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fontana-masson stain kit (melanin stain) 100 tests  (Advisains)


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    Advisains fontana-masson stain kit (melanin stain) 100 tests
    Fontana Masson Stain Kit (Melanin Stain) 100 Tests, supplied by Advisains, used in various techniques. Bioz Stars score: 99/100, based on 92 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/test+kit/Fontana-Masson+Stain+Kit+(Melanin+Stain)+100+tests/custom%40ab150669%4042278371
    Average 99 stars, based on 92 article reviews
    fontana-masson stain kit (melanin stain) 100 tests - by Bioz Stars, 2026-11
    99/100 stars

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    Related Articles

    Software:

    Article Title: Translational Evaluation of a Disodium Adenosine Monophosphate (AMP2Na)-Based Topical Formulation for Physiology-Aligned Skin Rejuvenation: Integrated In Vitro, Ex Vivo, and Clinical Evidence.
    Article Snippet: d, imaged at 400× (BX43F), and elastic fiber density (%) was quantified using Zen software. • Skin-whitening efficacy (FM): Deparaffinized sections were stained with the Fontana– Masson Kit (ab150669; Abcam, Cambridge, UK), dehydrated, mounted, and imaged at 400×. Melanin content (black) was quantified with ImageJ as % melanin-positive area relative to total epidermal and dermal area. 4.3.3. Gene E

    Quantitative RT-PCR:

    Article Title: Translational Evaluation of a Disodium Adenosine Monophosphate (AMP2Na)-Based Topical Formulation for Physiology-Aligned Skin Rejuvenation: Integrated In Vitro, Ex Vivo, and Clinical Evidence.
    Article Snippet: d, imaged at 400× (BX43F), and elastic fiber density (%) was quantified using Zen software. • Skin-whitening efficacy (FM): Deparaffinized sections were stained with the Fontana– Masson Kit (ab150669; Abcam, Cambridge, UK), dehydrated, mounted, and imaged at 400×. Melanin content (black) was quantified with ImageJ as % melanin-positive area relative to total epidermal and dermal area. 4.3.3. Gene E

    Gene Expression:

    Article Title: Translational Evaluation of a Disodium Adenosine Monophosphate (AMP2Na)-Based Topical Formulation for Physiology-Aligned Skin Rejuvenation: Integrated In Vitro, Ex Vivo, and Clinical Evidence.
    Article Snippet: d, imaged at 400× (BX43F), and elastic fiber density (%) was quantified using Zen software. • Skin-whitening efficacy (FM): Deparaffinized sections were stained with the Fontana– Masson Kit (ab150669; Abcam, Cambridge, UK), dehydrated, mounted, and imaged at 400×. Melanin content (black) was quantified with ImageJ as % melanin-positive area relative to total epidermal and dermal area. 4.3.3. Gene E

    Expressing:

    Article Title: Translational Evaluation of a Disodium Adenosine Monophosphate (AMP2Na)-Based Topical Formulation for Physiology-Aligned Skin Rejuvenation: Integrated In Vitro, Ex Vivo, and Clinical Evidence.
    Article Snippet: d, imaged at 400× (BX43F), and elastic fiber density (%) was quantified using Zen software. • Skin-whitening efficacy (FM): Deparaffinized sections were stained with the Fontana– Masson Kit (ab150669; Abcam, Cambridge, UK), dehydrated, mounted, and imaged at 400×. Melanin content (black) was quantified with ImageJ as % melanin-positive area relative to total epidermal and dermal area. 4.3.3. Gene E

    Staining:

    Article Title: Translational Evaluation of a Disodium Adenosine Monophosphate (AMP2Na)-Based Topical Formulation for Physiology-Aligned Skin Rejuvenation: Integrated In Vitro, Ex Vivo, and Clinical Evidence.
    Article Snippet: d, imaged at 400× (BX43F), and elastic fiber density (%) was quantified using Zen software. • Skin-whitening efficacy (FM): Deparaffinized sections were stained with the Fontana– Masson Kit (ab150669; Abcam, Cambridge, UK), dehydrated, mounted, and imaged at 400×. Melanin content (black) was quantified with ImageJ as % melanin-positive area relative to total epidermal and dermal area. 4.3.3. Gene E

    Microscopy:

    Article Title: Translational Evaluation of a Disodium Adenosine Monophosphate (AMP2Na)-Based Topical Formulation for Physiology-Aligned Skin Rejuvenation: Integrated In Vitro, Ex Vivo, and Clinical Evidence.
    Article Snippet: d, imaged at 400× (BX43F), and elastic fiber density (%) was quantified using Zen software. • Skin-whitening efficacy (FM): Deparaffinized sections were stained with the Fontana– Masson Kit (ab150669; Abcam, Cambridge, UK), dehydrated, mounted, and imaged at 400×. Melanin content (black) was quantified with ImageJ as % melanin-positive area relative to total epidermal and dermal area. 4.3.3. Gene E

    Fluorescence Microscopy:

    Article Title: Translational Evaluation of a Disodium Adenosine Monophosphate (AMP2Na)-Based Topical Formulation for Physiology-Aligned Skin Rejuvenation: Integrated In Vitro, Ex Vivo, and Clinical Evidence.
    Article Snippet: d, imaged at 400× (BX43F), and elastic fiber density (%) was quantified using Zen software. • Skin-whitening efficacy (FM): Deparaffinized sections were stained with the Fontana– Masson Kit (ab150669; Abcam, Cambridge, UK), dehydrated, mounted, and imaged at 400×. Melanin content (black) was quantified with ImageJ as % melanin-positive area relative to total epidermal and dermal area. 4.3.3. Gene E

    Fluorescence:

    Article Title: Translational Evaluation of a Disodium Adenosine Monophosphate (AMP2Na)-Based Topical Formulation for Physiology-Aligned Skin Rejuvenation: Integrated In Vitro, Ex Vivo, and Clinical Evidence.
    Article Snippet: d, imaged at 400× (BX43F), and elastic fiber density (%) was quantified using Zen software. • Skin-whitening efficacy (FM): Deparaffinized sections were stained with the Fontana– Masson Kit (ab150669; Abcam, Cambridge, UK), dehydrated, mounted, and imaged at 400×. Melanin content (black) was quantified with ImageJ as % melanin-positive area relative to total epidermal and dermal area. 4.3.3. Gene E

    Immunohistochemistry:

    Article Title: Translational Evaluation of a Disodium Adenosine Monophosphate (AMP2Na)-Based Topical Formulation for Physiology-Aligned Skin Rejuvenation: Integrated In Vitro, Ex Vivo, and Clinical Evidence.
    Article Snippet: d, imaged at 400× (BX43F), and elastic fiber density (%) was quantified using Zen software. • Skin-whitening efficacy (FM): Deparaffinized sections were stained with the Fontana– Masson Kit (ab150669; Abcam, Cambridge, UK), dehydrated, mounted, and imaged at 400×. Melanin content (black) was quantified with ImageJ as % melanin-positive area relative to total epidermal and dermal area. 4.3.3. Gene E

    Imaging:

    Article Title: Translational Evaluation of a Disodium Adenosine Monophosphate (AMP2Na)-Based Topical Formulation for Physiology-Aligned Skin Rejuvenation: Integrated In Vitro, Ex Vivo, and Clinical Evidence.
    Article Snippet: d, imaged at 400× (BX43F), and elastic fiber density (%) was quantified using Zen software. • Skin-whitening efficacy (FM): Deparaffinized sections were stained with the Fontana– Masson Kit (ab150669; Abcam, Cambridge, UK), dehydrated, mounted, and imaged at 400×. Melanin content (black) was quantified with ImageJ as % melanin-positive area relative to total epidermal and dermal area. 4.3.3. Gene E

    Live Cell Imaging:

    Article Title: Translational Evaluation of a Disodium Adenosine Monophosphate (AMP2Na)-Based Topical Formulation for Physiology-Aligned Skin Rejuvenation: Integrated In Vitro, Ex Vivo, and Clinical Evidence.
    Article Snippet: d, imaged at 400× (BX43F), and elastic fiber density (%) was quantified using Zen software. • Skin-whitening efficacy (FM): Deparaffinized sections were stained with the Fontana– Masson Kit (ab150669; Abcam, Cambridge, UK), dehydrated, mounted, and imaged at 400×. Melanin content (black) was quantified with ImageJ as % melanin-positive area relative to total epidermal and dermal area. 4.3.3. Gene E

    Formalin-fixed Paraffin-Embedded:

