dmem high glucose medium Search Results


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Cytiva Europe modified eagle medium high glucose dmem
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Cytiva Europe medium
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Danaher Inc dmem high glucose medium
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Danaher Inc high glucose dulbecco s modified eagle s medium dmem
FIGURE 7 25HC suppresses HPV infection by restricting small GTPase prenylation. (A) Pan‐prenylation level was suppressed by 25HC. (B) Membrane proteins were collected for Western blot. Membrane‐bound, prenylated Rac1, Cdc42, RhoA and Rap1 expressions were reduced by 25HC. Na+/K+ ATPase (ATP1a1) was used as membrane loading control. (C) The prenylation inhibitors (a) GGTI‐298 and (b) FTI‐277 revealed anti‐HPV16 PsV effect in inhibitory assays. GGTI‐298 and FTI‐277 were serially diluted (0−10 μM) in <t>DMEM</t> and incubated with HPV16 PsV. Mixtures were added to cells and incubated for 16 h for inhibition assay. (D) Farnesylation substrate FPP rescued anti‐HPV capability of 25HC. FPP (10 μM) were mixed with serially diluted 25HC, and added to cells with HPV16 PsV. (E) Prenylation inhibitor GGTI‐298 inhibited LIMK1/cofilin phosphorylation.
High Glucose Dulbecco S Modified Eagle S Medium Dmem, supplied by Danaher Inc, 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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Valiant Co Ltd glucose dulbecco
FIGURE 7 25HC suppresses HPV infection by restricting small GTPase prenylation. (A) Pan‐prenylation level was suppressed by 25HC. (B) Membrane proteins were collected for Western blot. Membrane‐bound, prenylated Rac1, Cdc42, RhoA and Rap1 expressions were reduced by 25HC. Na+/K+ ATPase (ATP1a1) was used as membrane loading control. (C) The prenylation inhibitors (a) GGTI‐298 and (b) FTI‐277 revealed anti‐HPV16 PsV effect in inhibitory assays. GGTI‐298 and FTI‐277 were serially diluted (0−10 μM) in <t>DMEM</t> and incubated with HPV16 PsV. Mixtures were added to cells and incubated for 16 h for inhibition assay. (D) Farnesylation substrate FPP rescued anti‐HPV capability of 25HC. FPP (10 μM) were mixed with serially diluted 25HC, and added to cells with HPV16 PsV. (E) Prenylation inhibitor GGTI‐298 inhibited LIMK1/cofilin phosphorylation.
Glucose Dulbecco, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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VivaCell Biotechnology GmbH dmem low-sugar medium
FIGURE 7 25HC suppresses HPV infection by restricting small GTPase prenylation. (A) Pan‐prenylation level was suppressed by 25HC. (B) Membrane proteins were collected for Western blot. Membrane‐bound, prenylated Rac1, Cdc42, RhoA and Rap1 expressions were reduced by 25HC. Na+/K+ ATPase (ATP1a1) was used as membrane loading control. (C) The prenylation inhibitors (a) GGTI‐298 and (b) FTI‐277 revealed anti‐HPV16 PsV effect in inhibitory assays. GGTI‐298 and FTI‐277 were serially diluted (0−10 μM) in <t>DMEM</t> and incubated with HPV16 PsV. Mixtures were added to cells and incubated for 16 h for inhibition assay. (D) Farnesylation substrate FPP rescued anti‐HPV capability of 25HC. FPP (10 μM) were mixed with serially diluted 25HC, and added to cells with HPV16 PsV. (E) Prenylation inhibitor GGTI‐298 inhibited LIMK1/cofilin phosphorylation.
Dmem Low Sugar Medium, supplied by VivaCell Biotechnology GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Dominique DUTSCHER SAS dmem
FIGURE 7 25HC suppresses HPV infection by restricting small GTPase prenylation. (A) Pan‐prenylation level was suppressed by 25HC. (B) Membrane proteins were collected for Western blot. Membrane‐bound, prenylated Rac1, Cdc42, RhoA and Rap1 expressions were reduced by 25HC. Na+/K+ ATPase (ATP1a1) was used as membrane loading control. (C) The prenylation inhibitors (a) GGTI‐298 and (b) FTI‐277 revealed anti‐HPV16 PsV effect in inhibitory assays. GGTI‐298 and FTI‐277 were serially diluted (0−10 μM) in <t>DMEM</t> and incubated with HPV16 PsV. Mixtures were added to cells and incubated for 16 h for inhibition assay. (D) Farnesylation substrate FPP rescued anti‐HPV capability of 25HC. FPP (10 μM) were mixed with serially diluted 25HC, and added to cells with HPV16 PsV. (E) Prenylation inhibitor GGTI‐298 inhibited LIMK1/cofilin phosphorylation.
