34085 Search Results


93
Santa Cruz Biotechnology phosphorylated p met
Characteristics of MKN-45 human gastric cancer cells and KRC-108-resistant clones (MKN-R1, -R2 and -R3). (A) MKN-45, MKN-R1, MKN-R2 and MKN-R3 cells were treated with KRC-108 at the indicated concentrations for 72 h before subjection to a cell viability assay. Data are presented as the means from three independent experiments and bars represent standard error. *P<0.05 vs. DMSO control. (B) Cells were seeded into a 24-well plate, and the cell numbers were counted each day until day 4 to establish a growth curve. Data are presented as the mean and standard error of three independent experiments. *P<0.05 vs. MKN-45 cells (C) The expression levels of c-Met and <t>p-Met</t> following KRC-108 treatment were measured by western blotting in MKN-45 and MKN-R cells. (D) The expression of c-Met and the phosphorylation of c-Met were analyzed by immunofluorescence (magnification, ×630). Red, c-Met (top row) or p-Met (bottom row); blue, DAPI. p-Met, <t>phosphorylated</t> c-Met.
Phosphorylated P Met, supplied by Santa Cruz Biotechnology, 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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90
SERVA Electrophoresis pyruvate kinase from rabbit muscle
Characteristics of MKN-45 human gastric cancer cells and KRC-108-resistant clones (MKN-R1, -R2 and -R3). (A) MKN-45, MKN-R1, MKN-R2 and MKN-R3 cells were treated with KRC-108 at the indicated concentrations for 72 h before subjection to a cell viability assay. Data are presented as the means from three independent experiments and bars represent standard error. *P<0.05 vs. DMSO control. (B) Cells were seeded into a 24-well plate, and the cell numbers were counted each day until day 4 to establish a growth curve. Data are presented as the mean and standard error of three independent experiments. *P<0.05 vs. MKN-45 cells (C) The expression levels of c-Met and <t>p-Met</t> following KRC-108 treatment were measured by western blotting in MKN-45 and MKN-R cells. (D) The expression of c-Met and the phosphorylation of c-Met were analyzed by immunofluorescence (magnification, ×630). Red, c-Met (top row) or p-Met (bottom row); blue, DAPI. p-Met, <t>phosphorylated</t> c-Met.
Pyruvate Kinase From Rabbit Muscle, supplied by SERVA Electrophoresis, 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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93
Santa Cruz Biotechnology phosphorylated c met sc 34085 expressions
Characteristics of MKN-45 human gastric cancer cells and KRC-108-resistant clones (MKN-R1, -R2 and -R3). (A) MKN-45, MKN-R1, MKN-R2 and MKN-R3 cells were treated with KRC-108 at the indicated concentrations for 72 h before subjection to a cell viability assay. Data are presented as the means from three independent experiments and bars represent standard error. *P<0.05 vs. DMSO control. (B) Cells were seeded into a 24-well plate, and the cell numbers were counted each day until day 4 to establish a growth curve. Data are presented as the mean and standard error of three independent experiments. *P<0.05 vs. MKN-45 cells (C) The expression levels of c-Met and <t>p-Met</t> following KRC-108 treatment were measured by western blotting in MKN-45 and MKN-R cells. (D) The expression of c-Met and the phosphorylation of c-Met were analyzed by immunofluorescence (magnification, ×630). Red, c-Met (top row) or p-Met (bottom row); blue, DAPI. p-Met, <t>phosphorylated</t> c-Met.
Phosphorylated C Met Sc 34085 Expressions, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/phosphorylated c met sc 34085 expressions/product/Santa Cruz Biotechnology
Average 93 stars, based on 1 article reviews
phosphorylated c met sc 34085 expressions - by Bioz Stars, 2026-02
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90
Biomol GmbH ecules max mousseron
Characteristics of MKN-45 human gastric cancer cells and KRC-108-resistant clones (MKN-R1, -R2 and -R3). (A) MKN-45, MKN-R1, MKN-R2 and MKN-R3 cells were treated with KRC-108 at the indicated concentrations for 72 h before subjection to a cell viability assay. Data are presented as the means from three independent experiments and bars represent standard error. *P<0.05 vs. DMSO control. (B) Cells were seeded into a 24-well plate, and the cell numbers were counted each day until day 4 to establish a growth curve. Data are presented as the mean and standard error of three independent experiments. *P<0.05 vs. MKN-45 cells (C) The expression levels of c-Met and <t>p-Met</t> following KRC-108 treatment were measured by western blotting in MKN-45 and MKN-R cells. (D) The expression of c-Met and the phosphorylation of c-Met were analyzed by immunofluorescence (magnification, ×630). Red, c-Met (top row) or p-Met (bottom row); blue, DAPI. p-Met, <t>phosphorylated</t> c-Met.
Ecules Max Mousseron, supplied by Biomol 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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Lenti ORF clone of Ppp2r1b mGFP tagged Mouse protein phosphatase 2 formerly 2A regulatory subunit A PR 65 beta isoform Ppp2r1b transcript variant 1
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EMD534085 is a kinesin inhibitor currently in clinical development
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The CD4 antibody clone SK3 is derived from the hybridization of mouse NS 1 myeloma cells with spleen cells from BALB c mice immunized with human peripheral blood T lymphocytes The CD4 antibody clone SK3
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N/A
Inhibits kinesin spindle protein Eg5. Inhibits kinesin spindle protein Eg5.
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Image Search Results


