wizard genomic dna purification kit Search Results


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Promega wizard genomic dna purification kit a1120
a Genomic PCR for the floxed site in F1 heterozygous KI mice (intact, 2.5 kbp; recombined, 1.5 kbp). These mice were injected with three doses (3D) or six doses (6D) of tamoxifen or the solvent corn oil alone (TAM−) two weeks before limb sample collection ( n = 3 each). Lane numbers indicate the ID of the individual. WT: <t>genomic</t> <t>DNA</t> of a wild-type C57BL/6J mouse. P: plasmid DNA (control). M: size marker. Pink arrowheads: 1.5 kbp (recombined). b − e Representative images showing tamoxifen-dependent induction of mCherry expression in SMF cells ( n = 3 for each). F1 heterozygous KI mice were injected with either six doses of tamoxifen (TAM+) or the solvent corn oil alone (TAM−). The limb samples were cross-sectioned in the middle of the zeugopod (20 µm thick). mCherry fluorescence was detected in the TAM+ mice ( b , c ) but not in the TAM− mice ( d , e ). Note that EGFP fluorescence in the TAM+ mice was weaker than in the TAM− mice, suggesting recombination of the floxed site. The optical sections (1.3–2.0 µm thick) of the boxed areas of the merged images in ( b ) and ( d ), acquired by laser confocal microscopy, are shown in ( c ) and ( e ), respectively. Scale bars: b and d 1 mm for upper panels, 200 µm for lower panel; c and e 100 µm.
Wizard Genomic Dna Purification Kit A1120, 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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Promega wizard genomic dna purification kit for plant tissue
a Genomic PCR for the floxed site in F1 heterozygous KI mice (intact, 2.5 kbp; recombined, 1.5 kbp). These mice were injected with three doses (3D) or six doses (6D) of tamoxifen or the solvent corn oil alone (TAM−) two weeks before limb sample collection ( n = 3 each). Lane numbers indicate the ID of the individual. WT: <t>genomic</t> <t>DNA</t> of a wild-type C57BL/6J mouse. P: plasmid DNA (control). M: size marker. Pink arrowheads: 1.5 kbp (recombined). b − e Representative images showing tamoxifen-dependent induction of mCherry expression in SMF cells ( n = 3 for each). F1 heterozygous KI mice were injected with either six doses of tamoxifen (TAM+) or the solvent corn oil alone (TAM−). The limb samples were cross-sectioned in the middle of the zeugopod (20 µm thick). mCherry fluorescence was detected in the TAM+ mice ( b , c ) but not in the TAM− mice ( d , e ). Note that EGFP fluorescence in the TAM+ mice was weaker than in the TAM− mice, suggesting recombination of the floxed site. The optical sections (1.3–2.0 µm thick) of the boxed areas of the merged images in ( b ) and ( d ), acquired by laser confocal microscopy, are shown in ( c ) and ( e ), respectively. Scale bars: b and d 1 mm for upper panels, 200 µm for lower panel; c and e 100 µm.
Wizard Genomic Dna Purification Kit For Plant Tissue, 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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a Genomic PCR for the floxed site in F1 heterozygous KI mice (intact, 2.5 kbp; recombined, 1.5 kbp). These mice were injected with three doses (3D) or six doses (6D) of tamoxifen or the solvent corn oil alone (TAM−) two weeks before limb sample collection ( n = 3 each). Lane numbers indicate the ID of the individual. WT: <t>genomic</t> <t>DNA</t> of a wild-type C57BL/6J mouse. P: plasmid DNA (control). M: size marker. Pink arrowheads: 1.5 kbp (recombined). b − e Representative images showing tamoxifen-dependent induction of mCherry expression in SMF cells ( n = 3 for each). F1 heterozygous KI mice were injected with either six doses of tamoxifen (TAM+) or the solvent corn oil alone (TAM−). The limb samples were cross-sectioned in the middle of the zeugopod (20 µm thick). mCherry fluorescence was detected in the TAM+ mice ( b , c ) but not in the TAM− mice ( d , e ). Note that EGFP fluorescence in the TAM+ mice was weaker than in the TAM− mice, suggesting recombination of the floxed site. The optical sections (1.3–2.0 µm thick) of the boxed areas of the merged images in ( b ) and ( d ), acquired by laser confocal microscopy, are shown in ( c ) and ( e ), respectively. Scale bars: b and d 1 mm for upper panels, 200 µm for lower panel; c and e 100 µm.
Wizard Tm Genomic Dna Purification Kit Promega H, 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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Promega nuclei lysis solution from promega's wizardtm genomic dna purification kit
a Genomic PCR for the floxed site in F1 heterozygous KI mice (intact, 2.5 kbp; recombined, 1.5 kbp). These mice were injected with three doses (3D) or six doses (6D) of tamoxifen or the solvent corn oil alone (TAM−) two weeks before limb sample collection ( n = 3 each). Lane numbers indicate the ID of the individual. WT: <t>genomic</t> <t>DNA</t> of a wild-type C57BL/6J mouse. P: plasmid DNA (control). M: size marker. Pink arrowheads: 1.5 kbp (recombined). b − e Representative images showing tamoxifen-dependent induction of mCherry expression in SMF cells ( n = 3 for each). F1 heterozygous KI mice were injected with either six doses of tamoxifen (TAM+) or the solvent corn oil alone (TAM−). The limb samples were cross-sectioned in the middle of the zeugopod (20 µm thick). mCherry fluorescence was detected in the TAM+ mice ( b , c ) but not in the TAM− mice ( d , e ). Note that EGFP fluorescence in the TAM+ mice was weaker than in the TAM− mice, suggesting recombination of the floxed site. The optical sections (1.3–2.0 µm thick) of the boxed areas of the merged images in ( b ) and ( d ), acquired by laser confocal microscopy, are shown in ( c ) and ( e ), respectively. Scale bars: b and d 1 mm for upper panels, 200 µm for lower panel; c and e 100 µm.
Nuclei Lysis Solution From Promega's Wizardtm Genomic Dna Purification 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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Promega wizard genomic dna purification kit 12
a Genomic PCR for the floxed site in F1 heterozygous KI mice (intact, 2.5 kbp; recombined, 1.5 kbp). These mice were injected with three doses (3D) or six doses (6D) of tamoxifen or the solvent corn oil alone (TAM−) two weeks before limb sample collection ( n = 3 each). Lane numbers indicate the ID of the individual. WT: <t>genomic</t> <t>DNA</t> of a wild-type C57BL/6J mouse. P: plasmid DNA (control). M: size marker. Pink arrowheads: 1.5 kbp (recombined). b − e Representative images showing tamoxifen-dependent induction of mCherry expression in SMF cells ( n = 3 for each). F1 heterozygous KI mice were injected with either six doses of tamoxifen (TAM+) or the solvent corn oil alone (TAM−). The limb samples were cross-sectioned in the middle of the zeugopod (20 µm thick). mCherry fluorescence was detected in the TAM+ mice ( b , c ) but not in the TAM− mice ( d , e ). Note that EGFP fluorescence in the TAM+ mice was weaker than in the TAM− mice, suggesting recombination of the floxed site. The optical sections (1.3–2.0 µm thick) of the boxed areas of the merged images in ( b ) and ( d ), acquired by laser confocal microscopy, are shown in ( c ) and ( e ), respectively. Scale bars: b and d 1 mm for upper panels, 200 µm for lower panel; c and e 100 µm.
Wizard Genomic Dna Purification Kit 12, 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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Promega wizard dna isolation
