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rabbit polyclonal anti gfp antiserum  (Bio-Rad)


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    Bio-Rad rabbit polyclonal anti gfp antiserum
    Rabbit Polyclonal Anti Gfp Antiserum, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 94/100, based on 66 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal anti gfp antiserum/product/Bio-Rad
    Average 94 stars, based on 66 article reviews
    rabbit polyclonal anti gfp antiserum - by Bioz Stars, 2026-06
    94/100 stars

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    Thermo Fisher anti-gfp polyclonal rabbit antiserum
    PARP is active and necessary for efficient apoptosis in NS1-transfected cells. A. Immunoprecipitated <t>GFP/NS1</t> protein was poly(ADP ribose)ylated, as shown by a band at 100 kd on the blot probed with anti-poly ADP ribose (PAR, left blot) antibodies. The blots were stripped and reprobed <t>with</t> <t>anti-GFP</t> (right), showing that PAR colocalizes with the GFP/NS1 fusion protein. GFP alone is not ribosylated, as evidenced by the lack of a PAR band corresponding to GFP at 37 kD. Blots shown are representative of three independent experiments. B. PARP activity is necessary for optimal NS1-induced apoptosis. Addition of the PARP inhibitor 5-aminoisoquinolinone (5AIQ) to GFP/NS1 expressing HepG2 cells reduced apoptosis by 57% ( p <0.003). Addition of 5-aminoisoquinolinone had no effect on the GFP transfected cells. N=3, error bars indicate the range of values.
    Anti Gfp Polyclonal Rabbit Antiserum, supplied by Thermo Fisher, 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/anti-gfp polyclonal rabbit antiserum/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
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    90
    Thermo Fisher polyclonal rabbit anti-gfp antiserum
    PARP is active and necessary for efficient apoptosis in NS1-transfected cells. A. Immunoprecipitated <t>GFP/NS1</t> protein was poly(ADP ribose)ylated, as shown by a band at 100 kd on the blot probed with anti-poly ADP ribose (PAR, left blot) antibodies. The blots were stripped and reprobed <t>with</t> <t>anti-GFP</t> (right), showing that PAR colocalizes with the GFP/NS1 fusion protein. GFP alone is not ribosylated, as evidenced by the lack of a PAR band corresponding to GFP at 37 kD. Blots shown are representative of three independent experiments. B. PARP activity is necessary for optimal NS1-induced apoptosis. Addition of the PARP inhibitor 5-aminoisoquinolinone (5AIQ) to GFP/NS1 expressing HepG2 cells reduced apoptosis by 57% ( p <0.003). Addition of 5-aminoisoquinolinone had no effect on the GFP transfected cells. N=3, error bars indicate the range of values.
    Polyclonal Rabbit Anti Gfp Antiserum, supplied by Thermo Fisher, 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/polyclonal rabbit anti-gfp antiserum/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    polyclonal rabbit anti-gfp antiserum - by Bioz Stars, 2026-06
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    Thermo Fisher rabbit polyclonal anti gfp antiserum
    PARP is active and necessary for efficient apoptosis in NS1-transfected cells. A. Immunoprecipitated <t>GFP/NS1</t> protein was poly(ADP ribose)ylated, as shown by a band at 100 kd on the blot probed with anti-poly ADP ribose (PAR, left blot) antibodies. The blots were stripped and reprobed <t>with</t> <t>anti-GFP</t> (right), showing that PAR colocalizes with the GFP/NS1 fusion protein. GFP alone is not ribosylated, as evidenced by the lack of a PAR band corresponding to GFP at 37 kD. Blots shown are representative of three independent experiments. B. PARP activity is necessary for optimal NS1-induced apoptosis. Addition of the PARP inhibitor 5-aminoisoquinolinone (5AIQ) to GFP/NS1 expressing HepG2 cells reduced apoptosis by 57% ( p <0.003). Addition of 5-aminoisoquinolinone had no effect on the GFP transfected cells. N=3, error bars indicate the range of values.
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    Synaptic Systems anti-gfp polyclonal rabbit antiserum
    PARP is active and necessary for efficient apoptosis in NS1-transfected cells. A. Immunoprecipitated <t>GFP/NS1</t> protein was poly(ADP ribose)ylated, as shown by a band at 100 kd on the blot probed with anti-poly ADP ribose (PAR, left blot) antibodies. The blots were stripped and reprobed <t>with</t> <t>anti-GFP</t> (right), showing that PAR colocalizes with the GFP/NS1 fusion protein. GFP alone is not ribosylated, as evidenced by the lack of a PAR band corresponding to GFP at 37 kD. Blots shown are representative of three independent experiments. B. PARP activity is necessary for optimal NS1-induced apoptosis. Addition of the PARP inhibitor 5-aminoisoquinolinone (5AIQ) to GFP/NS1 expressing HepG2 cells reduced apoptosis by 57% ( p <0.003). Addition of 5-aminoisoquinolinone had no effect on the GFP transfected cells. N=3, error bars indicate the range of values.
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    Bio-Rad rabbit polyclonal anti gfp antiserum
    PARP is active and necessary for efficient apoptosis in NS1-transfected cells. A. Immunoprecipitated <t>GFP/NS1</t> protein was poly(ADP ribose)ylated, as shown by a band at 100 kd on the blot probed with anti-poly ADP ribose (PAR, left blot) antibodies. The blots were stripped and reprobed <t>with</t> <t>anti-GFP</t> (right), showing that PAR colocalizes with the GFP/NS1 fusion protein. GFP alone is not ribosylated, as evidenced by the lack of a PAR band corresponding to GFP at 37 kD. Blots shown are representative of three independent experiments. B. PARP activity is necessary for optimal NS1-induced apoptosis. Addition of the PARP inhibitor 5-aminoisoquinolinone (5AIQ) to GFP/NS1 expressing HepG2 cells reduced apoptosis by 57% ( p <0.003). Addition of 5-aminoisoquinolinone had no effect on the GFP transfected cells. N=3, error bars indicate the range of values.
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    https://www.bioz.com/result/rabbit polyclonal anti gfp antiserum/product/Bio-Rad
    Average 94 stars, based on 1 article reviews
    rabbit polyclonal anti gfp antiserum - by Bioz Stars, 2026-06
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    Torrey Pines Biolabs rabbit anti-gfp polyclonal antiserum tp401
    KEY RESOURCES TABLE
    Rabbit Anti Gfp Polyclonal Antiserum Tp401, supplied by Torrey Pines Biolabs, 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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    95
    Torrey Pines Biolabs rabbit anti gfp polyclonal antiserum
    KEY RESOURCES TABLE
    Rabbit Anti Gfp Polyclonal Antiserum, supplied by Torrey Pines Biolabs, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit anti gfp polyclonal antiserum/product/Torrey Pines Biolabs
    Average 95 stars, based on 1 article reviews
    rabbit anti gfp polyclonal antiserum - by Bioz Stars, 2026-06
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    PARP is active and necessary for efficient apoptosis in NS1-transfected cells. A. Immunoprecipitated GFP/NS1 protein was poly(ADP ribose)ylated, as shown by a band at 100 kd on the blot probed with anti-poly ADP ribose (PAR, left blot) antibodies. The blots were stripped and reprobed with anti-GFP (right), showing that PAR colocalizes with the GFP/NS1 fusion protein. GFP alone is not ribosylated, as evidenced by the lack of a PAR band corresponding to GFP at 37 kD. Blots shown are representative of three independent experiments. B. PARP activity is necessary for optimal NS1-induced apoptosis. Addition of the PARP inhibitor 5-aminoisoquinolinone (5AIQ) to GFP/NS1 expressing HepG2 cells reduced apoptosis by 57% ( p <0.003). Addition of 5-aminoisoquinolinone had no effect on the GFP transfected cells. N=3, error bars indicate the range of values.

