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Cov644

Manufactured by Merck Group

COV644 is a laboratory equipment designed for scientific research and analysis. It is a multi-function device capable of performing various tasks, such as sample preparation, measurement, and data collection. The core function of COV644 is to support researchers and scientists in their work, but a detailed description of its intended use is not available at this time.

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2 protocols using cov644

1

Cell Culture Conditions for Cancer Research

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RPE1-hTERT p53−/− Cas9
(Zimmermann et al., 2018 (link)) and
293T cells were grown in DMEM supplemented with 10% FBS (Wisent
#080150), GlutaMAX (life Technologies #35050–061) and 1%
Pen/Strep (Wisent #450–201-EL). UWB1.28, SKOV3 and OV90 cells
were purchased from ATCC. UWB1.28 cells were grown in RPMI: MEGM (1:1)
supplemented with 3% FBS and 1% Pen/Strep. SKOV3 cells were grown in
McCoys 5a supplemented with 10% FBS and 1% Pen/Strep. OV90 cells were
grown in MCDB 105: Medium 99 (1:1) supplemented with 1% sodium
bicarbonate (0.75 g/L), 15% FBS and 1% Pen/Step. JHOS2 were purchased
from Riken BRC and grown in DMEM: F-12(1:1) supplemented with 10%FBS,
0.1mM NEAA. SUM149PT cells were purchased from Asterand BioScience and
grown in a DMEM/F12 medium mixture supplemented with 5% FBS, 1%
Pen/Strep, 1 μg/mL hydrocortisone and 5 μg/mL insulin.
COV362 and COV644 were purchased from Sigma and grown in DMEM
supplemented with 10% FBS and 1% Pen/Strep. RMUGS cells were purchased
from JCRC cell bank and grown in Ham’s 12 supplemented with 10%
FBS and 1% Pen/Strep. Wild-type and
BRCA2−/−DLD-1 cells were purchased from Horizon and maintained in RPMI medium
supplemented with 10% FBS, 1% Pen/Strep and 2 mM sodium pyruvate. All
cell lines were grown at 37 °C and 5% CO2.
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2

Cell Culture Conditions for Cancer Research

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OVCAR-3 cells were maintained in Roswell Park Memorial Institute (RPMI) 1640 media supplemented with 20% fetal bovine serum. hTERT-RPE1 cells were maintained in Dulbecco's Modified Eagle Medium: F12 (DMEM: F12) supplemented with 10% fetal bovine serum and 0.01 mg/ml hygromycin B. A549 cells were maintained in F-12K Medium supplemented with 10% fetal bovine serum. COV644 and COV318 cells were maintained in DMEM supplemented with 10% fetal bovine serum. FUOV1 cells were maintained in Ham's F12 + DMEM at 1:1, and supplemented with 10% fetal bovine serum. MCF-7 cells were maintained in Eagle's Minimum Essential Medium (EMEM), and supplemented with 0.01 mg/ml human recombinant insulin and 10% fetal bovine serum. OVCAR-3, hTERT-RPE1, A549, and MCF-7 cells were purchased from the American Type Culture Collection. COV644 and COV318 were purchased from Sigma Aldrich. FUOV1 cells were purchased from DSMZ. Cell line identity was confirmed with short tandem repeat (STR) testing (Charles River). All cells were maintained in a humidified incubator at 37°C with 5% CO2.
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