The Nuclear Membrane Methods and Protocols /
| مؤلف مشترك: | |
|---|---|
| مؤلفون آخرون: | , |
| الملخص: | XI, 346 p. 62 illus., 58 illus. in color. text |
| اللغة: | الإنجليزية |
| منشور في: |
New York, NY :
Springer US : Imprint: Humana,
2025.
|
| الطبعة: | 1st ed. 2025. |
| سلاسل: | Methods in Molecular Biology,
2958 |
| الموضوعات: | |
| الوصول للمادة أونلاين: | https://doi.org/10.1007/978-1-0716-4714-1 |
| التنسيق: | الكتروني كتاب |
جدول المحتويات:
- Lipidomic profiling of isolated nuclei from mice and cultured cells
- Profiling plant nuclear envelope composition using subtractive proteomics
- Ultrastructural visualization of the nuclearenvelope in HeLa cells
- Imaging nuclear envelopes using correlative AFM/fluorescence microscopy
- Fast super-resolution live cell imaging of nuclear membrane-endoplasmic reticulum dynamicsImmunostaining the yeast nuclear membrane for imaging by super-resolution fluorescence microscopy
- Visualizing phosphatidic acid and diacylglycerol at the nuclear envelope in fission yeast
- Measuring molecular mass densities at subcellular resolution using optical diffraction tomography
- Quantification and comparison of protein distribution on nuclear membrane
- Quantifying nuclear shape fluctuations along the cell cycle, with a focus on early mitosis
- Micropost arrays to model ECM fiber obstacles during cell migration in confinement
- Use of nucleoporin-conjugated beads to study the nuclear pore complex assembly on the nuclear membrane
- T4 DNA-induced reconstruction of artificial nuclei in living mouse oocyte
- Preparation of nucleoplasmic extract and its application in DNA end processing
- Liposome floatation assays to study membrane interactions of nucleoporins
- Giant unilamellar vesicles (GUVs) to study membrane interaction of nucleoporins
- One-pot reconstitution of GPCRs into unilamellar vesicles for fluorescence-based phospholipid scramblase activity assay
- Identifying genomic DNA sequences near the nuclear lamina using proximity biotinylation with Ascorbate Peroxidase
- Pairing LaminB1-DamID and Immuno-3D-FISH to resolve and verify peripheral genome organization of adipogenesis
- Measurement of spatial contact map using sequential FISH.