[3636 Search Results


f solani atcc  (ATCC)
93
ATCC f solani atcc
F Solani Atcc, supplied by ATCC, 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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falciforme atcc  (ATCC)
93
ATCC falciforme atcc
Falciforme Atcc, supplied by ATCC, 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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mouse anti phospho histone h2ax  (Cell Signaling Technology Inc)
94
Cell Signaling Technology Inc mouse anti phospho histone h2ax
A . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring <t>g-H2AX</t> (yellow). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; ** p<0.01. B . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring 53BP1 (grey). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; *** p<0.001. C . Western blot analysis showing protein expression of TEAD4 and p53 family of proteins in HCT116 treated (Oxa), or not (NT) with oxaliplatin (0.5 μM). GAPDH was used as a loading control (n=3). D. Heat map corresponding to the genes differentially expressed in HCT116 cells after 24h of oxaliplatin treatment at IC50 (see Supplemental Table 1). The three replicates for the non-treated (NT) and treated (Oxa) are shown.
Mouse Anti Phospho Histone H2ax, supplied by Cell Signaling Technology Inc, 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
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ova 323 339 peptide new england peptide  (Biosynth Carbosynth)
92
Biosynth Carbosynth ova 323 339 peptide new england peptide
A . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring <t>g-H2AX</t> (yellow). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; ** p<0.01. B . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring 53BP1 (grey). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; *** p<0.001. C . Western blot analysis showing protein expression of TEAD4 and p53 family of proteins in HCT116 treated (Oxa), or not (NT) with oxaliplatin (0.5 μM). GAPDH was used as a loading control (n=3). D. Heat map corresponding to the genes differentially expressed in HCT116 cells after 24h of oxaliplatin treatment at IC50 (see Supplemental Table 1). The three replicates for the non-treated (NT) and treated (Oxa) are shown.
Ova 323 339 Peptide New England Peptide, supplied by Biosynth Carbosynth, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pendotech press s 000 pressure sensor  (Cole-Parmer)
92
Cole-Parmer pendotech press s 000 pressure sensor
A . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring <t>g-H2AX</t> (yellow). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; ** p<0.01. B . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring 53BP1 (grey). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; *** p<0.001. C . Western blot analysis showing protein expression of TEAD4 and p53 family of proteins in HCT116 treated (Oxa), or not (NT) with oxaliplatin (0.5 μM). GAPDH was used as a loading control (n=3). D. Heat map corresponding to the genes differentially expressed in HCT116 cells after 24h of oxaliplatin treatment at IC50 (see Supplemental Table 1). The three replicates for the non-treated (NT) and treated (Oxa) are shown.
Pendotech Press S 000 Pressure Sensor, supplied by Cole-Parmer, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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methanobacterium formicicum  (DSMZ)
93
DSMZ methanobacterium formicicum
A . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring <t>g-H2AX</t> (yellow). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; ** p<0.01. B . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring 53BP1 (grey). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; *** p<0.001. C . Western blot analysis showing protein expression of TEAD4 and p53 family of proteins in HCT116 treated (Oxa), or not (NT) with oxaliplatin (0.5 μM). GAPDH was used as a loading control (n=3). D. Heat map corresponding to the genes differentially expressed in HCT116 cells after 24h of oxaliplatin treatment at IC50 (see Supplemental Table 1). The three replicates for the non-treated (NT) and treated (Oxa) are shown.
Methanobacterium Formicicum, supplied by DSMZ, 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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φx174 dsm4497  (DSMZ)
97
DSMZ φx174 dsm4497
A . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring <t>g-H2AX</t> (yellow). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; ** p<0.01. B . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring 53BP1 (grey). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; *** p<0.001. C . Western blot analysis showing protein expression of TEAD4 and p53 family of proteins in HCT116 treated (Oxa), or not (NT) with oxaliplatin (0.5 μM). GAPDH was used as a loading control (n=3). D. Heat map corresponding to the genes differentially expressed in HCT116 cells after 24h of oxaliplatin treatment at IC50 (see Supplemental Table 1). The three replicates for the non-treated (NT) and treated (Oxa) are shown.
φx174 Dsm4497, supplied by DSMZ, 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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dicyanazide adeka hardener eh-3636  (ADEKA CORPORATION)
90
ADEKA CORPORATION dicyanazide adeka hardener eh-3636
A . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring <t>g-H2AX</t> (yellow). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; ** p<0.01. B . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring 53BP1 (grey). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; *** p<0.001. C . Western blot analysis showing protein expression of TEAD4 and p53 family of proteins in HCT116 treated (Oxa), or not (NT) with oxaliplatin (0.5 μM). GAPDH was used as a loading control (n=3). D. Heat map corresponding to the genes differentially expressed in HCT116 cells after 24h of oxaliplatin treatment at IC50 (see Supplemental Table 1). The three replicates for the non-treated (NT) and treated (Oxa) are shown.
Dicyanazide Adeka Hardener Eh 3636, supplied by ADEKA CORPORATION, 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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type-t thermocouple 5sc-tt-t36-36  (OMEGA Engineering)
90
OMEGA Engineering type-t thermocouple 5sc-tt-t36-36
A . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring <t>g-H2AX</t> (yellow). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; ** p<0.01. B . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring 53BP1 (grey). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; *** p<0.001. C . Western blot analysis showing protein expression of TEAD4 and p53 family of proteins in HCT116 treated (Oxa), or not (NT) with oxaliplatin (0.5 μM). GAPDH was used as a loading control (n=3). D. Heat map corresponding to the genes differentially expressed in HCT116 cells after 24h of oxaliplatin treatment at IC50 (see Supplemental Table 1). The three replicates for the non-treated (NT) and treated (Oxa) are shown.
Type T Thermocouple 5sc Tt T36 36, supplied by OMEGA Engineering, 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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shaker shake-xr mounted with wr-3636  (Taitec Corp)
90
Taitec Corp shaker shake-xr mounted with wr-3636
A . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring <t>g-H2AX</t> (yellow). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; ** p<0.01. B . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring 53BP1 (grey). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; *** p<0.001. C . Western blot analysis showing protein expression of TEAD4 and p53 family of proteins in HCT116 treated (Oxa), or not (NT) with oxaliplatin (0.5 μM). GAPDH was used as a loading control (n=3). D. Heat map corresponding to the genes differentially expressed in HCT116 cells after 24h of oxaliplatin treatment at IC50 (see Supplemental Table 1). The three replicates for the non-treated (NT) and treated (Oxa) are shown.
Shaker Shake Xr Mounted With Wr 3636, supplied by Taitec Corp, 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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uv-c leds oslon uv 3636  (Osram Sylvania)
90
Osram Sylvania uv-c leds oslon uv 3636
A . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring <t>g-H2AX</t> (yellow). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; ** p<0.01. B . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring 53BP1 (grey). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; *** p<0.001. C . Western blot analysis showing protein expression of TEAD4 and p53 family of proteins in HCT116 treated (Oxa), or not (NT) with oxaliplatin (0.5 μM). GAPDH was used as a loading control (n=3). D. Heat map corresponding to the genes differentially expressed in HCT116 cells after 24h of oxaliplatin treatment at IC50 (see Supplemental Table 1). The three replicates for the non-treated (NT) and treated (Oxa) are shown.
Uv C Leds Oslon Uv 3636, supplied by Osram Sylvania, 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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irmm-3636 u double spike ( 233 u- 236 u)  (Teva)
90
Teva irmm-3636 u double spike ( 233 u- 236 u)
A . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring <t>g-H2AX</t> (yellow). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; ** p<0.01. B . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring 53BP1 (grey). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; *** p<0.001. C . Western blot analysis showing protein expression of TEAD4 and p53 family of proteins in HCT116 treated (Oxa), or not (NT) with oxaliplatin (0.5 μM). GAPDH was used as a loading control (n=3). D. Heat map corresponding to the genes differentially expressed in HCT116 cells after 24h of oxaliplatin treatment at IC50 (see Supplemental Table 1). The three replicates for the non-treated (NT) and treated (Oxa) are shown.
Irmm 3636 U Double Spike ( 233 U 236 U), supplied by Teva, 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


A . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring g-H2AX (yellow). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; ** p<0.01. B . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring 53BP1 (grey). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; *** p<0.001. C . Western blot analysis showing protein expression of TEAD4 and p53 family of proteins in HCT116 treated (Oxa), or not (NT) with oxaliplatin (0.5 μM). GAPDH was used as a loading control (n=3). D. Heat map corresponding to the genes differentially expressed in HCT116 cells after 24h of oxaliplatin treatment at IC50 (see Supplemental Table 1). The three replicates for the non-treated (NT) and treated (Oxa) are shown.

Journal: bioRxiv

Article Title: The Hippo pathway terminal effector TAZ/WWTR1 mediates oxaliplatin sensitivity in HCT116 colon cancer cells

doi: 10.1101/2023.03.17.533075

Figure Lengend Snippet: A . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring g-H2AX (yellow). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; ** p<0.01. B . Immunofluorescence experiments performed on HCT116 cells treated, or not, with oxaliplatin (0.5 μM) monitoring 53BP1 (grey). DAPI (blue) was used to stain DNA and the nuclei. Quantification of the staining is shown on the right side and is represented as the corrected nuclear fluorescence. Data are represented as the mean ± SEM. (n=3). Unpaired two-tailed Student’s t-test; *** p<0.001. C . Western blot analysis showing protein expression of TEAD4 and p53 family of proteins in HCT116 treated (Oxa), or not (NT) with oxaliplatin (0.5 μM). GAPDH was used as a loading control (n=3). D. Heat map corresponding to the genes differentially expressed in HCT116 cells after 24h of oxaliplatin treatment at IC50 (see Supplemental Table 1). The three replicates for the non-treated (NT) and treated (Oxa) are shown.

Article Snippet: Antibodies used were rabbit anti-53BP1 (1/100; CST #4937), mouse anti-phospho-Histone H2AX clone JBW301 (1/200; Millipore #05-636), anti-TAZ (1/100; CST #4883), mouse anti-TEAD4 (1/50; Santa Cruz #sc101184), and rabbit anti-YAP (1/100; CST #14074).

Techniques: Immunofluorescence, Staining, Fluorescence, Two Tailed Test, Western Blot, Expressing