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aunp 12  (MedChemExpress)


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    Structured Review

    MedChemExpress aunp 12
    Figure 1. Characterization of <t>AUNP-12-Cy5.5</t> and AUNP-12-CH1055. (A, B) Absorbance spectra and fluorescence intensities of AUNP-12-Cy5.5 and AUNP-12-CH1055. (C) ζ-Potential of AUNP-12-Cy5.5 in different solvents. (D) NIR-I fluorescence intensities of AUNP-12-Cy5.5 with different concentrations. (E) Fluorescence intensities under different long-pass filters of AUNP-12-CH1055. (F) NIR-II fluorescence intensity of AUNP-12-CH1055 at different concentrations.
    Aunp 12, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 92/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hy-p1812/AUNP-12/pm38980173-166-39-41
    Average 92 stars, based on 2 article reviews
    aunp 12 - by Bioz Stars, 2026-10
    92/100 stars

    Images

    1) Product Images from "AUNP-12 Near-Infrared Fluorescence Probes across NIR-I to NIR-II Enable In Vivo Detection of PD-1/PD-L1 Axis in the Tumor Microenvironment."

    Article Title: AUNP-12 Near-Infrared Fluorescence Probes across NIR-I to NIR-II Enable In Vivo Detection of PD-1/PD-L1 Axis in the Tumor Microenvironment.

    Journal: Bioconjugate chemistry

    doi: 10.1021/acs.bioconjchem.4c00266

    Figure 1. Characterization of AUNP-12-Cy5.5 and AUNP-12-CH1055. (A, B) Absorbance spectra and fluorescence intensities of AUNP-12-Cy5.5 and AUNP-12-CH1055. (C) ζ-Potential of AUNP-12-Cy5.5 in different solvents. (D) NIR-I fluorescence intensities of AUNP-12-Cy5.5 with different concentrations. (E) Fluorescence intensities under different long-pass filters of AUNP-12-CH1055. (F) NIR-II fluorescence intensity of AUNP-12-CH1055 at different concentrations.
    Figure Legend Snippet: Figure 1. Characterization of AUNP-12-Cy5.5 and AUNP-12-CH1055. (A, B) Absorbance spectra and fluorescence intensities of AUNP-12-Cy5.5 and AUNP-12-CH1055. (C) ζ-Potential of AUNP-12-Cy5.5 in different solvents. (D) NIR-I fluorescence intensities of AUNP-12-Cy5.5 with different concentrations. (E) Fluorescence intensities under different long-pass filters of AUNP-12-CH1055. (F) NIR-II fluorescence intensity of AUNP-12-CH1055 at different concentrations.

    Techniques Used: Fluorescence

    Figure 2. Expression characteristics of PD-L1 and targeting of AUNP-12-Cy5.5 in vitro. (A, B) PD-L1 showed varying expression levels across several cancer cell lines: higher in B16F10, CT26, and MDA-MB-231 and lower in 4T1 and MCF-7. (C) Flow cytometry indicated that AUNP-12- Cy5.5 more effectively targeted CT26 cells (high PD-L1 expression) in the AUNP-12-Cy5.5 group.
    Figure Legend Snippet: Figure 2. Expression characteristics of PD-L1 and targeting of AUNP-12-Cy5.5 in vitro. (A, B) PD-L1 showed varying expression levels across several cancer cell lines: higher in B16F10, CT26, and MDA-MB-231 and lower in 4T1 and MCF-7. (C) Flow cytometry indicated that AUNP-12- Cy5.5 more effectively targeted CT26 cells (high PD-L1 expression) in the AUNP-12-Cy5.5 group.

