ipg strips Search Results


rehydration buffer  (Bio-Rad)
96
Bio-Rad rehydration buffer
Rehydration Buffer, 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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ipg strips  (Bio-Rad)
93
Bio-Rad ipg strips
Ipg Strips, supplied by Bio-Rad, 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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ipg strips  (Amersham Life Sciences Inc)
90
Amersham Life Sciences Inc ipg strips
2DE of yeast whole cell lysates using <t>IPG</t> (A-C) and NEPHGE (D-F) based methods at standard protein load. The same samples from control cells ( transformed with empty vector pFGG3; A , D) and MeH ( pFGG3-MeH transformant; B , E) or MeN ( pFGG3-MeN; C , F) expressing cells were loaded onto <t>IPG</t> <t>strips</t> (50 μg of total protein in each strip) and NEPHGE gels (30 μg of total protein in each gel). Approximate pI values are indicated below the gels (pH 3–10 gradient was used in both methods). Dashed line indicates approximate zone of neutral pI 7.0, which separates acidic (on the left, pI < 7) and basic (on the right, pI > 7) protein spots. Protein molecular weight markers (M) are loaded onto IPG-based 2D gels, their masses are indicated at the right (kDa). Arrows point to the spots described in Table . Solid arrows indicate protein spots that were identified in our previous work , whereas dotted arrows point to additional spots identified by MS in this study. Quantitative analysis of each indicated protein spot is presented in Table .
Ipg Strips, supplied by Amersham Life Sciences 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/result/ipg strips/product/Amersham Life Sciences Inc
Average 90 stars, based on 1 article reviews
ipg strips - by Bioz Stars, 2026-03
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immobline drystrips ipg strip continuous ph 4–7 gradient  (Amersham Life Sciences Inc)
90
Amersham Life Sciences Inc immobline drystrips ipg strip continuous ph 4–7 gradient
2DE of yeast whole cell lysates using <t>IPG</t> (A-C) and NEPHGE (D-F) based methods at standard protein load. The same samples from control cells ( transformed with empty vector pFGG3; A , D) and MeH ( pFGG3-MeH transformant; B , E) or MeN ( pFGG3-MeN; C , F) expressing cells were loaded onto <t>IPG</t> <t>strips</t> (50 μg of total protein in each strip) and NEPHGE gels (30 μg of total protein in each gel). Approximate pI values are indicated below the gels (pH 3–10 gradient was used in both methods). Dashed line indicates approximate zone of neutral pI 7.0, which separates acidic (on the left, pI < 7) and basic (on the right, pI > 7) protein spots. Protein molecular weight markers (M) are loaded onto IPG-based 2D gels, their masses are indicated at the right (kDa). Arrows point to the spots described in Table . Solid arrows indicate protein spots that were identified in our previous work , whereas dotted arrows point to additional spots identified by MS in this study. Quantitative analysis of each indicated protein spot is presented in Table .
Immobline Drystrips Ipg Strip Continuous Ph 4–7 Gradient, supplied by Amersham Life Sciences 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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ipg strips  (Amersham Pharmacia Biotech Ltd)
90
Amersham Pharmacia Biotech Ltd ipg strips
2DE of yeast whole cell lysates using <t>IPG</t> (A-C) and NEPHGE (D-F) based methods at standard protein load. The same samples from control cells ( transformed with empty vector pFGG3; A , D) and MeH ( pFGG3-MeH transformant; B , E) or MeN ( pFGG3-MeN; C , F) expressing cells were loaded onto <t>IPG</t> <t>strips</t> (50 μg of total protein in each strip) and NEPHGE gels (30 μg of total protein in each gel). Approximate pI values are indicated below the gels (pH 3–10 gradient was used in both methods). Dashed line indicates approximate zone of neutral pI 7.0, which separates acidic (on the left, pI < 7) and basic (on the right, pI > 7) protein spots. Protein molecular weight markers (M) are loaded onto IPG-based 2D gels, their masses are indicated at the right (kDa). Arrows point to the spots described in Table . Solid arrows indicate protein spots that were identified in our previous work , whereas dotted arrows point to additional spots identified by MS in this study. Quantitative analysis of each indicated protein spot is presented in Table .
Ipg Strips, supplied by Amersham Pharmacia Biotech Ltd, 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/result/ipg strips/product/Amersham Pharmacia Biotech Ltd
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ipg immobiline dry strips nl  (Amersham Pharmacia Biotech Ltd)
90
Amersham Pharmacia Biotech Ltd ipg immobiline dry strips nl
