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C11095500bt

Manufactured by Thermo Fisher Scientific
Sourced in United States

The C11095500BT is a laboratory equipment product offered by Thermo Fisher Scientific. It is a compact, benchtop centrifuge designed for general-purpose applications in research and clinical laboratories. The centrifuge can accommodate a variety of sample tube sizes and volumes, enabling efficient sample preparation and separation. The product specifications and core functionalities are presented in a factual and unbiased manner, without interpretation or extrapolation.

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7 protocols using c11095500bt

1

Cultivation and Characterization of Cell Lines and Viruses

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HeLa, human rhabdomyosarcoma RD cells, human neuroblastoma SK-N-SH cells, human glioblastoma U251 cells, and HEK293T cells were obtained from the American Type Culture Collection (ATCC). SK-N-SH cells were cultured in MEM (C11095500BT; Gibco) containing 10% fetal bovine serum (FBS; Sunrise) and 100 U/ml of penicillin and streptomycin (10378016; Gibco). The other cells were cultured in DMEM (C11995500BT; Gibco) containing 10% FBS and 100 U/ml of penicillin and streptomycin. All cells were maintained in a humidified incubator with 5% CO2 at 37°C.
EV71 strain VR-784 was purchased from China Center for Type Culture Collection (CCTCC). EV71 strain SHAPHC695F/SH/CHN/10 (EV71-695F; GenBank: JQ736684.2) was isolated from fecal sample of a 1.8-yr-old patient in Shanghai public health clinical centre (SHPHC) in 2010 and provided by Dr. Zhigang Yi (Fudan University, Shanghai, China; Zhang et al., 2013 (link)). Coxsackievirus A16 (CVA16-G10; GeneBank: U05876.1) was provided by Dr. Dan Xu (Fudan University, Shanghai, China). VSV was from Genhong Cheng Laboratory (University of California, Los Angeles, CA, USA). HSV virus was kindly provided by Dr. Chunfu Zheng (Soochow University, Suzhou, China). Viral titers were determined using the TCID50 assay according to standard procedures.
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2

Cultivation and Characterization of Cell Lines and Viruses

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HeLa, human rhabdomyosarcoma RD cells, human neuroblastoma SK-N-SH cells, human glioblastoma U251 cells, and HEK293T cells were obtained from the American Type Culture Collection (ATCC). SK-N-SH cells were cultured in MEM (C11095500BT; Gibco) containing 10% fetal bovine serum (FBS; Sunrise) and 100 U/ml of penicillin and streptomycin (10378016; Gibco). The other cells were cultured in DMEM (C11995500BT; Gibco) containing 10% FBS and 100 U/ml of penicillin and streptomycin. All cells were maintained in a humidified incubator with 5% CO2 at 37°C.
EV71 strain VR-784 was purchased from China Center for Type Culture Collection (CCTCC). EV71 strain SHAPHC695F/SH/CHN/10 (EV71-695F; GenBank: JQ736684.2) was isolated from fecal sample of a 1.8-yr-old patient in Shanghai public health clinical centre (SHPHC) in 2010 and provided by Dr. Zhigang Yi (Fudan University, Shanghai, China; Zhang et al., 2013 (link)). Coxsackievirus A16 (CVA16-G10; GeneBank: U05876.1) was provided by Dr. Dan Xu (Fudan University, Shanghai, China). VSV was from Genhong Cheng Laboratory (University of California, Los Angeles, CA, USA). HSV virus was kindly provided by Dr. Chunfu Zheng (Soochow University, Suzhou, China). Viral titers were determined using the TCID50 assay according to standard procedures.
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3