    Article Title: Translational Evaluation of a Disodium Adenosine Monophosphate (AMP2Na)-Based Topical Formulation for Physiology-Aligned Skin Rejuvenation: Integrated In Vitro, Ex Vivo, and Clinical Evidence.
    Article Snippet: d, imaged at 400× (BX43F), and elastic fiber density (%) was quantified using Zen software. • Skin-whitening efficacy (FM): Deparaffinized sections were stained with the Fontana– Masson Kit (ab150669; Abcam, Cambridge, UK), dehydrated, mounted, and imaged at 400×. Melanin content (black) was quantified with ImageJ as % melanin-positive area relative to total epidermal and dermal area. 4.3.3. Gene E

    Immunohistochemical staining:

    Article Title: Translational Evaluation of a Disodium Adenosine Monophosphate (AMP2Na)-Based Topical Formulation for Physiology-Aligned Skin Rejuvenation: Integrated In Vitro, Ex Vivo, and Clinical Evidence.
    Article Snippet: d, imaged at 400× (BX43F), and elastic fiber density (%) was quantified using Zen software. • Skin-whitening efficacy (FM): Deparaffinized sections were stained with the Fontana– Masson Kit (ab150669; Abcam, Cambridge, UK), dehydrated, mounted, and imaged at 400×. Melanin content (black) was quantified with ImageJ as % melanin-positive area relative to total epidermal and dermal area. 4.3.3. Gene E



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    Image Search Results


    Genetic and Pharmacological Inhibition of Nupr1 Attenuates Ang II Induced Mitochondrial Apoptosis in VSMCs. (A) Cell ability was evaluated by CCK8 assay ( n = 8 per group). (B) Lactate production of indicated groups ( n = 6 per group). (C) Representative images of TEM in VSMCs from the indicated groups. (D) Quantification of mitochondrial size in VSMCs from indicated groups ( n = 6 per group). (E) Quantification of circularity index in VSMC from indicated groups ( n = 6 per group). (F) Real‐time monitoring of oxygen consumption rate (OCR) in indicated groups detected by O2k. (G–I) Quantification of ATP‐coupled respiration, mitochondrial basal respiration, and maximal respiration from indicated groups ( n = 6 per group). (J) Representative images of calcein and Annexin V fluorescence results showing mPTP opening and apoptosis in indicated groups. Stronger green fluorescence represents a lower degree of mPTP opening, while diminished fluorescence indicates increased mPTP opening. Stronger red fluorescence represents a higher apoptosis rate. (K, L) Quantification of fluorescence intensity, including Annexin V and Calcein ( n = 6 per group). (M) Flow cytometry analysis of Annexin and PI staining of apoptosis from indicated groups. (N) Quantification of early apoptosis, late apoptosis, and total apoptosis by flow cytometry ( n = 3 per group). (O) Quantification of maximal respiration from indicated groups ( n = 6 per group). (P) Real‐time monitoring of OCR in indicated groups detected by O2k. (Q, R) Quantification of ATP‐coupled respiration and mitochondrial basal respiration from indicated groups ( n = 6 per group). (S) Flow cytometry analysis of Annexin and PI staining of apoptosis from indicated groups. (T) Quantification of early apoptosis, late apoptosis, and total apoptosis by flow cytometry ( n = 3 per group).

    Journal: Advanced Science

    Article Title: Targeting Nupr1‐Mediated p53 Mitochondrial Sequestration Alleviates Aortic Dissection by Restoring the Gadd45b‐Dependent Survival Program

    doi: 10.1002/advs.78143

    Figure Lengend Snippet: Genetic and Pharmacological Inhibition of Nupr1 Attenuates Ang II Induced Mitochondrial Apoptosis in VSMCs. (A) Cell ability was evaluated by CCK8 assay ( n = 8 per group). (B) Lactate production of indicated groups ( n = 6 per group). (C) Representative images of TEM in VSMCs from the indicated groups. (D) Quantification of mitochondrial size in VSMCs from indicated groups ( n = 6 per group). (E) Quantification of circularity index in VSMC from indicated groups ( n = 6 per group). (F) Real‐time monitoring of oxygen consumption rate (OCR) in indicated groups detected by O2k. (G–I) Quantification of ATP‐coupled respiration, mitochondrial basal respiration, and maximal respiration from indicated groups ( n = 6 per group). (J) Representative images of calcein and Annexin V fluorescence results showing mPTP opening and apoptosis in indicated groups. Stronger green fluorescence represents a lower degree of mPTP opening, while diminished fluorescence indicates increased mPTP opening. Stronger red fluorescence represents a higher apoptosis rate. (K, L) Quantification of fluorescence intensity, including Annexin V and Calcein ( n = 6 per group). (M) Flow cytometry analysis of Annexin and PI staining of apoptosis from indicated groups. (N) Quantification of early apoptosis, late apoptosis, and total apoptosis by flow cytometry ( n = 3 per group). (O) Quantification of maximal respiration from indicated groups ( n = 6 per group). (P) Real‐time monitoring of OCR in indicated groups detected by O2k. (Q, R) Quantification of ATP‐coupled respiration and mitochondrial basal respiration from indicated groups ( n = 6 per group). (S) Flow cytometry analysis of Annexin and PI staining of apoptosis from indicated groups. (T) Quantification of early apoptosis, late apoptosis, and total apoptosis by flow cytometry ( n = 3 per group).

