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dihydrochloride  (Thermo Fisher)


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    Structured Review

    Thermo Fisher dihydrochloride
    Dihydrochloride, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 96/100, based on 12264 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/dihydrochloride/product/Thermo Fisher
    Average 96 stars, based on 12264 article reviews
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    Characterization of AMCMOFs. (a) Size distribution and (b) TEM image of AMCMOFs. Scale bar: 200 nm. (c) FT-IR spectrum. (d) Corresponding elemental mapping of AMCMOFs. Scale bar: 50 nm. (e) XPS spectrum of AMCMOFs. (f) UV–vis absorption spectra and (g) XRD patterns. (h) Stability of AMCMOFs in H 2 O, RPMI 1640, or PBS containing 10 % FBS (n = 3). (i) TEM and size distribution of AMCMOFs at pH 5.0. Scale bar: 25 nm. (j) <t>AQ4N</t> release from AMCMOFs under different conditions (n = 3).
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    Hepatocyte growth factor (HGF)/MET signaling activation in human acute liver failure (ALF). A: Predicted alterations in canonical signaling pathways in human hepatocytes from acetaminophen (APAP)-induced ALF versus healthy livers identified by Ingenuity Pathways Analysis of publicly available single-nuclei RNA-sequencing data set (positive z score indicates predicted activation of a pathway). B: The dot plot illustrates average expression along with percentage of cells showing significant expression of cell proliferation genes in APAP-induced ALF livers versus healthy controls, based on analysis of publicly available spatial transcriptomics data set. C: Downstream gene network of HGF predicted to be activated in hepatocytes of APAP-induced ALF livers based on single-nuclei RNA-sequencing data analysis. D: Pie-chart illustrating that a large proportion (approximately 35%) of genes altered in human ALF were regulated by MET in the mouse APAP-induced liver injury (AILI) model [ie, differentially expressed genes (DEGs) in MET knockout (KO) vs wild-type (WT) mice]. E: Enrichment analysis using DAVID analysis software showing altered biological processes (Gene Ontology terms) in the MET-regulated genes from the mouse AILI model linked to human ALF (ie, 781 genes shown in orange color in D ). The number of genes associated with each pathway is indicated on the right side of the corresponding bar. F: Heat map depicting comparison analysis of altered canonical pathway in human ALF (vs HEA) and MET KO (vs WT) mice. G: Effect of MET inhibition on APAP-treated primary human hepatocytes. Representative images of propidium iodide (PI)-stained primary human hepatocytes, illustrating the percentage of cell death after 24 hours of treatment with 10 mM APAP alone or in combination with <t>capmatinib</t> (CAP) (MET inhibitor: 0.1 and 1 μM). ∗∗ P < 0.01 and ∗∗∗ P < 0.001 versus APAP 10 mM. Scale bar: 300 μm ( G ). ERAD, endoplasmic reticulum–associated protein degradation; HEA, healthy human liver tissue; TGF-β, transforming growth factor-β.
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    Image Search Results


    Characterization of AMCMOFs. (a) Size distribution and (b) TEM image of AMCMOFs. Scale bar: 200 nm. (c) FT-IR spectrum. (d) Corresponding elemental mapping of AMCMOFs. Scale bar: 50 nm. (e) XPS spectrum of AMCMOFs. (f) UV–vis absorption spectra and (g) XRD patterns. (h) Stability of AMCMOFs in H 2 O, RPMI 1640, or PBS containing 10 % FBS (n = 3). (i) TEM and size distribution of AMCMOFs at pH 5.0. Scale bar: 25 nm. (j) AQ4N release from AMCMOFs under different conditions (n = 3).

