tem image of the crumpled 2-dimensional carbon thin film material Search Results


pdquesttm 2d gel analysis software  (Bio-Rad)
96
Bio-Rad pdquesttm 2d gel analysis software
Pdquesttm 2d Gel Analysis Software, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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2d gel analysis software  (Bio-Rad)
96
Bio-Rad 2d gel analysis software
Comparative <t>2D</t> <t>gel</t> electrophoresis analyses of total E. coli proteins expressed in response to selenium oxide treatment. Autoradiograms of 2D gels performed with total E. coli extracts from [35S] methionine-labeled cells as described in Materials and Methods are shown. The extracts were prepared from control untreated cells (A), from cells exposed to SeO42− (2 mM) for 30 min (B), and from cells exposed to SeO32− (2 mM) for 30 min (C). Proteins whose synthesis rate is stimulated upon SeO42− or SeO32− exposure were identified by mass spectrometry and are indicated on the map. Protein spots induced but not characterized are also indicated by an arrow. Proteins repressed by SeO42− or SeO32− are indicated by a black bar in panel A.
2d Gel Analysis Software, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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2d gel analysis software - by Bioz Stars, 2026-09
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matrigel  (Becton Dickinson)
90
Becton Dickinson matrigel
Comparative <t>2D</t> <t>gel</t> electrophoresis analyses of total E. coli proteins expressed in response to selenium oxide treatment. Autoradiograms of 2D gels performed with total E. coli extracts from [35S] methionine-labeled cells as described in Materials and Methods are shown. The extracts were prepared from control untreated cells (A), from cells exposed to SeO42− (2 mM) for 30 min (B), and from cells exposed to SeO32− (2 mM) for 30 min (C). Proteins whose synthesis rate is stimulated upon SeO42− or SeO32− exposure were identified by mass spectrometry and are indicated on the map. Protein spots induced but not characterized are also indicated by an arrow. Proteins repressed by SeO42− or SeO32− are indicated by a black bar in panel A.
Matrigel, supplied by Becton Dickinson, 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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2d gel analysis software phoretix 2005  (PHORETIX INTERNATIONAL LIMITED)
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PHORETIX INTERNATIONAL LIMITED 2d gel analysis software phoretix 2005
Comparative <t>2D</t> <t>gel</t> electrophoresis analyses of total E. coli proteins expressed in response to selenium oxide treatment. Autoradiograms of 2D gels performed with total E. coli extracts from [35S] methionine-labeled cells as described in Materials and Methods are shown. The extracts were prepared from control untreated cells (A), from cells exposed to SeO42− (2 mM) for 30 min (B), and from cells exposed to SeO32− (2 mM) for 30 min (C). Proteins whose synthesis rate is stimulated upon SeO42− or SeO32− exposure were identified by mass spectrometry and are indicated on the map. Protein spots induced but not characterized are also indicated by an arrow. Proteins repressed by SeO42− or SeO32− are indicated by a black bar in panel A.
2d Gel Analysis Software Phoretix 2005, supplied by PHORETIX INTERNATIONAL LIMITED, 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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2d gel analysis software phoretix 2005 - by Bioz Stars, 2026-09
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tracking software wall motion 2-dimensional tracking  (TOSHIBA Medical)
90
TOSHIBA Medical tracking software wall motion 2-dimensional tracking
Comparative <t>2D</t> <t>gel</t> electrophoresis analyses of total E. coli proteins expressed in response to selenium oxide treatment. Autoradiograms of 2D gels performed with total E. coli extracts from [35S] methionine-labeled cells as described in Materials and Methods are shown. The extracts were prepared from control untreated cells (A), from cells exposed to SeO42− (2 mM) for 30 min (B), and from cells exposed to SeO32− (2 mM) for 30 min (C). Proteins whose synthesis rate is stimulated upon SeO42− or SeO32− exposure were identified by mass spectrometry and are indicated on the map. Protein spots induced but not characterized are also indicated by an arrow. Proteins repressed by SeO42− or SeO32− are indicated by a black bar in panel A.
Tracking Software Wall Motion 2 Dimensional Tracking, supplied by TOSHIBA Medical, 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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2-dimensional numerical model  (COMSOL Inc)
90
COMSOL Inc 2-dimensional numerical model
