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human afp matched elisa antibody pair  (Sino Biological)


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    Structured Review

    Sino Biological human afp matched elisa antibody pair
    Figure 6. Verification of detection accuracy using the nano-ELISPR sensor. a) <t>ELISA</t> detection platform process. b) Nano-ELISPR biosensor detection platform process. c) Differential spectra of CEA at 500–700 nm at different concentrations (0–320 pg/mL). d) Relative OD values at 580 nm with different sample concentrations. e) Standard curve of CEA detection by the nano-ELISPR platform (R2 = 0.996). Each value represents the mean of three independent experiments (n = 3). f) Differential spectra of CA125 at 500–700 nm at different concentrations (0–4000 mU/mL). g) Relative OD values at 580 nm with different sample concentrations. h) Standard curve of CA125 detection by the nano-ELISPR platform (R2 = 0.996). Each value represents the mean of three independent experiments (n = 3).
    Human Afp Matched Elisa Antibody Pair, supplied by Sino Biological, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/afp+antibody+pair/Human+AFP+alpha-fetoprotein+ELISA+Pair+Set/pm37358326-294-0-13
    Average 94 stars, based on 1 article reviews
    human afp matched elisa antibody pair - by Bioz Stars, 2026-09
    94/100 stars

    Images

    1) Product Images from "Nanozyme-Catalyzed Metasurface Plasmon Sensor-Based Portable Ultrasensitive Optical Quantification Platform for Cancer Biomarker Screening."

    Article Title: Nanozyme-Catalyzed Metasurface Plasmon Sensor-Based Portable Ultrasensitive Optical Quantification Platform for Cancer Biomarker Screening.

    Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

    doi: 10.1002/advs.202301658

    Figure 6. Verification of detection accuracy using the nano-ELISPR sensor. a) ELISA detection platform process. b) Nano-ELISPR biosensor detection platform process. c) Differential spectra of CEA at 500–700 nm at different concentrations (0–320 pg/mL). d) Relative OD values at 580 nm with different sample concentrations. e) Standard curve of CEA detection by the nano-ELISPR platform (R2 = 0.996). Each value represents the mean of three independent experiments (n = 3). f) Differential spectra of CA125 at 500–700 nm at different concentrations (0–4000 mU/mL). g) Relative OD values at 580 nm with different sample concentrations. h) Standard curve of CA125 detection by the nano-ELISPR platform (R2 = 0.996). Each value represents the mean of three independent experiments (n = 3).
    Figure Legend Snippet: Figure 6. Verification of detection accuracy using the nano-ELISPR sensor. a) ELISA detection platform process. b) Nano-ELISPR biosensor detection platform process. c) Differential spectra of CEA at 500–700 nm at different concentrations (0–320 pg/mL). d) Relative OD values at 580 nm with different sample concentrations. e) Standard curve of CEA detection by the nano-ELISPR platform (R2 = 0.996). Each value represents the mean of three independent experiments (n = 3). f) Differential spectra of CA125 at 500–700 nm at different concentrations (0–4000 mU/mL). g) Relative OD values at 580 nm with different sample concentrations. h) Standard curve of CA125 detection by the nano-ELISPR platform (R2 = 0.996). Each value represents the mean of three independent experiments (n = 3).

    Techniques Used: Enzyme-linked Immunosorbent Assay

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    Article Snippet: AFP antibody pair set including a capture antibody (Capture Ab) and a detection antibody (Detection Ab) with and without horseradish peroxidase (HRP) were purchased from Sino Biological (Inc. Beijing, China).



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    Figure 6. Verification of detection accuracy using the nano-ELISPR sensor. a) <t>ELISA</t> detection platform process. b) Nano-ELISPR biosensor detection platform process. c) Differential spectra of CEA at 500–700 nm at different concentrations (0–320 pg/mL). d) Relative OD values at 580 nm with different sample concentrations. e) Standard curve of CEA detection by the nano-ELISPR platform (R2 = 0.996). Each value represents the mean of three independent experiments (n = 3). f) Differential spectra of CA125 at 500–700 nm at different concentrations (0–4000 mU/mL). g) Relative OD values at 580 nm with different sample concentrations. h) Standard curve of CA125 detection by the nano-ELISPR platform (R2 = 0.996). Each value represents the mean of three independent experiments (n = 3).
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    Figure 6. Verification of detection accuracy using the nano-ELISPR sensor. a) <t>ELISA</t> detection platform process. b) Nano-ELISPR biosensor detection platform process. c) Differential spectra of CEA at 500–700 nm at different concentrations (0–320 pg/mL). d) Relative OD values at 580 nm with different sample concentrations. e) Standard curve of CEA detection by the nano-ELISPR platform (R2 = 0.996). Each value represents the mean of three independent experiments (n = 3). f) Differential spectra of CA125 at 500–700 nm at different concentrations (0–4000 mU/mL). g) Relative OD values at 580 nm with different sample concentrations. h) Standard curve of CA125 detection by the nano-ELISPR platform (R2 = 0.996). Each value represents the mean of three independent experiments (n = 3).
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    Image Search Results


    Figure 6. Verification of detection accuracy using the nano-ELISPR sensor. a) ELISA detection platform process. b) Nano-ELISPR biosensor detection platform process. c) Differential spectra of CEA at 500–700 nm at different concentrations (0–320 pg/mL). d) Relative OD values at 580 nm with different sample concentrations. e) Standard curve of CEA detection by the nano-ELISPR platform (R2 = 0.996). Each value represents the mean of three independent experiments (n = 3). f) Differential spectra of CA125 at 500–700 nm at different concentrations (0–4000 mU/mL). g) Relative OD values at 580 nm with different sample concentrations. h) Standard curve of CA125 detection by the nano-ELISPR platform (R2 = 0.996). Each value represents the mean of three independent experiments (n = 3).

    Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

    Article Title: Nanozyme-Catalyzed Metasurface Plasmon Sensor-Based Portable Ultrasensitive Optical Quantification Platform for Cancer Biomarker Screening.

    doi: 10.1002/advs.202301658

    Figure Lengend Snippet: Figure 6. Verification of detection accuracy using the nano-ELISPR sensor. a) ELISA detection platform process. b) Nano-ELISPR biosensor detection platform process. c) Differential spectra of CEA at 500–700 nm at different concentrations (0–320 pg/mL). d) Relative OD values at 580 nm with different sample concentrations. e) Standard curve of CEA detection by the nano-ELISPR platform (R2 = 0.996). Each value represents the mean of three independent experiments (n = 3). f) Differential spectra of CA125 at 500–700 nm at different concentrations (0–4000 mU/mL). g) Relative OD values at 580 nm with different sample concentrations. h) Standard curve of CA125 detection by the nano-ELISPR platform (R2 = 0.996). Each value represents the mean of three independent experiments (n = 3).

    Article Snippet: Human AFP Matched ELISA Antibody Pair Set (catalog no. 12177) was purchased from Sino Biological Co., Ltd. (Beijing, China).

    Techniques: Enzyme-linked Immunosorbent Assay