    Journal: Materials Today Bio

    Article Title: Hypoxia-specific metal-organic frameworks combined with lactate immunometabolism regulation augment anti-tumor immunity of HIFU

    doi: 10.1016/j.mtbio.2025.102695

    Figure Lengend Snippet: Characterization of AMCMOFs. (a) Size distribution and (b) TEM image of AMCMOFs. Scale bar: 200 nm. (c) FT-IR spectrum. (d) Corresponding elemental mapping of AMCMOFs. Scale bar: 50 nm. (e) XPS spectrum of AMCMOFs. (f) UV–vis absorption spectra and (g) XRD patterns. (h) Stability of AMCMOFs in H 2 O, RPMI 1640, or PBS containing 10 % FBS (n = 3). (i) TEM and size distribution of AMCMOFs at pH 5.0. Scale bar: 25 nm. (j) AQ4N release from AMCMOFs under different conditions (n = 3).

    Article Snippet: Sodium carbonate (Na 2 CO 3 ), calcium chloride (CaCl 2 ), and manganese chloride (MnCl 2 ) were procured from Aladdin (China), while banoxantrone dihydrochloride (AQ4N) was sourced from MedChemExpress (USA).

    Techniques:

    Cellular uptake and cytotoxicity assays of AMCMOFs. (a–d) CLSM images and flow cytometry analysis of cell uptake. Scale bar: 50 μm. (e, g) CLSM images of intracellular Ca 2+ in 4T1 cells. Scale bar: 50 μm. (f) Cell viability of 4T1 cells under different conditions. (h) Live (green)/dead (red) staining images and their mean fluorescence intensity (MFI). Scale bar: 100 μm. (j, k) Flow cytometry analysis of apoptosis. I: PBS under normoxia; II: AQ4N under normoxia; III: AMMOFs under normoxia; IV: AMCMOFs under normoxia; V: PBS under hypoxia; AQ4N under hypoxia; VI: AQ4N under hypoxia; VII: AMMOFs under hypoxia; VIII: AMCMOFs under hypoxia. Data are presented as mean ± SD. For comparisons between two groups, statistical significance was assessed using a two-tailed Student's t-test. For experiments involving multiple groups, one-way ANOVA followed by Tukey's post-hoc test was applied, with n = 3, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Hypoxia-specific metal-organic frameworks combined with lactate immunometabolism regulation augment anti-tumor immunity of HIFU

    doi: 10.1016/j.mtbio.2025.102695

    Figure Lengend Snippet: Cellular uptake and cytotoxicity assays of AMCMOFs. (a–d) CLSM images and flow cytometry analysis of cell uptake. Scale bar: 50 μm. (e, g) CLSM images of intracellular Ca 2+ in 4T1 cells. Scale bar: 50 μm. (f) Cell viability of 4T1 cells under different conditions. (h) Live (green)/dead (red) staining images and their mean fluorescence intensity (MFI). Scale bar: 100 μm. (j, k) Flow cytometry analysis of apoptosis. I: PBS under normoxia; II: AQ4N under normoxia; III: AMMOFs under normoxia; IV: AMCMOFs under normoxia; V: PBS under hypoxia; AQ4N under hypoxia; VI: AQ4N under hypoxia; VII: AMMOFs under hypoxia; VIII: AMCMOFs under hypoxia. Data are presented as mean ± SD. For comparisons between two groups, statistical significance was assessed using a two-tailed Student's t-test. For experiments involving multiple groups, one-way ANOVA followed by Tukey's post-hoc test was applied, with n = 3, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001.

    Article Snippet: Sodium carbonate (Na 2 CO 3 ), calcium chloride (CaCl 2 ), and manganese chloride (MnCl 2 ) were procured from Aladdin (China), while banoxantrone dihydrochloride (AQ4N) was sourced from MedChemExpress (USA).