2DE of yeast whole cell lysates using <t>IPG</t> (A-C) and NEPHGE (D-F) based methods at standard protein load. The same samples from control cells ( transformed with empty vector pFGG3; A , D) and MeH ( pFGG3-MeH transformant; B , E) or MeN ( pFGG3-MeN; C , F) expressing cells were loaded onto <t>IPG</t> <t>strips</t> (50 μg of total protein in each strip) and NEPHGE gels (30 μg of total protein in each gel). Approximate pI values are indicated below the gels (pH 3–10 gradient was used in both methods). Dashed line indicates approximate zone of neutral pI 7.0, which separates acidic (on the left, pI < 7) and basic (on the right, pI > 7) protein spots. Protein molecular weight markers (M) are loaded onto IPG-based 2D gels, their masses are indicated at the right (kDa). Arrows point to the spots described in Table . Solid arrows indicate protein spots that were identified in our previous work , whereas dotted arrows point to additional spots identified by MS in this study. Quantitative analysis of each indicated protein spot is presented in Table .
Ipg Immobiline Dry Strips Nl, supplied by Amersham Pharmacia Biotech Ltd, 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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ipg dry strips (ph 4–10)  (GenoMine Inc)
90
GenoMine Inc ipg dry strips (ph 4–10)
2DE of yeast whole cell lysates using <t>IPG</t> (A-C) and NEPHGE (D-F) based methods at standard protein load. The same samples from control cells ( transformed with empty vector pFGG3; A , D) and MeH ( pFGG3-MeH transformant; B , E) or MeN ( pFGG3-MeN; C , F) expressing cells were loaded onto <t>IPG</t> <t>strips</t> (50 μg of total protein in each strip) and NEPHGE gels (30 μg of total protein in each gel). Approximate pI values are indicated below the gels (pH 3–10 gradient was used in both methods). Dashed line indicates approximate zone of neutral pI 7.0, which separates acidic (on the left, pI < 7) and basic (on the right, pI > 7) protein spots. Protein molecular weight markers (M) are loaded onto IPG-based 2D gels, their masses are indicated at the right (kDa). Arrows point to the spots described in Table . Solid arrows indicate protein spots that were identified in our previous work , whereas dotted arrows point to additional spots identified by MS in this study. Quantitative analysis of each indicated protein spot is presented in Table .
Ipg Dry Strips (Ph 4–10), supplied by GenoMine 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/result/ipg dry strips (ph 4–10)/product/GenoMine Inc
Average 90 stars, based on 1 article reviews
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dimension-immobilized ph gradient (ipg) strips  (Amersham Pharmacia Biotech Ltd)
90
Amersham Pharmacia Biotech Ltd dimension-immobilized ph gradient (ipg) strips
2DE of yeast whole cell lysates using <t>IPG</t> (A-C) and NEPHGE (D-F) based methods at standard protein load. The same samples from control cells ( transformed with empty vector pFGG3; A , D) and MeH ( pFGG3-MeH transformant; B , E) or MeN ( pFGG3-MeN; C , F) expressing cells were loaded onto <t>IPG</t> <t>strips</t> (50 μg of total protein in each strip) and NEPHGE gels (30 μg of total protein in each gel). Approximate pI values are indicated below the gels (pH 3–10 gradient was used in both methods). Dashed line indicates approximate zone of neutral pI 7.0, which separates acidic (on the left, pI < 7) and basic (on the right, pI > 7) protein spots. Protein molecular weight markers (M) are loaded onto IPG-based 2D gels, their masses are indicated at the right (kDa). Arrows point to the spots described in Table . Solid arrows indicate protein spots that were identified in our previous work , whereas dotted arrows point to additional spots identified by MS in this study. Quantitative analysis of each indicated protein spot is presented in Table .
Dimension Immobilized Ph Gradient (Ipg) Strips, supplied by Amersham Pharmacia Biotech Ltd, 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/result/dimension-immobilized ph gradient (ipg) strips/product/Amersham Pharmacia Biotech Ltd
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24-cm immobilin dry strips, ph 4–7  (Amersham Life Sciences Inc)
90
Amersham Life Sciences Inc 24-cm immobilin dry strips, ph 4–7
