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ATCC
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Millipore
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Merck KGaA
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Novus Biologicals
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Cell Signaling Technology Inc
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Millipore
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Danaher Inc
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Santa Cruz Biotechnology
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Millipore
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Millipore
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Image Search Results
Journal: PLoS ONE
Article Title: Involvement of B2 Receptor in Bradykinin-Induced Proliferation and Proinflammatory Effects in Human Nasal Mucosa-Derived Fibroblasts Isolated from Chronic Rhinosinusitis Patients
doi: 10.1371/journal.pone.0126853
Figure Lengend Snippet: (A) Immunohistochemical staining showing fibroblast distribution in the normal and CRSsNP nasal mucosa. Inferior turbinates (control) and CRSsNP nasal mucosa were stained with anti-fibroblast Ab. Please note that immunoreactivity for fibroblasts was stronger in the submucosal stroma of CRSsNP specimens than in the nasal septal deviation controls. The arrow indicates a positive staining for fibroblast. ep: epithelial cells; v: blood vessels; g: submucosal glands. Scale bar = 100 μm. (B) Immunocytochemical staining of primary cultured NMDFs. Cells grown on chamber slides in subconfluent and confluent conditions were fixed, stained with anti-vimentin Ab, and analyzed under phase-contrast and fluorescence microscopy. This is representative of three similar experiments.
Article Snippet: The sections were then washed in TBS (Tris-buffered saline containing 1% CaCl 2 ), immersed in sodium citrate buffer (pH 6.0), and heated on a water bath for 20 min. After blocking with buffer containing 10% FBS, the slides were incubated at 4 ° C overnight with primary Ab specific for
Techniques: Immunohistochemical staining, Staining, Control, Cell Culture, Fluorescence, Microscopy
Journal: PLoS ONE
Article Title: Involvement of B2 Receptor in Bradykinin-Induced Proliferation and Proinflammatory Effects in Human Nasal Mucosa-Derived Fibroblasts Isolated from Chronic Rhinosinusitis Patients
doi: 10.1371/journal.pone.0126853
Figure Lengend Snippet: NMDFs were treated with the indicated concentrations of BK for 16 h, and (A) cell proliferation was determined by the MTT assay and direct cell counting assay (n = 3–4). (B) The expression of CAMs and COXs was determined by western blotting (n = 4). (C) Effect of BK on monocytes adhesion to fibroblasts. Twenty-four well plates seeded with or without NMDFs were treated with BK (1 μM) for 16 h. Then, BCECF/AM-labeled monocytes were allowed to adhere to the wells for 1 h. After a brief wash, monocytes adhered to wells (green spots) were determined by direct cell counting under the high-powered field (HPF) (n = 4). * P <0.05, ** P <0.01, *** p < 0.001 versus basal (BK 0 μM).
Article Snippet: The sections were then washed in TBS (Tris-buffered saline containing 1% CaCl 2 ), immersed in sodium citrate buffer (pH 6.0), and heated on a water bath for 20 min. After blocking with buffer containing 10% FBS, the slides were incubated at 4 ° C overnight with primary Ab specific for
Techniques: MTT Assay, Cell Counting, Expressing, Western Blot, Labeling
Journal: Cell metabolism
Article Title: Human skeletal muscle CD90 + fibro-adipogenic progenitors are associated with muscle degeneration in type 2 diabetic patients
doi: 10.1016/j.cmet.2021.10.001
Figure Lengend Snippet: KEY RESOURCES TABLE
Article Snippet:
Techniques: Recombinant, Blocking Assay, Staining, Imaging, Sample Prep, Software, Flow Cytometry, RNA Sequencing, Quantitative Proteomics
Journal: Cell metabolism
Article Title: Human skeletal muscle CD90 + fibro-adipogenic progenitors are associated with muscle degeneration in type 2 diabetic patients
doi: 10.1016/j.cmet.2021.10.001
Figure Lengend Snippet: KEY RESOURCES TABLE
Article Snippet:
Techniques: Recombinant, Blocking Assay, Staining, Imaging, Sample Prep, Software, Flow Cytometry, RNA Sequencing, Quantitative Proteomics
Journal: Science Advances
Article Title: Modeling long QT syndrome type 2 on-a-chip via in-depth assessment of isogenic gene-edited 3D cardiac tissues
doi: 10.1126/sciadv.abq6720
Figure Lengend Snippet: ( A to C ) Characterization of CM differentiation of WT and edited hiPSCs, including (A) immunostaining for sarcomeric α-actinin (SAA, green) and CX43 (red), (B) lack of pluripotency marker expression, and (C) expression of CM-specific genes. ( D to F ) Characterization of CF differentiation of WT and edited hiPSCs, including (D) immunostaining for TE7 (green) and vimentin (red), (E) lack of pluripotency marker expression, and (F) expression of fibroblast-specific genes. Scale bars, 50 μm.
Article Snippet: Primary antibodies [mouse anti-SAA (A7811, Sigma-Aldrich), mouse anti-TNNT2 (MA512960, Thermo Fisher Scientific),
Techniques: Immunostaining, Marker, Expressing
Journal: Journal of Visualized Experiments : JoVE
Article Title: Isolation and Quantitative Immunocytochemical Characterization of Primary Myogenic Cells and Fibroblasts from Human Skeletal Muscle
doi: 10.3791/52049
Figure Lengend Snippet:
Article Snippet: Name/antigen Antibody species and isotype Clone name Dilution for use Catalogue no. Company Myogenic markers: CD56 (N-CAM) Mouse mc IgG 1 MY-31 (1:100) 347740 BD Desmin Rabbit mc IgG 1 D93F5 (XP) (1:250) 5332S NEB Myogenin Mouse mc IgG 1 F5D (1:50) F5D DSHB Myosin Heavy Chain Mouse mc IgG2b, kappa light chain MF20 (1:200) MF20 DSHB Fibroblast/connective tissue markers:
Techniques:
Journal: Frontiers in Physiology
Article Title: 3D Proximal Tubule Tissues Recapitulate Key Aspects of Renal Physiology to Enable Nephrotoxicity Testing
doi: 10.3389/fphys.2017.00123
Figure Lengend Snippet: List of antibodies used .
Article Snippet:
Techniques: