The largest database of trusted experimental protocols

10 protocols using cfpac 1

1

Pancreatic Cancer Cell Line Culture

Check if the same lab product or an alternative is used in the 5 most similar protocols
Four human pancreatic cancer cell lines (MiaPaCa-2, BxPC-3, CFPAC-1 and PANC-1) and a normal human pancreatic ductal cell line (HPNE) were purchased from the Shanghai Cell Bank (Shanghai, China). Cells stably overexpressing YY1 or with YY1 knockdown had already been transfected into the BxPC-3 and PANC-1 cell lines (BxPC-3-YY1, BxPC-3-YY1 shRNA, PANC-1-YY1, PANC-1-YY1 shRNA). The corresponding control cell lines (BxPC-3-Vector, BxPC-3-Scramble shRNA, PANC-1-Vector, PANC-1-Scramble shRNA) had also already been prepared.21 (link)As described previously, PDAC cells were grown in Dulbecco’s modified Eagle’s medium (DMEM) (Life Technologies) supplemented with 10% foetal calf serum (FBS) (Wisent Inc., Montreal, Qc, Canada), 10 mM HEPES (Sigma, St. Louis, MO, USA), 2 mM L-glutamine (Sigma), 1 mM pyruvate sodium (Sigma), 100 U/ml penicillin (Life Technologies), and 100 μg/ml streptomycin (Life Technologies). HPNE cells were grown in keratinocyte serum-free medium supplemented with epidermal growth factor and bovine pituitary extract at 37 °C in a humidified atmosphere containing 95% air and 5% CO210 (link)
+ Open protocol
+ Expand
2

Pancreatic Cancer Cell Line Culturing

Check if the same lab product or an alternative is used in the 5 most similar protocols
Three human PDAC cell lines (PANC-1, CFPAC-1, MIAPACA-2) and a normal human pancreatic ductal cell line (HPNE) were purchased from Shanghai Cell Bank (Shanghai, China). PDAC cell lines were cultured in Dulbecco’s modified medium (Wisent, Canada) supplemented with 10% fetal calf serum (Wisent, Canada). The HPNE cell line was grown in keratinocyte serum-free medium supplemented with epidermal growth factor and bovine pituitary extract according to the recommendations of the ATCC.
+ Open protocol
+ Expand
3

Culturing Human Pancreatic Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
Five human pancreatic ductal adenocarcinoma (PDAC) cell lines (PANC-1, BxPC-3, AsPC-1, CFPAC-1, and MIA-PaCa-2) and a normal human pancreatic ductal cell line (hTERT-HPNE) were purchased from the Shanghai Cell Bank (Shanghai, China). According to the recommendation of ATCC, both BxPC-3 and AsPC-1 cell lines were cultured in RPMI­1640 Medium (Life Technologies; Carlsbad, CA, USA) supplemented with 10% fetal bovine serum (FBS) (Life Technologies; Carlsbad, CA, USA) and 1% penicillin-streptomycin (HyClone, USA). However, PANC-1, CFPAC-1, and MIA-PaCa-2 were grown in Dulbecco's modified Eagle's medium (DMEM) (Life Technologies; Carlsbad, CA, USA) containing 10% FBS and 1% penicillin-streptomycin (HyClone, USA). In addition, the hTERT-HPNE cell line was maintained in DMEM, supplemented with 5% FBS, 10 ng/ml human recombinant epidermal growth factor (EGF), 5.5 mMD glucose (1 g/L), and 750 ng/ml puromycin. All cell lines were routinely cultured in a humidified incubator with 5% CO2 at 37°C.
+ Open protocol
+ Expand
4

Culturing Pancreatic Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
PC cell lines (BXPC-3, CFPAC-1, COLO-357, MIAPACA-2, and PANC-1) and the normal human pancreatic ductal cell line hTERT-HPNE (HPNE) were purchased from Shanghai Cell Bank (Shanghai, China). Cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM) (Life Technologies) containing 10% fetal bovine serum (FBS) (Wisent, Inc., Montreal, QC, Canada), 1% glutamine (Sigma), and 1% penicillin/streptomycin (Life Technologies) at 37 °C in a humidified incubator with 95% air and 5% CO2.
+ Open protocol
+ Expand
5