    Journal: International Journal of Medical Sciences

    Article Title: Parvovirus B19 Nonstructural Protein-Induced Damage of Cellular DNA and Resultant Apoptosis

    doi:

    Figure Lengend Snippet: PARP is active and necessary for efficient apoptosis in NS1-transfected cells. A. Immunoprecipitated GFP/NS1 protein was poly(ADP ribose)ylated, as shown by a band at 100 kd on the blot probed with anti-poly ADP ribose (PAR, left blot) antibodies. The blots were stripped and reprobed with anti-GFP (right), showing that PAR colocalizes with the GFP/NS1 fusion protein. GFP alone is not ribosylated, as evidenced by the lack of a PAR band corresponding to GFP at 37 kD. Blots shown are representative of three independent experiments. B. PARP activity is necessary for optimal NS1-induced apoptosis. Addition of the PARP inhibitor 5-aminoisoquinolinone (5AIQ) to GFP/NS1 expressing HepG2 cells reduced apoptosis by 57% ( p <0.003). Addition of 5-aminoisoquinolinone had no effect on the GFP transfected cells. N=3, error bars indicate the range of values.

    Article Snippet: Proteins were transferred to nitrocellulose membranes and bound with anti-GFP polyclonal rabbit antiserum (Invitrogen) or poly(ADP ribose) (PAR) monoclonal antibody (Pharmingen, San Diego, CA) at 1:5000 dilution.

    Techniques: Transfection, Immunoprecipitation, Activity Assay, Expressing

    KEY RESOURCES TABLE

    Journal: Cell reports

    Article Title: The miR-216a -Dot1l Regulatory Axis Is Necessary and Sufficient for Müller Glia Reprogramming during Retina Regeneration

    doi: 10.1016/j.celrep.2019.07.061

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Rabbit anti-GFP polyclonal antiserum , Torrey Pines Biolabs , TP401; RRID: AB_10013661.

    Techniques: Recombinant, Plasmid Preparation, cDNA Synthesis, SYBR Green Assay, Mutagenesis, Software

    KEY RESOURCES TABLE

    Journal: Cell reports

    Article Title: The miR-216a -Dot1l Regulatory Axis Is Necessary and Sufficient for Müller Glia Reprogramming during Retina Regeneration

    doi: 10.1016/j.celrep.2019.07.061

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Rabbit anti-GFP polyclonal antiserum , Torrey Pines Biolabs , TP401; RRID: AB_10013661.

    Techniques: Recombinant, Plasmid Preparation, SYBR Green Assay, Mutagenesis, Software