Characteristics of MKN-45 human gastric cancer cells and KRC-108-resistant clones (MKN-R1, -R2 and -R3). (A) MKN-45, MKN-R1, MKN-R2 and MKN-R3 cells were treated with KRC-108 at the indicated concentrations for 72 h before subjection to a cell viability assay. Data are presented as the means from three independent experiments and bars represent standard error. *P<0.05 vs. DMSO control. (B) Cells were seeded into a 24-well plate, and the cell numbers were counted each day until day 4 to establish a growth curve. Data are presented as the mean and standard error of three independent experiments. *P<0.05 vs. MKN-45 cells (C) The expression levels of c-Met and p-Met following KRC-108 treatment were measured by western blotting in MKN-45 and MKN-R cells. (D) The expression of c-Met and the phosphorylation of c-Met were analyzed by immunofluorescence (magnification, ×630). Red, c-Met (top row) or p-Met (bottom row); blue, DAPI. p-Met, phosphorylated c-Met.

Journal: Oncology Letters

Article Title: Resistance to the c-Met inhibitor KRC-108 induces the epithelial transition of gastric cancer cells

doi: 10.3892/ol.2015.4029

Figure Lengend Snippet: Characteristics of MKN-45 human gastric cancer cells and KRC-108-resistant clones (MKN-R1, -R2 and -R3). (A) MKN-45, MKN-R1, MKN-R2 and MKN-R3 cells were treated with KRC-108 at the indicated concentrations for 72 h before subjection to a cell viability assay. Data are presented as the means from three independent experiments and bars represent standard error. *P<0.05 vs. DMSO control. (B) Cells were seeded into a 24-well plate, and the cell numbers were counted each day until day 4 to establish a growth curve. Data are presented as the mean and standard error of three independent experiments. *P<0.05 vs. MKN-45 cells (C) The expression levels of c-Met and p-Met following KRC-108 treatment were measured by western blotting in MKN-45 and MKN-R cells. (D) The expression of c-Met and the phosphorylation of c-Met were analyzed by immunofluorescence (magnification, ×630). Red, c-Met (top row) or p-Met (bottom row); blue, DAPI. p-Met, phosphorylated c-Met.

Article Snippet: Primary antibodies against human c-Met (rabbit polyclonal IgG; #sc-10; 1:1,000), phosphorylated (p-)Met (rabbit polyclonal IgG; #sc-34085; 1:1,000), E-cadherin (mouse monoclonal IgG; #sc-21791; 1:1,000), N-cadherin (rabbit polyclonal IgG; #sc-7939; 1:1,000; all from Santa Cruz Biotechnology, Inc., Dallas, TX, USA) and β-actin (mouse monoclonal IgG; #A5441; 1:5,000; Sigma-Aldrich, St. Louis, MO, USA) were used.

Techniques: Clone Assay, Viability Assay, Control, Expressing, Western Blot, Phospho-proteomics, Immunofluorescence