light cycler 480 probes master mix Search Results


light cycler r 480 system  (Roche)
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Roche light cycler r 480 system
Light Cycler R 480 System, supplied by Roche, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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light cycler roche 480 rt qpcr instrument  (Roche)
86
Roche light cycler roche 480 rt qpcr instrument
Light Cycler Roche 480 Rt Qpcr Instrument, supplied by Roche, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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light cycler 480  (Roche)
86
Roche light cycler 480
Light Cycler 480, supplied by Roche, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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light cycler 480 noroxmaster mix  (Kaneka Corp)
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Kaneka Corp light cycler 480 noroxmaster mix
Light Cycler 480 Noroxmaster Mix, supplied by Kaneka 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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reactions light cycler 480 roche diagnostics  (Roche)
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Roche reactions light cycler 480 roche diagnostics
Reactions Light Cycler 480 Roche Diagnostics, supplied by Roche, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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light cycler 480 sybr green i master  (Roche)
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Roche light cycler 480 sybr green i master
Light Cycler 480 Sybr Green I Master, supplied by Roche, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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light cycler rna amplification kit hybridization probes  (Boehringer Mannheim)
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Boehringer Mannheim light cycler rna amplification kit hybridization probes
Light Cycler Rna Amplification Kit Hybridization Probes, supplied by Boehringer Mannheim, 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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roche light cycler 480  (Roche)
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Roche roche light cycler 480
Roche Light Cycler 480, supplied by Roche, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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480 light cycler rt qpcr instrument  (Roche)
86
Roche 480 light cycler rt qpcr instrument
Activation of MAPK signaling pathway promoted the proliferation of PGCLCs. a Schematic diagram of the research design. b Bright field of cultures with 400 mIU LH, 25 μM MLT, or 5 μM RA for 16 days. Scale bar, 100 μm. c Flow cytometry analysis of SOX17 (FITC) and PCNA (CY3) double staining with 400 mIU LH, 25 μM MLT, or 5 μM RA. d Correlation matrix heatmap for control group, LH group, and MLT group. e The KEGG pathway enrichment of DEGs for LH vs control group and MLT vs control. f Venn diagram showed the number of enriched genes in MAPK signaling pathway for LH vs control group and MLT vs control. g Heatmap analysis of DEGs associated with cell proliferation and cell cycle for LH vs control group and MLT vs control. h The protein levels of the p‐MEK (MEK) and p‐ERK (ERK) detected by WB in culturing with LH, MLT, or RA groups for 16 days. i The expression levels of proliferation-related genes were detected by <t>RT-qPCR</t> in culturing with LH, MLT, or RA groups for 16 days. j Bright field of 10 μM U0126 culture for 16 days. Scale bar, 100 μm. k Flow cytometry analysis of SOX17 (FITC) staining with 10 μM U0126. The results are presented as mean ± SD. All the experiments were repeated at least three times. *0.01 < P < 0.05; **P < 0.01
480 Light Cycler Rt Qpcr Instrument, supplied by Roche, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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light cycler fast start dna master hybridization probe mix  (TIB MOLBIOL)
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TIB MOLBIOL light cycler fast start dna master hybridization probe mix
Activation of MAPK signaling pathway promoted the proliferation of PGCLCs. a Schematic diagram of the research design. b Bright field of cultures with 400 mIU LH, 25 μM MLT, or 5 μM RA for 16 days. Scale bar, 100 μm. c Flow cytometry analysis of SOX17 (FITC) and PCNA (CY3) double staining with 400 mIU LH, 25 μM MLT, or 5 μM RA. d Correlation matrix heatmap for control group, LH group, and MLT group. e The KEGG pathway enrichment of DEGs for LH vs control group and MLT vs control. f Venn diagram showed the number of enriched genes in MAPK signaling pathway for LH vs control group and MLT vs control. g Heatmap analysis of DEGs associated with cell proliferation and cell cycle for LH vs control group and MLT vs control. h The protein levels of the p‐MEK (MEK) and p‐ERK (ERK) detected by WB in culturing with LH, MLT, or RA groups for 16 days. i The expression levels of proliferation-related genes were detected by <t>RT-qPCR</t> in culturing with LH, MLT, or RA groups for 16 days. j Bright field of 10 μM U0126 culture for 16 days. Scale bar, 100 μm. k Flow cytometry analysis of SOX17 (FITC) staining with 10 μM U0126. The results are presented as mean ± SD. All the experiments were repeated at least three times. *0.01 < P < 0.05; **P < 0.01
Light Cycler Fast Start Dna Master Hybridization Probe Mix, supplied by TIB MOLBIOL, 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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light cycler probe design software, version 1.0  (Idaho Technology Inc)
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Idaho Technology Inc light cycler probe design software, version 1.0
Activation of MAPK signaling pathway promoted the proliferation of PGCLCs. a Schematic diagram of the research design. b Bright field of cultures with 400 mIU LH, 25 μM MLT, or 5 μM RA for 16 days. Scale bar, 100 μm. c Flow cytometry analysis of SOX17 (FITC) and PCNA (CY3) double staining with 400 mIU LH, 25 μM MLT, or 5 μM RA. d Correlation matrix heatmap for control group, LH group, and MLT group. e The KEGG pathway enrichment of DEGs for LH vs control group and MLT vs control. f Venn diagram showed the number of enriched genes in MAPK signaling pathway for LH vs control group and MLT vs control. g Heatmap analysis of DEGs associated with cell proliferation and cell cycle for LH vs control group and MLT vs control. h The protein levels of the p‐MEK (MEK) and p‐ERK (ERK) detected by WB in culturing with LH, MLT, or RA groups for 16 days. i The expression levels of proliferation-related genes were detected by <t>RT-qPCR</t> in culturing with LH, MLT, or RA groups for 16 days. j Bright field of 10 μM U0126 culture for 16 days. Scale bar, 100 μm. k Flow cytometry analysis of SOX17 (FITC) staining with 10 μM U0126. The results are presented as mean ± SD. All the experiments were repeated at least three times. *0.01 < P < 0.05; **P < 0.01
Light Cycler Probe Design Software, Version 1.0, supplied by Idaho Technology Inc, 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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light cycler 480 instrument ii  (Roche)
86
Roche light cycler 480 instrument ii
Activation of MAPK signaling pathway promoted the proliferation of PGCLCs. a Schematic diagram of the research design. b Bright field of cultures with 400 mIU LH, 25 μM MLT, or 5 μM RA for 16 days. Scale bar, 100 μm. c Flow cytometry analysis of SOX17 (FITC) and PCNA (CY3) double staining with 400 mIU LH, 25 μM MLT, or 5 μM RA. d Correlation matrix heatmap for control group, LH group, and MLT group. e The KEGG pathway enrichment of DEGs for LH vs control group and MLT vs control. f Venn diagram showed the number of enriched genes in MAPK signaling pathway for LH vs control group and MLT vs control. g Heatmap analysis of DEGs associated with cell proliferation and cell cycle for LH vs control group and MLT vs control. h The protein levels of the p‐MEK (MEK) and p‐ERK (ERK) detected by WB in culturing with LH, MLT, or RA groups for 16 days. i The expression levels of proliferation-related genes were detected by <t>RT-qPCR</t> in culturing with LH, MLT, or RA groups for 16 days. j Bright field of 10 μM U0126 culture for 16 days. Scale bar, 100 μm. k Flow cytometry analysis of SOX17 (FITC) staining with 10 μM U0126. The results are presented as mean ± SD. All the experiments were repeated at least three times. *0.01 < P < 0.05; **P < 0.01
Light Cycler 480 Instrument Ii, supplied by Roche, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/light cycler 480 instrument ii/product/Roche
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light cycler 480 instrument ii - by Bioz Stars, 2026-03
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Image Search Results


