The largest database of trusted experimental protocols
Sourced in United States

The LASCPC-01 is a laboratory equipment product provided by American Type Culture Collection. It is a device designed for the cultivation and maintenance of cell cultures. The core function of this product is to create a controlled environment suitable for the growth and preservation of various cell lines.

Automatically generated - may contain errors

5 protocols using lascpc 01

1

Cell Line Characterization for Cancer Research

Check if the same lab product or an alternative is used in the 5 most similar protocols
293 T (ATCC, CRL-3216), HCT116 (ATCC, CCL-247EMT), PrEC LH (ATCC, PCS-440-010), LNCaP (ATCC, CRL-1740), C4-2 (ATCC, CRL-3314), PC3 (ATCC, CRL-1435), DU145 (ATCC, HTB-81), NCI-H660 (ATCC, CRL-5813), and LASCPC-01 (ATCC, CRL-3356) were originally purchased from ATCC (American Type Culture Collection) and have been confirmed by STR genotyping in our previous studies15 (link),49 (link)–51 (link). We conduct routine testing for Mycoplasma every few months. PrEC LH, LNCaP, C4-2, and PC3 were cultured in RPMI 1640. 293 T, HCT116 and DU145 was cultured in Dulbecco’s modified Eagle’s medium (Gibco, USA), supplemented with 10% fetal bovine serum (Invitrogen, USA) and 1% pen/strep (Gibco, USA). NCI-H660 and LASCPC-01 were cultured in RPMI 1640 medium, supplemented with 0.005 mg/ml Insulin, 0.01 mg/ml Transferrin, 30 nM Sodium selenite, 10 nM Hydrocortisone, 10 nM beta-estradiol, 4 mM l-glutamine (HyCloneTM, USA) and 10% FBS. Cells were maintained at 5% CO2 in a 37 °C humidified incubator.
+ Open protocol
+ Expand
2

Cell Culture Protocols for Cancer Research

Check if the same lab product or an alternative is used in the 5 most similar protocols
LASCPC-01 (ATCC® CRL-3356) was from ATCC (Manssas, VA, USA). LASCPC-01 cells were cultured in modified HITES medium as described [45 (link)]. Briefly, HITES media containing RPMI, 5% FBS, 10 nM hydrocortisone, 10 nM beta-estradiol (Millipore Sigma, Burlington, MA, USA), insulin–transferrin–selenium, and Glutamax (Life Technologies, Carlsbad, CA, USA). HEK293T cells were cultured in DMEM (Hyclone, #SH30243.01, Logan, UT, USA) containing 10% FBS and supplemented with 1% penicillin/streptomycin. Fludarabine phosphate (#S1229, Selleckchem, Houston, TX, USA). N-acetyl-L-cysteine (A7250, Sigma), Bortizomeb (#S1013, Selleckchem). The cell line LNCaP, and LNCaP-N-MYC as well as 22Rv1, and 22Rv1-N-MYC cells were kindly provided by the Rickman Lab from Cornell Medical College. Cells were cultured in the RPMI 1640 medium (Hyclone, #SH30027.01) containing 10% Fetal Bovine Serum (FBS) (Hyclone, F1051), 1% penicillin/streptomycin (Hyclone, #SV30010) at 37 °C with 5% CO2.
+ Open protocol
+ Expand
3

Prostate Cancer Cell Line Acquisition and Culturing

Check if the same lab product or an alternative is used in the 5 most similar protocols
Human prostate cancer cell lines PC3, DU145, 22Rv1, LNCaP, and LASCPC-01 were purchased from ATCC (Manassas, VA, USA). The Doce-resistant PC3-DR and DU145-DR cell lines, generated by the long-term exposure to increasing sub-lethal concentration of Doce as previously described [37 (link)], were donated by Prof. Z. Culig, Innsbruck Medical University, Austria. All cell lines were recently authenticated and cultured according to the manufacturers’ protocols.
+ Open protocol
+ Expand
4

Cell Line Acquisition for Cancer Research

Check if the same lab product or an alternative is used in the 5 most similar protocols
E0771/Pa breast and TRAMP-C1 prostate carcinoma cells were obtained from ATCC. E0771/Bone cells were obtained from Toru Hiraga (Matsumoto Dental University, Shiojiri, Japan).12 (link) B16F10 malignant melanoma cell lines were obtained from ATCC. LLC Lewis lung carcinoma cells were obtained from Klaus Okkenhaug (University of Cambridge, Cambridge, United Kingdom), with permission from Matthew Kraman (F-star Biotechnology, Cambridge, United Kingdom). MC38 colon carcinoma cell line was obtained from Klaus Okkenhaug (University of Cambridge, Cambridge, United Kingdom), with permission from Mark Smyth (QIMR Berghofer, Brisbane, Australia). Human cell lines A375, MDA-MB-435S, A549, NCI-H1299, NCI-H460, DU145, LNCaP, PC-3, Hs895.T, SK-MEL-28, BEAS-2B, NCI-H2126, NCI-H128, HCC70, MCF-10A, MDA-PCa-2b, LASCPC-01, RWPE-1, MCF-7 and MDA-MB-231 were obtained from ATCC.
+ Open protocol
+ Expand
5

Cell Culture Protocol for Prostate and T-ALL Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
PC3, LNCaP, and DU145 were purchased from the American Type Culture Collection (ATCC, Baltimore, MD, USA); PC3‐LN4 and human prostate fibroblast cell line BHPrS1 (Zemskova et al., 2015) were cultured in RPMI supplemented with 2 mmol·L−1 GlutaMAX (Life Technologies, Rockville, MD, USA) and 10% FBS (BioAbChem, Ladson, SC, USA) at 37 °C under 5% CO2 as reported previously. The T‐ALL cell lines HSB‐2, DU.528, KOPT‐K1, CUTLL1, HPB‐ALL, and SUP‐T1 (Padi et al., 2017) were cultured in RPMI 1640 supplemented with 2 mm GlutaMAX (Life Technologies) and 10% FBS (BioAbChem) at 37 °C under 5% CO2. LASCPC‐01 (ATCC) was grown in HITES media containing RPMI, 5% FBS, 10 nm hydrocortisone, 10 nm beta‐estradiol (Sigma‐aldrich, St. Louis, MO, USA), insulin–transferrin–selenium (Life Technologies), and GlutaMAX (Life Technologies). hPrEC and murine prostate epithelial tumor cells (mPrEC) cells were cultured as described previously (Song et al., 2018). Phoenix‐Eco cells (a gift from J. Schatz, University of Miami Health System) and fibrosarcoma cell line FLYRD18/mCAT‐IRES‐Bleo (a gift from H.G. Wendel, Memorial Sloan Kettering Cancer Center) were cultured in DMEM + 2 mm glutamine + 10% FBS. All cell lines were maintained for no more than 6 months in culture and were routinely tested for Mycoplasma.
+ 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!