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mouse embryonic fibroblast mef cells  (ATCC)


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    Structured Review

    ATCC mouse embryonic fibroblast mef cells
    Mouse Embryonic Fibroblast Mef Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 563 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+embryonic+fibroblasts+mef+cells/MEF/pm41811437-212-20-25
    Average 95 stars, based on 563 article reviews
    mouse embryonic fibroblast mef cells - by Bioz Stars, 2026-09
    95/100 stars

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    Cell Culture:

    Article Title: Constitutive heterochromatin controls nuclear mechanics, morphology, and integrity through H3K9me3 mediated chromocenter compaction
    Article Snippet: .. Mouse Embryonic Fibroblasts (MEF) cells and Human HT1080 cells (ATCC) were cultured in DMEM (Corning) complete with 10% fetal bovine serum (FBS; HyClone) and 1% penicillin/streptomycin (Corning). ..

    Article Title: Identification of an N-terminal Truncation of the NF-?B p65 Subunit That Specifically Modulates Ribosomal Protein S3-dependent NF-?B Gene Expression
    Article Snippet: .. Jurkat A3, HEK293T, and mouse embryonic fibroblasts (MEF) cells (ATCC) were cultured in RPMI 1640 and DMEM, respectively, supplemented with 10% fetal calf serum, 2 m m glutamine, and 100 units/ml each of penicillin and streptomycin. .. IκBα (C-21, sc-371), C-terminal p65 (C-20, sc-372), N-terminal p65 (F-6, sc-8008x), and Sam68 (Src-associated in mitosis 68 kDa; C-20, sc-333) antibodies were from Santa Cruz Biotechnology; GFP (7.1 and 13.1, 11814460001) antibody was from Roche Applied Science; RNA polymerase II (CTD4H8, 05-623) antibody was from Millipore; β-actin (AC-15, A5441) and importin-α (IM-75, I1784) antibodies were from Sigma; poly(ADP-ribose) polymerase (C2–10, 556362), Hsp90 (68, 610418), caspase 3 (19, 610322), CD3 (HIT3a, 550367), and CD28 (CD28.2, 555726) antibodies were from BD; phospho-IκBα (5A5, 9246) and cleaved caspase 3 (Asp-175, 9661) antibodies were from Cell Signaling Technology; RPS3 and Ser-209 phosphorylated RPS3 antibodies were generated and affinity-purified by Primm Biotech, as previously described ( 16 , 17 ).

    Article Title: Constitutive heterochromatin controls nuclear mechanics, morphology, and integrity through H3K9me3 mediated chromocenter compaction
    Article Snippet: .. Mouse Embryonic Fibroblasts (MEF) cells and Human HT1080 cells (ATCC) were cultured in DMEM (Corning) complete with 10% fetal bovine serum (FBS; HyClone) and 1% penicillin/streptomycin (Corning). ..

    Control:

    Article Title: Rap1-GTPases control mTORC1 activity by coordinating lysosome organization with amino acid availability
    Article Snippet: .. HELA, HEK293T, U2OS, mouse embryonic fibroblasts (MEF) cells deficient in GCN2 and their littermate-derived wild-type control cells were obtained from ATCC. .. HEK293A cells were purchased from Thermo Fisher Scientific.

    Article Title: Rap1-GTPases control mTORC1 activity by coordinating lysosome organization with amino acid availability.
    Article Snippet: .. HELA, HEK293T, U2OS, mouse embryonic fibroblasts (MEF) cells deficient in GCN2 and their littermate-derived wild-type control cells were obtained from ATCC. .. HEK293A cells were purchased from Thermo Fisher Scientific.

    Mutagenesis:

    Article Title: Base Excision Repair in Mitotic Cells and the Role of Apurinic/Apyrimidinic Endonuclease 1 (APE1) in Post-Mitotic Transcriptional Reactivation of Genes
    Article Snippet: For nascent RNA detection in the cells, a Click-iT TM RNA Alexa Fluor 594 Imaging kit (ThermoFisher Scientific; Cat # C10330) was used. .. The human mutant KRAS expressing pancreatic ductal adenocarcinoma MIA PaCa-2 (ATCC, Manassas, VA, USA, Cat # CRM-CRL-1420) cell line, mouse embryonic fibroblasts (MEF) cells, and BJ-5ta (BJ-hTERT; ATCC, Manassas, VA, USA, Cat # CRL-4001) cells were all maintained in high-glucose Dulbecco’s Modified Eagle’s Medium (DMEM; ThermoFisher Scientific, Cat # 11965084) supplemented with 10% fetal bovine serum (FBS; Sigma, Catalog # F2442) and an antibiotic mixture of 100 U/mL penicillin and 100 μg/mL streptomycin (Gibco-BRL, Grand Island, NY, USA). .. The human colon cancer cell line HCT116 (ATCC, Cat # CCL-247) was maintained in McCoy’s 5A (modified) medium (Gibco; Grand Island, NY, USA, Cat # 16600082) supplemented with 10% fetal bovine serum and an antibiotic mixture of 100 U/mL penicillin and 100 μg/mL streptomycin.