    Techniques: Flow Cytometry, Staining, Fluorescence, Two Tailed Test

    In vitro ICD-inducing effects of AMCMOF and HIFU-induced hypoxia. Immunofluorescence images showing (a) CRT and (c) HMGB1 expression in 4T1 cells post-treatment. Scale bar: 50 μm. MFI of (b) CRT expression and (d) HMGB1 release. (e) Quantification of ATP release. (f) Immunofluorescent detection of HIF-1α in tumor tissues at indicated time points post-HIFU irradiation. Scale bar: 100 μm. (g) MFI of HIF-1α immunofluorescence in tumor sites at 0, 4, 12, or 24 h after HIFU irradiation. I: PBS under normoxia; II: AQ4N under normoxia; III: AMMOFs under normoxia; IV: AMCMOFs under normoxia; V: PBS under hypoxia; AQ4N under hypoxia; VI: AQ4N under hypoxia; VII: AMMOFs under hypoxia; VIII: AMCMOFs under hypoxia. Data are presented as mean ± SD. For comparisons between two groups, statistical significance was assessed using a two-tailed Student's t-test. For experiments involving multiple groups, one-way ANOVA followed by Tukey's post-hoc test was applied, with n = 3, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Hypoxia-specific metal-organic frameworks combined with lactate immunometabolism regulation augment anti-tumor immunity of HIFU

    doi: 10.1016/j.mtbio.2025.102695

    Figure Lengend Snippet: In vitro ICD-inducing effects of AMCMOF and HIFU-induced hypoxia. Immunofluorescence images showing (a) CRT and (c) HMGB1 expression in 4T1 cells post-treatment. Scale bar: 50 μm. MFI of (b) CRT expression and (d) HMGB1 release. (e) Quantification of ATP release. (f) Immunofluorescent detection of HIF-1α in tumor tissues at indicated time points post-HIFU irradiation. Scale bar: 100 μm. (g) MFI of HIF-1α immunofluorescence in tumor sites at 0, 4, 12, or 24 h after HIFU irradiation. I: PBS under normoxia; II: AQ4N under normoxia; III: AMMOFs under normoxia; IV: AMCMOFs under normoxia; V: PBS under hypoxia; AQ4N under hypoxia; VI: AQ4N under hypoxia; VII: AMMOFs under hypoxia; VIII: AMCMOFs under hypoxia. Data are presented as mean ± SD. For comparisons between two groups, statistical significance was assessed using a two-tailed Student's t-test. For experiments involving multiple groups, one-way ANOVA followed by Tukey's post-hoc test was applied, with n = 3, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001.

    Article Snippet: Sodium carbonate (Na 2 CO 3 ), calcium chloride (CaCl 2 ), and manganese chloride (MnCl 2 ) were procured from Aladdin (China), while banoxantrone dihydrochloride (AQ4N) was sourced from MedChemExpress (USA).

    Techniques: In Vitro, Immunofluorescence, Expressing, Irradiation, Two Tailed Test

    Drug distribution and antitumor effects of AMCMOFs in vivo. (a) Pharmacokinetics of Sprague-Dawley rats following intravenous injection of AMCMOFs and free AQ4N (n = 3). (b) AQ4N content in major organs and tumors at different time points after drug injection (n = 3). (c, d) Intratumoral release of CLSM and analysis following different treatments. Scale bar: 100 μm. (e) Primary and (f) distant tumor inhibition curves (n = 5). Weight of primary tumors (g) and distant tumors (h) excised on day 15 (n = 5). (i) PCNA, TUNEL, and H&E staining of tumor sections from each group. Scale bar: 100 μm. (j, k) MFI of PCNA and TUNEL in the tumor sections. I: PBS; II: AQ4N; III: AMMOFs; IV: AMCMOFs; V: HIFU; VI: AMCMOFs + HIFU (with an AQ4N concentration of 10 mg/kg). Data are presented as mean ± SD. For comparisons between two groups, statistical significance was assessed using a two-tailed Student's t-test. For experiments involving multiple groups, one-way ANOVA followed by Tukey's post-hoc test was applied, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001 and ∗∗∗∗p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Hypoxia-specific metal-organic frameworks combined with lactate immunometabolism regulation augment anti-tumor immunity of HIFU

