solid phase micro extraction spme probe Search Results


solid phase micro extraction spme probe  (Gerstel GmbH)
96
Gerstel GmbH solid phase micro extraction spme probe
Solid Phase Micro Extraction Spme Probe, supplied by Gerstel GmbH, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/solid+phase+micro+extraction+spme+probe/SPME/us11618864-502-29-23
Average 96 stars, based on 1 article reviews
solid phase micro extraction spme probe - by Bioz Stars, 2026-10
96/100 stars
  Buy from Supplier
electron probe micro analyzer epma  (JEOL)
96
JEOL electron probe micro analyzer epma
Electron Probe Micro Analyzer Epma, supplied by JEOL, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/solid+phase+micro+extraction+spme+probe/JXA-8500F+Electron+Probe+Microanalyzer/pmc11012869-130-9-16
Average 96 stars, based on 1 article reviews
electron probe micro analyzer epma - by Bioz Stars, 2026-10
96/100 stars
  Buy from Supplier
electron probe micro analysis sx51  (CAMECA Inc)
90
CAMECA Inc electron probe micro analysis sx51
Electron Probe Micro Analysis Sx51, supplied by CAMECA Inc, 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/product/solid+phase+micro+extraction+spme+probe/sx100+electron+microprobe/us07005191-299-6-11
Average 90 stars, based on 1 article reviews
electron probe micro analysis sx51 - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier
cancer signaling phospho-antibody microarray slides  (Full Moon BioSystems)
90
Full Moon BioSystems cancer signaling phospho-antibody microarray slides
Analysis of CXCR6-mediated phosphorylation of cell signaling molecules using antibody <t>microarray.</t> Phosphorylation-specific antibody array was performed for the qualitative analysis of differentially phosphorylated proteins after treating BrCa cells with CXCL16 (100 ng/mL for 5 min). The BrCa cells treated with vehicle were used as the control. The antibody array consisted of 273 highly specific antibodies against proteins significant for cancer signaling pathways, with β-actin and GAPDH serving as internal positive controls. The median signal intensity for each antibody was obtained using six replicate spots ( n = 6) and was normalized to the median signal of GAPDH. The heat map shown in Panel ( A ) represents a fold change in the phosphorylation status of specified proteins in CXCL16-treated BrCa cells. Heat map was generated from normalized intensity data using the CIMminer tool. Each cell in the heat map shows the ratio of phosphorylated (P) to non-phosphorylated (N) protein in a treated vs. nontreated sample. Red indicates an increase, while green represents a decrease in phosphorylation signaling molecules. The intensity of the color is dependent on the degree of phosphorylation. Panel ( B ) shows the predicted signaling pathway induced by CXCR6-CXCL16 activation leading to neoplastic progression. Changes in the phosphorylation of signaling molecules obtained from antibody microarray analysis were uploaded into Ingenuity Pathways Knowledge Database as text files containing GenBank accession numbers. The chart shows possible activation (red) of the FAK-Src, PI3K/Akt, and Jak/Stat pathways along with the reorganization of the cytoskeleton, which would increase the potential of BrCa cells to survive and invade.
