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multi image light cabinet  (Alpha Innotech)
86
Alpha Innotech multi image light cabinet
Figure 2. Comparison of FAP-1 protein levels in ovarian cancer cell lines. Lysates from cell lines (100 g total protein) were subjected to SDS-PAGE/ immunoblot assay using rabbit polyclonal no. 1730. Jurkat and HEK 293 cells served as negative and positive controls, respectively. A nonspecific band is also observed (asterisk), serving as a loading control. Densitometrical anal- ysis was performed using a <t>Multi</t> <t>Image</t> <t>light</t> <t>cabinet</t> and the ChemiImager software version 4000 yielding values based on integrated density (#). Data were arbitrarily normalized relative to FAP-1 levels of HEK 293 cells that were included on all blots as an internal control.
Multi Image Light Cabinet, supplied by Alpha Innotech, 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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multi image ii  (Alpha Innotech)
86
Alpha Innotech multi image ii
Figure 2. Comparison of FAP-1 protein levels in ovarian cancer cell lines. Lysates from cell lines (100 g total protein) were subjected to SDS-PAGE/ immunoblot assay using rabbit polyclonal no. 1730. Jurkat and HEK 293 cells served as negative and positive controls, respectively. A nonspecific band is also observed (asterisk), serving as a loading control. Densitometrical anal- ysis was performed using a <t>Multi</t> <t>Image</t> <t>light</t> <t>cabinet</t> and the ChemiImager software version 4000 yielding values based on integrated density (#). Data were arbitrarily normalized relative to FAP-1 levels of HEK 293 cells that were included on all blots as an internal control.
Multi Image Ii, supplied by Alpha Innotech, 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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horseradish peroxidase–conjugated goat anti-rabbit igg  (MultiSciences Biotech Co Ltd)
90
MultiSciences Biotech Co Ltd horseradish peroxidase–conjugated goat anti-rabbit igg
Figure 2. Comparison of FAP-1 protein levels in ovarian cancer cell lines. Lysates from cell lines (100 g total protein) were subjected to SDS-PAGE/ immunoblot assay using rabbit polyclonal no. 1730. Jurkat and HEK 293 cells served as negative and positive controls, respectively. A nonspecific band is also observed (asterisk), serving as a loading control. Densitometrical anal- ysis was performed using a <t>Multi</t> <t>Image</t> <t>light</t> <t>cabinet</t> and the ChemiImager software version 4000 yielding values based on integrated density (#). Data were arbitrarily normalized relative to FAP-1 levels of HEK 293 cells that were included on all blots as an internal control.
Horseradish Peroxidase–Conjugated Goat Anti Rabbit Igg, supplied by MultiSciences Biotech Co 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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multi color chemiluminescence imaging system  (Alpha Innotech)
86
Alpha Innotech multi color chemiluminescence imaging system
Figure 2. Comparison of FAP-1 protein levels in ovarian cancer cell lines. Lysates from cell lines (100 g total protein) were subjected to SDS-PAGE/ immunoblot assay using rabbit polyclonal no. 1730. Jurkat and HEK 293 cells served as negative and positive controls, respectively. A nonspecific band is also observed (asterisk), serving as a loading control. Densitometrical anal- ysis was performed using a <t>Multi</t> <t>Image</t> <t>light</t> <t>cabinet</t> and the ChemiImager software version 4000 yielding values based on integrated density (#). Data were arbitrarily normalized relative to FAP-1 levels of HEK 293 cells that were included on all blots as an internal control.
Multi Color Chemiluminescence Imaging System, supplied by Alpha Innotech, 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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multi color chemiluminescence imaging system - by Bioz Stars, 2026-10
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chemiluminescence solution  (Alpha Innotech)
86
Alpha Innotech chemiluminescence solution
Figure 2. Comparison of FAP-1 protein levels in ovarian cancer cell lines. Lysates from cell lines (100 g total protein) were subjected to SDS-PAGE/ immunoblot assay using rabbit polyclonal no. 1730. Jurkat and HEK 293 cells served as negative and positive controls, respectively. A nonspecific band is also observed (asterisk), serving as a loading control. Densitometrical anal- ysis was performed using a <t>Multi</t> <t>Image</t> <t>light</t> <t>cabinet</t> and the ChemiImager software version 4000 yielding values based on integrated density (#). Data were arbitrarily normalized relative to FAP-1 levels of HEK 293 cells that were included on all blots as an internal control.
Chemiluminescence Solution, supplied by Alpha Innotech, 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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multi gauge v3.0 software  (FUJIFILM)
90
FUJIFILM multi gauge v3.0 software
Figure 2. Comparison of FAP-1 protein levels in ovarian cancer cell lines. Lysates from cell lines (100 g total protein) were subjected to SDS-PAGE/ immunoblot assay using rabbit polyclonal no. 1730. Jurkat and HEK 293 cells served as negative and positive controls, respectively. A nonspecific band is also observed (asterisk), serving as a loading control. Densitometrical anal- ysis was performed using a <t>Multi</t> <t>Image</t> <t>light</t> <t>cabinet</t> and the ChemiImager software version 4000 yielding values based on integrated density (#). Data were arbitrarily normalized relative to FAP-1 levels of HEK 293 cells that were included on all blots as an internal control.
