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Image Search Results
Journal: Scientific Reports
Article Title: Tracing the invisible mutant ADNP protein in Helsmoortel-Van der Aa syndrome patients
doi: 10.1038/s41598-024-65608-x
Figure Lengend Snippet: Overview of the reported ADNP antibodies with indication of the observed molecular weights and tested sample materials.
Article Snippet: Adult human brain (NB820-59177), human brain cerebellum (NB820-59180), human brain frontal lobe (NB820- 59186), and
Techniques: Molecular Weight, Transfection, Expressing, Construct
Journal: Scientific Reports
Article Title: Tracing the invisible mutant ADNP protein in Helsmoortel-Van der Aa syndrome patients
doi: 10.1038/s41598-024-65608-x
Figure Lengend Snippet: A polyclonal N-terminal ADNP antibody from Aviva Systems detects ADNP specifically in murine and rat tissues and suggests proteolytic processing of the protein in the human brain. Cerebellum, frontal cortex or lobe, hippocampus and whole brains of control mice, rats and humans were lysed in RIPA buffer and used as protein samples for the assessment of N-terminal antibody of Aviva systems. (A – C) The predicted molecular weight of ADNP is 124 kDa. The antibody recognizes ADNP in a range of 145 kDa with (E) additional lower mass signal of 85 kDa in all human brain regions. (B – D – F) Western blot analysis of the blocking peptide competition assay. Supplementation of the immunization peptide in a 5 × excess to antibody concentration reduced the signal observed at 145 kDa in all tested cell lines. Importantly, the 85 kDa band suggestive for proteolytic cleavage as well as degraded ADNP signal disappeared completely after immunization peptide supplementation. GAPDH was used as a loading control.
Article Snippet: Adult human brain (NB820-59177), human brain cerebellum (NB820-59180), human brain frontal lobe (NB820- 59186), and
Techniques: Control, Molecular Weight, Western Blot, Blocking Assay, Competitive Binding Assay, Concentration Assay
Journal: Scientific Reports
Article Title: Tracing the invisible mutant ADNP protein in Helsmoortel-Van der Aa syndrome patients
doi: 10.1038/s41598-024-65608-x
Figure Lengend Snippet: Different C-terminal ADNP antibodies detect ADNP in the range of 150 kDa and suggest proteolytic processing of the protein in the brain. Cerebellum, frontal cortex or lobe, hippocampus and whole brains of control mice, rats, and humans were lysed in RIPA buffer and used as protein samples for the assessment with three C-terminal antibodies with the optimized dilutions listed in Table . GAPDH was used as a loading control. The predicted molecular weight of ADNP is 124 kDa. ( A ) C ) Murine samples indicate detection of ADNP in the range of 150 kDa with bands suggesting proteolytic processing at 50 kDa. ( D – F ) Rat samples indicate detection of ADNP in the range of 150 kDa with bands indicating proteolytic processing at 82 kDa after incubation with the C-terminal Abcam antibody. ( G – I ) Human brain samples indicate detection of ADNP at different molecular weights of 124 – 150 kDa in the adult frontal lobe and hippocampus and highlight the antibody differences in detection of ADNP. The three tested antibodies showed strong band signals at lower molecular weights, which could indicate proteolytic cleavage or degradation of the protein.
Article Snippet: Adult human brain (NB820-59177), human brain cerebellum (NB820-59180), human brain frontal lobe (NB820- 59186), and
Techniques: Control, Molecular Weight, Incubation
Journal: Nature Communications
Article Title: Mammalian brain glycoproteins exhibit diminished glycan complexity compared to other tissues
doi: 10.1038/s41467-021-27781-9
Figure Lengend Snippet: Protein lysate from a representative male mouse cortex and cerebellum with human plasma as a positive control was treated with or without PNGase F and visualized using biotinylated lectins (ConA, GNL, PHA-E, AAL, RCA, and SNA) in addition to immunoblotting for actin and staining for total protein. Non-specific binding of lectins to PNGase F is noted by an asterisk (*) near 35 kDa, as shown in the Total Protein stain. Protein blotting of brain lysate with each lectin has been repeated at least three times each with similar results. A schematic with common lectin-binding sites is shown for reference. Source data are provided as a Source Data file.
Article Snippet:
Techniques: Clinical Proteomics, Positive Control, Western Blot, Staining, Binding Assay
Journal: Cell reports
Article Title: A PINK1 input threshold arises from positive feedback in the PINK1/Parkin mitophagy decision circuit
doi: 10.1016/j.celrep.2023.113260
Figure Lengend Snippet: KEY RESOURCES TABLE
Article Snippet: Healthy human brain lysate, whole (
Techniques: Recombinant, Bradford Assay, Mutagenesis, Plasmid Preparation, Microscopy, Cell Culture, Software, Sequencing
Journal: iScience
Article Title: Inhibition of the pseudokinase MLKL alters extracellular vesicle release and reduces tumor growth in glioblastoma
doi: 10.1016/j.isci.2022.105118
Figure Lengend Snippet:
Article Snippet:
Techniques: Recombinant, Enzyme-linked Immunosorbent Assay, EdU Assay, Flow Cytometry, Imaging, Cell Counting, Luciferase, Viability Assay, Isolation
Journal: Experimental Neurobiology
Article Title: LGR5 and Downstream Intracellular Signaling Proteins Play Critical Roles in the Cell Proliferation of Neuroblastoma, Meningioma and Pituitary Adenoma
doi: 10.5607/en.2019.28.5.628
Figure Lengend Snippet: Patient description and tumor sample characteristics
Article Snippet:
Techniques: Concentration Assay
Journal: Experimental Neurobiology
Article Title: LGR5 and Downstream Intracellular Signaling Proteins Play Critical Roles in the Cell Proliferation of Neuroblastoma, Meningioma and Pituitary Adenoma
doi: 10.5607/en.2019.28.5.628
Figure Lengend Snippet: Expression of LGR5, hnRNPA2B1, and hnRNPH3 proteins in human normal, benign meningioma, and pituitary adenoma tissues, and immunohistochemistry for LGR5 and hnRNPH3 in meningioma and pituitary adenoma tissues with immunofluorescence confocal microscopy. (A) Comparison of expression levels of LGR5, hnRNPA2B1, and hnRNPH3 between normal, benign meningioma, and pituitary adenoma by western blotting. (B) Confocal images of the human normal brain (top), meningioma (middle) and pituitary adenoma (bottom) tissues stained with antibodies against LGR5 (green) and hnRNPH3 (red). Scale bar: 20 μm. The number of LGR5 + /hnRNPH3 + cells per DAPI positive cells and hnRNPH3 + cells per LGR5 positive cells was counted and expressed as %.
Article Snippet:
Techniques: Expressing, Immunohistochemistry, Immunofluorescence, Confocal Microscopy, Comparison, Western Blot, Staining