Cancer Signaling Phospho Antibody Microarray Slides, supplied by Full Moon BioSystems, 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/product/solid+phase+micro+extraction+spme+probe/antibody+microarray+slide/pmc08306453-51-7-17
Average 90 stars, based on 1 article reviews
cancer signaling phospho-antibody microarray slides - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier
field emission electron probe micro analyzer  (JEOL)
97
JEOL field emission electron probe micro analyzer
Analysis of CXCR6-mediated phosphorylation of cell signaling molecules using antibody <t>microarray.</t> Phosphorylation-specific antibody array was performed for the qualitative analysis of differentially phosphorylated proteins after treating BrCa cells with CXCL16 (100 ng/mL for 5 min). The BrCa cells treated with vehicle were used as the control. The antibody array consisted of 273 highly specific antibodies against proteins significant for cancer signaling pathways, with β-actin and GAPDH serving as internal positive controls. The median signal intensity for each antibody was obtained using six replicate spots ( n = 6) and was normalized to the median signal of GAPDH. The heat map shown in Panel ( A ) represents a fold change in the phosphorylation status of specified proteins in CXCL16-treated BrCa cells. Heat map was generated from normalized intensity data using the CIMminer tool. Each cell in the heat map shows the ratio of phosphorylated (P) to non-phosphorylated (N) protein in a treated vs. nontreated sample. Red indicates an increase, while green represents a decrease in phosphorylation signaling molecules. The intensity of the color is dependent on the degree of phosphorylation. Panel ( B ) shows the predicted signaling pathway induced by CXCR6-CXCL16 activation leading to neoplastic progression. Changes in the phosphorylation of signaling molecules obtained from antibody microarray analysis were uploaded into Ingenuity Pathways Knowledge Database as text files containing GenBank accession numbers. The chart shows possible activation (red) of the FAK-Src, PI3K/Akt, and Jak/Stat pathways along with the reorganization of the cytoskeleton, which would increase the potential of BrCa cells to survive and invade.
Field Emission Electron Probe Micro Analyzer, supplied by JEOL, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/solid+phase+micro+extraction+spme+probe/JXA-8530F+Electron+Probe+Microanalyzer/10__2355_slash_isijinternational__isijint___2016___737-31-9-14
Average 97 stars, based on 1 article reviews
field emission electron probe micro analyzer - by Bioz Stars, 2026-10
97/100 stars
  Buy from Supplier
tnfα quantikine solid phase immunoassay enzyme linked immunoassay  (R&D Systems)
96
R&D Systems tnfα quantikine solid phase immunoassay enzyme linked immunoassay
Analysis of CXCR6-mediated phosphorylation of cell signaling molecules using antibody <t>microarray.</t> Phosphorylation-specific antibody array was performed for the qualitative analysis of differentially phosphorylated proteins after treating BrCa cells with CXCL16 (100 ng/mL for 5 min). The BrCa cells treated with vehicle were used as the control. The antibody array consisted of 273 highly specific antibodies against proteins significant for cancer signaling pathways, with β-actin and GAPDH serving as internal positive controls. The median signal intensity for each antibody was obtained using six replicate spots ( n = 6) and was normalized to the median signal of GAPDH. The heat map shown in Panel ( A ) represents a fold change in the phosphorylation status of specified proteins in CXCL16-treated BrCa cells. Heat map was generated from normalized intensity data using the CIMminer tool. Each cell in the heat map shows the ratio of phosphorylated (P) to non-phosphorylated (N) protein in a treated vs. nontreated sample. Red indicates an increase, while green represents a decrease in phosphorylation signaling molecules. The intensity of the color is dependent on the degree of phosphorylation. Panel ( B ) shows the predicted signaling pathway induced by CXCR6-CXCL16 activation leading to neoplastic progression. Changes in the phosphorylation of signaling molecules obtained from antibody microarray analysis were uploaded into Ingenuity Pathways Knowledge Database as text files containing GenBank accession numbers. The chart shows possible activation (red) of the FAK-Src, PI3K/Akt, and Jak/Stat pathways along with the reorganization of the cytoskeleton, which would increase the potential of BrCa cells to survive and invade.