    doi: 10.1016/j.mtbio.2025.102695

    Figure Lengend Snippet: Drug distribution and antitumor effects of AMCMOFs in vivo. (a) Pharmacokinetics of Sprague-Dawley rats following intravenous injection of AMCMOFs and free AQ4N (n = 3). (b) AQ4N content in major organs and tumors at different time points after drug injection (n = 3). (c, d) Intratumoral release of CLSM and analysis following different treatments. Scale bar: 100 μm. (e) Primary and (f) distant tumor inhibition curves (n = 5). Weight of primary tumors (g) and distant tumors (h) excised on day 15 (n = 5). (i) PCNA, TUNEL, and H&E staining of tumor sections from each group. Scale bar: 100 μm. (j, k) MFI of PCNA and TUNEL in the tumor sections. I: PBS; II: AQ4N; III: AMMOFs; IV: AMCMOFs; V: HIFU; VI: AMCMOFs + HIFU (with an AQ4N concentration of 10 mg/kg). Data are presented as mean ± SD. For comparisons between two groups, statistical significance was assessed using a two-tailed Student's t-test. For experiments involving multiple groups, one-way ANOVA followed by Tukey's post-hoc test was applied, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001 and ∗∗∗∗p < 0.0001.

    Article Snippet: Sodium carbonate (Na 2 CO 3 ), calcium chloride (CaCl 2 ), and manganese chloride (MnCl 2 ) were procured from Aladdin (China), while banoxantrone dihydrochloride (AQ4N) was sourced from MedChemExpress (USA).

    Techniques: In Vivo, Drug discovery, Injection, Inhibition, TUNEL Assay, Staining, Concentration Assay, Two Tailed Test

    Induction of ICD and Tumor Microenvironment Modulation. (a–d) CLSM and analysis of CRT and HMGB1 staining in tumor sections. Scale bar: 100 μm. (e) Lactate content in each group following co-incubation with 3 mM lactate. (f) Lactate content within tumor tissues. (g, h) Levels of IFN-γ and TNF-α in primary tumors. (i, j) Western blotting analysis in the tumor tissue. I: PBS; II: AQ4N; III: AMMOFs; IV: AMCMOFs; V: HIFU; VI: AMCMOFs + HIFU at an AQ4N concentration of 10 mg/kg). Data are presented as mean ± SD. For comparisons between two groups, statistical significance was assessed using a two-tailed Student's t-test. For experiments involving multiple groups, one-way ANOVA followed by Tukey's post-hoc test was applied, with n = 3, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001 and ∗∗∗∗p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Hypoxia-specific metal-organic frameworks combined with lactate immunometabolism regulation augment anti-tumor immunity of HIFU

    doi: 10.1016/j.mtbio.2025.102695

    Figure Lengend Snippet: Induction of ICD and Tumor Microenvironment Modulation. (a–d) CLSM and analysis of CRT and HMGB1 staining in tumor sections. Scale bar: 100 μm. (e) Lactate content in each group following co-incubation with 3 mM lactate. (f) Lactate content within tumor tissues. (g, h) Levels of IFN-γ and TNF-α in primary tumors. (i, j) Western blotting analysis in the tumor tissue. I: PBS; II: AQ4N; III: AMMOFs; IV: AMCMOFs; V: HIFU; VI: AMCMOFs + HIFU at an AQ4N concentration of 10 mg/kg). Data are presented as mean ± SD. For comparisons between two groups, statistical significance was assessed using a two-tailed Student's t-test. For experiments involving multiple groups, one-way ANOVA followed by Tukey's post-hoc test was applied, with n = 3, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001 and ∗∗∗∗p < 0.0001.

    Article Snippet: Sodium carbonate (Na 2 CO 3 ), calcium chloride (CaCl 2 ), and manganese chloride (MnCl 2 ) were procured from Aladdin (China), while banoxantrone dihydrochloride (AQ4N) was sourced from MedChemExpress (USA).