a Genomic PCR for the floxed site in F1 heterozygous KI mice (intact, 2.5 kbp; recombined, 1.5 kbp). These mice were injected with three doses (3D) or six doses (6D) of tamoxifen or the solvent corn oil alone (TAM−) two weeks before limb sample collection ( n = 3 each). Lane numbers indicate the ID of the individual. WT: <t>genomic</t> <t>DNA</t> of a wild-type C57BL/6J mouse. P: plasmid DNA (control). M: size marker. Pink arrowheads: 1.5 kbp (recombined). b − e Representative images showing tamoxifen-dependent induction of mCherry expression in SMF cells ( n = 3 for each). F1 heterozygous KI mice were injected with either six doses of tamoxifen (TAM+) or the solvent corn oil alone (TAM−). The limb samples were cross-sectioned in the middle of the zeugopod (20 µm thick). mCherry fluorescence was detected in the TAM+ mice ( b , c ) but not in the TAM− mice ( d , e ). Note that EGFP fluorescence in the TAM+ mice was weaker than in the TAM− mice, suggesting recombination of the floxed site. The optical sections (1.3–2.0 µm thick) of the boxed areas of the merged images in ( b ) and ( d ), acquired by laser confocal microscopy, are shown in ( c ) and ( e ), respectively. Scale bars: b and d 1 mm for upper panels, 200 µm for lower panel; c and e 100 µm.
Wizard Dna Isolation, 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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a Genomic PCR for the floxed site in F1 heterozygous KI mice (intact, 2.5 kbp; recombined, 1.5 kbp). These mice were injected with three doses (3D) or six doses (6D) of tamoxifen or the solvent corn oil alone (TAM−) two weeks before limb sample collection ( n = 3 each). Lane numbers indicate the ID of the individual. WT: <t>genomic</t> <t>DNA</t> of a wild-type C57BL/6J mouse. P: plasmid DNA (control). M: size marker. Pink arrowheads: 1.5 kbp (recombined). b − e Representative images showing tamoxifen-dependent induction of mCherry expression in SMF cells ( n = 3 for each). F1 heterozygous KI mice were injected with either six doses of tamoxifen (TAM+) or the solvent corn oil alone (TAM−). The limb samples were cross-sectioned in the middle of the zeugopod (20 µm thick). mCherry fluorescence was detected in the TAM+ mice ( b , c ) but not in the TAM− mice ( d , e ). Note that EGFP fluorescence in the TAM+ mice was weaker than in the TAM− mice, suggesting recombination of the floxed site. The optical sections (1.3–2.0 µm thick) of the boxed areas of the merged images in ( b ) and ( d ), acquired by laser confocal microscopy, are shown in ( c ) and ( e ), respectively. Scale bars: b and d 1 mm for upper panels, 200 µm for lower panel; c and e 100 µm.
Cell Lysis Solution Wizard Genomic Dna Purification 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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Promega wizard genomic dna purification kit # 1120
a Genomic PCR for the floxed site in F1 heterozygous KI mice (intact, 2.5 kbp; recombined, 1.5 kbp). These mice were injected with three doses (3D) or six doses (6D) of tamoxifen or the solvent corn oil alone (TAM−) two weeks before limb sample collection ( n = 3 each). Lane numbers indicate the ID of the individual. WT: <t>genomic</t> <t>DNA</t> of a wild-type C57BL/6J mouse. P: plasmid DNA (control). M: size marker. Pink arrowheads: 1.5 kbp (recombined). b − e Representative images showing tamoxifen-dependent induction of mCherry expression in SMF cells ( n = 3 for each). F1 heterozygous KI mice were injected with either six doses of tamoxifen (TAM+) or the solvent corn oil alone (TAM−). The limb samples were cross-sectioned in the middle of the zeugopod (20 µm thick). mCherry fluorescence was detected in the TAM+ mice ( b , c ) but not in the TAM− mice ( d , e ). Note that EGFP fluorescence in the TAM+ mice was weaker than in the TAM− mice, suggesting recombination of the floxed site. The optical sections (1.3–2.0 µm thick) of the boxed areas of the merged images in ( b ) and ( d ), acquired by laser confocal microscopy, are shown in ( c ) and ( e ), respectively. Scale bars: b and d 1 mm for upper panels, 200 µm for lower panel; c and e 100 µm.
Wizard Genomic Dna Purification Kit # 1120, 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
https://www.bioz.com/result/wizard genomic dna purification kit # 1120/product/Promega
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Promega dna rehydration solution wizard genomic dna purification kit
a Genomic PCR for the floxed site in F1 heterozygous KI mice (intact, 2.5 kbp; recombined, 1.5 kbp). These mice were injected with three doses (3D) or six doses (6D) of tamoxifen or the solvent corn oil alone (TAM−) two weeks before limb sample collection ( n = 3 each). Lane numbers indicate the ID of the individual. WT: <t>genomic</t> <t>DNA</t> of a wild-type C57BL/6J mouse. P: plasmid DNA (control). M: size marker. Pink arrowheads: 1.5 kbp (recombined). b − e Representative images showing tamoxifen-dependent induction of mCherry expression in SMF cells ( n = 3 for each). F1 heterozygous KI mice were injected with either six doses of tamoxifen (TAM+) or the solvent corn oil alone (TAM−). The limb samples were cross-sectioned in the middle of the zeugopod (20 µm thick). mCherry fluorescence was detected in the TAM+ mice ( b , c ) but not in the TAM− mice ( d , e ). Note that EGFP fluorescence in the TAM+ mice was weaker than in the TAM− mice, suggesting recombination of the floxed site. The optical sections (1.3–2.0 µm thick) of the boxed areas of the merged images in ( b ) and ( d ), acquired by laser confocal microscopy, are shown in ( c ) and ( e ), respectively. Scale bars: b and d 1 mm for upper panels, 200 µm for lower panel; c and e 100 µm.
Dna Rehydration Solution Wizard Genomic Dna Purification 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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Promega wizard genomic dna purification kit
a Genomic PCR for the floxed site in F1 heterozygous KI mice (intact, 2.5 kbp; recombined, 1.5 kbp). These mice were injected with three doses (3D) or six doses (6D) of tamoxifen or the solvent corn oil alone (TAM−) two weeks before limb sample collection ( n = 3 each). Lane numbers indicate the ID of the individual. WT: <t>genomic</t> <t>DNA</t> of a wild-type C57BL/6J mouse. P: plasmid DNA (control). M: size marker. Pink arrowheads: 1.5 kbp (recombined). b − e Representative images showing tamoxifen-dependent induction of mCherry expression in SMF cells ( n = 3 for each). F1 heterozygous KI mice were injected with either six doses of tamoxifen (TAM+) or the solvent corn oil alone (TAM−). The limb samples were cross-sectioned in the middle of the zeugopod (20 µm thick). mCherry fluorescence was detected in the TAM+ mice ( b , c ) but not in the TAM− mice ( d , e ). Note that EGFP fluorescence in the TAM+ mice was weaker than in the TAM− mice, suggesting recombination of the floxed site. The optical sections (1.3–2.0 µm thick) of the boxed areas of the merged images in ( b ) and ( d ), acquired by laser confocal microscopy, are shown in ( c ) and ( e ), respectively. Scale bars: b and d 1 mm for upper panels, 200 µm for lower panel; c and e 100 µm.
Wizard Genomic Dna Purification 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
https://www.bioz.com/result/wizard genomic dna purification kit/product/Promega
Average 90 stars, based on 1 article reviews
wizard genomic dna purification kit - by Bioz Stars, 2026-06
90/100 stars
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Image Search Results


