l2 fibroblast cell line Search Results


rat lung fibroblast l2 cells  (ATCC)
96
ATCC rat lung fibroblast l2 cells
Rat Lung Fibroblast L2 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
rat lung fibroblast l2 cells - by Bioz Stars, 2026-04
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murine l 2 cells  (ATCC)
99
ATCC murine l 2 cells
Murine L 2 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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murine l 2 cells - by Bioz Stars, 2026-04
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nat cell biol 2017 cell lines  (ATCC)
97
ATCC nat cell biol 2017 cell lines
Nat Cell Biol 2017 Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 97 stars, based on 1 article reviews
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murine l lr7 cell  (ATCC)
94
ATCC murine l lr7 cell
Murine L Lr7 Cell, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
murine l lr7 cell - by Bioz Stars, 2026-04
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l2 fibroblast cell line  (Thermo Fisher)
90
Thermo Fisher l2 fibroblast cell line
(A) Intracellular growth of WT, Δ glpD /Δ golD , Δ uhpT, Δ glpD /Δ golD /Δ uhpT was determined in BMDMs following infection at an MOI of 0.2. Growth curves are representative of at least three independent experiments. Error bars represent the standard deviation of the means of technical triplicates within the representative experiment. (B) <t>L2</t> <t>fibroblasts</t> were infected with indicated L. monocytogenes strains at an MOI of 0.5 and were examined for plaque formation 4 days post infection. Assays were performed in biological triplicate and data displayed is the median and SEM of a strain’s plaque size relative to WT in one of three representative biological replicates. (C) Bacterial burdens from the spleen and liver were enumerated at 48 hours post-intravenous infection with 1x10 5 bacteria. Data are representative of results from two separate experiments. Horizontal dashed lines represent the limits of detection, and the bars associated with the individual strains represents the mean and SEM of the group.
L2 Fibroblast Cell Line, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/l2 fibroblast cell line/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
l2 fibroblast cell line - by Bioz Stars, 2026-04
90/100 stars
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nat commun 3t3 l1 cells  (ATCC)
99
ATCC nat commun 3t3 l1 cells
(A) Intracellular growth of WT, Δ glpD /Δ golD , Δ uhpT, Δ glpD /Δ golD /Δ uhpT was determined in BMDMs following infection at an MOI of 0.2. Growth curves are representative of at least three independent experiments. Error bars represent the standard deviation of the means of technical triplicates within the representative experiment. (B) <t>L2</t> <t>fibroblasts</t> were infected with indicated L. monocytogenes strains at an MOI of 0.5 and were examined for plaque formation 4 days post infection. Assays were performed in biological triplicate and data displayed is the median and SEM of a strain’s plaque size relative to WT in one of three representative biological replicates. (C) Bacterial burdens from the spleen and liver were enumerated at 48 hours post-intravenous infection with 1x10 5 bacteria. Data are representative of results from two separate experiments. Horizontal dashed lines represent the limits of detection, and the bars associated with the individual strains represents the mean and SEM of the group.
Nat Commun 3t3 L1 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/nat commun 3t3 l1 cells/product/ATCC
Average 99 stars, based on 1 article reviews
nat commun 3t3 l1 cells - by Bioz Stars, 2026-04
99/100 stars
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shh light 2 cells are nih3t3 cells  (ATCC)
99
ATCC shh light 2 cells are nih3t3 cells
(A) Intracellular growth of WT, Δ glpD /Δ golD , Δ uhpT, Δ glpD /Δ golD /Δ uhpT was determined in BMDMs following infection at an MOI of 0.2. Growth curves are representative of at least three independent experiments. Error bars represent the standard deviation of the means of technical triplicates within the representative experiment. (B) <t>L2</t> <t>fibroblasts</t> were infected with indicated L. monocytogenes strains at an MOI of 0.5 and were examined for plaque formation 4 days post infection. Assays were performed in biological triplicate and data displayed is the median and SEM of a strain’s plaque size relative to WT in one of three representative biological replicates. (C) Bacterial burdens from the spleen and liver were enumerated at 48 hours post-intravenous infection with 1x10 5 bacteria. Data are representative of results from two separate experiments. Horizontal dashed lines represent the limits of detection, and the bars associated with the individual strains represents the mean and SEM of the group.
Shh Light 2 Cells Are Nih3t3 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/shh light 2 cells are nih3t3 cells/product/ATCC
Average 99 stars, based on 1 article reviews
shh light 2 cells are nih3t3 cells - by Bioz Stars, 2026-04
99/100 stars
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mccoy cells  (ATCC)
98
ATCC mccoy cells
(A) Intracellular growth of WT, Δ glpD /Δ golD , Δ uhpT, Δ glpD /Δ golD /Δ uhpT was determined in BMDMs following infection at an MOI of 0.2. Growth curves are representative of at least three independent experiments. Error bars represent the standard deviation of the means of technical triplicates within the representative experiment. (B) <t>L2</t> <t>fibroblasts</t> were infected with indicated L. monocytogenes strains at an MOI of 0.5 and were examined for plaque formation 4 days post infection. Assays were performed in biological triplicate and data displayed is the median and SEM of a strain’s plaque size relative to WT in one of three representative biological replicates. (C) Bacterial burdens from the spleen and liver were enumerated at 48 hours post-intravenous infection with 1x10 5 bacteria. Data are representative of results from two separate experiments. Horizontal dashed lines represent the limits of detection, and the bars associated with the individual strains represents the mean and SEM of the group.
Mccoy Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mccoy cells/product/ATCC
Average 98 stars, based on 1 article reviews
mccoy cells - by Bioz Stars, 2026-04
98/100 stars
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Image Search Results