Activation of MAPK signaling pathway promoted the proliferation of PGCLCs. a Schematic diagram of the research design. b Bright field of cultures with 400 mIU LH, 25 μM MLT, or 5 μM RA for 16 days. Scale bar, 100 μm. c Flow cytometry analysis of SOX17 (FITC) and PCNA (CY3) double staining with 400 mIU LH, 25 μM MLT, or 5 μM RA. d Correlation matrix heatmap for control group, LH group, and MLT group. e The KEGG pathway enrichment of DEGs for LH vs control group and MLT vs control. f Venn diagram showed the number of enriched genes in MAPK signaling pathway for LH vs control group and MLT vs control. g Heatmap analysis of DEGs associated with cell proliferation and cell cycle for LH vs control group and MLT vs control. h The protein levels of the p‐MEK (MEK) and p‐ERK (ERK) detected by WB in culturing with LH, MLT, or RA groups for 16 days. i The expression levels of proliferation-related genes were detected by RT-qPCR in culturing with LH, MLT, or RA groups for 16 days. j Bright field of 10 μM U0126 culture for 16 days. Scale bar, 100 μm. k Flow cytometry analysis of SOX17 (FITC) staining with 10 μM U0126. The results are presented as mean ± SD. All the experiments were repeated at least three times. *0.01 < P < 0.05; **P < 0.01

Journal: Cellular and Molecular Life Sciences: CMLS

Article Title: Transcriptomic landscape reveals germline potential of porcine skin-derived multipotent dermal fibroblast progenitors

doi: 10.1007/s00018-023-04869-7

Figure Lengend Snippet: Activation of MAPK signaling pathway promoted the proliferation of PGCLCs. a Schematic diagram of the research design. b Bright field of cultures with 400 mIU LH, 25 μM MLT, or 5 μM RA for 16 days. Scale bar, 100 μm. c Flow cytometry analysis of SOX17 (FITC) and PCNA (CY3) double staining with 400 mIU LH, 25 μM MLT, or 5 μM RA. d Correlation matrix heatmap for control group, LH group, and MLT group. e The KEGG pathway enrichment of DEGs for LH vs control group and MLT vs control. f Venn diagram showed the number of enriched genes in MAPK signaling pathway for LH vs control group and MLT vs control. g Heatmap analysis of DEGs associated with cell proliferation and cell cycle for LH vs control group and MLT vs control. h The protein levels of the p‐MEK (MEK) and p‐ERK (ERK) detected by WB in culturing with LH, MLT, or RA groups for 16 days. i The expression levels of proliferation-related genes were detected by RT-qPCR in culturing with LH, MLT, or RA groups for 16 days. j Bright field of 10 μM U0126 culture for 16 days. Scale bar, 100 μm. k Flow cytometry analysis of SOX17 (FITC) staining with 10 μM U0126. The results are presented as mean ± SD. All the experiments were repeated at least three times. *0.01 < P < 0.05; **P < 0.01

Article Snippet: The reaction was performed by Roche 480 Light Cycler RT-qPCR instrument (Roche, Germany) as previously described [ 36 ].

Techniques: Activation Assay, Flow Cytometry, Double Staining, Expressing, Quantitative RT-PCR, Staining