native double stranded calf thymus ct dna  (Worthington Biochemical)


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    Structured Review

    Worthington Biochemical native double stranded calf thymus ct dna
    The ability of polymers PAMAM, HDMBr, and CDP to inhibit binding of a murine monoclonal <t>anti-DNA</t> antibody QB1 to DNA was tested <t>by</t> <t>ELISA.</t> Binding of QB1 at 35 ng/ml final concentration was assayed by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 10 ng/ml to 1,250 ng/ml. Control wells had buffer alone. Antibody was measured as described in Experimental Procedures. The OD 450 values of 3 wells of each polymer concentration or of 6 wells without polymer were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for PAMAM; squares show data for HDMBr; triangles show data for CDP.
    Native Double Stranded Calf Thymus Ct Dna, supplied by Worthington Biochemical, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/native double stranded calf thymus ct dna/product/Worthington Biochemical
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    native double stranded calf thymus ct dna - by Bioz Stars, 2024-07
    93/100 stars

    Images

    1) Product Images from "The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers"

    Article Title: The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0040862

    The ability of polymers PAMAM, HDMBr, and CDP to inhibit binding of a murine monoclonal anti-DNA antibody QB1 to DNA was tested by ELISA. Binding of QB1 at 35 ng/ml final concentration was assayed by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 10 ng/ml to 1,250 ng/ml. Control wells had buffer alone. Antibody was measured as described in Experimental Procedures. The OD 450 values of 3 wells of each polymer concentration or of 6 wells without polymer were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for PAMAM; squares show data for HDMBr; triangles show data for CDP.
    Figure Legend Snippet: The ability of polymers PAMAM, HDMBr, and CDP to inhibit binding of a murine monoclonal anti-DNA antibody QB1 to DNA was tested by ELISA. Binding of QB1 at 35 ng/ml final concentration was assayed by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 10 ng/ml to 1,250 ng/ml. Control wells had buffer alone. Antibody was measured as described in Experimental Procedures. The OD 450 values of 3 wells of each polymer concentration or of 6 wells without polymer were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for PAMAM; squares show data for HDMBr; triangles show data for CDP.

    Techniques Used: Binding Assay, Enzyme-linked Immunosorbent Assay, Concentration Assay

    The ability of polymers PAMAM, HDMBr, and CDP to inhibit DNA binding by anti-DNA antibodies in three SLE patient plasmas to DNA was tested by ELISA. Binding by antibodies in Plasma 1 (final dilution 1/1,000), Plasma 2 (final dilution 1/2,800), and Plasma 3 (final dilution 1/3,000) was assayed in the presence of PAMAM, HDMBr, or CDP at final concentrations ranging from 300 ng/ml to 10,000 ng/ml or with dilution buffer alone. Antibody levels were determined by ELISA as described in . The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.
    Figure Legend Snippet: The ability of polymers PAMAM, HDMBr, and CDP to inhibit DNA binding by anti-DNA antibodies in three SLE patient plasmas to DNA was tested by ELISA. Binding by antibodies in Plasma 1 (final dilution 1/1,000), Plasma 2 (final dilution 1/2,800), and Plasma 3 (final dilution 1/3,000) was assayed in the presence of PAMAM, HDMBr, or CDP at final concentrations ranging from 300 ng/ml to 10,000 ng/ml or with dilution buffer alone. Antibody levels were determined by ELISA as described in . The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.

    Techniques Used: Binding Assay, Enzyme-linked Immunosorbent Assay

    Native CT DNA was biotinylated and then captured in ELISA plate wells coated with streptavidin. The binding of Plasma 1 (final dilution 1/3,500), Plasma 2 (final dilution 1/8,000), and Plasma 3 (final dilution 1/4,500) was measured by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 80 ng/ml to 10,000 ng/ml or with dilution buffer alone. The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.
    Figure Legend Snippet: Native CT DNA was biotinylated and then captured in ELISA plate wells coated with streptavidin. The binding of Plasma 1 (final dilution 1/3,500), Plasma 2 (final dilution 1/8,000), and Plasma 3 (final dilution 1/4,500) was measured by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 80 ng/ml to 10,000 ng/ml or with dilution buffer alone. The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.