Dmem, supplied by Dominique DUTSCHER SAS, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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TransGen biotech co cartilage induction medium (dmem high glucose
FIGURE 7 25HC suppresses HPV infection by restricting small GTPase prenylation. (A) Pan‐prenylation level was suppressed by 25HC. (B) Membrane proteins were collected for Western blot. Membrane‐bound, prenylated Rac1, Cdc42, RhoA and Rap1 expressions were reduced by 25HC. Na+/K+ ATPase (ATP1a1) was used as membrane loading control. (C) The prenylation inhibitors (a) GGTI‐298 and (b) FTI‐277 revealed anti‐HPV16 PsV effect in inhibitory assays. GGTI‐298 and FTI‐277 were serially diluted (0−10 μM) in <t>DMEM</t> and incubated with HPV16 PsV. Mixtures were added to cells and incubated for 16 h for inhibition assay. (D) Farnesylation substrate FPP rescued anti‐HPV capability of 25HC. FPP (10 μM) were mixed with serially diluted 25HC, and added to cells with HPV16 PsV. (E) Prenylation inhibitor GGTI‐298 inhibited LIMK1/cofilin phosphorylation.
Cartilage Induction Medium (Dmem High Glucose, supplied by TransGen biotech co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Corning Life Sciences high glucose dmem medium containing 25% corning matrigel matrix
FIGURE 7 25HC suppresses HPV infection by restricting small GTPase prenylation. (A) Pan‐prenylation level was suppressed by 25HC. (B) Membrane proteins were collected for Western blot. Membrane‐bound, prenylated Rac1, Cdc42, RhoA and Rap1 expressions were reduced by 25HC. Na+/K+ ATPase (ATP1a1) was used as membrane loading control. (C) The prenylation inhibitors (a) GGTI‐298 and (b) FTI‐277 revealed anti‐HPV16 PsV effect in inhibitory assays. GGTI‐298 and FTI‐277 were serially diluted (0−10 μM) in <t>DMEM</t> and incubated with HPV16 PsV. Mixtures were added to cells and incubated for 16 h for inhibition assay. (D) Farnesylation substrate FPP rescued anti‐HPV capability of 25HC. FPP (10 μM) were mixed with serially diluted 25HC, and added to cells with HPV16 PsV. (E) Prenylation inhibitor GGTI‐298 inhibited LIMK1/cofilin phosphorylation.
High Glucose Dmem Medium Containing 25% Corning Matrigel Matrix, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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iCell Gene Therapeutics high glucose dmem medium
FIGURE 7 25HC suppresses HPV infection by restricting small GTPase prenylation. (A) Pan‐prenylation level was suppressed by 25HC. (B) Membrane proteins were collected for Western blot. Membrane‐bound, prenylated Rac1, Cdc42, RhoA and Rap1 expressions were reduced by 25HC. Na+/K+ ATPase (ATP1a1) was used as membrane loading control. (C) The prenylation inhibitors (a) GGTI‐298 and (b) FTI‐277 revealed anti‐HPV16 PsV effect in inhibitory assays. GGTI‐298 and FTI‐277 were serially diluted (0−10 μM) in <t>DMEM</t> and incubated with HPV16 PsV. Mixtures were added to cells and incubated for 16 h for inhibition assay. (D) Farnesylation substrate FPP rescued anti‐HPV capability of 25HC. FPP (10 μM) were mixed with serially diluted 25HC, and added to cells with HPV16 PsV. (E) Prenylation inhibitor GGTI‐298 inhibited LIMK1/cofilin phosphorylation.
High Glucose Dmem Medium, supplied by iCell Gene Therapeutics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Dominique DUTSCHER SAS dulbecco´s modified eagle´s medium (dmem-high glucose
FIGURE 7 25HC suppresses HPV infection by restricting small GTPase prenylation. (A) Pan‐prenylation level was suppressed by 25HC. (B) Membrane proteins were collected for Western blot. Membrane‐bound, prenylated Rac1, Cdc42, RhoA and Rap1 expressions were reduced by 25HC. Na+/K+ ATPase (ATP1a1) was used as membrane loading control. (C) The prenylation inhibitors (a) GGTI‐298 and (b) FTI‐277 revealed anti‐HPV16 PsV effect in inhibitory assays. GGTI‐298 and FTI‐277 were serially diluted (0−10 μM) in <t>DMEM</t> and incubated with HPV16 PsV. Mixtures were added to cells and incubated for 16 h for inhibition assay. (D) Farnesylation substrate FPP rescued anti‐HPV capability of 25HC. FPP (10 μM) were mixed with serially diluted 25HC, and added to cells with HPV16 PsV. (E) Prenylation inhibitor GGTI‐298 inhibited LIMK1/cofilin phosphorylation.
Dulbecco´S Modified Eagle´S Medium (Dmem High Glucose, supplied by Dominique DUTSCHER SAS, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


