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qiaex extraction kit  (Qiagen)


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    Qiagen qiaex extraction kit
    Qiaex Extraction Kit, supplied by Qiagen, used in various techniques. Bioz Stars score: 99/100, based on 18985 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lambda-zap+express+vector/QIAEX+II+Gel+Extraction+Kit/pm12070074-139-16-19
    Average 99 stars, based on 18985 article reviews
    qiaex extraction kit - by Bioz Stars, 2026-11
    99/100 stars

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    Related Articles

    Sequencing:

    Article Title: STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness
    Article Snippet: Immunoprecipitations were carried out overnight at 4 °C using 4 μg of antibody for transcription factor ChIP or 2 μg for histone ChIP, and immune complexes were washed and eluted according to the kit protocol, with DNA purification using the iPure kit V2 (Diagenode). .. Sequencing libraries were prepared from 1 to 10 ng of ChIP DNA with an Illumina-compatible library preparation workflow that included end repair, addition of a 3′ A overhang, adaptor ligation, PCR amplification, and size selection on 3% NuSieve 3:1 agarose (Lonza), followed by QIAEX II gel extraction (QIAGEN). .. Library size distribution and concentration were assessed on an Agilent 2100 Bioanalyzer before sequencing.

    Article Title: STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness.
    Article Snippet: Immunoprecipitations were carried out overnight at 4 °C using 4 μg of antibody for transcription factor ChIP or 2 μg for histone ChIP, and immune complexes were washed and eluted according to the kit protocol, with DNA purification using the iPure kit V2 (Diagenode). .. Sequencing libraries were prepared from 1 to 10 ng of ChIP DNA with an Illumina- compatible library preparation workflow that included end repair, addition of a 3′ A overhang, adaptor ligation, PCR amplification, and size selection on 3% NuSieve 3:1 agarose (Lonza), followed by QIAEX II gel extraction (QIAGEN). ..

    Chromatin Immunoprecipitation:

    Article Title: STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness
    Article Snippet: Immunoprecipitations were carried out overnight at 4 °C using 4 μg of antibody for transcription factor ChIP or 2 μg for histone ChIP, and immune complexes were washed and eluted according to the kit protocol, with DNA purification using the iPure kit V2 (Diagenode). .. Sequencing libraries were prepared from 1 to 10 ng of ChIP DNA with an Illumina-compatible library preparation workflow that included end repair, addition of a 3′ A overhang, adaptor ligation, PCR amplification, and size selection on 3% NuSieve 3:1 agarose (Lonza), followed by QIAEX II gel extraction (QIAGEN). .. Library size distribution and concentration were assessed on an Agilent 2100 Bioanalyzer before sequencing.

    Article Title: STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness.
    Article Snippet: Immunoprecipitations were carried out overnight at 4 °C using 4 μg of antibody for transcription factor ChIP or 2 μg for histone ChIP, and immune complexes were washed and eluted according to the kit protocol, with DNA purification using the iPure kit V2 (Diagenode). .. Sequencing libraries were prepared from 1 to 10 ng of ChIP DNA with an Illumina- compatible library preparation workflow that included end repair, addition of a 3′ A overhang, adaptor ligation, PCR amplification, and size selection on 3% NuSieve 3:1 agarose (Lonza), followed by QIAEX II gel extraction (QIAGEN). ..

    Ligation:

    Article Title: STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness
    Article Snippet: Immunoprecipitations were carried out overnight at 4 °C using 4 μg of antibody for transcription factor ChIP or 2 μg for histone ChIP, and immune complexes were washed and eluted according to the kit protocol, with DNA purification using the iPure kit V2 (Diagenode). .. Sequencing libraries were prepared from 1 to 10 ng of ChIP DNA with an Illumina-compatible library preparation workflow that included end repair, addition of a 3′ A overhang, adaptor ligation, PCR amplification, and size selection on 3% NuSieve 3:1 agarose (Lonza), followed by QIAEX II gel extraction (QIAGEN). .. Library size distribution and concentration were assessed on an Agilent 2100 Bioanalyzer before sequencing.