    Techniques: Staining, Incubation, Western Blot, Concentration Assay, Two Tailed Test

    Enhancement of systemic anti-tumor immunity and suppression of tumor metastasis. (a–d) M1 and M2 macrophages in the primary tumors of each group. (e–h) DCs and CD8 + T cell populations in primary tumors in each group. (i) Representative flow cytometry plots of memory T cell subsets in spleens from different treatment groups. (j) Quantification of CD8 + central memory T cells (CD44 + CD62L + ). (k) Quantification of CD8 + effector memory T cells (CD44 + CD62L − ). (l) Lung metastasis in different groups. Scale bar: 3000 μm or 500 μm. I: PBS; II: AQ4N; III: AMMOFs; IV: AMCMOFs; V: HIFU; VI: AMCMOFs + HIFU at an AQ4N concentration of 10 mg/kg. Data are presented as mean ± SD. For comparisons between two groups, statistical significance was assessed using a two-tailed Student's t-test. For experiments involving multiple groups, one-way ANOVA followed by Tukey's post-hoc test was applied, with n = 3, ∗∗p < 0.01, ∗∗∗p < 0.001 and ∗∗∗∗p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Hypoxia-specific metal-organic frameworks combined with lactate immunometabolism regulation augment anti-tumor immunity of HIFU

    doi: 10.1016/j.mtbio.2025.102695

    Figure Lengend Snippet: Enhancement of systemic anti-tumor immunity and suppression of tumor metastasis. (a–d) M1 and M2 macrophages in the primary tumors of each group. (e–h) DCs and CD8 + T cell populations in primary tumors in each group. (i) Representative flow cytometry plots of memory T cell subsets in spleens from different treatment groups. (j) Quantification of CD8 + central memory T cells (CD44 + CD62L + ). (k) Quantification of CD8 + effector memory T cells (CD44 + CD62L − ). (l) Lung metastasis in different groups. Scale bar: 3000 μm or 500 μm. I: PBS; II: AQ4N; III: AMMOFs; IV: AMCMOFs; V: HIFU; VI: AMCMOFs + HIFU at an AQ4N concentration of 10 mg/kg. Data are presented as mean ± SD. For comparisons between two groups, statistical significance was assessed using a two-tailed Student's t-test. For experiments involving multiple groups, one-way ANOVA followed by Tukey's post-hoc test was applied, with n = 3, ∗∗p < 0.01, ∗∗∗p < 0.001 and ∗∗∗∗p < 0.0001.

    Article Snippet: Sodium carbonate (Na 2 CO 3 ), calcium chloride (CaCl 2 ), and manganese chloride (MnCl 2 ) were procured from Aladdin (China), while banoxantrone dihydrochloride (AQ4N) was sourced from MedChemExpress (USA).