2DE of yeast whole cell lysates using <t>IPG</t> (A-C) and NEPHGE (D-F) based methods at standard protein load. The same samples from control cells ( transformed with empty vector pFGG3; A , D) and MeH ( pFGG3-MeH transformant; B , E) or MeN ( pFGG3-MeN; C , F) expressing cells were loaded onto <t>IPG</t> <t>strips</t> (50 μg of total protein in each strip) and NEPHGE gels (30 μg of total protein in each gel). Approximate pI values are indicated below the gels (pH 3–10 gradient was used in both methods). Dashed line indicates approximate zone of neutral pI 7.0, which separates acidic (on the left, pI < 7) and basic (on the right, pI > 7) protein spots. Protein molecular weight markers (M) are loaded onto IPG-based 2D gels, their masses are indicated at the right (kDa). Arrows point to the spots described in Table . Solid arrows indicate protein spots that were identified in our previous work , whereas dotted arrows point to additional spots identified by MS in this study. Quantitative analysis of each indicated protein spot is presented in Table .
24 Cm Immobilin Dry Strips, Ph 4–7, supplied by Amersham Life Sciences 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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ipg strips immobiline drystrips  (Amersham Life Sciences Inc)
90
Amersham Life Sciences Inc ipg strips immobiline drystrips
2DE of yeast whole cell lysates using <t>IPG</t> (A-C) and NEPHGE (D-F) based methods at standard protein load. The same samples from control cells ( transformed with empty vector pFGG3; A , D) and MeH ( pFGG3-MeH transformant; B , E) or MeN ( pFGG3-MeN; C , F) expressing cells were loaded onto <t>IPG</t> <t>strips</t> (50 μg of total protein in each strip) and NEPHGE gels (30 μg of total protein in each gel). Approximate pI values are indicated below the gels (pH 3–10 gradient was used in both methods). Dashed line indicates approximate zone of neutral pI 7.0, which separates acidic (on the left, pI < 7) and basic (on the right, pI > 7) protein spots. Protein molecular weight markers (M) are loaded onto IPG-based 2D gels, their masses are indicated at the right (kDa). Arrows point to the spots described in Table . Solid arrows indicate protein spots that were identified in our previous work , whereas dotted arrows point to additional spots identified by MS in this study. Quantitative analysis of each indicated protein spot is presented in Table .
Ipg Strips Immobiline Drystrips, supplied by Amersham Life Sciences 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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immobilized ph gradient (ipg) strips 4–7 ph linear gradient  (Amersham Life Sciences Inc)
90
Amersham Life Sciences Inc immobilized ph gradient (ipg) strips 4–7 ph linear gradient
2DE of yeast whole cell lysates using <t>IPG</t> (A-C) and NEPHGE (D-F) based methods at standard protein load. The same samples from control cells ( transformed with empty vector pFGG3; A , D) and MeH ( pFGG3-MeH transformant; B , E) or MeN ( pFGG3-MeN; C , F) expressing cells were loaded onto <t>IPG</t> <t>strips</t> (50 μg of total protein in each strip) and NEPHGE gels (30 μg of total protein in each gel). Approximate pI values are indicated below the gels (pH 3–10 gradient was used in both methods). Dashed line indicates approximate zone of neutral pI 7.0, which separates acidic (on the left, pI < 7) and basic (on the right, pI > 7) protein spots. Protein molecular weight markers (M) are loaded onto IPG-based 2D gels, their masses are indicated at the right (kDa). Arrows point to the spots described in Table . Solid arrows indicate protein spots that were identified in our previous work , whereas dotted arrows point to additional spots identified by MS in this study. Quantitative analysis of each indicated protein spot is presented in Table .
Immobilized Ph Gradient (Ipg) Strips 4–7 Ph Linear Gradient, supplied by Amersham Life Sciences 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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ipg strips  (EuroClone)
90
EuroClone ipg strips
2DE of yeast whole cell lysates using <t>IPG</t> (A-C) and NEPHGE (D-F) based methods at standard protein load. The same samples from control cells ( transformed with empty vector pFGG3; A , D) and MeH ( pFGG3-MeH transformant; B , E) or MeN ( pFGG3-MeN; C , F) expressing cells were loaded onto <t>IPG</t> <t>strips</t> (50 μg of total protein in each strip) and NEPHGE gels (30 μg of total protein in each gel). Approximate pI values are indicated below the gels (pH 3–10 gradient was used in both methods). Dashed line indicates approximate zone of neutral pI 7.0, which separates acidic (on the left, pI < 7) and basic (on the right, pI > 7) protein spots. Protein molecular weight markers (M) are loaded onto IPG-based 2D gels, their masses are indicated at the right (kDa). Arrows point to the spots described in Table . Solid arrows indicate protein spots that were identified in our previous work , whereas dotted arrows point to additional spots identified by MS in this study. Quantitative analysis of each indicated protein spot is presented in Table .
Ipg Strips, supplied by EuroClone, 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