PDAC Cohort and Cell Line Culture

Check if the same lab product or an alternative is used in the 5 most similar protocols
We collected a cohort of 64 paraffin-embedded specimens from patients with resectable primary PDAC who underwent pancreaticoduodenectomy at Nanfang Hospital, Southern Medical University from 2016 to 2018. Prior patient consent and approval were obtained from the Institutional Research Ethics Committee. PDAC cell lines, including SW1990, PANC-1, BXPC-3, and CFPAC-1, and the normal human pancreatic duct epithelium cell line HPDE6-c7 were provided by Shanghai Cell Bank (Chinese Academy of Sciences, Shanghai, China). All cell lines (8 × 105 cells/plate) were seeded in Dulbecco’s modified Eagle’s medium (DMEM) (HyClone, Logan, UT, USA) with 10% fetal bovine serum (FBS, Gibco, Brazil) at 37°C in a 5% CO2 incubator.
+ Open protocol
+ Expand
6

Establishing Pancreatic Cancer Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
Six human pancreatic cancer cell lines (BxPC-3, CFPAC-1, Colo-357, MiaPaCa-2, PANC-1, and SW1990) were purchased from the Shanghai Cell Bank (Shanghai, China). The normal human pancreatic ductal cell line, HPNE, was purchased from the American Type Culture Collection (ATCC, USA). Cell lines that stably overexpress YY1 (BxPC-3 and PANC-1), cell lines in which YY1 is knocked down, and control cell lines were prepared and cultured as previously described [20 (link)]. Human pancreatic cancer cell lines were cultured in DMEM supplemented with 10% FBS, penicillin (100 U/mL), and streptomycin (100 μg/mL). The HPNE cell line was cultured according to the recommendations of the ATCC.
+ Open protocol
+ Expand
7

Culturing Human Pancreatic Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
Human PC cell lines BXPC‐3, Capan‐2, CFPAC‐1, COLO‐357, MIA PaCa‐2, and PANC‐1 were purchased from the Shanghai Cell Bank. The cell line hTERT‐HPNE was obtained from the American Type Culture Collection (ATCC, CRL‐4037). All these cell lines were cultured according to their manufacturer's instructions.
+ Open protocol
+ Expand
8

Culturing Pancreatic Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
HEK293T, HPDE pancreatic duct epithelial cell line and human PAAD cell lines (AsPC-1, BXPC3, CFPAC1, PANC-1, and SW1990) cells were obtained from the Shanghai Cell Bank. Cells were cultured in DMEM media supplemented with 10% fetal bovine serum (FBS), 100 units/mL penicillin and 100 μg/mL streptomycin.
+ Open protocol
+ Expand
9

Culturing Human Pancreatic Cancer Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Six human PDAC cell lines (BXPC-3, PANC-1, HPAC, CFPAC-1, SW1990 and COLO-357) were purchased from the Shanghai Cell Bank (Shanghai, China). The cells were grown in Dulbecco’s modified Eagle’s medium (DMEM) (Life Technologies) supplemented with 10% fetal calf serum (FBS) (Wisent Inc., Montreal, Qc, Canada), 10 mM HEPES (Sigma, St Louis, MO, USA), 2 mM L-glutamine (Sigma), 1 mM pyruvate sodium (Sigma), 100 units/ml penicillin (Life Technologies), and 100 μg/ml streptomycin (Life Technologies) at 37°C in a humidified atmosphere containing 95% air and 5% CO2.
+ Open protocol
+ Expand
10

PDAC Cell Lines and Mycoplasma Screening

Check if the same lab product or an alternative is used in the 5 most similar protocols
PDAC cell lines (PANC-1, CFPAC-1, BXPC-3, and MiaPaCa-2) and a normal human pancreatic ductal cell line (hTERT-HPNE, also known as HPNE) were obtained from Shanghai Cell Bank. Cells were cultured in DMEM (Thermo Fisher Scientific, Inc.) supplemented with 10% FBS (Wisent Inc.) and 1% penicillin/streptomycin (Thermo Fisher Scientific, Inc.). Cell lines underwent routine testing for mycoplasma contamination every 3 months. The genetic identity of the cell lines was confirmed by short tandem repeat profiling.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!