a Genomic PCR for the floxed site in F1 heterozygous KI mice (intact, 2.5 kbp; recombined, 1.5 kbp). These mice were injected with three doses (3D) or six doses (6D) of tamoxifen or the solvent corn oil alone (TAM−) two weeks before limb sample collection ( n = 3 each). Lane numbers indicate the ID of the individual. WT: genomic DNA of a wild-type C57BL/6J mouse. P: plasmid DNA (control). M: size marker. Pink arrowheads: 1.5 kbp (recombined). b − e Representative images showing tamoxifen-dependent induction of mCherry expression in SMF cells ( n = 3 for each). F1 heterozygous KI mice were injected with either six doses of tamoxifen (TAM+) or the solvent corn oil alone (TAM−). The limb samples were cross-sectioned in the middle of the zeugopod (20 µm thick). mCherry fluorescence was detected in the TAM+ mice ( b , c ) but not in the TAM− mice ( d , e ). Note that EGFP fluorescence in the TAM+ mice was weaker than in the TAM− mice, suggesting recombination of the floxed site. The optical sections (1.3–2.0 µm thick) of the boxed areas of the merged images in ( b ) and ( d ), acquired by laser confocal microscopy, are shown in ( c ) and ( e ), respectively. Scale bars: b and d 1 mm for upper panels, 200 µm for lower panel; c and e 100 µm.