FIGURE 7 25HC suppresses HPV infection by restricting small GTPase prenylation. (A) Pan‐prenylation level was suppressed by 25HC. (B) Membrane proteins were collected for Western blot. Membrane‐bound, prenylated Rac1, Cdc42, RhoA and Rap1 expressions were reduced by 25HC. Na+/K+ ATPase (ATP1a1) was used as membrane loading control. (C) The prenylation inhibitors (a) GGTI‐298 and (b) FTI‐277 revealed anti‐HPV16 PsV effect in inhibitory assays. GGTI‐298 and FTI‐277 were serially diluted (0−10 μM) in DMEM and incubated with HPV16 PsV. Mixtures were added to cells and incubated for 16 h for inhibition assay. (D) Farnesylation substrate FPP rescued anti‐HPV capability of 25HC. FPP (10 μM) were mixed with serially diluted 25HC, and added to cells with HPV16 PsV. (E) Prenylation inhibitor GGTI‐298 inhibited LIMK1/cofilin phosphorylation.

Journal: Journal of medical virology

Article Title: 25-hydroxycholesterol inhibits human papillomavirus infection in cervical epithelial cells by perturbing cytoskeletal remodeling.

doi: 10.1002/jmv.28834

Figure Lengend Snippet: FIGURE 7 25HC suppresses HPV infection by restricting small GTPase prenylation. (A) Pan‐prenylation level was suppressed by 25HC. (B) Membrane proteins were collected for Western blot. Membrane‐bound, prenylated Rac1, Cdc42, RhoA and Rap1 expressions were reduced by 25HC. Na+/K+ ATPase (ATP1a1) was used as membrane loading control. (C) The prenylation inhibitors (a) GGTI‐298 and (b) FTI‐277 revealed anti‐HPV16 PsV effect in inhibitory assays. GGTI‐298 and FTI‐277 were serially diluted (0−10 μM) in DMEM and incubated with HPV16 PsV. Mixtures were added to cells and incubated for 16 h for inhibition assay. (D) Farnesylation substrate FPP rescued anti‐HPV capability of 25HC. FPP (10 μM) were mixed with serially diluted 25HC, and added to cells with HPV16 PsV. (E) Prenylation inhibitor GGTI‐298 inhibited LIMK1/cofilin phosphorylation.

Article Snippet: Cells were cultured in high‐ glucose Dulbecco's modified Eagle's medium (DMEM) (HyClone) supplemented with 10% fetal bovine serum (FBS) (Yeasen), and incubated in a humidified environment containing 5% CO2 at 37°C.

Techniques: Infection, Membrane, Western Blot, Control, Incubation, Inhibition, Phospho-proteomics