2DE of yeast whole cell lysates using IPG (A-C) and NEPHGE (D-F) based methods at standard protein load. The same samples from control cells ( transformed with empty vector pFGG3; A , D) and MeH ( pFGG3-MeH transformant; B , E) or MeN ( pFGG3-MeN; C , F) expressing cells were loaded onto IPG strips (50 μg of total protein in each strip) and NEPHGE gels (30 μg of total protein in each gel). Approximate pI values are indicated below the gels (pH 3–10 gradient was used in both methods). Dashed line indicates approximate zone of neutral pI 7.0, which separates acidic (on the left, pI < 7) and basic (on the right, pI > 7) protein spots. Protein molecular weight markers (M) are loaded onto IPG-based 2D gels, their masses are indicated at the right (kDa). Arrows point to the spots described in Table . Solid arrows indicate protein spots that were identified in our previous work , whereas dotted arrows point to additional spots identified by MS in this study. Quantitative analysis of each indicated protein spot is presented in Table .

Journal: Proteome Science

Article Title: Comparison of first dimension IPG and NEPHGE techniques in two-dimensional gel electrophoresis experiment with cytosolic unfolded protein response in Saccharomyces cerevisiae

doi: 10.1186/1477-5956-11-36

Figure Lengend Snippet: 2DE of yeast whole cell lysates using IPG (A-C) and NEPHGE (D-F) based methods at standard protein load. The same samples from control cells ( transformed with empty vector pFGG3; A , D) and MeH ( pFGG3-MeH transformant; B , E) or MeN ( pFGG3-MeN; C , F) expressing cells were loaded onto IPG strips (50 μg of total protein in each strip) and NEPHGE gels (30 μg of total protein in each gel). Approximate pI values are indicated below the gels (pH 3–10 gradient was used in both methods). Dashed line indicates approximate zone of neutral pI 7.0, which separates acidic (on the left, pI < 7) and basic (on the right, pI > 7) protein spots. Protein molecular weight markers (M) are loaded onto IPG-based 2D gels, their masses are indicated at the right (kDa). Arrows point to the spots described in Table . Solid arrows indicate protein spots that were identified in our previous work , whereas dotted arrows point to additional spots identified by MS in this study. Quantitative analysis of each indicated protein spot is presented in Table .

Article Snippet: Cited study was performed using IPG strips produced by Amersham (now GE Healthcare).

Techniques: Control, Transformation Assay, Plasmid Preparation, Expressing, Stripping Membranes, Molecular Weight

2DE of yeast whole cell lysates using IPG (A-C) and NEPHGE (D-F) based methods at high protein load. The same concentrated samples from control cells ( transformed with empty vector pFGG3; A , D) and MeH ( pFGG3-MeH transformant; B , E) or MeN ( pFGG3-MeN; C , F) expressing cells were loaded onto IPG strips (100 μg of total protein in each strip) and NEPHGE gels (100 μg of total protein in each gel). Original scan of one of the replicas is shown for comparison (six gels were being scanned in parallel at the same time). The references are the same as in Figure .

Journal: Proteome Science

Article Title: Comparison of first dimension IPG and NEPHGE techniques in two-dimensional gel electrophoresis experiment with cytosolic unfolded protein response in Saccharomyces cerevisiae

doi: 10.1186/1477-5956-11-36

Figure Lengend Snippet: 2DE of yeast whole cell lysates using IPG (A-C) and NEPHGE (D-F) based methods at high protein load. The same concentrated samples from control cells ( transformed with empty vector pFGG3; A , D) and MeH ( pFGG3-MeH transformant; B , E) or MeN ( pFGG3-MeN; C , F) expressing cells were loaded onto IPG strips (100 μg of total protein in each strip) and NEPHGE gels (100 μg of total protein in each gel). Original scan of one of the replicas is shown for comparison (six gels were being scanned in parallel at the same time). The references are the same as in Figure .

Article Snippet: Cited study was performed using IPG strips produced by Amersham (now GE Healthcare).

Techniques: Control, Transformation Assay, Plasmid Preparation, Expressing, Stripping Membranes, Comparison