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pdquest advanced 8 0 1 software  (Bio-Rad)


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    Structured Review

    Bio-Rad pdquest advanced 8 0 1 software
    Experimental design to elucidate liver proteomic profile in mice fed four fat-varied diets. PUFA – polyunsaturated fatty acids; STD – standard diet; SFA – diet high in saturated fatty acids; 14 :1 – diet high in PUFA with this linoleic acid to α-linolenic acid ratio; 5 : 1 – diet high in PUFA with this linoleic acid to α-linolenic acid ratio; qPCR – real-time quantitative polymerase chain reaction; 2DE – two-dimensional electrophoresis. <t>PDQuest</t> Advanced 8.0.1 (Bio-Rad Laboratories, Hercules, CA, USA) software used for analysis of protein profiles. MALDI-TOF/TOF – matrix-assisted laser desorption/ionisation–time-of-flight tandem mass spectrometry
    Pdquest Advanced 8 0 1 Software, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 3292 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pdquest+8%2E0%2E1+software/pmc11418388-66-17-21?v=Bio-Rad
    Average 96 stars, based on 3292 article reviews
    pdquest advanced 8 0 1 software - by Bioz Stars, 2026-08
    96/100 stars

    Images

    1) Product Images from "Murine hepatic proteome adaptation to high-fat diets with different contents of saturated fatty acids and linoleic acid : α-linolenic acid polyunsaturated fatty acid ratios"

    Article Title: Murine hepatic proteome adaptation to high-fat diets with different contents of saturated fatty acids and linoleic acid : α-linolenic acid polyunsaturated fatty acid ratios

    Journal: Journal of Veterinary Research

    doi: 10.2478/jvetres-2024-0041

    Experimental design to elucidate liver proteomic profile in mice fed four fat-varied diets. PUFA – polyunsaturated fatty acids; STD – standard diet; SFA – diet high in saturated fatty acids; 14 :1 – diet high in PUFA with this linoleic acid to α-linolenic acid ratio; 5 : 1 – diet high in PUFA with this linoleic acid to α-linolenic acid ratio; qPCR – real-time quantitative polymerase chain reaction; 2DE – two-dimensional electrophoresis. PDQuest Advanced 8.0.1 (Bio-Rad Laboratories, Hercules, CA, USA) software used for analysis of protein profiles. MALDI-TOF/TOF – matrix-assisted laser desorption/ionisation–time-of-flight tandem mass spectrometry
    Figure Legend Snippet: Experimental design to elucidate liver proteomic profile in mice fed four fat-varied diets. PUFA – polyunsaturated fatty acids; STD – standard diet; SFA – diet high in saturated fatty acids; 14 :1 – diet high in PUFA with this linoleic acid to α-linolenic acid ratio; 5 : 1 – diet high in PUFA with this linoleic acid to α-linolenic acid ratio; qPCR – real-time quantitative polymerase chain reaction; 2DE – two-dimensional electrophoresis. PDQuest Advanced 8.0.1 (Bio-Rad Laboratories, Hercules, CA, USA) software used for analysis of protein profiles. MALDI-TOF/TOF – matrix-assisted laser desorption/ionisation–time-of-flight tandem mass spectrometry

    Techniques Used: Real-time Polymerase Chain Reaction, Electrophoresis, Software, Mass Spectrometry