Tnfα Quantikine Solid Phase Immunoassay Enzyme Linked Immunoassay, supplied by R&D Systems, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/solid+phase+micro+extraction+spme+probe/Mouse+TNF-alpha+Quantikine+ELISA+Kit/pm35723764-95-14-21
Average 96 stars, based on 1 article reviews
tnfα quantikine solid phase immunoassay enzyme linked immunoassay - by Bioz Stars, 2026-10
96/100 stars
  Buy from Supplier
solid phase dna probe method  (Thermo Fisher)
99
Thermo Fisher solid phase dna probe method
Analysis of CXCR6-mediated phosphorylation of cell signaling molecules using antibody <t>microarray.</t> Phosphorylation-specific antibody array was performed for the qualitative analysis of differentially phosphorylated proteins after treating BrCa cells with CXCL16 (100 ng/mL for 5 min). The BrCa cells treated with vehicle were used as the control. The antibody array consisted of 273 highly specific antibodies against proteins significant for cancer signaling pathways, with β-actin and GAPDH serving as internal positive controls. The median signal intensity for each antibody was obtained using six replicate spots ( n = 6) and was normalized to the median signal of GAPDH. The heat map shown in Panel ( A ) represents a fold change in the phosphorylation status of specified proteins in CXCL16-treated BrCa cells. Heat map was generated from normalized intensity data using the CIMminer tool. Each cell in the heat map shows the ratio of phosphorylated (P) to non-phosphorylated (N) protein in a treated vs. nontreated sample. Red indicates an increase, while green represents a decrease in phosphorylation signaling molecules. The intensity of the color is dependent on the degree of phosphorylation. Panel ( B ) shows the predicted signaling pathway induced by CXCR6-CXCL16 activation leading to neoplastic progression. Changes in the phosphorylation of signaling molecules obtained from antibody microarray analysis were uploaded into Ingenuity Pathways Knowledge Database as text files containing GenBank accession numbers. The chart shows possible activation (red) of the FAK-Src, PI3K/Akt, and Jak/Stat pathways along with the reorganization of the cytoskeleton, which would increase the potential of BrCa cells to survive and invade.
Solid Phase Dna Probe Method, supplied by Thermo Fisher, 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/product/solid+phase+micro+extraction+spme+probe/DNA/pm16876193-160-21-47
Average 99 stars, based on 1 article reviews
solid phase dna probe method - by Bioz Stars, 2026-10
99/100 stars
  Buy from Supplier
expedite 8900 nucleic acid synthesis system  (PerSeptive Biosystems Inc)
90
PerSeptive Biosystems Inc expedite 8900 nucleic acid synthesis system
Analysis of CXCR6-mediated phosphorylation of cell signaling molecules using antibody <t>microarray.</t> Phosphorylation-specific antibody array was performed for the qualitative analysis of differentially phosphorylated proteins after treating BrCa cells with CXCL16 (100 ng/mL for 5 min). The BrCa cells treated with vehicle were used as the control. The antibody array consisted of 273 highly specific antibodies against proteins significant for cancer signaling pathways, with β-actin and GAPDH serving as internal positive controls. The median signal intensity for each antibody was obtained using six replicate spots ( n = 6) and was normalized to the median signal of GAPDH. The heat map shown in Panel ( A ) represents a fold change in the phosphorylation status of specified proteins in CXCL16-treated BrCa cells. Heat map was generated from normalized intensity data using the CIMminer tool. Each cell in the heat map shows the ratio of phosphorylated (P) to non-phosphorylated (N) protein in a treated vs. nontreated sample. Red indicates an increase, while green represents a decrease in phosphorylation signaling molecules. The intensity of the color is dependent on the degree of phosphorylation. Panel ( B ) shows the predicted signaling pathway induced by CXCR6-CXCL16 activation leading to neoplastic progression. Changes in the phosphorylation of signaling molecules obtained from antibody microarray analysis were uploaded into Ingenuity Pathways Knowledge Database as text files containing GenBank accession numbers. The chart shows possible activation (red) of the FAK-Src, PI3K/Akt, and Jak/Stat pathways along with the reorganization of the cytoskeleton, which would increase the potential of BrCa cells to survive and invade.