Comparative <t>2D</t> <t>gel</t> electrophoresis analyses of total E. coli proteins expressed in response to selenium oxide treatment. Autoradiograms of 2D gels performed with total E. coli extracts from [35S] methionine-labeled cells as described in Materials and Methods are shown. The extracts were prepared from control untreated cells (A), from cells exposed to SeO42− (2 mM) for 30 min (B), and from cells exposed to SeO32− (2 mM) for 30 min (C). Proteins whose synthesis rate is stimulated upon SeO42− or SeO32− exposure were identified by mass spectrometry and are indicated on the map. Protein spots induced but not characterized are also indicated by an arrow. Proteins repressed by SeO42− or SeO32− are indicated by a black bar in panel A.
2 Dimensional Numerical Model, supplied by COMSOL 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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image analysis software  (Gatan Inc)
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Gatan Inc image analysis software
Comparative <t>2D</t> <t>gel</t> electrophoresis analyses of total E. coli proteins expressed in response to selenium oxide treatment. Autoradiograms of 2D gels performed with total E. coli extracts from [35S] methionine-labeled cells as described in Materials and Methods are shown. The extracts were prepared from control untreated cells (A), from cells exposed to SeO42− (2 mM) for 30 min (B), and from cells exposed to SeO32− (2 mM) for 30 min (C). Proteins whose synthesis rate is stimulated upon SeO42− or SeO32− exposure were identified by mass spectrometry and are indicated on the map. Protein spots induced but not characterized are also indicated by an arrow. Proteins repressed by SeO42− or SeO32− are indicated by a black bar in panel A.
Image Analysis Software, supplied by Gatan Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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image analysis software - by Bioz Stars, 2026-09
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2d gel electrophoresis  (Fangman Specialties)
90
Fangman Specialties 2d gel electrophoresis
Analysis of low-copy-rDNA strains. (A) Southern hybridization analysis of rDNA copy numbers. DNA was digested with BglII and subjected to <t>electrophoresis</t> followed by Southern analysis using the rDNA probe (Fig. 1). A single-copy gene, MCM2, was used as an internal control for normalization. (B) Quantitation of the intensities of the bands. NOY408-1b (wild-type strain), NOY408-1bf (fob1), TAK300 (fob1; low-copy rDNA strain), TAK301 (fob1 pol1; low-copy rDNA strain). (C) Collision between the transcription and the replication machineries analyzed by <t>2D</t> gel analysis. DNA was prepared from the strains indicated, digested with BglII and SphI, and subjected to 2D agarose gel electrophoresis followed by Southern hybridization using the rDNA probe (see Fig. 1). A spot indicated by an arrowhead shows accumulation of Y-shaped DNA molecules at the RFB site (panel a). The slowdown region (SDR) is located between two arrows (panel c). The numbers in parentheses are copy numbers of rDNA in each strain. (Panel a) NOY408-1b (wild-type strain). (Panel b) NOY408-1bf (fob1). (Panel c) TAK300 (fob1; low-copy rDNA strain). (Panel d) TAK301 (fob1 pol1; low-copy rDNA strain). (Panel e) TAK301, complemented by a plasmid-borne RPA135 gene (fob1 POLI; low-copy rDNA strain).
2d Gel Electrophoresis, supplied by Fangman Specialties, 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/tem+image+of+the+crumpled+2-dimensional+carbon+thin+film+material/2d+gel+electrophoresis/pmc00196080-347-9-18
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two-dimensional gel electrophoresis  (Fangman Specialties)
90
Fangman Specialties two-dimensional gel electrophoresis
Analysis of low-copy-rDNA strains. (A) Southern hybridization analysis of rDNA copy numbers. DNA was digested with BglII and subjected to <t>electrophoresis</t> followed by Southern analysis using the rDNA probe (Fig. 1). A single-copy gene, MCM2, was used as an internal control for normalization. (B) Quantitation of the intensities of the bands. NOY408-1b (wild-type strain), NOY408-1bf (fob1), TAK300 (fob1; low-copy rDNA strain), TAK301 (fob1 pol1; low-copy rDNA strain). (C) Collision between the transcription and the replication machineries analyzed by <t>2D</t> gel analysis. DNA was prepared from the strains indicated, digested with BglII and SphI, and subjected to 2D agarose gel electrophoresis followed by Southern hybridization using the rDNA probe (see Fig. 1). A spot indicated by an arrowhead shows accumulation of Y-shaped DNA molecules at the RFB site (panel a). The slowdown region (SDR) is located between two arrows (panel c). The numbers in parentheses are copy numbers of rDNA in each strain. (Panel a) NOY408-1b (wild-type strain). (Panel b) NOY408-1bf (fob1). (Panel c) TAK300 (fob1; low-copy rDNA strain). (Panel d) TAK301 (fob1 pol1; low-copy rDNA strain). (Panel e) TAK301, complemented by a plasmid-borne RPA135 gene (fob1 POLI; low-copy rDNA strain).
Two Dimensional Gel Electrophoresis, supplied by Fangman Specialties, 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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two-dimensional gel electrophoresis - by Bioz Stars, 2026-09