    Expressing:

    Article Title: Base Excision Repair in Mitotic Cells and the Role of Apurinic/Apyrimidinic Endonuclease 1 (APE1) in Post-Mitotic Transcriptional Reactivation of Genes
    Article Snippet: For nascent RNA detection in the cells, a Click-iT TM RNA Alexa Fluor 594 Imaging kit (ThermoFisher Scientific; Cat # C10330) was used. .. The human mutant KRAS expressing pancreatic ductal adenocarcinoma MIA PaCa-2 (ATCC, Manassas, VA, USA, Cat # CRM-CRL-1420) cell line, mouse embryonic fibroblasts (MEF) cells, and BJ-5ta (BJ-hTERT; ATCC, Manassas, VA, USA, Cat # CRL-4001) cells were all maintained in high-glucose Dulbecco’s Modified Eagle’s Medium (DMEM; ThermoFisher Scientific, Cat # 11965084) supplemented with 10% fetal bovine serum (FBS; Sigma, Catalog # F2442) and an antibiotic mixture of 100 U/mL penicillin and 100 μg/mL streptomycin (Gibco-BRL, Grand Island, NY, USA). .. The human colon cancer cell line HCT116 (ATCC, Cat # CCL-247) was maintained in McCoy’s 5A (modified) medium (Gibco; Grand Island, NY, USA, Cat # 16600082) supplemented with 10% fetal bovine serum and an antibiotic mixture of 100 U/mL penicillin and 100 μg/mL streptomycin.

    Modification:

    Article Title: Base Excision Repair in Mitotic Cells and the Role of Apurinic/Apyrimidinic Endonuclease 1 (APE1) in Post-Mitotic Transcriptional Reactivation of Genes
    Article Snippet: For nascent RNA detection in the cells, a Click-iT TM RNA Alexa Fluor 594 Imaging kit (ThermoFisher Scientific; Cat # C10330) was used. .. The human mutant KRAS expressing pancreatic ductal adenocarcinoma MIA PaCa-2 (ATCC, Manassas, VA, USA, Cat # CRM-CRL-1420) cell line, mouse embryonic fibroblasts (MEF) cells, and BJ-5ta (BJ-hTERT; ATCC, Manassas, VA, USA, Cat # CRL-4001) cells were all maintained in high-glucose Dulbecco’s Modified Eagle’s Medium (DMEM; ThermoFisher Scientific, Cat # 11965084) supplemented with 10% fetal bovine serum (FBS; Sigma, Catalog # F2442) and an antibiotic mixture of 100 U/mL penicillin and 100 μg/mL streptomycin (Gibco-BRL, Grand Island, NY, USA). .. The human colon cancer cell line HCT116 (ATCC, Cat # CCL-247) was maintained in McCoy’s 5A (modified) medium (Gibco; Grand Island, NY, USA, Cat # 16600082) supplemented with 10% fetal bovine serum and an antibiotic mixture of 100 U/mL penicillin and 100 μg/mL streptomycin.



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    ATCC mouse embryonic fibroblast cells
    (A) Cryo-soft X-ray (SXT) tomography ortho-slices of noninfected (NI) and infected mouse embryonic <t>fibroblast</t> (MEF) cells at 8 hpi. Molecular densities are presented in a continuous grey scale representing linear absorption coefficient values ranging from 0.1 to 0.4 μm -1 (calibration bar). Scale bars, 2 μm. (B) Cross-sections of 3D SXT reconstructions of a noninfected and an infected cell. The high-density region (heterochromatin) is shown in blue, the low-density region (euchromatin) in yellow, the viral replication compartment (VRC/euchromatin) area in green, and the cytoplasm in grey. See also . Quantitative analysis of linear absorption coefficient (LAC) of the (C) low-density and (D) high-density region in noninfected and infected cells at 4 and 8 hpi (n = 6). (E) Representative cross-sections of focused ion beam scanning electron microscopy (FIB-SEM) images of noninfected and infected MEF cells at 8 hpi. The viral capsid (arrows) and nuclear pore complexes (arrowheads) are shown. Scale bars, 0.5 µm. See also . (F) Reconstruction of chromatin fiber thickness and (G) chromatin density as a function of the distance from the nuclear envelope in noninfected and infected cells. The color scale in (F) indicates high and low chromatin thickness (yellow-blue), and in (G) high and low density (yellow-blue). The error bars show the standard deviation. Statistical significance was determined using Tukey’s test, and the significance values are denoted as * (p < 0.05). Nonsignificant differences (p ≥ 0.05) are not labeled.
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    ATCC mef cells mouse embryonic fibroblasts cf 1
    (A) Cryo-soft X-ray (SXT) tomography ortho-slices of noninfected (NI) and infected mouse embryonic <t>fibroblast</t> (MEF) cells at 8 hpi. Molecular densities are presented in a continuous grey scale representing linear absorption coefficient values ranging from 0.1 to 0.4 μm -1 (calibration bar). Scale bars, 2 μm. (B) Cross-sections of 3D SXT reconstructions of a noninfected and an infected cell. The high-density region (heterochromatin) is shown in blue, the low-density region (euchromatin) in yellow, the viral replication compartment (VRC/euchromatin) area in green, and the cytoplasm in grey. See also . Quantitative analysis of linear absorption coefficient (LAC) of the (C) low-density and (D) high-density region in noninfected and infected cells at 4 and 8 hpi (n = 6). (E) Representative cross-sections of focused ion beam scanning electron microscopy (FIB-SEM) images of noninfected and infected MEF cells at 8 hpi. The viral capsid (arrows) and nuclear pore complexes (arrowheads) are shown. Scale bars, 0.5 µm. See also . (F) Reconstruction of chromatin fiber thickness and (G) chromatin density as a function of the distance from the nuclear envelope in noninfected and infected cells. The color scale in (F) indicates high and low chromatin thickness (yellow-blue), and in (G) high and low density (yellow-blue). The error bars show the standard deviation. Statistical significance was determined using Tukey’s test, and the significance values are denoted as * (p < 0.05). Nonsignificant differences (p ≥ 0.05) are not labeled.
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    Image Search Results


