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au np afp antibody  (Biosynth Carbosynth)


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    Structured Review

    Biosynth Carbosynth au np afp antibody
    Figure 3. Scanometric identification of three protein cancer markers for eight different samples in buffer after two gold depositions. The concentration of each antigen was 1.4 pM. (1) All targets present; <t>(2)</t> <t>hCG</t> and PSA; (3) hCG and <t>AFP;</t> (4) PSA and AFP; (5) AFP; (6) PSA; (7) hCG; (8) no targets present. The gray scale images from the Verigene Reader system were converted into colored ones using GenePix Pro 6 software (Molecular Devices), and the exposure time was 200 ms.
    Au Np Afp Antibody, supplied by Biosynth Carbosynth, 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/product/au+np+afp+antibody/AFP+antibody/10__1021_slash_ac9018389-88-45-50
    Average 90 stars, based on 1 article reviews
    au np afp antibody - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "Microarray-Based Multiplexed Scanometric Immunoassay for Protein Cancer Markers Using Gold Nanoparticle Probes"

    Article Title: Microarray-Based Multiplexed Scanometric Immunoassay for Protein Cancer Markers Using Gold Nanoparticle Probes

    Journal: Analytical Chemistry

    doi: 10.1021/ac9018389

    Figure 3. Scanometric identification of three protein cancer markers for eight different samples in buffer after two gold depositions. The concentration of each antigen was 1.4 pM. (1) All targets present; (2) hCG and PSA; (3) hCG and AFP; (4) PSA and AFP; (5) AFP; (6) PSA; (7) hCG; (8) no targets present. The gray scale images from the Verigene Reader system were converted into colored ones using GenePix Pro 6 software (Molecular Devices), and the exposure time was 200 ms.
    Figure Legend Snippet: Figure 3. Scanometric identification of three protein cancer markers for eight different samples in buffer after two gold depositions. The concentration of each antigen was 1.4 pM. (1) All targets present; (2) hCG and PSA; (3) hCG and AFP; (4) PSA and AFP; (5) AFP; (6) PSA; (7) hCG; (8) no targets present. The gray scale images from the Verigene Reader system were converted into colored ones using GenePix Pro 6 software (Molecular Devices), and the exposure time was 200 ms.

    Techniques Used: Concentration Assay, Software

    Related Articles

    Concentration Assay:

    Article Title: Microarray-Based Multiplexed Scanometric Immunoassay for Protein Cancer Markers Using Gold Nanoparticle Probes
    Article Snippet: Antibodies and Antigens.Antibodies and Antigens.. The proteins used in the study were prostate specific antigen (PSA) (P3338, Sigma-Aldrich), the spotted PSA antibody (ab403, Abcam), the Au NP PSA antibody (AF1344, R&D Systems), R-fetoprotein antigen (APF) (A32260H, Biodesign International), the spotted AFP antibody (10-A05, clone M19301, Fitzgerald Industries International, Inc.), the Au NP AFP antibody (70-XG05, Fitzgerald Industries International, Inc.), human chorionic gonadotropin (HCG) (A81355M, Biodesign International), the spotted HCG antibody (E20579, Biodesign International), and the Au NP-monoclonal HCG antibody (E20106, Biodesign International).. Preparation of Antibody and Oligonucleotide Modified Gold Nanoparticles (Au NPs).Preparation of Antibody and Oligonucleotide Modified Gold Nanoparticles (Au NPs).

    Software:

    Article Title: Microarray-Based Multiplexed Scanometric Immunoassay for Protein Cancer Markers Using Gold Nanoparticle Probes
    Article Snippet: Antibodies and Antigens.Antibodies and Antigens.. The proteins used in the study were prostate specific antigen (PSA) (P3338, Sigma-Aldrich), the spotted PSA antibody (ab403, Abcam), the Au NP PSA antibody (AF1344, R&D Systems), R-fetoprotein antigen (APF) (A32260H, Biodesign International), the spotted AFP antibody (10-A05, clone M19301, Fitzgerald Industries International, Inc.), the Au NP AFP antibody (70-XG05, Fitzgerald Industries International, Inc.), human chorionic gonadotropin (HCG) (A81355M, Biodesign International), the spotted HCG antibody (E20579, Biodesign International), and the Au NP-monoclonal HCG antibody (E20106, Biodesign International).. Preparation of Antibody and Oligonucleotide Modified Gold Nanoparticles (Au NPs).Preparation of Antibody and Oligonucleotide Modified Gold Nanoparticles (Au NPs).



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    Biosynth Carbosynth au np afp antibody
    Figure 3. Scanometric identification of three protein cancer markers for eight different samples in buffer after two gold depositions. The concentration of each antigen was 1.4 pM. (1) All targets present; <t>(2)</t> <t>hCG</t> and PSA; (3) hCG and <t>AFP;</t> (4) PSA and AFP; (5) AFP; (6) PSA; (7) hCG; (8) no targets present. The gray scale images from the Verigene Reader system were converted into colored ones using GenePix Pro 6 software (Molecular Devices), and the exposure time was 200 ms.
    Au Np Afp Antibody, supplied by Biosynth Carbosynth, 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/product/au+np+afp+antibody/AFP+antibody/10__1021_slash_ac9018389-88-45-50
    Average 90 stars, based on 1 article reviews
    au np afp antibody - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

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    Figure 3. Scanometric identification of three protein cancer markers for eight different samples in buffer after two gold depositions. The concentration of each antigen was 1.4 pM. (1) All targets present; (2) hCG and PSA; (3) hCG and AFP; (4) PSA and AFP; (5) AFP; (6) PSA; (7) hCG; (8) no targets present. The gray scale images from the Verigene Reader system were converted into colored ones using GenePix Pro 6 software (Molecular Devices), and the exposure time was 200 ms.

    Journal: Analytical Chemistry

    Article Title: Microarray-Based Multiplexed Scanometric Immunoassay for Protein Cancer Markers Using Gold Nanoparticle Probes

    doi: 10.1021/ac9018389

    Figure Lengend Snippet: Figure 3. Scanometric identification of three protein cancer markers for eight different samples in buffer after two gold depositions. The concentration of each antigen was 1.4 pM. (1) All targets present; (2) hCG and PSA; (3) hCG and AFP; (4) PSA and AFP; (5) AFP; (6) PSA; (7) hCG; (8) no targets present. The gray scale images from the Verigene Reader system were converted into colored ones using GenePix Pro 6 software (Molecular Devices), and the exposure time was 200 ms.

    Article Snippet: The proteins used in the study were prostate specific antigen (PSA) (P3338, Sigma-Aldrich), the spotted PSA antibody (ab403, Abcam), the Au NP PSA antibody (AF1344, R&D Systems), R-fetoprotein antigen (APF) (A32260H, Biodesign International), the spotted AFP antibody (10-A05, clone M19301, Fitzgerald Industries International, Inc.), the Au NP AFP antibody (70-XG05, Fitzgerald Industries International, Inc.), human chorionic gonadotropin (HCG) (A81355M, Biodesign International), the spotted HCG antibody (E20579, Biodesign International), and the Au NP-monoclonal HCG antibody (E20106, Biodesign International).

    Techniques: Concentration Assay, Software