    Techniques Used: Enzyme-linked Immunosorbent Assay, Binding Assay

    In this assay, 50 µl/well of Plasma 1 diluted 1/1,700, Plasma 2 diluted 1/3,950, and Plasma 3 diluted 1/2,250 were incubated in wells of microtiter plates with biotinylated DNA bound to streptavidin. After 1 hour to allow the formation of immune complexes, 50 µl of dilutions of PAMAM, HDMBr, or CDP or 50 µl of dilution buffer alone were then added to produce concentrations of the polymers of 10,000 ng/ml, 2,500 ng/ml, 620 ng/ml, 160 ng/ml or 0 ng/ml. Antibody binding was then determined by ELISA. The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.
    Figure Legend Snippet: In this assay, 50 µl/well of Plasma 1 diluted 1/1,700, Plasma 2 diluted 1/3,950, and Plasma 3 diluted 1/2,250 were incubated in wells of microtiter plates with biotinylated DNA bound to streptavidin. After 1 hour to allow the formation of immune complexes, 50 µl of dilutions of PAMAM, HDMBr, or CDP or 50 µl of dilution buffer alone were then added to produce concentrations of the polymers of 10,000 ng/ml, 2,500 ng/ml, 620 ng/ml, 160 ng/ml or 0 ng/ml. Antibody binding was then determined by ELISA. The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.

    Techniques Used: Incubation, Binding Assay, Enzyme-linked Immunosorbent Assay

    native double stranded calf thymus ct dna  (Worthington Biochemical)


    Bioz Verified Symbol Worthington Biochemical is a verified supplier
    Bioz Manufacturer Symbol Worthington Biochemical manufactures this product  
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  • 93

    Structured Review

    Worthington Biochemical native double stranded calf thymus ct dna
    The ability of polymers PAMAM, HDMBr, and CDP to inhibit binding of a murine monoclonal <t>anti-DNA</t> antibody QB1 to DNA was tested <t>by</t> <t>ELISA.</t> Binding of QB1 at 35 ng/ml final concentration was assayed by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 10 ng/ml to 1,250 ng/ml. Control wells had buffer alone. Antibody was measured as described in Experimental Procedures. The OD 450 values of 3 wells of each polymer concentration or of 6 wells without polymer were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for PAMAM; squares show data for HDMBr; triangles show data for CDP.
    Native Double Stranded Calf Thymus Ct Dna, supplied by Worthington Biochemical, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/native double stranded calf thymus ct dna/product/Worthington Biochemical
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    native double stranded calf thymus ct dna - by Bioz Stars, 2024-07
    93/100 stars

    Images

    1) Product Images from "The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers"

    Article Title: The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0040862

    The ability of polymers PAMAM, HDMBr, and CDP to inhibit binding of a murine monoclonal anti-DNA antibody QB1 to DNA was tested by ELISA. Binding of QB1 at 35 ng/ml final concentration was assayed by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 10 ng/ml to 1,250 ng/ml. Control wells had buffer alone. Antibody was measured as described in Experimental Procedures. The OD 450 values of 3 wells of each polymer concentration or of 6 wells without polymer were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for PAMAM; squares show data for HDMBr; triangles show data for CDP.
    Figure Legend Snippet: The ability of polymers PAMAM, HDMBr, and CDP to inhibit binding of a murine monoclonal anti-DNA antibody QB1 to DNA was tested by ELISA. Binding of QB1 at 35 ng/ml final concentration was assayed by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 10 ng/ml to 1,250 ng/ml. Control wells had buffer alone. Antibody was measured as described in Experimental Procedures. The OD 450 values of 3 wells of each polymer concentration or of 6 wells without polymer were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for PAMAM; squares show data for HDMBr; triangles show data for CDP.

    Techniques Used: Binding Assay, Enzyme-linked Immunosorbent Assay, Concentration Assay

    The ability of polymers PAMAM, HDMBr, and CDP to inhibit DNA binding by anti-DNA antibodies in three SLE patient plasmas to DNA was tested by ELISA. Binding by antibodies in Plasma 1 (final dilution 1/1,000), Plasma 2 (final dilution 1/2,800), and Plasma 3 (final dilution 1/3,000) was assayed in the presence of PAMAM, HDMBr, or CDP at final concentrations ranging from 300 ng/ml to 10,000 ng/ml or with dilution buffer alone. Antibody levels were determined by ELISA as described in . The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.
    Figure Legend Snippet: The ability of polymers PAMAM, HDMBr, and CDP to inhibit DNA binding by anti-DNA antibodies in three SLE patient plasmas to DNA was tested by ELISA. Binding by antibodies in Plasma 1 (final dilution 1/1,000), Plasma 2 (final dilution 1/2,800), and Plasma 3 (final dilution 1/3,000) was assayed in the presence of PAMAM, HDMBr, or CDP at final concentrations ranging from 300 ng/ml to 10,000 ng/ml or with dilution buffer alone. Antibody levels were determined by ELISA as described in . The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.