Expedite 8900 Nucleic Acid Synthesis System, supplied by PerSeptive Biosystems Inc, 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/product/solid+phase+micro+extraction+spme+probe/expedite+8909+nucleic+acid+synthesis+system/pmc01233981-71-12-18
Average 90 stars, based on 1 article reviews
expedite 8900 nucleic acid synthesis system - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier
electron probe micro analysis  (JEOL)
97
JEOL electron probe micro analysis
Analysis of CXCR6-mediated phosphorylation of cell signaling molecules using antibody <t>microarray.</t> Phosphorylation-specific antibody array was performed for the qualitative analysis of differentially phosphorylated proteins after treating BrCa cells with CXCL16 (100 ng/mL for 5 min). The BrCa cells treated with vehicle were used as the control. The antibody array consisted of 273 highly specific antibodies against proteins significant for cancer signaling pathways, with β-actin and GAPDH serving as internal positive controls. The median signal intensity for each antibody was obtained using six replicate spots ( n = 6) and was normalized to the median signal of GAPDH. The heat map shown in Panel ( A ) represents a fold change in the phosphorylation status of specified proteins in CXCL16-treated BrCa cells. Heat map was generated from normalized intensity data using the CIMminer tool. Each cell in the heat map shows the ratio of phosphorylated (P) to non-phosphorylated (N) protein in a treated vs. nontreated sample. Red indicates an increase, while green represents a decrease in phosphorylation signaling molecules. The intensity of the color is dependent on the degree of phosphorylation. Panel ( B ) shows the predicted signaling pathway induced by CXCR6-CXCL16 activation leading to neoplastic progression. Changes in the phosphorylation of signaling molecules obtained from antibody microarray analysis were uploaded into Ingenuity Pathways Knowledge Database as text files containing GenBank accession numbers. The chart shows possible activation (red) of the FAK-Src, PI3K/Akt, and Jak/Stat pathways along with the reorganization of the cytoskeleton, which would increase the potential of BrCa cells to survive and invade.
Electron Probe Micro Analysis, supplied by JEOL, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/solid+phase+micro+extraction+spme+probe/JXA-8230+Electron+Probe+Microanalyzer/10__1016_slash_j__jmrt__2023__11__183-60-14-19
Average 97 stars, based on 1 article reviews
electron probe micro analysis - by Bioz Stars, 2026-10
97/100 stars
  Buy from Supplier
solid phase sandwich elisa kit  (Monobind)
96
Monobind solid phase sandwich elisa kit
Analysis of CXCR6-mediated phosphorylation of cell signaling molecules using antibody <t>microarray.</t> Phosphorylation-specific antibody array was performed for the qualitative analysis of differentially phosphorylated proteins after treating BrCa cells with CXCL16 (100 ng/mL for 5 min). The BrCa cells treated with vehicle were used as the control. The antibody array consisted of 273 highly specific antibodies against proteins significant for cancer signaling pathways, with β-actin and GAPDH serving as internal positive controls. The median signal intensity for each antibody was obtained using six replicate spots ( n = 6) and was normalized to the median signal of GAPDH. The heat map shown in Panel ( A ) represents a fold change in the phosphorylation status of specified proteins in CXCL16-treated BrCa cells. Heat map was generated from normalized intensity data using the CIMminer tool. Each cell in the heat map shows the ratio of phosphorylated (P) to non-phosphorylated (N) protein in a treated vs. nontreated sample. Red indicates an increase, while green represents a decrease in phosphorylation signaling molecules. The intensity of the color is dependent on the degree of phosphorylation. Panel ( B ) shows the predicted signaling pathway induced by CXCR6-CXCL16 activation leading to neoplastic progression. Changes in the phosphorylation of signaling molecules obtained from antibody microarray analysis were uploaded into Ingenuity Pathways Knowledge Database as text files containing GenBank accession numbers. The chart shows possible activation (red) of the FAK-Src, PI3K/Akt, and Jak/Stat pathways along with the reorganization of the cytoskeleton, which would increase the potential of BrCa cells to survive and invade.