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2-dimensional polyacrylamide gel electrophoresis 2-de  (DuPont de Nemours)
90
DuPont de Nemours 2-dimensional polyacrylamide gel electrophoresis 2-de
Analysis of low-copy-rDNA strains. (A) Southern hybridization analysis of rDNA copy numbers. DNA was digested with BglII and subjected to <t>electrophoresis</t> followed by Southern analysis using the rDNA probe (Fig. 1). A single-copy gene, MCM2, was used as an internal control for normalization. (B) Quantitation of the intensities of the bands. NOY408-1b (wild-type strain), NOY408-1bf (fob1), TAK300 (fob1; low-copy rDNA strain), TAK301 (fob1 pol1; low-copy rDNA strain). (C) Collision between the transcription and the replication machineries analyzed by <t>2D</t> gel analysis. DNA was prepared from the strains indicated, digested with BglII and SphI, and subjected to 2D agarose gel electrophoresis followed by Southern hybridization using the rDNA probe (see Fig. 1). A spot indicated by an arrowhead shows accumulation of Y-shaped DNA molecules at the RFB site (panel a). The slowdown region (SDR) is located between two arrows (panel c). The numbers in parentheses are copy numbers of rDNA in each strain. (Panel a) NOY408-1b (wild-type strain). (Panel b) NOY408-1bf (fob1). (Panel c) TAK300 (fob1; low-copy rDNA strain). (Panel d) TAK301 (fob1 pol1; low-copy rDNA strain). (Panel e) TAK301, complemented by a plasmid-borne RPA135 gene (fob1 POLI; low-copy rDNA strain).
2 Dimensional Polyacrylamide Gel Electrophoresis 2 De, supplied by DuPont de Nemours, 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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high-resolution echocardiography system vevo 770tm  (FUJIFILM VisualSonics Inc)
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FUJIFILM VisualSonics Inc high-resolution echocardiography system vevo 770tm
Analysis of low-copy-rDNA strains. (A) Southern hybridization analysis of rDNA copy numbers. DNA was digested with BglII and subjected to <t>electrophoresis</t> followed by Southern analysis using the rDNA probe (Fig. 1). A single-copy gene, MCM2, was used as an internal control for normalization. (B) Quantitation of the intensities of the bands. NOY408-1b (wild-type strain), NOY408-1bf (fob1), TAK300 (fob1; low-copy rDNA strain), TAK301 (fob1 pol1; low-copy rDNA strain). (C) Collision between the transcription and the replication machineries analyzed by <t>2D</t> gel analysis. DNA was prepared from the strains indicated, digested with BglII and SphI, and subjected to 2D agarose gel electrophoresis followed by Southern hybridization using the rDNA probe (see Fig. 1). A spot indicated by an arrowhead shows accumulation of Y-shaped DNA molecules at the RFB site (panel a). The slowdown region (SDR) is located between two arrows (panel c). The numbers in parentheses are copy numbers of rDNA in each strain. (Panel a) NOY408-1b (wild-type strain). (Panel b) NOY408-1bf (fob1). (Panel c) TAK300 (fob1; low-copy rDNA strain). (Panel d) TAK301 (fob1 pol1; low-copy rDNA strain). (Panel e) TAK301, complemented by a plasmid-borne RPA135 gene (fob1 POLI; low-copy rDNA strain).
High Resolution Echocardiography System Vevo 770tm, supplied by FUJIFILM VisualSonics 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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ultrasound biomicroscopy system vevo 660  (FUJIFILM VisualSonics Inc)
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FUJIFILM VisualSonics Inc ultrasound biomicroscopy system vevo 660
Analysis of low-copy-rDNA strains. (A) Southern hybridization analysis of rDNA copy numbers. DNA was digested with BglII and subjected to <t>electrophoresis</t> followed by Southern analysis using the rDNA probe (Fig. 1). A single-copy gene, MCM2, was used as an internal control for normalization. (B) Quantitation of the intensities of the bands. NOY408-1b (wild-type strain), NOY408-1bf (fob1), TAK300 (fob1; low-copy rDNA strain), TAK301 (fob1 pol1; low-copy rDNA strain). (C) Collision between the transcription and the replication machineries analyzed by <t>2D</t> gel analysis. DNA was prepared from the strains indicated, digested with BglII and SphI, and subjected to 2D agarose gel electrophoresis followed by Southern hybridization using the rDNA probe (see Fig. 1). A spot indicated by an arrowhead shows accumulation of Y-shaped DNA molecules at the RFB site (panel a). The slowdown region (SDR) is located between two arrows (panel c). The numbers in parentheses are copy numbers of rDNA in each strain. (Panel a) NOY408-1b (wild-type strain). (Panel b) NOY408-1bf (fob1). (Panel c) TAK300 (fob1; low-copy rDNA strain). (Panel d) TAK301 (fob1 pol1; low-copy rDNA strain). (Panel e) TAK301, complemented by a plasmid-borne RPA135 gene (fob1 POLI; low-copy rDNA strain).
Ultrasound Biomicroscopy System Vevo 660, supplied by FUJIFILM VisualSonics 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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Image Search Results