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    Bio-Rad pdquest advanced 8 0 1 software
    Experimental design to elucidate liver proteomic profile in mice fed four fat-varied diets. PUFA – polyunsaturated fatty acids; STD – standard diet; SFA – diet high in saturated fatty acids; 14 :1 – diet high in PUFA with this linoleic acid to α-linolenic acid ratio; 5 : 1 – diet high in PUFA with this linoleic acid to α-linolenic acid ratio; qPCR – real-time quantitative polymerase chain reaction; 2DE – two-dimensional electrophoresis. <t>PDQuest</t> Advanced 8.0.1 (Bio-Rad Laboratories, Hercules, CA, USA) software used for analysis of protein profiles. MALDI-TOF/TOF – matrix-assisted laser desorption/ionisation–time-of-flight tandem mass spectrometry
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    Figure 1. AtCPK1-Ca-triggered increased and decreased amounts of the proteins associated with signaling. Fragments of two-dimensional gels of protein fractions from the control (Va) and AtCPK1-Ca-transformed VaCa calli obtained in three separate experiments are presented in the left panel. Proteins were separated on gels by isoelectric mobility and by mass. Gels were scanned using a VersaDoc MP 4000 system with <t>PDQuest</t> 8.0.1 Advanced software, as described in Section 4.3. Protein expression is presented in Table 1 as the average total spot intensity in a group of three repeated gels. Mass spectra were acquired with a MALDI-TOF mass spectrometer and presented on the right panel. (a) bifunctional nitrilase/nitrilehydratase NIT4B; (b) calreticulin; (c) annexin; (d) protein EXORDIUM. Up-regulated proteins are marked with a green circle, down-regulated proteins are marked with a red circle, and newly arising proteins are marked with a blue circle.
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    Figure 1. AtCPK1-Ca-triggered increased and decreased amounts of the proteins associated with signaling. Fragments of two-dimensional gels of protein fractions from the control (Va) and AtCPK1-Ca-transformed VaCa calli obtained in three separate experiments are presented in the left panel. Proteins were separated on gels by isoelectric mobility and by mass. Gels were scanned using a VersaDoc MP 4000 system with <t>PDQuest</t> 8.0.1 Advanced software, as described in Section 4.3. Protein expression is presented in Table 1 as the average total spot intensity in a group of three repeated gels. Mass spectra were acquired with a MALDI-TOF mass spectrometer and presented on the right panel. (a) bifunctional nitrilase/nitrilehydratase NIT4B; (b) calreticulin; (c) annexin; (d) protein EXORDIUM. Up-regulated proteins are marked with a green circle, down-regulated proteins are marked with a red circle, and newly arising proteins are marked with a blue circle.
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    Obs. pI and Mr, observed pI, Mr calculated from the 2D-gels with PDQuest 8.0.1 software according to standard marker proteins.
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    Image Search Results


    Experimental design to elucidate liver proteomic profile in mice fed four fat-varied diets. PUFA – polyunsaturated fatty acids; STD – standard diet; SFA – diet high in saturated fatty acids; 14 :1 – diet high in PUFA with this linoleic acid to α-linolenic acid ratio; 5 : 1 – diet high in PUFA with this linoleic acid to α-linolenic acid ratio; qPCR – real-time quantitative polymerase chain reaction; 2DE – two-dimensional electrophoresis. PDQuest Advanced 8.0.1 (Bio-Rad Laboratories, Hercules, CA, USA) software used for analysis of protein profiles. MALDI-TOF/TOF – matrix-assisted laser desorption/ionisation–time-of-flight tandem mass spectrometry

    Journal: Journal of Veterinary Research

    Article Title: Murine hepatic proteome adaptation to high-fat diets with different contents of saturated fatty acids and linoleic acid : α-linolenic acid polyunsaturated fatty acid ratios

    doi: 10.2478/jvetres-2024-0041

    Figure Lengend Snippet: Experimental design to elucidate liver proteomic profile in mice fed four fat-varied diets. PUFA – polyunsaturated fatty acids; STD – standard diet; SFA – diet high in saturated fatty acids; 14 :1 – diet high in PUFA with this linoleic acid to α-linolenic acid ratio; 5 : 1 – diet high in PUFA with this linoleic acid to α-linolenic acid ratio; qPCR – real-time quantitative polymerase chain reaction; 2DE – two-dimensional electrophoresis. PDQuest Advanced 8.0.1 (Bio-Rad Laboratories, Hercules, CA, USA) software used for analysis of protein profiles. MALDI-TOF/TOF – matrix-assisted laser desorption/ionisation–time-of-flight tandem mass spectrometry

    Article Snippet: Sample preparation, isoelectrofocusing, sodium dodecyl sulphate–polyacrylamide gel electrophoresis (SDS-PAGE), image staining and protein profiles analysis in the PDQuest Advanced 8.0.1 software (Bio-Rad Laboratories, Inc Hercules, CA, USA) were carried out as previously described ( ).