    Techniques Used: Expressing, In Vitro, Flow Cytometry

    Figure 3. In vivo NIR-I imaging and biodistribution of AUNP-12-Cy5.5 for the subcutaneous mouse tumor models. (A) Fluorescence images of the 4T1 subcutaneous mouse tumor models in vivo at different time points (n = 3). (B) Ex vivo fluorescence images of the 4T1 subcutaneous mouse tumor models. (C) Quantitative analysis of TBR over 24 h. (D) Fluorescence images of the CT26 subcutaneous mouse tumor models in vivo at different time points (n = 3). (E) Ex vivo fluorescence images of the CT26 subcutaneous mouse tumor models. (F) Quantitative analysis of TBR over 24 h. (G) 3D LSFM images of tumors in the 4T1 and CT26 subcutaneous mouse tumor models. Scale bars: 200 μm. TBR: tumor-to- background ratio. The data were presented as mean ± standard error of the mean (SEM) *p < 0.05, **p < 0.01, ***p < 0.001.
    Figure Legend Snippet: Figure 3. In vivo NIR-I imaging and biodistribution of AUNP-12-Cy5.5 for the subcutaneous mouse tumor models. (A) Fluorescence images of the 4T1 subcutaneous mouse tumor models in vivo at different time points (n = 3). (B) Ex vivo fluorescence images of the 4T1 subcutaneous mouse tumor models. (C) Quantitative analysis of TBR over 24 h. (D) Fluorescence images of the CT26 subcutaneous mouse tumor models in vivo at different time points (n = 3). (E) Ex vivo fluorescence images of the CT26 subcutaneous mouse tumor models. (F) Quantitative analysis of TBR over 24 h. (G) 3D LSFM images of tumors in the 4T1 and CT26 subcutaneous mouse tumor models. Scale bars: 200 μm. TBR: tumor-to- background ratio. The data were presented as mean ± standard error of the mean (SEM) *p < 0.05, **p < 0.01, ***p < 0.001.

    Techniques Used: In Vivo, Imaging, Fluorescence, Ex Vivo

    Figure 4. In vivo NIR-I imaging and biodistribution of AUNP-12-Cy5.5 in the MDA-MB-231 tumor (left) and MCF-7 tumor (right). (A) In vivo fluorescence images of bilateral mammary gland mouse tumor models at different time points (n = 3). (B−D) Quantitative analysis of TBR in MDA-MB-231 and MCF-7 tumors over 24 h. (E) Ex vivo fluorescence images of bilateral mammary gland mouse tumor models. TBR: tumor-to- background ratio. The data were presented as mean ± SEM *p < 0.05, **p < 0.01, ***p < 0.001.
    Figure Legend Snippet: Figure 4. In vivo NIR-I imaging and biodistribution of AUNP-12-Cy5.5 in the MDA-MB-231 tumor (left) and MCF-7 tumor (right). (A) In vivo fluorescence images of bilateral mammary gland mouse tumor models at different time points (n = 3). (B−D) Quantitative analysis of TBR in MDA-MB-231 and MCF-7 tumors over 24 h. (E) Ex vivo fluorescence images of bilateral mammary gland mouse tumor models. TBR: tumor-to- background ratio. The data were presented as mean ± SEM *p < 0.05, **p < 0.01, ***p < 0.001.

    Techniques Used: In Vivo, Imaging, Fluorescence, Ex Vivo

    Figure 5. In vivo NIR-II imaging and biodistribution of AUNP-12-CH1055 in the 4T1 subcutaneous mouse tumor models. (A) Fluorescence images of the 4T1 subcutaneous mouse tumor models in vivo at different time points (n = 3). (B) Quantitative analysis of mean fluorescence intensity over 48 h. The fluorescence intensity of tumors in AUNP-12-CH1055 groups was higher than that in the two block groups after injection of AUNP-12-CH1055. (C) Ex vivo fluorescence images of tumors and major organs. The data were presented as mean ± SEM *p < 0.05, **p < 0.01, ***p < 0.001.
    Figure Legend Snippet: Figure 5. In vivo NIR-II imaging and biodistribution of AUNP-12-CH1055 in the 4T1 subcutaneous mouse tumor models. (A) Fluorescence images of the 4T1 subcutaneous mouse tumor models in vivo at different time points (n = 3). (B) Quantitative analysis of mean fluorescence intensity over 48 h. The fluorescence intensity of tumors in AUNP-12-CH1055 groups was higher than that in the two block groups after injection of AUNP-12-CH1055. (C) Ex vivo fluorescence images of tumors and major organs. The data were presented as mean ± SEM *p < 0.05, **p < 0.01, ***p < 0.001.