    Article Title: STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness.
    Article Snippet: Immunoprecipitations were carried out overnight at 4 °C using 4 μg of antibody for transcription factor ChIP or 2 μg for histone ChIP, and immune complexes were washed and eluted according to the kit protocol, with DNA purification using the iPure kit V2 (Diagenode). .. Sequencing libraries were prepared from 1 to 10 ng of ChIP DNA with an Illumina- compatible library preparation workflow that included end repair, addition of a 3′ A overhang, adaptor ligation, PCR amplification, and size selection on 3% NuSieve 3:1 agarose (Lonza), followed by QIAEX II gel extraction (QIAGEN). ..

    Polymerase Chain Reaction:

    Article Title: STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness
    Article Snippet: Immunoprecipitations were carried out overnight at 4 °C using 4 μg of antibody for transcription factor ChIP or 2 μg for histone ChIP, and immune complexes were washed and eluted according to the kit protocol, with DNA purification using the iPure kit V2 (Diagenode). .. Sequencing libraries were prepared from 1 to 10 ng of ChIP DNA with an Illumina-compatible library preparation workflow that included end repair, addition of a 3′ A overhang, adaptor ligation, PCR amplification, and size selection on 3% NuSieve 3:1 agarose (Lonza), followed by QIAEX II gel extraction (QIAGEN). .. Library size distribution and concentration were assessed on an Agilent 2100 Bioanalyzer before sequencing.

    Article Title: STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness.
    Article Snippet: Immunoprecipitations were carried out overnight at 4 °C using 4 μg of antibody for transcription factor ChIP or 2 μg for histone ChIP, and immune complexes were washed and eluted according to the kit protocol, with DNA purification using the iPure kit V2 (Diagenode). .. Sequencing libraries were prepared from 1 to 10 ng of ChIP DNA with an Illumina- compatible library preparation workflow that included end repair, addition of a 3′ A overhang, adaptor ligation, PCR amplification, and size selection on 3% NuSieve 3:1 agarose (Lonza), followed by QIAEX II gel extraction (QIAGEN). ..

    Article Title: New Haplotype of Bartonella sp. in Haematopota pluvialis (Linnaeus, 1758).
    Article Snippet: ; Gdańsk; Poland) using a ChemiDoc MP imaging system (Bio-Rad, Hercules, CA, USA). .. PCR products were purified using the QIAEX II Gel Extraction Kit (Qiagen, Hilden, Germany) according to the manufacturer’s protocol and then sequenced by Genomed (Warsaw, Poland). ..

    Article Title: Emergence and evolution of chimeric pseudogenes (φgenes) contribute to genetic and functional diversity of the human genome
    Article Snippet: RNA extraction from cell lines and primary cultures performed using TRIzol reagent (RNAiso Plus TAKARA, 9108) was followed by complementary DNA (cDNA) synthesis and quantification (DeNovix spectrophotometer). .. PCR amplification was performed with TaKaRa DNA Polymerase (#R050B); amplified products were resolved on a 1.8% agarose gel (Sigma–Aldrich, #A9539-100G), and resulting bands were excised and purified using the QIAEX II Gel Extraction Kit (Qiagen #20021, #20051). .. 5′/3′ RACE kit (TAKARA, Cat. No. 634858) was used for synthesis of cDNA synthesis and RACE PCR.

    Amplification:

    Article Title: STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness
    Article Snippet: Immunoprecipitations were carried out overnight at 4 °C using 4 μg of antibody for transcription factor ChIP or 2 μg for histone ChIP, and immune complexes were washed and eluted according to the kit protocol, with DNA purification using the iPure kit V2 (Diagenode). .. Sequencing libraries were prepared from 1 to 10 ng of ChIP DNA with an Illumina-compatible library preparation workflow that included end repair, addition of a 3′ A overhang, adaptor ligation, PCR amplification, and size selection on 3% NuSieve 3:1 agarose (Lonza), followed by QIAEX II gel extraction (QIAGEN). .. Library size distribution and concentration were assessed on an Agilent 2100 Bioanalyzer before sequencing.