Multi Gauge V3.0 Software, supplied by FUJIFILM, 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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alphaimager 2000  (Alpha Innotech)
86
Alpha Innotech alphaimager 2000
Figure 2. Comparison of FAP-1 protein levels in ovarian cancer cell lines. Lysates from cell lines (100 g total protein) were subjected to SDS-PAGE/ immunoblot assay using rabbit polyclonal no. 1730. Jurkat and HEK 293 cells served as negative and positive controls, respectively. A nonspecific band is also observed (asterisk), serving as a loading control. Densitometrical anal- ysis was performed using a <t>Multi</t> <t>Image</t> <t>light</t> <t>cabinet</t> and the ChemiImager software version 4000 yielding values based on integrated density (#). Data were arbitrarily normalized relative to FAP-1 levels of HEK 293 cells that were included on all blots as an internal control.
Alphaimager 2000, supplied by Alpha Innotech, 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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enhanced chemiluminescence detection kit  (Promega)
90
Promega enhanced chemiluminescence detection kit
Figure 2. Comparison of FAP-1 protein levels in ovarian cancer cell lines. Lysates from cell lines (100 g total protein) were subjected to SDS-PAGE/ immunoblot assay using rabbit polyclonal no. 1730. Jurkat and HEK 293 cells served as negative and positive controls, respectively. A nonspecific band is also observed (asterisk), serving as a loading control. Densitometrical anal- ysis was performed using a <t>Multi</t> <t>Image</t> <t>light</t> <t>cabinet</t> and the ChemiImager software version 4000 yielding values based on integrated density (#). Data were arbitrarily normalized relative to FAP-1 levels of HEK 293 cells that were included on all blots as an internal control.
Enhanced Chemiluminescence Detection Kit, supplied by Promega, 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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bio rad dna engine  (Bio-Rad)
99
Bio-Rad bio rad dna engine
Fig. 2 . A typical MLPA Reaction. In testing MLPA probes, we test with both positive and negative controls. The MLPA amplification products were separated on a 3% NuSieve, 1% <t>agarose</t> <t>electrophoresis</t> gel and stained with Sybr Gold. The first lane contained a 100-bp ladder. The MLPA was conducted with probes designed for A. absinthium and tested with A. absinthium ( lane 2 ), A. vulgaris ( lane 3 ), and C. thalictroides ( lane 4 ) genomic <t>DNA.</t> The product in the lane for A. vulgaris genomic DNA indicates that these MLPA probes were not specific to A. absinthium.
Bio Rad Dna Engine, supplied by Bio-Rad, 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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secondary goat antirabbit  (Bio-Rad)
99
Bio-Rad secondary goat antirabbit
Fig. 2 . A typical MLPA Reaction. In testing MLPA probes, we test with both positive and negative controls. The MLPA amplification products were separated on a 3% NuSieve, 1% <t>agarose</t> <t>electrophoresis</t> gel and stained with Sybr Gold. The first lane contained a 100-bp ladder. The MLPA was conducted with probes designed for A. absinthium and tested with A. absinthium ( lane 2 ), A. vulgaris ( lane 3 ), and C. thalictroides ( lane 4 ) genomic <t>DNA.</t> The product in the lane for A. vulgaris genomic DNA indicates that these MLPA probes were not specific to A. absinthium.
Secondary Goat Antirabbit, supplied by Bio-Rad, 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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secondary goat anti rabbit  (Bio-Rad)
97
Bio-Rad secondary goat anti rabbit
Fig. 2 . A typical MLPA Reaction. In testing MLPA probes, we test with both positive and negative controls. The MLPA amplification products were separated on a 3% NuSieve, 1% <t>agarose</t> <t>electrophoresis</t> gel and stained with Sybr Gold. The first lane contained a 100-bp ladder. The MLPA was conducted with probes designed for A. absinthium and tested with A. absinthium ( lane 2 ), A. vulgaris ( lane 3 ), and C. thalictroides ( lane 4 ) genomic <t>DNA.</t> The product in the lane for A. vulgaris genomic DNA indicates that these MLPA probes were not specific to A. absinthium.
Secondary Goat Anti Rabbit, supplied by Bio-Rad, 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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coomassie brilliant blue  (Bio-Rad)
96
Bio-Rad coomassie brilliant blue
Fig. 2 . A typical MLPA Reaction. In testing MLPA probes, we test with both positive and negative controls. The MLPA amplification products were separated on a 3% NuSieve, 1% <t>agarose</t> <t>electrophoresis</t> gel and stained with Sybr Gold. The first lane contained a 100-bp ladder. The MLPA was conducted with probes designed for A. absinthium and tested with A. absinthium ( lane 2 ), A. vulgaris ( lane 3 ), and C. thalictroides ( lane 4 ) genomic <t>DNA.</t> The product in the lane for A. vulgaris genomic DNA indicates that these MLPA probes were not specific to A. absinthium.
Coomassie Brilliant Blue, 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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Image Search Results