(A) Intracellular growth of WT, Δ glpD /Δ golD , Δ uhpT, Δ glpD /Δ golD /Δ uhpT was determined in BMDMs following infection at an MOI of 0.2. Growth curves are representative of at least three independent experiments. Error bars represent the standard deviation of the means of technical triplicates within the representative experiment. (B) L2 fibroblasts were infected with indicated L. monocytogenes strains at an MOI of 0.5 and were examined for plaque formation 4 days post infection. Assays were performed in biological triplicate and data displayed is the median and SEM of a strain’s plaque size relative to WT in one of three representative biological replicates. (C) Bacterial burdens from the spleen and liver were enumerated at 48 hours post-intravenous infection with 1x10 5 bacteria. Data are representative of results from two separate experiments. Horizontal dashed lines represent the limits of detection, and the bars associated with the individual strains represents the mean and SEM of the group.

Journal: PLOS Pathogens

Article Title: Listeria monocytogenes requires phosphotransferase systems to facilitate intracellular growth and virulence

doi: 10.1371/journal.ppat.1012492

Figure Lengend Snippet: (A) Intracellular growth of WT, Δ glpD /Δ golD , Δ uhpT, Δ glpD /Δ golD /Δ uhpT was determined in BMDMs following infection at an MOI of 0.2. Growth curves are representative of at least three independent experiments. Error bars represent the standard deviation of the means of technical triplicates within the representative experiment. (B) L2 fibroblasts were infected with indicated L. monocytogenes strains at an MOI of 0.5 and were examined for plaque formation 4 days post infection. Assays were performed in biological triplicate and data displayed is the median and SEM of a strain’s plaque size relative to WT in one of three representative biological replicates. (C) Bacterial burdens from the spleen and liver were enumerated at 48 hours post-intravenous infection with 1x10 5 bacteria. Data are representative of results from two separate experiments. Horizontal dashed lines represent the limits of detection, and the bars associated with the individual strains represents the mean and SEM of the group.

Article Snippet: Plaque assays were conducted using a L2 fibroblast cell line grown in Dulbecco’s Minimal Essential Media (DMEM) based media (Thermo Fischer: 11965092) as previously described with minor modifications for visualization and quantification of plaques [ , ].

Techniques: Infection, Standard Deviation, Bacteria

(A) PTS mediated free sugar import and phosphorylation by phosphocarrier protein phospho-cycling from the terminal conversion of phosphoenol-pyruvate (PEP) to pyruvate. (B) Intracellular growth of WT, Δ glpD /Δ golD /Δ uhpT , Δ ptsI , and Δ glpD /Δ golD /Δ uhpT /Δ ptsI was determined in BMDMs following infection at an MOI of 0.2. Growth curves are representative of at least three independent experiments. Error bars represent the standard deviation of the means of technical triplicates within the representative experiment. (C) L2 fibroblasts were infected with indicated L. monocytogenes strains at an MOI of 0.5 and were examined for plaque formation 4 days post infection. Assays were performed in biological triplicate and data displayed is the median and SEM of a strain’s plaque size relative to WT in one of three representative biological replicates. (D) Bacterial burdens from the spleen and liver were enumerated at 48 hours post-intravenous infection with 1x10 5 bacteria. Data are representative of results from two separate experiments. Horizontal dashed lines represent the limits of detection, and the bars associated with the individual strains represents the mean and SEM of the group.

Journal: PLOS Pathogens

Article Title: Listeria monocytogenes requires phosphotransferase systems to facilitate intracellular growth and virulence

doi: 10.1371/journal.ppat.1012492

Figure Lengend Snippet: (A) PTS mediated free sugar import and phosphorylation by phosphocarrier protein phospho-cycling from the terminal conversion of phosphoenol-pyruvate (PEP) to pyruvate. (B) Intracellular growth of WT, Δ glpD /Δ golD /Δ uhpT , Δ ptsI , and Δ glpD /Δ golD /Δ uhpT /Δ ptsI was determined in BMDMs following infection at an MOI of 0.2. Growth curves are representative of at least three independent experiments. Error bars represent the standard deviation of the means of technical triplicates within the representative experiment. (C) L2 fibroblasts were infected with indicated L. monocytogenes strains at an MOI of 0.5 and were examined for plaque formation 4 days post infection. Assays were performed in biological triplicate and data displayed is the median and SEM of a strain’s plaque size relative to WT in one of three representative biological replicates. (D) Bacterial burdens from the spleen and liver were enumerated at 48 hours post-intravenous infection with 1x10 5 bacteria. Data are representative of results from two separate experiments. Horizontal dashed lines represent the limits of detection, and the bars associated with the individual strains represents the mean and SEM of the group.

Article Snippet: Plaque assays were conducted using a L2 fibroblast cell line grown in Dulbecco’s Minimal Essential Media (DMEM) based media (Thermo Fischer: 11965092) as previously described with minor modifications for visualization and quantification of plaques [ , ].

Techniques: Phospho-proteomics, Infection, Standard Deviation, Bacteria