    Article Title: STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness.
    Article Snippet: Immunoprecipitations were carried out overnight at 4 °C using 4 μg of antibody for transcription factor ChIP or 2 μg for histone ChIP, and immune complexes were washed and eluted according to the kit protocol, with DNA purification using the iPure kit V2 (Diagenode). .. Sequencing libraries were prepared from 1 to 10 ng of ChIP DNA with an Illumina- compatible library preparation workflow that included end repair, addition of a 3′ A overhang, adaptor ligation, PCR amplification, and size selection on 3% NuSieve 3:1 agarose (Lonza), followed by QIAEX II gel extraction (QIAGEN). ..

    Article Title: Mosaic variants in the LIM homeobox 1 (LHX1) gene contribute to Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.
    Article Snippet: Infertility is a common reproductive problem affecting 10–15% of individuals (Collins and Van Steirteghem 2004).. Causes may include ovulation disorders, endometriosis, sperm abnormalities, and/or uterine/tubal conditions.. Müllerian duct (MD) anomalies are relatively common congenital disorders that cause abnormal uterine and vaginal development, which may predispose to infertility and miscarriage.

    Article Title: Emergence and evolution of chimeric pseudogenes (φgenes) contribute to genetic and functional diversity of the human genome
    Article Snippet: RNA extraction from cell lines and primary cultures performed using TRIzol reagent (RNAiso Plus TAKARA, 9108) was followed by complementary DNA (cDNA) synthesis and quantification (DeNovix spectrophotometer). .. PCR amplification was performed with TaKaRa DNA Polymerase (#R050B); amplified products were resolved on a 1.8% agarose gel (Sigma–Aldrich, #A9539-100G), and resulting bands were excised and purified using the QIAEX II Gel Extraction Kit (Qiagen #20021, #20051). .. 5′/3′ RACE kit (TAKARA, Cat. No. 634858) was used for synthesis of cDNA synthesis and RACE PCR.

    Size Selection:

    Article Title: STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness
    Article Snippet: Immunoprecipitations were carried out overnight at 4 °C using 4 μg of antibody for transcription factor ChIP or 2 μg for histone ChIP, and immune complexes were washed and eluted according to the kit protocol, with DNA purification using the iPure kit V2 (Diagenode). .. Sequencing libraries were prepared from 1 to 10 ng of ChIP DNA with an Illumina-compatible library preparation workflow that included end repair, addition of a 3′ A overhang, adaptor ligation, PCR amplification, and size selection on 3% NuSieve 3:1 agarose (Lonza), followed by QIAEX II gel extraction (QIAGEN). .. Library size distribution and concentration were assessed on an Agilent 2100 Bioanalyzer before sequencing.

    Article Title: STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness.
    Article Snippet: Immunoprecipitations were carried out overnight at 4 °C using 4 μg of antibody for transcription factor ChIP or 2 μg for histone ChIP, and immune complexes were washed and eluted according to the kit protocol, with DNA purification using the iPure kit V2 (Diagenode). .. Sequencing libraries were prepared from 1 to 10 ng of ChIP DNA with an Illumina- compatible library preparation workflow that included end repair, addition of a 3′ A overhang, adaptor ligation, PCR amplification, and size selection on 3% NuSieve 3:1 agarose (Lonza), followed by QIAEX II gel extraction (QIAGEN). ..

    Gel Extraction:

    Article Title: STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness
    Article Snippet: Immunoprecipitations were carried out overnight at 4 °C using 4 μg of antibody for transcription factor ChIP or 2 μg for histone ChIP, and immune complexes were washed and eluted according to the kit protocol, with DNA purification using the iPure kit V2 (Diagenode). .. Sequencing libraries were prepared from 1 to 10 ng of ChIP DNA with an Illumina-compatible library preparation workflow that included end repair, addition of a 3′ A overhang, adaptor ligation, PCR amplification, and size selection on 3% NuSieve 3:1 agarose (Lonza), followed by QIAEX II gel extraction (QIAGEN). .. Library size distribution and concentration were assessed on an Agilent 2100 Bioanalyzer before sequencing.