    Techniques Used: Binding Assay, Enzyme-linked Immunosorbent Assay

    Native CT DNA was biotinylated and then captured in ELISA plate wells coated with streptavidin. The binding of Plasma 1 (final dilution 1/3,500), Plasma 2 (final dilution 1/8,000), and Plasma 3 (final dilution 1/4,500) was measured by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 80 ng/ml to 10,000 ng/ml or with dilution buffer alone. The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.
    Figure Legend Snippet: Native CT DNA was biotinylated and then captured in ELISA plate wells coated with streptavidin. The binding of Plasma 1 (final dilution 1/3,500), Plasma 2 (final dilution 1/8,000), and Plasma 3 (final dilution 1/4,500) was measured by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 80 ng/ml to 10,000 ng/ml or with dilution buffer alone. The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.

    Techniques Used: Enzyme-linked Immunosorbent Assay, Binding Assay

    In this assay, 50 µl/well of Plasma 1 diluted 1/1,700, Plasma 2 diluted 1/3,950, and Plasma 3 diluted 1/2,250 were incubated in wells of microtiter plates with biotinylated DNA bound to streptavidin. After 1 hour to allow the formation of immune complexes, 50 µl of dilutions of PAMAM, HDMBr, or CDP or 50 µl of dilution buffer alone were then added to produce concentrations of the polymers of 10,000 ng/ml, 2,500 ng/ml, 620 ng/ml, 160 ng/ml or 0 ng/ml. Antibody binding was then determined by ELISA. The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.
    Figure Legend Snippet: In this assay, 50 µl/well of Plasma 1 diluted 1/1,700, Plasma 2 diluted 1/3,950, and Plasma 3 diluted 1/2,250 were incubated in wells of microtiter plates with biotinylated DNA bound to streptavidin. After 1 hour to allow the formation of immune complexes, 50 µl of dilutions of PAMAM, HDMBr, or CDP or 50 µl of dilution buffer alone were then added to produce concentrations of the polymers of 10,000 ng/ml, 2,500 ng/ml, 620 ng/ml, 160 ng/ml or 0 ng/ml. Antibody binding was then determined by ELISA. The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.

    Techniques Used: Incubation, Binding Assay, Enzyme-linked Immunosorbent Assay

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    Worthington Biochemical native double stranded calf thymus ct dna
    The ability of polymers PAMAM, HDMBr, and CDP to inhibit binding of a murine monoclonal <t>anti-DNA</t> antibody QB1 to DNA was tested <t>by</t> <t>ELISA.</t> Binding of QB1 at 35 ng/ml final concentration was assayed by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 10 ng/ml to 1,250 ng/ml. Control wells had buffer alone. Antibody was measured as described in Experimental Procedures. The OD 450 values of 3 wells of each polymer concentration or of 6 wells without polymer were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for PAMAM; squares show data for HDMBr; triangles show data for CDP.
    Native Double Stranded Calf Thymus Ct Dna, supplied by Worthington Biochemical, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/native double stranded calf thymus ct dna/product/Worthington Biochemical
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    native double stranded calf thymus ct dna - by Bioz Stars, 2024-07
    93/100 stars
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    The ability of polymers PAMAM, HDMBr, and CDP to inhibit binding of a murine monoclonal anti-DNA antibody QB1 to DNA was tested by ELISA. Binding of QB1 at 35 ng/ml final concentration was assayed by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 10 ng/ml to 1,250 ng/ml. Control wells had buffer alone. Antibody was measured as described in Experimental Procedures. The OD 450 values of 3 wells of each polymer concentration or of 6 wells without polymer were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for PAMAM; squares show data for HDMBr; triangles show data for CDP.

    Journal: PLoS ONE

    Article Title: The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers

    doi: 10.1371/journal.pone.0040862

    Figure Lengend Snippet: The ability of polymers PAMAM, HDMBr, and CDP to inhibit binding of a murine monoclonal anti-DNA antibody QB1 to DNA was tested by ELISA. Binding of QB1 at 35 ng/ml final concentration was assayed by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 10 ng/ml to 1,250 ng/ml. Control wells had buffer alone. Antibody was measured as described in Experimental Procedures. The OD 450 values of 3 wells of each polymer concentration or of 6 wells without polymer were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for PAMAM; squares show data for HDMBr; triangles show data for CDP.

    Article Snippet: For the direct binding assay, wells of ELISA plates were coated with 5 µg/ml native double stranded calf thymus (CT) DNA (Worthington Biochemical, Lakewood, NJ) in 1 x SSC (150 mM NaCl, 15 mM Na citrate, pH 7) overnight at 4°C.

    Techniques: Binding Assay, Enzyme-linked Immunosorbent Assay, Concentration Assay

    The ability of polymers PAMAM, HDMBr, and CDP to inhibit DNA binding by anti-DNA antibodies in three SLE patient plasmas to DNA was tested by ELISA. Binding by antibodies in Plasma 1 (final dilution 1/1,000), Plasma 2 (final dilution 1/2,800), and Plasma 3 (final dilution 1/3,000) was assayed in the presence of PAMAM, HDMBr, or CDP at final concentrations ranging from 300 ng/ml to 10,000 ng/ml or with dilution buffer alone. Antibody levels were determined by ELISA as described in . The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.