    Techniques: Real-time Polymerase Chain Reaction, Electrophoresis, Software, Mass Spectrometry

    Figure 1. AtCPK1-Ca-triggered increased and decreased amounts of the proteins associated with signaling. Fragments of two-dimensional gels of protein fractions from the control (Va) and AtCPK1-Ca-transformed VaCa calli obtained in three separate experiments are presented in the left panel. Proteins were separated on gels by isoelectric mobility and by mass. Gels were scanned using a VersaDoc MP 4000 system with PDQuest 8.0.1 Advanced software, as described in Section 4.3. Protein expression is presented in Table 1 as the average total spot intensity in a group of three repeated gels. Mass spectra were acquired with a MALDI-TOF mass spectrometer and presented on the right panel. (a) bifunctional nitrilase/nitrilehydratase NIT4B; (b) calreticulin; (c) annexin; (d) protein EXORDIUM. Up-regulated proteins are marked with a green circle, down-regulated proteins are marked with a red circle, and newly arising proteins are marked with a blue circle.

    Journal: International journal of molecular sciences

    Article Title: Proteome-Level Investigation of Vitis amurensis Calli Transformed with a Constitutively Active, Ca 2+ -Independent Form of the Arabidopsis AtCPK1 Gene.

    doi: 10.3390/ijms241713184

    Figure Lengend Snippet: Figure 1. AtCPK1-Ca-triggered increased and decreased amounts of the proteins associated with signaling. Fragments of two-dimensional gels of protein fractions from the control (Va) and AtCPK1-Ca-transformed VaCa calli obtained in three separate experiments are presented in the left panel. Proteins were separated on gels by isoelectric mobility and by mass. Gels were scanned using a VersaDoc MP 4000 system with PDQuest 8.0.1 Advanced software, as described in Section 4.3. Protein expression is presented in Table 1 as the average total spot intensity in a group of three repeated gels. Mass spectra were acquired with a MALDI-TOF mass spectrometer and presented on the right panel. (a) bifunctional nitrilase/nitrilehydratase NIT4B; (b) calreticulin; (c) annexin; (d) protein EXORDIUM. Up-regulated proteins are marked with a green circle, down-regulated proteins are marked with a red circle, and newly arising proteins are marked with a blue circle.

    Article Snippet: PDQuest 8.0.1 Advanced software (Bio-Rad Laboratories Inc., Hercules, CA, USA) was used for the analysis of the protein maps.

    Techniques: Control, Transformation Assay, Software, Expressing, Mass Spectrometry

    Figure 3. AtCPK1-Ca-triggered increased and decreased amounts of the PR-proteins. Fragments of two-dimensional gels of protein fractions from the control (Va) and AtCPK1-Ca-transformed VaCa calli obtained in three separate experiments are presented in the left panel. Proteins were separated on gels by isoelectric mobility and by mass. Gels were scanned using a VersaDoc MP 4000 system with PDQuest 8.0.1 Advanced software, as described in Section 4.3. Protein expression is presented in Table 1 as the average total spot intensity in a group of three repeated gels. Mass spectra were acquired with a MALDI-TOF mass spectrometer and presented on the right panel. (a) betvI/major latex protein; (b) osmotin-like protein 13; (c) thaumatin-like protein; (d) beta-D-xylosidase 1; (e) class IV chitinase. Up-regulated proteins are marked with a green circle, down-regulated proteins are marked with a red circle, and newly arising proteins are marked with a blue circle.

