The largest database of trusted experimental protocols

Atcc 30 2020

Manufactured by LGC
Sourced in Germany, France

The ATCC 30-2020 is a laboratory instrument designed for the detection and quantification of nucleic acids. It utilizes real-time polymerase chain reaction (qPCR) technology to amplify and detect specific target sequences in a sample. The core function of the ATCC 30-2020 is to provide accurate and reliable results for applications such as gene expression analysis, pathogen detection, and genetic profiling.

Automatically generated - may contain errors

2 protocols using atcc 30 2020

1

Cell Culture and Transfection of HeLa and HepG2 Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
The human cervix epithelial adenocarcinoma cell line HeLa was purchased from the American Type Culture Collection, and the liver carcinoma cell line HepG2 from the European Collection of Authenticated Cell Cultures (Sigma-Aldrich Chemie N.V., Zwijndrecht, the Netherlands). General cell culture supplies were from Gibco (Life Technologies Europe B.V., Bleiswijk, the Netherlands) if not indicated otherwise: HeLa cells were cultured in Dulbecco's Modified Eagle Medium (DMEM) + 4.5 g/l d-glucose + l-glutamine + 25 mm HEPES (4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid) without pyruvate (42430-025) to which MEM nonessential amino acids (11140-035) were added and 10% fetal bovine serum (Sigma, F7524, Sigma-Aldrich Chemie N.V). HepG2 cells were cultured in Eagle's Minimum Essential Medium (EMEM) + Earle’s salts without l-glutamine (21090-022) to which MEM nonessential amino acids (11140-035) were added and 10% fetal bovine serum (American Type Culture Collection, ATCC 30-2020, LGC Standards GmbH, Wesel, Germany).
For transfections, HeLa and HepG2 cells were seeded at approximately 80% density in 96-well plates (Greiner Bio-One 655180). HeLa cells were transfected using the TransIT-HeLaMONSTER Transfection Kit (MIR 2904) and HepG2 cells with TransIT-LT1 Transfection Reagent (MIR 2304) applying the standard protocols (both from Mirus Bio LLC, Sopachem B.V., Ochten, the Netherlands).
+ Open protocol
+ Expand
2

Breast Cancer Cell Line Cultivation and Modification

Check if the same lab product or an alternative is used in the 5 most similar protocols
MDA-MB-231 breast cancer cells were purchased from DSMZ (Braunschweig, Germany) and grown in 10% fetal bovine serum (FBS) (ATCC® 30-2020™, LGC, Molsheim, France) DMEM (1 g/L of glucose). The cells were stably transfected with the pOPRSV-1/MCS expression plasmid (Agilent Technologies, Courtaboeuf, Les Ulis, France), containing a coding LRP-1-interfering RNA sequence: AAG CAG TT GCC TGC AGA GAT (shLRP-1) or a scramble control sequence: CCA GTC GCC ATTA ATT ATG CAA (shCtrl). We used 0.8 mg/mL of geneticin (G418; Sigma Aldrich, St. Louis, MI, USA) for the selection. For the screening needs, MCF-7, T-47D, SK-Br3, Hs-578T, BT-20, and 4T1 breast cancer cell lines have also been used. HUVECs (C-12203) were purchased from Promocell (Handschuhsheimer, Germany) and HUVECs-GFP labeled with GFP (ZHC-2402) from Cellworks (Buckingham, UK). The cells were cultivated in EBMTM-2 Basal Medium (CC-3156) supplemented with EGMTM-2 SingleQuotsTM (CC-4176; Lonza, Walkersville, MD, USA). The cells at the passage from P3 to P5 were used.
For all procedures, the cells were harvested using a 1X Trypsin-EDTA solution (Sigma Aldrich, St. Louis, MI, USA) or Accutase® (C-41310; Promocell, Handschuhsheimer, Germany) and were maintained at 37 °C in a humidified atmosphere of 5% CO2.
+ 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!