Figure 2. Comparison of FAP-1 protein levels in ovarian cancer cell lines. Lysates from cell lines (100 g total protein) were subjected to SDS-PAGE/ immunoblot assay using rabbit polyclonal no. 1730. Jurkat and HEK 293 cells served as negative and positive controls, respectively. A nonspecific band is also observed (asterisk), serving as a loading control. Densitometrical anal- ysis was performed using a Multi Image light cabinet and the ChemiImager software version 4000 yielding values based on integrated density (#). Data were arbitrarily normalized relative to FAP-1 levels of HEK 293 cells that were included on all blots as an internal control.

Journal: The American Journal of Pathology

Article Title: Expression and Potential Role of Fas-Associated Phosphatase-1 in Ovarian Cancer

doi: 10.1016/s0002-9440(10)64084-9

Figure Lengend Snippet: Figure 2. Comparison of FAP-1 protein levels in ovarian cancer cell lines. Lysates from cell lines (100 g total protein) were subjected to SDS-PAGE/ immunoblot assay using rabbit polyclonal no. 1730. Jurkat and HEK 293 cells served as negative and positive controls, respectively. A nonspecific band is also observed (asterisk), serving as a loading control. Densitometrical anal- ysis was performed using a Multi Image light cabinet and the ChemiImager software version 4000 yielding values based on integrated density (#). Data were arbitrarily normalized relative to FAP-1 levels of HEK 293 cells that were included on all blots as an internal control.

Article Snippet: To quantify immunoblotting results, films were analyzed densitometrically using a Multi Image Light Cabinet and the ChemiImager software version 4000 (Alpha Innotech Corporation, San Leandro, CA).

Techniques: Comparison, SDS Page, Western Blot, Control, Software

Fig. 2 . A typical MLPA Reaction. In testing MLPA probes, we test with both positive and negative controls. The MLPA amplification products were separated on a 3% NuSieve, 1% agarose electrophoresis gel and stained with Sybr Gold. The first lane contained a 100-bp ladder. The MLPA was conducted with probes designed for A. absinthium and tested with A. absinthium ( lane 2 ), A. vulgaris ( lane 3 ), and C. thalictroides ( lane 4 ) genomic DNA. The product in the lane for A. vulgaris genomic DNA indicates that these MLPA probes were not specific to A. absinthium.

Journal: Methods in molecular biology (Clifton, N.J.)

Article Title: Protocols for in vitro cultures and secondary metabolite analysis of aromatic and medicinal plants. Preface.

doi: 10.1007/978-1-60327-287-2

Figure Lengend Snippet: Fig. 2 . A typical MLPA Reaction. In testing MLPA probes, we test with both positive and negative controls. The MLPA amplification products were separated on a 3% NuSieve, 1% agarose electrophoresis gel and stained with Sybr Gold. The first lane contained a 100-bp ladder. The MLPA was conducted with probes designed for A. absinthium and tested with A. absinthium ( lane 2 ), A. vulgaris ( lane 3 ), and C. thalictroides ( lane 4 ) genomic DNA. The product in the lane for A. vulgaris genomic DNA indicates that these MLPA probes were not specific to A. absinthium.

Article Snippet: Equipment: “Bio-Rad DNA Engine” (Peltier Thermal cycler); Gel electrophoresis unit (Bio-Rad Sub-Cell ® GT), power-pack (Gene Power Supply GPS 200/400; Pharmacia), gel documentation system Alphalmager ® EC (Alpha Innotech Corporation, ChemiImagerTM Ready).

Techniques: Amplification, Electrophoresis, Staining