    Techniques Used: In Vivo, Imaging, Fluorescence, Blocking Assay, Injection, Ex Vivo

    Figure 6. Assessment of the safety of two imaging probes. The mice were sacrificed after 7 days treatment, and serum and major organs were collected. Assessment of liver (A, B) and renal (C) functions in mice treated with PBS, AUNP-12-Cy5.5, or AUNP-12-CH1055. (D) H&E staining of major organs after treatment with PBS, AUNP-12-Cy5.5, or AUNP-12-CH1055. Scale bars: 50 μm.
    Figure Legend Snippet: Figure 6. Assessment of the safety of two imaging probes. The mice were sacrificed after 7 days treatment, and serum and major organs were collected. Assessment of liver (A, B) and renal (C) functions in mice treated with PBS, AUNP-12-Cy5.5, or AUNP-12-CH1055. (D) H&E staining of major organs after treatment with PBS, AUNP-12-Cy5.5, or AUNP-12-CH1055. Scale bars: 50 μm.

    Techniques Used: Imaging, Staining

    Related Articles

    Blocking Assay:

    Article Title: AUNP-12 Near-Infrared Fluorescence Probes across NIR-I to NIR-II Enable In Vivo Detection of PD-1/PD-L1 Axis in the Tumor Microenvironment
    Article Snippet: .. For blocking experiments, CT26 or B16F10 cells were divided into different groups: one group was incubated with 60 μg of aPD-L1 (no. BE0101, Bioxcell) to create the aPD-L1 block group, and another group was treated with 6 μg of AUNP-12 (HY-P1812, MedChemExpress) to form the AUNP-12 block group. ..

    Article Title: AUNP-12 Near-Infrared Fluorescence Probes across NIR-I to NIR-II Enable In Vivo Detection of PD-1/PD-L1 Axis in the Tumor Microenvironment.
    Article Snippet: .. For blocking experiments, CT26 or B16F10 cells were divided into different groups: one group was incubated with 60 μg of aPD-L1 (no. BE0101, Bioxcell) to create the aPD-L1 block group, and another group was treated with 6 μg of AUNP-12 (HY-P1812, MedChemExpress) to form the AUNP-12 block group. ..

    Incubation:

    Article Title: AUNP-12 Near-Infrared Fluorescence Probes across NIR-I to NIR-II Enable In Vivo Detection of PD-1/PD-L1 Axis in the Tumor Microenvironment
    Article Snippet: .. For blocking experiments, CT26 or B16F10 cells were divided into different groups: one group was incubated with 60 μg of aPD-L1 (no. BE0101, Bioxcell) to create the aPD-L1 block group, and another group was treated with 6 μg of AUNP-12 (HY-P1812, MedChemExpress) to form the AUNP-12 block group. ..

    Article Title: AUNP-12 Near-Infrared Fluorescence Probes across NIR-I to NIR-II Enable In Vivo Detection of PD-1/PD-L1 Axis in the Tumor Microenvironment.
    Article Snippet: .. For blocking experiments, CT26 or B16F10 cells were divided into different groups: one group was incubated with 60 μg of aPD-L1 (no. BE0101, Bioxcell) to create the aPD-L1 block group, and another group was treated with 6 μg of AUNP-12 (HY-P1812, MedChemExpress) to form the AUNP-12 block group. ..

    Article Title: AML cell-derived exosomes suppress the activation and cytotoxicity of NK cells in AML via PD-1/PD-L1 pathway.
    Article Snippet: Funding information Fundamental Research Funds for the Central Universities of China, Grant/Award Numbers: DUT15RC(3)051, DUT17ZD214, DUT21YG101 Abstract Exosomes are bilayer lipid bodies and contain a variety of bioactive molecules such as proteins, lipids, and nucleic acids, and so forth.. Exosomes derived from solid tumors may play critical roles in tumor development and immune evasion.. However, the underlying effects of tumor‐derived exosomes on immune function in modulating intercellular crosstalk within the bone marrow niche during acute myeloid leukemia (AML) development and immune evasion remain largely elusive.



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