Comparative 2D gel electrophoresis analyses of total E. coli proteins expressed in response to selenium oxide treatment. Autoradiograms of 2D gels performed with total E. coli extracts from [35S] methionine-labeled cells as described in Materials and Methods are shown. The extracts were prepared from control untreated cells (A), from cells exposed to SeO42− (2 mM) for 30 min (B), and from cells exposed to SeO32− (2 mM) for 30 min (C). Proteins whose synthesis rate is stimulated upon SeO42− or SeO32− exposure were identified by mass spectrometry and are indicated on the map. Protein spots induced but not characterized are also indicated by an arrow. Proteins repressed by SeO42− or SeO32− are indicated by a black bar in panel A.

Journal:

Article Title: Involvement of Superoxide Dismutases in the Response of Escherichia coli to Selenium Oxides

doi: 10.1128/JB.184.6.1556-1564.2002

Figure Lengend Snippet: Comparative 2D gel electrophoresis analyses of total E. coli proteins expressed in response to selenium oxide treatment. Autoradiograms of 2D gels performed with total E. coli extracts from [35S] methionine-labeled cells as described in Materials and Methods are shown. The extracts were prepared from control untreated cells (A), from cells exposed to SeO42− (2 mM) for 30 min (B), and from cells exposed to SeO32− (2 mM) for 30 min (C). Proteins whose synthesis rate is stimulated upon SeO42− or SeO32− exposure were identified by mass spectrometry and are indicated on the map. Protein spots induced but not characterized are also indicated by an arrow. Proteins repressed by SeO42− or SeO32− are indicated by a black bar in panel A.