Culturing Human Dermal Fibroblasts and Cell Lines

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Human dermal fibroblasts (HDFs) were obtained from circumcised foreskins of healthy human donors aged 5-20 years in Xiangya Hospital, Central South University, as described previously [29 (link),30 (link)]. Human embryonic lung fibroblasts IMR-90 and HEL were purchased from the American Type Culture Collection (ATCC) and Kunming Cell Bank (Chinese Academy of Sciences), respectively. The HDF, HEL, and IMR-90 cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM, C11995500BT, Gibco, USA) or Minimum Essential Medium (MEM, C11095500BT, Gibco, USA) supplemented with 10% fetal bovine serum (35-076-CV, Gibco, USA) and 1% penicillin/streptomycin (15140-122, Gibco, USA) in a 37 °C/5% CO2 humidified incubator. Human embryonic kidney HEK-293T cells were purchased from ATCC and cultured in DMEM (C11995500BT, Gibco, USA) supplemented with 10% fetal bovine serum (04-001-1ACS, BI, Israel) and 1% penicillin/streptomycin (15140-122, Gibco, USA) in a 37 °C/5% CO2 humidified incubator.
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4

Isolation and Culture of Mouse BMSCs

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Bone mesenchymal stem cells (BMSCs) were harvested from C57BL/6 aged 3–5 weeks. Briefly, the bone medullary cavities of the isolated tibia and femur were repeatedly flushed with α-MEM (C11095500BT, GIBCO, America). Then the bone marrow suspension was filtered using a 70 μm cell strainer (431,751, Corning, America) and centrifuged at 1000 rpm for 5 min. The cells were cultured in α-MEM supplemented with 10% fetal bovine serum (FBS; 10,099,141 C, GIBCO, America) and 1% Penicillin-Streptomycin (15,140,122, GIBCO, America) at 37 °C and 5% CO2. The following experiments employed the cells at passages 3 to 5.
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5

Overexpression and Knockdown of CDC27 in Neuroblastoma Cell Lines

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The cell lines SK-N-SH, and SH-SY5Y were purchased from Procell Life Science & Technology (CL-0214, CL-0208, Wuhan, China). SK-N-SH, SH-SY5Y, SK-N-BE(2) cells were cultured in MEM (C11095500BT, Gibco, NY, USA) containing 10% fetal bovine serum and an appropriate concentration of penicillin-streptomycin antibiotics (15140-122, Gibco, NY, USA). Cell line authentication was performed using short tandem repeat DNA profiling, and mycoplasma detection was regularly performed using a PCR-based method. All cell lines were cultured in a humidified atmosphere with 5% CO2 at 37°C.
Plasmids carrying CDC27 were constructed previously (17 (link)). Premixed siRNA was purchased from Santa Cruz (siCDC27:sc-77362, siNC: sc-37007). Growing cells were added to six-well plates and then transfected with plasmid or siRNA using Lipofectamine 2000 transfection reagent (Invitrogen) following the manufacturer’s instructions.
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6

Cell Culture Optimization for Lung Cancer Research

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SK-MES-1 cells were maintained in MEM medium (C11095500BT, Gibco) augmented with 1% PS (BL505A, Biosharp) and 10% FBS (10270106, Gibco).
NCI-H1703 cells were maintained in RPMI-1640 medium (C11875500BT, Gibco) augmented with 1% PS (BL505A, Biosharp) and 10% FBS (10270106, Gibco). To emulate the physiological environment, the cells were incubated in a CO2-rich environment (5% CO2) at a constant temperature of 37°C.
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7

Cell Culture and Transfection Protocol

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HT29 was purchased from the American Type Culture Collection (ATCC; Manassas, USA), and HCT-116, H4, and Hep3B cells were purchased from Cell Bank of the Type Culture Collection of the Chinese Academy of Sciences (Shanghai, China). The H4 cells was cultured in Dulbecco’s modified Eagle’s medium (DMEM; C11995500BT; Gibco, Grand Island, USA), the Hep3B cells were cultured in Minimum Essential Medium (MEM; C11095500BT; Gibco), and the HT-29 and HCT-116 cells were cultured in McCoy′s 5A Medium (16600082; Gibco), all supplemented with 10% FBS (10091148; Gibco) and 1% penicillin/streptomycin (15140-122; Gibco) at 37°C in a humidified 5% CO
2 atmosphere. The cells were grown on coverslips in 35-mm diameter culture dishes until they reached approximately 70%-80% confluence. Then, the cells were transfected with the indicated plasmids utilizing Lipofectamine 3000 (Invitrogen, Carlsbad, USA) according to the manufacturer’s instructions.
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