    Techniques: Flow Cytometry, Concentration Assay, Two Tailed Test

    Hepatocyte growth factor (HGF)/MET signaling activation in human acute liver failure (ALF). A: Predicted alterations in canonical signaling pathways in human hepatocytes from acetaminophen (APAP)-induced ALF versus healthy livers identified by Ingenuity Pathways Analysis of publicly available single-nuclei RNA-sequencing data set (positive z score indicates predicted activation of a pathway). B: The dot plot illustrates average expression along with percentage of cells showing significant expression of cell proliferation genes in APAP-induced ALF livers versus healthy controls, based on analysis of publicly available spatial transcriptomics data set. C: Downstream gene network of HGF predicted to be activated in hepatocytes of APAP-induced ALF livers based on single-nuclei RNA-sequencing data analysis. D: Pie-chart illustrating that a large proportion (approximately 35%) of genes altered in human ALF were regulated by MET in the mouse APAP-induced liver injury (AILI) model [ie, differentially expressed genes (DEGs) in MET knockout (KO) vs wild-type (WT) mice]. E: Enrichment analysis using DAVID analysis software showing altered biological processes (Gene Ontology terms) in the MET-regulated genes from the mouse AILI model linked to human ALF (ie, 781 genes shown in orange color in D ). The number of genes associated with each pathway is indicated on the right side of the corresponding bar. F: Heat map depicting comparison analysis of altered canonical pathway in human ALF (vs HEA) and MET KO (vs WT) mice. G: Effect of MET inhibition on APAP-treated primary human hepatocytes. Representative images of propidium iodide (PI)-stained primary human hepatocytes, illustrating the percentage of cell death after 24 hours of treatment with 10 mM APAP alone or in combination with capmatinib (CAP) (MET inhibitor: 0.1 and 1 μM). ∗∗ P < 0.01 and ∗∗∗ P < 0.001 versus APAP 10 mM. Scale bar: 300 μm ( G ). ERAD, endoplasmic reticulum–associated protein degradation; HEA, healthy human liver tissue; TGF-β, transforming growth factor-β.

    Journal: The American Journal of Pathology

    Article Title: Hepatocyte-Specific MET Deletion Exacerbates Acetaminophen-Induced Hepatotoxicity in Mice

    doi: 10.1016/j.ajpath.2025.09.010

    Figure Lengend Snippet: Hepatocyte growth factor (HGF)/MET signaling activation in human acute liver failure (ALF). A: Predicted alterations in canonical signaling pathways in human hepatocytes from acetaminophen (APAP)-induced ALF versus healthy livers identified by Ingenuity Pathways Analysis of publicly available single-nuclei RNA-sequencing data set (positive z score indicates predicted activation of a pathway). B: The dot plot illustrates average expression along with percentage of cells showing significant expression of cell proliferation genes in APAP-induced ALF livers versus healthy controls, based on analysis of publicly available spatial transcriptomics data set. C: Downstream gene network of HGF predicted to be activated in hepatocytes of APAP-induced ALF livers based on single-nuclei RNA-sequencing data analysis. D: Pie-chart illustrating that a large proportion (approximately 35%) of genes altered in human ALF were regulated by MET in the mouse APAP-induced liver injury (AILI) model [ie, differentially expressed genes (DEGs) in MET knockout (KO) vs wild-type (WT) mice]. E: Enrichment analysis using DAVID analysis software showing altered biological processes (Gene Ontology terms) in the MET-regulated genes from the mouse AILI model linked to human ALF (ie, 781 genes shown in orange color in D ). The number of genes associated with each pathway is indicated on the right side of the corresponding bar. F: Heat map depicting comparison analysis of altered canonical pathway in human ALF (vs HEA) and MET KO (vs WT) mice. G: Effect of MET inhibition on APAP-treated primary human hepatocytes. Representative images of propidium iodide (PI)-stained primary human hepatocytes, illustrating the percentage of cell death after 24 hours of treatment with 10 mM APAP alone or in combination with capmatinib (CAP) (MET inhibitor: 0.1 and 1 μM). ∗∗ P < 0.01 and ∗∗∗ P < 0.001 versus APAP 10 mM. Scale bar: 300 μm ( G ). ERAD, endoplasmic reticulum–associated protein degradation; HEA, healthy human liver tissue; TGF-β, transforming growth factor-β.

    Article Snippet: Next day, the hepatocytes were washed with sterile phosphate-buffered saline and treated for 24 hours with 10 mM APAP alone or in combination with 0.1 or 1 μM capmatinib dihydrochloride hydrate (a MET inhibitor) (#HY-13404C; MedChemExpress) in fetal bovine serum–free media in the presence of HGF (50 ng/mL).

    Techniques: Activation Assay, Protein-Protein interactions, RNA Sequencing, Expressing, Spatial Transcriptomics, Knock-Out, Software, Comparison, Inhibition, Staining