    Journal: PLoS ONE

    Article Title: The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers

    doi: 10.1371/journal.pone.0040862

    Figure Lengend Snippet: The ability of polymers PAMAM, HDMBr, and CDP to inhibit DNA binding by anti-DNA antibodies in three SLE patient plasmas to DNA was tested by ELISA. Binding by antibodies in Plasma 1 (final dilution 1/1,000), Plasma 2 (final dilution 1/2,800), and Plasma 3 (final dilution 1/3,000) was assayed in the presence of PAMAM, HDMBr, or CDP at final concentrations ranging from 300 ng/ml to 10,000 ng/ml or with dilution buffer alone. Antibody levels were determined by ELISA as described in . The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.

    Article Snippet: For the direct binding assay, wells of ELISA plates were coated with 5 µg/ml native double stranded calf thymus (CT) DNA (Worthington Biochemical, Lakewood, NJ) in 1 x SSC (150 mM NaCl, 15 mM Na citrate, pH 7) overnight at 4°C.

    Techniques: Binding Assay, Enzyme-linked Immunosorbent Assay

    Native CT DNA was biotinylated and then captured in ELISA plate wells coated with streptavidin. The binding of Plasma 1 (final dilution 1/3,500), Plasma 2 (final dilution 1/8,000), and Plasma 3 (final dilution 1/4,500) was measured by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 80 ng/ml to 10,000 ng/ml or with dilution buffer alone. The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.

    Journal: PLoS ONE

    Article Title: The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers

    doi: 10.1371/journal.pone.0040862

    Figure Lengend Snippet: Native CT DNA was biotinylated and then captured in ELISA plate wells coated with streptavidin. The binding of Plasma 1 (final dilution 1/3,500), Plasma 2 (final dilution 1/8,000), and Plasma 3 (final dilution 1/4,500) was measured by ELISA in the presence of PAMAM, HDMBr, or CDP at final concentrations from 80 ng/ml to 10,000 ng/ml or with dilution buffer alone. The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.

    Article Snippet: For the direct binding assay, wells of ELISA plates were coated with 5 µg/ml native double stranded calf thymus (CT) DNA (Worthington Biochemical, Lakewood, NJ) in 1 x SSC (150 mM NaCl, 15 mM Na citrate, pH 7) overnight at 4°C.

    Techniques: Enzyme-linked Immunosorbent Assay, Binding Assay

    In this assay, 50 µl/well of Plasma 1 diluted 1/1,700, Plasma 2 diluted 1/3,950, and Plasma 3 diluted 1/2,250 were incubated in wells of microtiter plates with biotinylated DNA bound to streptavidin. After 1 hour to allow the formation of immune complexes, 50 µl of dilutions of PAMAM, HDMBr, or CDP or 50 µl of dilution buffer alone were then added to produce concentrations of the polymers of 10,000 ng/ml, 2,500 ng/ml, 620 ng/ml, 160 ng/ml or 0 ng/ml. Antibody binding was then determined by ELISA. The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.

    Journal: PLoS ONE

    Article Title: The Inhibition of Anti-DNA Binding to DNA by Nucleic Acid Binding Polymers

    doi: 10.1371/journal.pone.0040862

    Figure Lengend Snippet: In this assay, 50 µl/well of Plasma 1 diluted 1/1,700, Plasma 2 diluted 1/3,950, and Plasma 3 diluted 1/2,250 were incubated in wells of microtiter plates with biotinylated DNA bound to streptavidin. After 1 hour to allow the formation of immune complexes, 50 µl of dilutions of PAMAM, HDMBr, or CDP or 50 µl of dilution buffer alone were then added to produce concentrations of the polymers of 10,000 ng/ml, 2,500 ng/ml, 620 ng/ml, 160 ng/ml or 0 ng/ml. Antibody binding was then determined by ELISA. The OD 450 values of 2 wells for each condition were averaged. Each point shown is 100% x average OD 450 with polymer/average OD 450 without polymer. Circles show data for Plasma 1; squares show data for Plasma 2; triangles show data for Plasma 3.

    Article Snippet: For the direct binding assay, wells of ELISA plates were coated with 5 µg/ml native double stranded calf thymus (CT) DNA (Worthington Biochemical, Lakewood, NJ) in 1 x SSC (150 mM NaCl, 15 mM Na citrate, pH 7) overnight at 4°C.

    Techniques: Incubation, Binding Assay, Enzyme-linked Immunosorbent Assay