    Article Title: STAG2 loss amplifies EWS-FLI1-driven microsatellite enhancer activity promoting Ewing sarcoma aggressiveness.
    Article Snippet: Immunoprecipitations were carried out overnight at 4 °C using 4 μg of antibody for transcription factor ChIP or 2 μg for histone ChIP, and immune complexes were washed and eluted according to the kit protocol, with DNA purification using the iPure kit V2 (Diagenode). .. Sequencing libraries were prepared from 1 to 10 ng of ChIP DNA with an Illumina- compatible library preparation workflow that included end repair, addition of a 3′ A overhang, adaptor ligation, PCR amplification, and size selection on 3% NuSieve 3:1 agarose (Lonza), followed by QIAEX II gel extraction (QIAGEN). ..

    Article Title: Use of Ligilactobacillus salivarius SP36 as an Adjunct Culture by an Artisan Dairy and Isolation of New Autochthonous Strains with Technological Potential for Cheesemaking
    Article Snippet: The concentration of PCR products was determined using a 2100 Bioanalyzer (Agilent, Santa Clara, CA, USA). .. Barcoded products were pooled at approximately equimolar concentrations and run on a preparative agarose gel, and the correct band size was excised and purified using a QIAEX II Gel Extraction Kit (Qiagen). .. The pooled amplicons were quantified with PicoGreen (BMG Labtech, Jena, Germany) and sequenced on an Illumina MiSeq platform (2 × 300 bp paired-end reads) at the facilities of the Scientific Park of Madrid (Spain).

    Article Title: New Haplotype of Bartonella sp. in Haematopota pluvialis (Linnaeus, 1758).
    Article Snippet: ; Gdańsk; Poland) using a ChemiDoc MP imaging system (Bio-Rad, Hercules, CA, USA). .. PCR products were purified using the QIAEX II Gel Extraction Kit (Qiagen, Hilden, Germany) according to the manufacturer’s protocol and then sequenced by Genomed (Warsaw, Poland). ..

    Article Title: Mosaic variants in the LIM homeobox 1 (LHX1) gene contribute to Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.
    Article Snippet: Infertility is a common reproductive problem affecting 10–15% of individuals (Collins and Van Steirteghem 2004).. Causes may include ovulation disorders, endometriosis, sperm abnormalities, and/or uterine/tubal conditions.. Müllerian duct (MD) anomalies are relatively common congenital disorders that cause abnormal uterine and vaginal development, which may predispose to infertility and miscarriage.

    Article Title: Emergence and evolution of chimeric pseudogenes (φgenes) contribute to genetic and functional diversity of the human genome
    Article Snippet: RNA extraction from cell lines and primary cultures performed using TRIzol reagent (RNAiso Plus TAKARA, 9108) was followed by complementary DNA (cDNA) synthesis and quantification (DeNovix spectrophotometer). .. PCR amplification was performed with TaKaRa DNA Polymerase (#R050B); amplified products were resolved on a 1.8% agarose gel (Sigma–Aldrich, #A9539-100G), and resulting bands were excised and purified using the QIAEX II Gel Extraction Kit (Qiagen #20021, #20051). .. 5′/3′ RACE kit (TAKARA, Cat. No. 634858) was used for synthesis of cDNA synthesis and RACE PCR.

    Agarose Gel Electrophoresis:

    Article Title: Use of Ligilactobacillus salivarius SP36 as an Adjunct Culture by an Artisan Dairy and Isolation of New Autochthonous Strains with Technological Potential for Cheesemaking
    Article Snippet: The concentration of PCR products was determined using a 2100 Bioanalyzer (Agilent, Santa Clara, CA, USA). .. Barcoded products were pooled at approximately equimolar concentrations and run on a preparative agarose gel, and the correct band size was excised and purified using a QIAEX II Gel Extraction Kit (Qiagen). .. The pooled amplicons were quantified with PicoGreen (BMG Labtech, Jena, Germany) and sequenced on an Illumina MiSeq platform (2 × 300 bp paired-end reads) at the facilities of the Scientific Park of Madrid (Spain).