    Journal: International journal of molecular sciences

    Article Title: Proteome-Level Investigation of Vitis amurensis Calli Transformed with a Constitutively Active, Ca 2+ -Independent Form of the Arabidopsis AtCPK1 Gene.

    doi: 10.3390/ijms241713184

    Figure Lengend Snippet: Figure 3. AtCPK1-Ca-triggered increased and decreased amounts of the PR-proteins. Fragments of two-dimensional gels of protein fractions from the control (Va) and AtCPK1-Ca-transformed VaCa calli obtained in three separate experiments are presented in the left panel. Proteins were separated on gels by isoelectric mobility and by mass. Gels were scanned using a VersaDoc MP 4000 system with PDQuest 8.0.1 Advanced software, as described in Section 4.3. Protein expression is presented in Table 1 as the average total spot intensity in a group of three repeated gels. Mass spectra were acquired with a MALDI-TOF mass spectrometer and presented on the right panel. (a) betvI/major latex protein; (b) osmotin-like protein 13; (c) thaumatin-like protein; (d) beta-D-xylosidase 1; (e) class IV chitinase. Up-regulated proteins are marked with a green circle, down-regulated proteins are marked with a red circle, and newly arising proteins are marked with a blue circle.

    Article Snippet: PDQuest 8.0.1 Advanced software (Bio-Rad Laboratories Inc., Hercules, CA, USA) was used for the analysis of the protein maps.

    Techniques: Control, Transformation Assay, Software, Expressing, Mass Spectrometry

    Figure 4. AtCPK1-Ca-triggered increased and decreased amounts of the HSP proteins. Fragments of two-dimensional gels of protein fractions from the control (Va) and AtCPK1-Ca-transformed VaCa calli obtained in three separate experiments are presented in the left panel. Protein was separated on gels by isoelectric mobility and by mass. Gels were scanned using a VersaDoc MP 4000 system with PDQuest 8.0.1 Advanced software, as described in Section 4.3. Protein expression is presented in Table 1 as the average total spot intensity in a group of three repeated gels. Mass spectra were acquired with a MALDI-TOF mass spectrometer and presented on the right panel. (a) heat shock cognate 70 kDa protein; (b) histidine kinase/HSP90-like ATPase domain-containing protein. Up-regulated proteins are marked with a green circle, down-regulated proteins are marked with a red circle, and newly arising proteins are marked with a blue circle.

    Journal: International journal of molecular sciences

    Article Title: Proteome-Level Investigation of Vitis amurensis Calli Transformed with a Constitutively Active, Ca 2+ -Independent Form of the Arabidopsis AtCPK1 Gene.

    doi: 10.3390/ijms241713184

    Figure Lengend Snippet: Figure 4. AtCPK1-Ca-triggered increased and decreased amounts of the HSP proteins. Fragments of two-dimensional gels of protein fractions from the control (Va) and AtCPK1-Ca-transformed VaCa calli obtained in three separate experiments are presented in the left panel. Protein was separated on gels by isoelectric mobility and by mass. Gels were scanned using a VersaDoc MP 4000 system with PDQuest 8.0.1 Advanced software, as described in Section 4.3. Protein expression is presented in Table 1 as the average total spot intensity in a group of three repeated gels. Mass spectra were acquired with a MALDI-TOF mass spectrometer and presented on the right panel. (a) heat shock cognate 70 kDa protein; (b) histidine kinase/HSP90-like ATPase domain-containing protein. Up-regulated proteins are marked with a green circle, down-regulated proteins are marked with a red circle, and newly arising proteins are marked with a blue circle.

    Article Snippet: PDQuest 8.0.1 Advanced software (Bio-Rad Laboratories Inc., Hercules, CA, USA) was used for the analysis of the protein maps.

    Techniques: Control, Transformation Assay, Software, Expressing, Mass Spectrometry

    Journal: PLoS ONE

    Article Title: Proteomic Analysis of the Low Mutation Rate of Diploid Male Gametes Induced by Colchicine in Ginkgo biloba L.

    doi: 10.1371/journal.pone.0076088

    Figure Lengend Snippet: Obs. pI and Mr, observed pI, Mr calculated from the 2D-gels with PDQuest 8.0.1 software according to standard marker proteins.

    Article Snippet: The image analysis was carried out by a combination of manual visualization and software calculations using PDQuest 8.0.1 Gel Analysis Software (Bio-Rad, Hercules, CA, USA).

    Techniques: Software, Marker, Transduction, Sequencing