Journal: Communications Biology

Article Title: One-step Cre- loxP organism creation by TAx9

doi: 10.1038/s42003-025-07759-9

Figure Lengend Snippet: a Genomic PCR for the floxed site in F1 heterozygous KI mice (intact, 2.5 kbp; recombined, 1.5 kbp). These mice were injected with three doses (3D) or six doses (6D) of tamoxifen or the solvent corn oil alone (TAM−) two weeks before limb sample collection ( n = 3 each). Lane numbers indicate the ID of the individual. WT: genomic DNA of a wild-type C57BL/6J mouse. P: plasmid DNA (control). M: size marker. Pink arrowheads: 1.5 kbp (recombined). b − e Representative images showing tamoxifen-dependent induction of mCherry expression in SMF cells ( n = 3 for each). F1 heterozygous KI mice were injected with either six doses of tamoxifen (TAM+) or the solvent corn oil alone (TAM−). The limb samples were cross-sectioned in the middle of the zeugopod (20 µm thick). mCherry fluorescence was detected in the TAM+ mice ( b , c ) but not in the TAM− mice ( d , e ). Note that EGFP fluorescence in the TAM+ mice was weaker than in the TAM− mice, suggesting recombination of the floxed site. The optical sections (1.3–2.0 µm thick) of the boxed areas of the merged images in ( b ) and ( d ), acquired by laser confocal microscopy, are shown in ( c ) and ( e ), respectively. Scale bars: b and d 1 mm for upper panels, 200 µm for lower panel; c and e 100 µm.

Article Snippet: Genomic DNA was obtained from the tail tips of larval newts (St. 59) and mice (1 month old) with a Wizard Genomic DNA Purification Kit (A1120; Promega).

Techniques: Injection, Solvent, Plasmid Preparation, Control, Marker, Expressing, Fluorescence, Confocal Microscopy