC, ASPC1, Colo357, Panc1 and BXPC3, were procured from ATCC (Manassas, VA) and maintained under normal culturing conditions as described previously (16 (link)). All the cells were tested and determined to be free from mycoplasma contamination every alternate month. Frozen pancreatic tissue samples (normal and malignant) were obtained through cooperative human tissue network (CHTN) at the University of Alabama at Birmingham (UAB) under an Institutional Review Board (IRB) approved protocol.
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10

Characterization of Pancreatic Cancer Cell Lines

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HPAF-II, AsPC-1, BxPC-3, CAPAN-1, CAPAN-2, CFPAC-1, Hs766T, MIAPaCa-2, Mpanc96, PANC-1, PSN-1, and SW1990 cells were obtained from ATCC (Manassas, VA, USA). Thirteen cell lines (KMP2, KMP3, KMP4, KMP5, KMP8, KP1L, KP1NL, KP2, KP3, KP3L, KP4, PH61N, and QGP-1) and normal human fibroblasts (WI-38, TIG-1, and IMR-90 cells) were obtained from JCRB cell bank (Tokyo, Japan). HPC-Y0, HPC-Y3, and HPC-Y25 were kindly given to us by Dr. Otsuji E (Kyoto Prefectural University of Medicine). PK-59 cells were obtained from RIKEN Bioresource Research Center (Ibaraki, Japan). All cell lines were cultured in RPMI-1640 medium or DMEM (Wako, Osaka, Japan) containing 10% fetal bovine serum (FBS) at 37°C with 5% CO2.
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