    Article Title: Emergence and evolution of chimeric pseudogenes (φgenes) contribute to genetic and functional diversity of the human genome
    Article Snippet: RNA extraction from cell lines and primary cultures performed using TRIzol reagent (RNAiso Plus TAKARA, 9108) was followed by complementary DNA (cDNA) synthesis and quantification (DeNovix spectrophotometer). .. PCR amplification was performed with TaKaRa DNA Polymerase (#R050B); amplified products were resolved on a 1.8% agarose gel (Sigma–Aldrich, #A9539-100G), and resulting bands were excised and purified using the QIAEX II Gel Extraction Kit (Qiagen #20021, #20051). .. 5′/3′ RACE kit (TAKARA, Cat. No. 634858) was used for synthesis of cDNA synthesis and RACE PCR.

    Purification:

    Article Title: Use of Ligilactobacillus salivarius SP36 as an Adjunct Culture by an Artisan Dairy and Isolation of New Autochthonous Strains with Technological Potential for Cheesemaking
    Article Snippet: The concentration of PCR products was determined using a 2100 Bioanalyzer (Agilent, Santa Clara, CA, USA). .. Barcoded products were pooled at approximately equimolar concentrations and run on a preparative agarose gel, and the correct band size was excised and purified using a QIAEX II Gel Extraction Kit (Qiagen). .. The pooled amplicons were quantified with PicoGreen (BMG Labtech, Jena, Germany) and sequenced on an Illumina MiSeq platform (2 × 300 bp paired-end reads) at the facilities of the Scientific Park of Madrid (Spain).

    Article Title: New Haplotype of Bartonella sp. in Haematopota pluvialis (Linnaeus, 1758).
    Article Snippet: ; Gdańsk; Poland) using a ChemiDoc MP imaging system (Bio-Rad, Hercules, CA, USA). .. PCR products were purified using the QIAEX II Gel Extraction Kit (Qiagen, Hilden, Germany) according to the manufacturer’s protocol and then sequenced by Genomed (Warsaw, Poland). ..

    Article Title: Emergence and evolution of chimeric pseudogenes (φgenes) contribute to genetic and functional diversity of the human genome
    Article Snippet: RNA extraction from cell lines and primary cultures performed using TRIzol reagent (RNAiso Plus TAKARA, 9108) was followed by complementary DNA (cDNA) synthesis and quantification (DeNovix spectrophotometer). .. PCR amplification was performed with TaKaRa DNA Polymerase (#R050B); amplified products were resolved on a 1.8% agarose gel (Sigma–Aldrich, #A9539-100G), and resulting bands were excised and purified using the QIAEX II Gel Extraction Kit (Qiagen #20021, #20051). .. 5′/3′ RACE kit (TAKARA, Cat. No. 634858) was used for synthesis of cDNA synthesis and RACE PCR.

    other:

    Article Title: RNA-binding proteins TDP-43 and FUS promote R-loop resolution and regulate transcription termination
    Article Snippet: Primary antibodies 1:50-1:100 in PBST + 30 mg/ml BSA (Roche, 10735108001) were added to cells for staining overnight at 4 °C.

    Article Title: Modulation of biomolecular condensation of alpha-synuclein variants by eprodisate.
    Article Snippet: Fetal bovine serum (FBS), Ham’s F-12 (Kaighn’s, F-12K), opti-MEM reduced serum medium, lipofectamine 3000, P3000, MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) were purchased from Invitrogen Corporation, California, USA.

    Variant Assay:

    Article Title: Mosaic variants in the LIM homeobox 1 (LHX1) gene contribute to Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.
    Article Snippet: Infertility is a common reproductive problem affecting 10–15% of individuals (Collins and Van Steirteghem 2004).. Causes may include ovulation disorders, endometriosis, sperm abnormalities, and/or uterine/tubal conditions.. Müllerian duct (MD) anomalies are relatively common congenital disorders that cause abnormal uterine and vaginal development, which may predispose to infertility and miscarriage.



