melan-a Search Results


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Bioss rabbit monoclonal antihuman melan a
OPN expression in normal human epidermal melanocytes (NHMs). (A) Relative expression level of OPNs was analyzed by qPCR. OPN level was normalized with GAPDH level ( n = 8). (B) The cell lysate was analyzed by Western blot using anti‐OPNs antibody and β‐actin. The relative protein level was quantified using Quantity One software ( n = 3). (C) Immunofluorescence of normal human epidermal melanocyte with specific antibodies against OPNs (yellow), and nuclei (blue) under the fluorescence microscope. Scale bar = 20 μm. (D) Immunofluorescence of normal human epidermal melanocyte with specific antibodies against OPN3 (yellow), and nuclei (blue) under the confocal microscope. Scale bar = 20 μm. (E) OPN3 colocalized with <t>melan‐A</t> in human epidermal melanocytes with immunofluorescence double staining method. Photomicrographs were taken with Cell Observer‐Living Cells (Zeiss) and pseudocolored with Axiovision software (Zeiss). Scale bar = 20 μm (400 × magnification).
Rabbit Monoclonal Antihuman Melan A, supplied by Bioss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems mouse anti melan a mab8008
OPN expression in normal human epidermal melanocytes (NHMs). (A) Relative expression level of OPNs was analyzed by qPCR. OPN level was normalized with GAPDH level ( n = 8). (B) The cell lysate was analyzed by Western blot using anti‐OPNs antibody and β‐actin. The relative protein level was quantified using Quantity One software ( n = 3). (C) Immunofluorescence of normal human epidermal melanocyte with specific antibodies against OPNs (yellow), and nuclei (blue) under the fluorescence microscope. Scale bar = 20 μm. (D) Immunofluorescence of normal human epidermal melanocyte with specific antibodies against OPN3 (yellow), and nuclei (blue) under the confocal microscope. Scale bar = 20 μm. (E) OPN3 colocalized with <t>melan‐A</t> in human epidermal melanocytes with immunofluorescence double staining method. Photomicrographs were taken with Cell Observer‐Living Cells (Zeiss) and pseudocolored with Axiovision software (Zeiss). Scale bar = 20 μm (400 × magnification).
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Boster Bio themelan a m02033 antibody
OPN expression in normal human epidermal melanocytes (NHMs). (A) Relative expression level of OPNs was analyzed by qPCR. OPN level was normalized with GAPDH level ( n = 8). (B) The cell lysate was analyzed by Western blot using anti‐OPNs antibody and β‐actin. The relative protein level was quantified using Quantity One software ( n = 3). (C) Immunofluorescence of normal human epidermal melanocyte with specific antibodies against OPNs (yellow), and nuclei (blue) under the fluorescence microscope. Scale bar = 20 μm. (D) Immunofluorescence of normal human epidermal melanocyte with specific antibodies against OPN3 (yellow), and nuclei (blue) under the confocal microscope. Scale bar = 20 μm. (E) OPN3 colocalized with <t>melan‐A</t> in human epidermal melanocytes with immunofluorescence double staining method. Photomicrographs were taken with Cell Observer‐Living Cells (Zeiss) and pseudocolored with Axiovision software (Zeiss). Scale bar = 20 μm (400 × magnification).
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Novus Biologicals alexa fluor 647 novus biologicals nbp2 46603af647 multiple lots
OPN expression in normal human epidermal melanocytes (NHMs). (A) Relative expression level of OPNs was analyzed by qPCR. OPN level was normalized with GAPDH level ( n = 8). (B) The cell lysate was analyzed by Western blot using anti‐OPNs antibody and β‐actin. The relative protein level was quantified using Quantity One software ( n = 3). (C) Immunofluorescence of normal human epidermal melanocyte with specific antibodies against OPNs (yellow), and nuclei (blue) under the fluorescence microscope. Scale bar = 20 μm. (D) Immunofluorescence of normal human epidermal melanocyte with specific antibodies against OPN3 (yellow), and nuclei (blue) under the confocal microscope. Scale bar = 20 μm. (E) OPN3 colocalized with <t>melan‐A</t> in human epidermal melanocytes with immunofluorescence double staining method. Photomicrographs were taken with Cell Observer‐Living Cells (Zeiss) and pseudocolored with Axiovision software (Zeiss). Scale bar = 20 μm (400 × magnification).
Alexa Fluor 647 Novus Biologicals Nbp2 46603af647 Multiple Lots, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


OPN expression in normal human epidermal melanocytes (NHMs). (A) Relative expression level of OPNs was analyzed by qPCR. OPN level was normalized with GAPDH level ( n = 8). (B) The cell lysate was analyzed by Western blot using anti‐OPNs antibody and β‐actin. The relative protein level was quantified using Quantity One software ( n = 3). (C) Immunofluorescence of normal human epidermal melanocyte with specific antibodies against OPNs (yellow), and nuclei (blue) under the fluorescence microscope. Scale bar = 20 μm. (D) Immunofluorescence of normal human epidermal melanocyte with specific antibodies against OPN3 (yellow), and nuclei (blue) under the confocal microscope. Scale bar = 20 μm. (E) OPN3 colocalized with melan‐A in human epidermal melanocytes with immunofluorescence double staining method. Photomicrographs were taken with Cell Observer‐Living Cells (Zeiss) and pseudocolored with Axiovision software (Zeiss). Scale bar = 20 μm (400 × magnification).

Journal: Photochemistry and Photobiology

Article Title: Opsin3 Downregulation Induces Apoptosis of Human Epidermal Melanocytes via Mitochondrial Pathway

doi: 10.1111/php.13178

Figure Lengend Snippet: OPN expression in normal human epidermal melanocytes (NHMs). (A) Relative expression level of OPNs was analyzed by qPCR. OPN level was normalized with GAPDH level ( n = 8). (B) The cell lysate was analyzed by Western blot using anti‐OPNs antibody and β‐actin. The relative protein level was quantified using Quantity One software ( n = 3). (C) Immunofluorescence of normal human epidermal melanocyte with specific antibodies against OPNs (yellow), and nuclei (blue) under the fluorescence microscope. Scale bar = 20 μm. (D) Immunofluorescence of normal human epidermal melanocyte with specific antibodies against OPN3 (yellow), and nuclei (blue) under the confocal microscope. Scale bar = 20 μm. (E) OPN3 colocalized with melan‐A in human epidermal melanocytes with immunofluorescence double staining method. Photomicrographs were taken with Cell Observer‐Living Cells (Zeiss) and pseudocolored with Axiovision software (Zeiss). Scale bar = 20 μm (400 × magnification).

Article Snippet: NHMs were also double labeled with mouse monoclonal antihuman OPN3 (1:50; MDL, MD6636‐100) and rabbit monoclonal antihuman melan‐A (1:50; Bioss, Beijing, China, bs‐7362R).

Techniques: Expressing, Western Blot, Software, Immunofluorescence, Fluorescence, Microscopy, Double Staining