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引用および参考文献 (16)
引用および参考文献
Abstract
The HECT domain ligase itch ubiquitinates endophilin and localizes to the trans-Golgi network and endosomal system.
Authors:Angers A, Ramjaun AR, McPherson PS
Journal:J Biol Chem
PubMed ID:14684745
'Endophilin A1 is an SH3 domain-containing protein functioning in membrane trafficking on the endocytic pathway. We have identified the E3 ubiquitin ligase itch/AIP4 as an endophilin A1-binding partner. Itch belongs to the Nedd4/Rsp5p family of proteins and contains an N-terminal C2 domain, four WW domains and a catalytic HECT domain. ... More
Ligands for clathrin-mediated endocytosis are differentially sorted into distinct populations of early endosomes.
Authors:Lakadamyali M, Rust MJ, Zhuang X
Journal:Cell
PubMed ID:16530046
'Cells rely on the correct sorting of endocytic ligands and receptors for proper function. Early endosomes have been considered as the initial sorting station where cargos for degradation separate from those for recycling. Using live-cell imaging to monitor individual endosomes and ligand particles in real time, we have discovered a ... More
Simultaneous prospective purification of adult subventricular zone neural stem cells and their progeny.
Authors:Pastrana E, Cheng LC, Doetsch F,
Journal:Proc Natl Acad Sci U S A
PubMed ID:19332781
'The ability to prospectively isolate adult neural stem cells and their progeny is crucial to study their biology and therapeutic potential. Stem cells in adult mammalian neurogenic niches are a subset of astrocytes. A major limitation in the field has been the inability to distinguish stem cell astrocytes from niche ... More
A fluid membrane-based soluble ligand-display system for live-cell assays.
Authors:Nam JM, Nair PM, Neve RM, Gray JW, Groves JT
Journal:Chembiochem
PubMed ID:16456901
Test samples for optimizing STORM super-resolution microscopy.
Authors:Metcalf DJ, Edwards R, Kumarswami N, Knight AE,
Journal:
PubMed ID:24056752
STORM is a recently developed super-resolution microscopy technique with up to 10 times better resolution than standard fluorescence microscopy techniques. However, as the image is acquired in a very different way than normal, by building up an image molecule-by-molecule, there are some significant challenges for users in trying to optimize ... More