    (A) Cryo-soft X-ray (SXT) tomography ortho-slices of noninfected (NI) and infected mouse embryonic fibroblast (MEF) cells at 8 hpi. Molecular densities are presented in a continuous grey scale representing linear absorption coefficient values ranging from 0.1 to 0.4 μm -1 (calibration bar). Scale bars, 2 μm. (B) Cross-sections of 3D SXT reconstructions of a noninfected and an infected cell. The high-density region (heterochromatin) is shown in blue, the low-density region (euchromatin) in yellow, the viral replication compartment (VRC/euchromatin) area in green, and the cytoplasm in grey. See also . Quantitative analysis of linear absorption coefficient (LAC) of the (C) low-density and (D) high-density region in noninfected and infected cells at 4 and 8 hpi (n = 6). (E) Representative cross-sections of focused ion beam scanning electron microscopy (FIB-SEM) images of noninfected and infected MEF cells at 8 hpi. The viral capsid (arrows) and nuclear pore complexes (arrowheads) are shown. Scale bars, 0.5 µm. See also . (F) Reconstruction of chromatin fiber thickness and (G) chromatin density as a function of the distance from the nuclear envelope in noninfected and infected cells. The color scale in (F) indicates high and low chromatin thickness (yellow-blue), and in (G) high and low density (yellow-blue). The error bars show the standard deviation. Statistical significance was determined using Tukey’s test, and the significance values are denoted as * (p < 0.05). Nonsignificant differences (p ≥ 0.05) are not labeled.

    Journal: PLOS Pathogens

    Article Title: Nucleus softens during herpesvirus infection

    doi: 10.1371/journal.ppat.1013873

    Figure Lengend Snippet: (A) Cryo-soft X-ray (SXT) tomography ortho-slices of noninfected (NI) and infected mouse embryonic fibroblast (MEF) cells at 8 hpi. Molecular densities are presented in a continuous grey scale representing linear absorption coefficient values ranging from 0.1 to 0.4 μm -1 (calibration bar). Scale bars, 2 μm. (B) Cross-sections of 3D SXT reconstructions of a noninfected and an infected cell. The high-density region (heterochromatin) is shown in blue, the low-density region (euchromatin) in yellow, the viral replication compartment (VRC/euchromatin) area in green, and the cytoplasm in grey. See also . Quantitative analysis of linear absorption coefficient (LAC) of the (C) low-density and (D) high-density region in noninfected and infected cells at 4 and 8 hpi (n = 6). (E) Representative cross-sections of focused ion beam scanning electron microscopy (FIB-SEM) images of noninfected and infected MEF cells at 8 hpi. The viral capsid (arrows) and nuclear pore complexes (arrowheads) are shown. Scale bars, 0.5 µm. See also . (F) Reconstruction of chromatin fiber thickness and (G) chromatin density as a function of the distance from the nuclear envelope in noninfected and infected cells. The color scale in (F) indicates high and low chromatin thickness (yellow-blue), and in (G) high and low density (yellow-blue). The error bars show the standard deviation. Statistical significance was determined using Tukey’s test, and the significance values are denoted as * (p < 0.05). Nonsignificant differences (p ≥ 0.05) are not labeled.

    Article Snippet: Mouse embryonic fibroblast cells (MEF, ATCC CRL-2991) and African green monkey kidney cells (Vero, ATCC CCL-81) were grown in Dulbecco’s modified Eagle medium (DMEM) supplemented with 10% fetal bovine serum, L-glutamine, and penicillin-streptomycin (Gibco-Invitrogen) at 37 °C in the presence of 5% CO 2.

    Techniques: Tomography, Infection, Electron Microscopy, Standard Deviation, Labeling