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    Image Search Results


    ( A ) The expression vector was subsequently inserted into the λ phage, generating the recombinant NBPs, ( B ) Different cell types were infected with the indicated recombinant λ NBPs at an MOI of 10 PFU/cell and apoptin transcription was analyzed by RT-PCR, ( C ) RT-PCR result for λ ZAP-CMV vector treated cells that have no expression of apoptin, ( D ) Western blot analysis to detect apoptin protein from cells supernatants and lysates. To analyze apoptin expression, the cells were infected with the indicated recombinant NBPs. Purified apoptin was used as a positive control and CAV infected BT-474 cell was used as a negative control.

    Journal: PLoS ONE

    Article Title: λ Phage Nanobioparticle Expressing Apoptin Efficiently Suppress Human Breast Carcinoma Tumor Growth In Vivo

    doi: 10.1371/journal.pone.0079907

    Figure Lengend Snippet: ( A ) The expression vector was subsequently inserted into the λ phage, generating the recombinant NBPs, ( B ) Different cell types were infected with the indicated recombinant λ NBPs at an MOI of 10 PFU/cell and apoptin transcription was analyzed by RT-PCR, ( C ) RT-PCR result for λ ZAP-CMV vector treated cells that have no expression of apoptin, ( D ) Western blot analysis to detect apoptin protein from cells supernatants and lysates. To analyze apoptin expression, the cells were infected with the indicated recombinant NBPs. Purified apoptin was used as a positive control and CAV infected BT-474 cell was used as a negative control.

    Article Snippet: Large scale NBPs containing λ ZAP-CMV-apoptin expressing vector was conducted in 1 l of M9 medium (Sigma-Aldrich, USA) containing ampicillin (Sigma, USA).

    Techniques: Expressing, Plasmid Preparation, Recombinant, Infection, Reverse Transcription Polymerase Chain Reaction, Western Blot, Purification, Positive Control, Negative Control

    Immunostaining of apoptin protein showed that in can express in breast carcinoma cell lines after 12λ ZAP-CMV vector have not any apoptosis after 36 h as same as untreated cells.

    Journal: PLoS ONE

    Article Title: λ Phage Nanobioparticle Expressing Apoptin Efficiently Suppress Human Breast Carcinoma Tumor Growth In Vivo

    doi: 10.1371/journal.pone.0079907

    Figure Lengend Snippet: Immunostaining of apoptin protein showed that in can express in breast carcinoma cell lines after 12λ ZAP-CMV vector have not any apoptosis after 36 h as same as untreated cells.

    Article Snippet: Large scale NBPs containing λ ZAP-CMV-apoptin expressing vector was conducted in 1 l of M9 medium (Sigma-Aldrich, USA) containing ampicillin (Sigma, USA).

    Techniques: Immunostaining, Plasmid Preparation

    BT-474, SKBR-3 and ZR-75 cells were examined after 36 h of transfection by flowcytometry. All the cell lines were susceptible to NBPs apoptin-induced apoptosis. We have not apoptosis in vector treated group and untreated group.

    Journal: PLoS ONE

    Article Title: λ Phage Nanobioparticle Expressing Apoptin Efficiently Suppress Human Breast Carcinoma Tumor Growth In Vivo

    doi: 10.1371/journal.pone.0079907

    Figure Lengend Snippet: BT-474, SKBR-3 and ZR-75 cells were examined after 36 h of transfection by flowcytometry. All the cell lines were susceptible to NBPs apoptin-induced apoptosis. We have not apoptosis in vector treated group and untreated group.

    Article Snippet: Large scale NBPs containing λ ZAP-CMV-apoptin expressing vector was conducted in 1 l of M9 medium (Sigma-Aldrich, USA) containing ampicillin (Sigma, USA).

    Techniques: Transfection, Plasmid Preparation

    BT-474 breast carcinoma cell line transfected with λ ZAP-CMV-apoptin, λ ZAP-CMV vector and λ phage (vehicle) construct stained with FITC immunostaining and then visualized by fluorescence microscopy. There was no sign of cell necrosis after the treatments. There is only apoptotic morphology of cells after treatment with λ ZAP-CMV-apoptin.