Solid Phase Sandwich Elisa Kit, supplied by Monobind, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/solid+phase+micro+extraction+spme+probe/Cortisol+AccuBind+ELISA+Kit/pmc10188054-60-32-36
Average 96 stars, based on 1 article reviews
solid phase sandwich elisa kit - by Bioz Stars, 2026-10
96/100 stars
  Buy from Supplier
solid-phase sandwich elisa kit  (Aviscera Bioscience Inc)
90
Aviscera Bioscience Inc solid-phase sandwich elisa kit
Analysis of CXCR6-mediated phosphorylation of cell signaling molecules using antibody <t>microarray.</t> Phosphorylation-specific antibody array was performed for the qualitative analysis of differentially phosphorylated proteins after treating BrCa cells with CXCL16 (100 ng/mL for 5 min). The BrCa cells treated with vehicle were used as the control. The antibody array consisted of 273 highly specific antibodies against proteins significant for cancer signaling pathways, with β-actin and GAPDH serving as internal positive controls. The median signal intensity for each antibody was obtained using six replicate spots ( n = 6) and was normalized to the median signal of GAPDH. The heat map shown in Panel ( A ) represents a fold change in the phosphorylation status of specified proteins in CXCL16-treated BrCa cells. Heat map was generated from normalized intensity data using the CIMminer tool. Each cell in the heat map shows the ratio of phosphorylated (P) to non-phosphorylated (N) protein in a treated vs. nontreated sample. Red indicates an increase, while green represents a decrease in phosphorylation signaling molecules. The intensity of the color is dependent on the degree of phosphorylation. Panel ( B ) shows the predicted signaling pathway induced by CXCR6-CXCL16 activation leading to neoplastic progression. Changes in the phosphorylation of signaling molecules obtained from antibody microarray analysis were uploaded into Ingenuity Pathways Knowledge Database as text files containing GenBank accession numbers. The chart shows possible activation (red) of the FAK-Src, PI3K/Akt, and Jak/Stat pathways along with the reorganization of the cytoskeleton, which would increase the potential of BrCa cells to survive and invade.
Solid Phase Sandwich Elisa Kit, supplied by Aviscera Bioscience Inc, 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/product/solid+phase+micro+extraction+spme+probe/elisa+kit/pmc04047921-181-22-26
Average 90 stars, based on 1 article reviews
solid-phase sandwich elisa kit - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier
solid-phase enzyme linked immunosorbent assay (elisa) method  (MyBiosource Biotechnology)
90
MyBiosource Biotechnology solid-phase enzyme linked immunosorbent assay (elisa) method
Analysis of CXCR6-mediated phosphorylation of cell signaling molecules using antibody <t>microarray.</t> Phosphorylation-specific antibody array was performed for the qualitative analysis of differentially phosphorylated proteins after treating BrCa cells with CXCL16 (100 ng/mL for 5 min). The BrCa cells treated with vehicle were used as the control. The antibody array consisted of 273 highly specific antibodies against proteins significant for cancer signaling pathways, with β-actin and GAPDH serving as internal positive controls. The median signal intensity for each antibody was obtained using six replicate spots ( n = 6) and was normalized to the median signal of GAPDH. The heat map shown in Panel ( A ) represents a fold change in the phosphorylation status of specified proteins in CXCL16-treated BrCa cells. Heat map was generated from normalized intensity data using the CIMminer tool. Each cell in the heat map shows the ratio of phosphorylated (P) to non-phosphorylated (N) protein in a treated vs. nontreated sample. Red indicates an increase, while green represents a decrease in phosphorylation signaling molecules. The intensity of the color is dependent on the degree of phosphorylation. Panel ( B ) shows the predicted signaling pathway induced by CXCR6-CXCL16 activation leading to neoplastic progression. Changes in the phosphorylation of signaling molecules obtained from antibody microarray analysis were uploaded into Ingenuity Pathways Knowledge Database as text files containing GenBank accession numbers. The chart shows possible activation (red) of the FAK-Src, PI3K/Akt, and Jak/Stat pathways along with the reorganization of the cytoskeleton, which would increase the potential of BrCa cells to survive and invade.