    Article Snippet: According to mPTP test kit instructions (C2009S, Beyotime), 200 μL of Calcein AM staining solution and fluorescence quenching working solution were added to each well after the respective cell treatments.

    Techniques: Inhibition, CCK-8 Assay, Real-time Monitoring, Fluorescence, Flow Cytometry, Analysis, Staining

    Gadd45b is Indispensable for the Protective Effects of Nupr1 Deficiency Against Mitochondrial Apoptosis. (A) Enrichment of KEGG pathways. (B) GSEA analysis in VSMCs treated with Ang II stimulation and Nupr1 deficiency. (C) Chordal diagram of GO pathways related with cell fate and the contributing DEPs. (D) Stem plot of DEPs in the apoptosis pathway from the indicated groups. (E) RT‐qPCR analysis of mRNA levels of candidate genes in VSMCs. Data were presented as relative fold change to controls ( n = 6 per group). (F) Expressions of Gadd45b in VSMCs measured by Western blot and its quantification from indicated groups measured by Western blot ( n = 5 per group). (G, H) Representative images of ROS staining in indicated groups. Semi‐quantitative analysis of mean fluorescence intensity in indicated groups ( n = 6 per group). (I) Representative images of calcein and Annexin V fluorescence results showing mPTP opening in indicated groups. (J) Quantification of fluorescence intensity, including Annexin V and mPTP ( n = 3 per group). (K) Co‐immunoprecipitation and Western blot assays of Myc‐Nupr1 and Gadd45b. (L) Co‐immunoprecipitation assays of Myc‐Gadd45b and Nupr1.

    Journal: Advanced Science

    Article Title: Targeting Nupr1‐Mediated p53 Mitochondrial Sequestration Alleviates Aortic Dissection by Restoring the Gadd45b‐Dependent Survival Program

    doi: 10.1002/advs.78143

    Figure Lengend Snippet: Gadd45b is Indispensable for the Protective Effects of Nupr1 Deficiency Against Mitochondrial Apoptosis. (A) Enrichment of KEGG pathways. (B) GSEA analysis in VSMCs treated with Ang II stimulation and Nupr1 deficiency. (C) Chordal diagram of GO pathways related with cell fate and the contributing DEPs. (D) Stem plot of DEPs in the apoptosis pathway from the indicated groups. (E) RT‐qPCR analysis of mRNA levels of candidate genes in VSMCs. Data were presented as relative fold change to controls ( n = 6 per group). (F) Expressions of Gadd45b in VSMCs measured by Western blot and its quantification from indicated groups measured by Western blot ( n = 5 per group). (G, H) Representative images of ROS staining in indicated groups. Semi‐quantitative analysis of mean fluorescence intensity in indicated groups ( n = 6 per group). (I) Representative images of calcein and Annexin V fluorescence results showing mPTP opening in indicated groups. (J) Quantification of fluorescence intensity, including Annexin V and mPTP ( n = 3 per group). (K) Co‐immunoprecipitation and Western blot assays of Myc‐Nupr1 and Gadd45b. (L) Co‐immunoprecipitation assays of Myc‐Gadd45b and Nupr1.

    Article Snippet: According to mPTP test kit instructions (C2009S, Beyotime), 200 μL of Calcein AM staining solution and fluorescence quenching working solution were added to each well after the respective cell treatments.

    Techniques: Analysis, Quantitative RT-PCR, Western Blot, Staining, Fluorescence, Co-Immunoprecipitation Assay, Significance Assay