    Journal: PLoS ONE

    Article Title: λ Phage Nanobioparticle Expressing Apoptin Efficiently Suppress Human Breast Carcinoma Tumor Growth In Vivo

    doi: 10.1371/journal.pone.0079907

    Figure Lengend Snippet: BT-474 breast carcinoma cell line transfected with λ ZAP-CMV-apoptin, λ ZAP-CMV vector and λ phage (vehicle) construct stained with FITC immunostaining and then visualized by fluorescence microscopy. There was no sign of cell necrosis after the treatments. There is only apoptotic morphology of cells after treatment with λ ZAP-CMV-apoptin.

    Article Snippet: Large scale NBPs containing λ ZAP-CMV-apoptin expressing vector was conducted in 1 l of M9 medium (Sigma-Aldrich, USA) containing ampicillin (Sigma, USA).

    Techniques: Transfection, Plasmid Preparation, Construct, Staining, Immunostaining, Fluorescence, Microscopy

    ( A ) Histochemistry analysis of tumor tissue sections showing apoptotic changes. The untreated tumor tissue contains many dividing cells. After 96 h treatment with NBPs there are a few cells maintained in the tumor tissue that could proliferate. Tumor growth was markedly suppressed in the apoptin treated group, ( B ) Histological examination of other organs (brain and heart) in tumor bearing mice that is not involved in the pathological changes of BT-474 cells. There are no changes in morphology of the brain and/or heart tissues and they are as same as control groups.

    Journal: PLoS ONE

    Article Title: λ Phage Nanobioparticle Expressing Apoptin Efficiently Suppress Human Breast Carcinoma Tumor Growth In Vivo

    doi: 10.1371/journal.pone.0079907

    Figure Lengend Snippet: ( A ) Histochemistry analysis of tumor tissue sections showing apoptotic changes. The untreated tumor tissue contains many dividing cells. After 96 h treatment with NBPs there are a few cells maintained in the tumor tissue that could proliferate. Tumor growth was markedly suppressed in the apoptin treated group, ( B ) Histological examination of other organs (brain and heart) in tumor bearing mice that is not involved in the pathological changes of BT-474 cells. There are no changes in morphology of the brain and/or heart tissues and they are as same as control groups.

    Article Snippet: Large scale NBPs containing λ ZAP-CMV-apoptin expressing vector was conducted in 1 l of M9 medium (Sigma-Aldrich, USA) containing ampicillin (Sigma, USA).

    Techniques:

    ( A ) TUNEL analysis revealed that apoptin induces the apoptotic activity in neoplasms (Magnification: ×400), ( B ) Analysis of survival. Mice treated with NBPs survived longer than the mice in the other 2 groups and the mean survival of NBPs-infected mice were >90 days (p<0.005). Fifty days after the beginning of the treatment, 90% of the animals infected by NBPs were alive, while at this time 100% of vector treated mice and 100% of saline-treated mice had died. Tumor-bearing mice treated with saline had a mean survival of 50 days.

    Journal: PLoS ONE

    Article Title: λ Phage Nanobioparticle Expressing Apoptin Efficiently Suppress Human Breast Carcinoma Tumor Growth In Vivo

    doi: 10.1371/journal.pone.0079907

    Figure Lengend Snippet: ( A ) TUNEL analysis revealed that apoptin induces the apoptotic activity in neoplasms (Magnification: ×400), ( B ) Analysis of survival. Mice treated with NBPs survived longer than the mice in the other 2 groups and the mean survival of NBPs-infected mice were >90 days (p<0.005). Fifty days after the beginning of the treatment, 90% of the animals infected by NBPs were alive, while at this time 100% of vector treated mice and 100% of saline-treated mice had died. Tumor-bearing mice treated with saline had a mean survival of 50 days.

    Article Snippet: Large scale NBPs containing λ ZAP-CMV-apoptin expressing vector was conducted in 1 l of M9 medium (Sigma-Aldrich, USA) containing ampicillin (Sigma, USA).

    Techniques: TUNEL Assay, Activity Assay, Infection, Plasmid Preparation