Solid Phase Enzyme Linked Immunosorbent Assay (Elisa) Method, supplied by MyBiosource Biotechnology, 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/product/solid+phase+micro+extraction+spme+probe/enzyme+linked+immunosorbent+assay++elisa++kit/10__1080_slash_20905068__2019__1662647-73-9-28
Average 90 stars, based on 1 article reviews
solid-phase enzyme linked immunosorbent assay (elisa) method - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier

Image Search Results


Analysis of CXCR6-mediated phosphorylation of cell signaling molecules using antibody microarray. Phosphorylation-specific antibody array was performed for the qualitative analysis of differentially phosphorylated proteins after treating BrCa cells with CXCL16 (100 ng/mL for 5 min). The BrCa cells treated with vehicle were used as the control. The antibody array consisted of 273 highly specific antibodies against proteins significant for cancer signaling pathways, with β-actin and GAPDH serving as internal positive controls. The median signal intensity for each antibody was obtained using six replicate spots ( n = 6) and was normalized to the median signal of GAPDH. The heat map shown in Panel ( A ) represents a fold change in the phosphorylation status of specified proteins in CXCL16-treated BrCa cells. Heat map was generated from normalized intensity data using the CIMminer tool. Each cell in the heat map shows the ratio of phosphorylated (P) to non-phosphorylated (N) protein in a treated vs. nontreated sample. Red indicates an increase, while green represents a decrease in phosphorylation signaling molecules. The intensity of the color is dependent on the degree of phosphorylation. Panel ( B ) shows the predicted signaling pathway induced by CXCR6-CXCL16 activation leading to neoplastic progression. Changes in the phosphorylation of signaling molecules obtained from antibody microarray analysis were uploaded into Ingenuity Pathways Knowledge Database as text files containing GenBank accession numbers. The chart shows possible activation (red) of the FAK-Src, PI3K/Akt, and Jak/Stat pathways along with the reorganization of the cytoskeleton, which would increase the potential of BrCa cells to survive and invade.

Journal: Cancers

Article Title: CXCR6-CXCL16 Axis Promotes Breast Cancer by Inducing Oncogenic Signaling

doi: 10.3390/cancers13143568

Figure Lengend Snippet: Analysis of CXCR6-mediated phosphorylation of cell signaling molecules using antibody microarray. Phosphorylation-specific antibody array was performed for the qualitative analysis of differentially phosphorylated proteins after treating BrCa cells with CXCL16 (100 ng/mL for 5 min). The BrCa cells treated with vehicle were used as the control. The antibody array consisted of 273 highly specific antibodies against proteins significant for cancer signaling pathways, with β-actin and GAPDH serving as internal positive controls. The median signal intensity for each antibody was obtained using six replicate spots ( n = 6) and was normalized to the median signal of GAPDH. The heat map shown in Panel ( A ) represents a fold change in the phosphorylation status of specified proteins in CXCL16-treated BrCa cells. Heat map was generated from normalized intensity data using the CIMminer tool. Each cell in the heat map shows the ratio of phosphorylated (P) to non-phosphorylated (N) protein in a treated vs. nontreated sample. Red indicates an increase, while green represents a decrease in phosphorylation signaling molecules. The intensity of the color is dependent on the degree of phosphorylation. Panel ( B ) shows the predicted signaling pathway induced by CXCR6-CXCL16 activation leading to neoplastic progression. Changes in the phosphorylation of signaling molecules obtained from antibody microarray analysis were uploaded into Ingenuity Pathways Knowledge Database as text files containing GenBank accession numbers. The chart shows possible activation (red) of the FAK-Src, PI3K/Akt, and Jak/Stat pathways along with the reorganization of the cytoskeleton, which would increase the potential of BrCa cells to survive and invade.

Article Snippet: Protein lysates were processed and probed onto cancer signaling phospho-antibody microarray slides as per the manufacturer’s protocol (Fullmoon Biosystems Inc., Sunnyvale, CA, USA).

Techniques: Phospho-proteomics, Microarray, Ab Array, Control, Protein-Protein interactions, Generated, Activation Assay