Article Snippet: The spots on the radioactive gels were recorded by PhosphorImager technology (Molecular Dynamics) and analyzed with a 2D gel analysis software (MelanieII; Bio-Rad).

Techniques: Two-Dimensional Gel Electrophoresis, Electrophoresis, Labeling, Mass Spectrometry

Analysis of low-copy-rDNA strains. (A) Southern hybridization analysis of rDNA copy numbers. DNA was digested with BglII and subjected to electrophoresis followed by Southern analysis using the rDNA probe (Fig. 1). A single-copy gene, MCM2, was used as an internal control for normalization. (B) Quantitation of the intensities of the bands. NOY408-1b (wild-type strain), NOY408-1bf (fob1), TAK300 (fob1; low-copy rDNA strain), TAK301 (fob1 pol1; low-copy rDNA strain). (C) Collision between the transcription and the replication machineries analyzed by 2D gel analysis. DNA was prepared from the strains indicated, digested with BglII and SphI, and subjected to 2D agarose gel electrophoresis followed by Southern hybridization using the rDNA probe (see Fig. 1). A spot indicated by an arrowhead shows accumulation of Y-shaped DNA molecules at the RFB site (panel a). The slowdown region (SDR) is located between two arrows (panel c). The numbers in parentheses are copy numbers of rDNA in each strain. (Panel a) NOY408-1b (wild-type strain). (Panel b) NOY408-1bf (fob1). (Panel c) TAK300 (fob1; low-copy rDNA strain). (Panel d) TAK301 (fob1 pol1; low-copy rDNA strain). (Panel e) TAK301, complemented by a plasmid-borne RPA135 gene (fob1 POLI; low-copy rDNA strain).

Journal:

Article Title: Transcription-dependent recombination and the role of fork collision in yeast rDNA

doi: 10.1101/gad.1085403

Figure Lengend Snippet: Analysis of low-copy-rDNA strains. (A) Southern hybridization analysis of rDNA copy numbers. DNA was digested with BglII and subjected to electrophoresis followed by Southern analysis using the rDNA probe (Fig. 1). A single-copy gene, MCM2, was used as an internal control for normalization. (B) Quantitation of the intensities of the bands. NOY408-1b (wild-type strain), NOY408-1bf (fob1), TAK300 (fob1; low-copy rDNA strain), TAK301 (fob1 pol1; low-copy rDNA strain). (C) Collision between the transcription and the replication machineries analyzed by 2D gel analysis. DNA was prepared from the strains indicated, digested with BglII and SphI, and subjected to 2D agarose gel electrophoresis followed by Southern hybridization using the rDNA probe (see Fig. 1). A spot indicated by an arrowhead shows accumulation of Y-shaped DNA molecules at the RFB site (panel a). The slowdown region (SDR) is located between two arrows (panel c). The numbers in parentheses are copy numbers of rDNA in each strain. (Panel a) NOY408-1b (wild-type strain). (Panel b) NOY408-1bf (fob1). (Panel c) TAK300 (fob1; low-copy rDNA strain). (Panel d) TAK301 (fob1 pol1; low-copy rDNA strain). (Panel e) TAK301, complemented by a plasmid-borne RPA135 gene (fob1 POLI; low-copy rDNA strain).

Article Snippet: Replication fork blocking and slowdown activities were analyzed using 2D gel electrophoresis as described previously ( Brewer and Fangman 1987 ).

Techniques: Hybridization, Electrophoresis, Control, Quantitation Assay, Two-Dimensional Gel Electrophoresis, Agarose Gel Electrophoresis, Plasmid Preparation