phosphorylation Search Results


94
Sino Biological variant
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Sino Biological gsk3β phosphorylated tau
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95
Chem Impex International fmoc ser po obzl oh oh pser
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93
Proteintech phospho marcks ser159 163 polyclonal antibody
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96
Rockland Immunochemicals rabbit p chk2 t68
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94
BioVendor Instruments phosphorylated neurofilament h human elisa kit
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Chem Impex International coenzyme a
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Chem Impex International nicotinamide adenine dinucleotide nad
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90
Boster Bio phospho s6k1
(A) Cytotoxicity of SK-Hep1 cells treated with IR (2Gy) alone or combined with PKI-587 (0.1 μM) at 0, 12, 24, 36, and 48 h. (B) Clonogenic survival assays of SK-Hep1 cells treated with PKI-587 (0.1μM) followed by irradiation in a range of radiation doses. (C and F) Representative images of the colony formation revealing the proliferation of SK-Kep1 cells treated with IR (2 Gy) alone or combined with PKI-587 (0.1 μM) for 24 h. The percentage of colony formation was calculated. (D and E) The level of <t>p-S6K1</t> and p70S6K proteins in SK-Hep1 cells after treatment with IR (2Gy) alone or combined with PKI-587 (0.1 μM) for 24 h determined by western blot assay. The semiquantitative data were represented as p-S6K1/p70S6K. The data are mean ± SD, n = 3. ** P <0.01, *** P <0.001 versus IR group. IR, ionizing radiation (6 MV-X ray).
Phospho S6k1, supplied by Boster Bio, 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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85
Proteintech cmlck
(A) Cytotoxicity of SK-Hep1 cells treated with IR (2Gy) alone or combined with PKI-587 (0.1 μM) at 0, 12, 24, 36, and 48 h. (B) Clonogenic survival assays of SK-Hep1 cells treated with PKI-587 (0.1μM) followed by irradiation in a range of radiation doses. (C and F) Representative images of the colony formation revealing the proliferation of SK-Kep1 cells treated with IR (2 Gy) alone or combined with PKI-587 (0.1 μM) for 24 h. The percentage of colony formation was calculated. (D and E) The level of <t>p-S6K1</t> and p70S6K proteins in SK-Hep1 cells after treatment with IR (2Gy) alone or combined with PKI-587 (0.1 μM) for 24 h determined by western blot assay. The semiquantitative data were represented as p-S6K1/p70S6K. The data are mean ± SD, n = 3. ** P <0.01, *** P <0.001 versus IR group. IR, ionizing radiation (6 MV-X ray).
Cmlck, supplied by Proteintech, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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95
Chem Impex International phospho threonine derivative fmoc thr hpo 3 bzl oh
(A) Cytotoxicity of SK-Hep1 cells treated with IR (2Gy) alone or combined with PKI-587 (0.1 μM) at 0, 12, 24, 36, and 48 h. (B) Clonogenic survival assays of SK-Hep1 cells treated with PKI-587 (0.1μM) followed by irradiation in a range of radiation doses. (C and F) Representative images of the colony formation revealing the proliferation of SK-Kep1 cells treated with IR (2 Gy) alone or combined with PKI-587 (0.1 μM) for 24 h. The percentage of colony formation was calculated. (D and E) The level of <t>p-S6K1</t> and p70S6K proteins in SK-Hep1 cells after treatment with IR (2Gy) alone or combined with PKI-587 (0.1 μM) for 24 h determined by western blot assay. The semiquantitative data were represented as p-S6K1/p70S6K. The data are mean ± SD, n = 3. ** P <0.01, *** P <0.001 versus IR group. IR, ionizing radiation (6 MV-X ray).
Phospho Threonine Derivative Fmoc Thr Hpo 3 Bzl Oh, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


(A) Cytotoxicity of SK-Hep1 cells treated with IR (2Gy) alone or combined with PKI-587 (0.1 μM) at 0, 12, 24, 36, and 48 h. (B) Clonogenic survival assays of SK-Hep1 cells treated with PKI-587 (0.1μM) followed by irradiation in a range of radiation doses. (C and F) Representative images of the colony formation revealing the proliferation of SK-Kep1 cells treated with IR (2 Gy) alone or combined with PKI-587 (0.1 μM) for 24 h. The percentage of colony formation was calculated. (D and E) The level of p-S6K1 and p70S6K proteins in SK-Hep1 cells after treatment with IR (2Gy) alone or combined with PKI-587 (0.1 μM) for 24 h determined by western blot assay. The semiquantitative data were represented as p-S6K1/p70S6K. The data are mean ± SD, n = 3. ** P <0.01, *** P <0.001 versus IR group. IR, ionizing radiation (6 MV-X ray).

Journal: PLoS ONE

Article Title: PKI-587 enhances radiosensitization of hepatocellular carcinoma by inhibiting the PI3K/AKT/mTOR pathways and DNA damage repair

doi: 10.1371/journal.pone.0258817

Figure Lengend Snippet: (A) Cytotoxicity of SK-Hep1 cells treated with IR (2Gy) alone or combined with PKI-587 (0.1 μM) at 0, 12, 24, 36, and 48 h. (B) Clonogenic survival assays of SK-Hep1 cells treated with PKI-587 (0.1μM) followed by irradiation in a range of radiation doses. (C and F) Representative images of the colony formation revealing the proliferation of SK-Kep1 cells treated with IR (2 Gy) alone or combined with PKI-587 (0.1 μM) for 24 h. The percentage of colony formation was calculated. (D and E) The level of p-S6K1 and p70S6K proteins in SK-Hep1 cells after treatment with IR (2Gy) alone or combined with PKI-587 (0.1 μM) for 24 h determined by western blot assay. The semiquantitative data were represented as p-S6K1/p70S6K. The data are mean ± SD, n = 3. ** P <0.01, *** P <0.001 versus IR group. IR, ionizing radiation (6 MV-X ray).

Article Snippet: Antibodies to p70S6K, phospho-S6K1 (T421 + S424), eIF4EBP1 and phospho-eIF4EBP1 were purchased from Boster Biological Technology, China. γ-H2AX was obtained from Biolegend Biological Technology, USA. β-actin was obtained from Biosharp Life Science, China.

Techniques: Irradiation, Western Blot