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human embryonic kidney hek 293ft cell line  (Thermo Fisher)


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    Structured Review

    Thermo Fisher human embryonic kidney hek 293ft cell line
    Cytotoxicity of formulation of 1% α -MG in orabase gel in <t> 293FT </t> cell line
    Human Embryonic Kidney Hek 293ft Cell Line, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human embryonic kidney hek 293ft cell line/product/Thermo Fisher
    Average 86 stars, based on 1 article reviews
    human embryonic kidney hek 293ft cell line - by Bioz Stars, 2026-02
    86/100 stars

    Images

    1) Product Images from "Formulation of 1% α-mangostin in orabase gel induces apoptosis in oral squamous cell carcinoma"

    Article Title: Formulation of 1% α-mangostin in orabase gel induces apoptosis in oral squamous cell carcinoma

    Journal: BMC Complementary Medicine and Therapies

    doi: 10.1186/s12906-024-04450-0

    Cytotoxicity of formulation of 1% α -MG in orabase gel in  293FT  cell line
    Figure Legend Snippet: Cytotoxicity of formulation of 1% α -MG in orabase gel in 293FT cell line

    Techniques Used: Formulation, Concentration Assay

    Effect of the formulation of 1% α-MG in orabase gel on HPV-16 pseudovirus infection in 293FT cell. HPV-16 pseudovirus at multiplicity of infection (MOI) at 0.05 was performed to infect 293FT cells. For pre-attachment step ( A ), the formulation of 1% α-MG in orabase gel (Formulation 2) at CC 20 and CC 50 was mixed to pseudovirus and incubated at 37 °C for 1 h. Subsequently, the mixture was incubated with 293FT cells for 4 h and then removed and replaced with complete medium incubated for 48 h. For adsorption step ( B ), the 293FT cells were adsorbed with pseudovirus at 20 °C for 2 h. The gel was added to the cells after removal of the pseudovirus and then incubated for 48 h. Heparin (400 µM) was used as a positive control. Total cells and green fluorescent cells were counted in the same area by hemocytometer. The number of green fluorescent cells was relative to total cells and compared to untreated cells. The different percentage of inhibition was statistically assessed by an unpaired t test. The significant value was indicated as ** ( P < 0.01) and *** ( P < 0.001), respectively
    Figure Legend Snippet: Effect of the formulation of 1% α-MG in orabase gel on HPV-16 pseudovirus infection in 293FT cell. HPV-16 pseudovirus at multiplicity of infection (MOI) at 0.05 was performed to infect 293FT cells. For pre-attachment step ( A ), the formulation of 1% α-MG in orabase gel (Formulation 2) at CC 20 and CC 50 was mixed to pseudovirus and incubated at 37 °C for 1 h. Subsequently, the mixture was incubated with 293FT cells for 4 h and then removed and replaced with complete medium incubated for 48 h. For adsorption step ( B ), the 293FT cells were adsorbed with pseudovirus at 20 °C for 2 h. The gel was added to the cells after removal of the pseudovirus and then incubated for 48 h. Heparin (400 µM) was used as a positive control. Total cells and green fluorescent cells were counted in the same area by hemocytometer. The number of green fluorescent cells was relative to total cells and compared to untreated cells. The different percentage of inhibition was statistically assessed by an unpaired t test. The significant value was indicated as ** ( P < 0.01) and *** ( P < 0.001), respectively

    Techniques Used: Formulation, Infection, Incubation, Adsorption, Positive Control, Inhibition



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    Cytotoxicity of formulation of 1% α -MG in orabase gel in  293FT  cell line

    Journal: BMC Complementary Medicine and Therapies

    Article Title: Formulation of 1% α-mangostin in orabase gel induces apoptosis in oral squamous cell carcinoma

    doi: 10.1186/s12906-024-04450-0

    Figure Lengend Snippet: Cytotoxicity of formulation of 1% α -MG in orabase gel in 293FT cell line

    Article Snippet: Human embryonic kidney (HEK) 293FT cell line was purchased from Invitrogen company (Carlsbad, CA, USA).

    Techniques: Formulation, Concentration Assay

    Effect of the formulation of 1% α-MG in orabase gel on HPV-16 pseudovirus infection in 293FT cell. HPV-16 pseudovirus at multiplicity of infection (MOI) at 0.05 was performed to infect 293FT cells. For pre-attachment step ( A ), the formulation of 1% α-MG in orabase gel (Formulation 2) at CC 20 and CC 50 was mixed to pseudovirus and incubated at 37 °C for 1 h. Subsequently, the mixture was incubated with 293FT cells for 4 h and then removed and replaced with complete medium incubated for 48 h. For adsorption step ( B ), the 293FT cells were adsorbed with pseudovirus at 20 °C for 2 h. The gel was added to the cells after removal of the pseudovirus and then incubated for 48 h. Heparin (400 µM) was used as a positive control. Total cells and green fluorescent cells were counted in the same area by hemocytometer. The number of green fluorescent cells was relative to total cells and compared to untreated cells. The different percentage of inhibition was statistically assessed by an unpaired t test. The significant value was indicated as ** ( P < 0.01) and *** ( P < 0.001), respectively

    Journal: BMC Complementary Medicine and Therapies

    Article Title: Formulation of 1% α-mangostin in orabase gel induces apoptosis in oral squamous cell carcinoma

    doi: 10.1186/s12906-024-04450-0

    Figure Lengend Snippet: Effect of the formulation of 1% α-MG in orabase gel on HPV-16 pseudovirus infection in 293FT cell. HPV-16 pseudovirus at multiplicity of infection (MOI) at 0.05 was performed to infect 293FT cells. For pre-attachment step ( A ), the formulation of 1% α-MG in orabase gel (Formulation 2) at CC 20 and CC 50 was mixed to pseudovirus and incubated at 37 °C for 1 h. Subsequently, the mixture was incubated with 293FT cells for 4 h and then removed and replaced with complete medium incubated for 48 h. For adsorption step ( B ), the 293FT cells were adsorbed with pseudovirus at 20 °C for 2 h. The gel was added to the cells after removal of the pseudovirus and then incubated for 48 h. Heparin (400 µM) was used as a positive control. Total cells and green fluorescent cells were counted in the same area by hemocytometer. The number of green fluorescent cells was relative to total cells and compared to untreated cells. The different percentage of inhibition was statistically assessed by an unpaired t test. The significant value was indicated as ** ( P < 0.01) and *** ( P < 0.001), respectively

    Article Snippet: Human embryonic kidney (HEK) 293FT cell line was purchased from Invitrogen company (Carlsbad, CA, USA).

    Techniques: Formulation, Infection, Incubation, Adsorption, Positive Control, Inhibition

    Key resources list.

    Journal: International Journal of Molecular Sciences

    Article Title: Mitochondrial Ribosomal Protein MRPS15 Is a Component of Cytosolic Ribosomes and Regulates Translation in Stressed Cardiomyocytes

    doi: 10.3390/ijms25063250

    Figure Lengend Snippet: Key resources list.

    Article Snippet: Female human embryonic HEK-293FT kidney cells (Invitrogen R700-07, Waltham, MA, USA), used to produce lentivectors, were cultivated in DMEM-GlutaMAX + Pyruvate (Life Technologies SAS, Saint-Aubin, France), supplemented with 10% fetal bovine serum (FBS) and MEM essential and non-essential amino acids (Sigma-Aldrich, St. Louis, MO, USA).

    Techniques: Bacteria, Virus, Recombinant, Plasmid Preparation, PCR Cloning, In Situ, Reporter Assay, Modification, Sequencing, Software, Microscopy, Western Blot