D8938
KIMBLE Dounce tissue grinder set
2 mL complete
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About This Item
Produtos recomendados
Materiais
glass
Características
autoclavable
fabricante/nome comercial
Kimble® 885300-0002
espaço do pilão A
0.0030-0.0050 in.
espaço do pilão B
0.0005-0.0025 in.
volume de trabalho × C
2 mL × 60 mm
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Descrição geral
Designed primarily for cellular work where the nucleus remains intact after homogenization. All-glass construction. Two pestles are supplied with each complete set. Large clearance pestle is used for the initial sample reduction. Small clearance pestle is used to form the final homogenate.
Informações legais
KIMBLE is a registered trademark of DWK Life Sciences
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Retina is a crucial tissue for capturing and processing light stimulus. It is critical to describe the characteristics of retina at the single-cell level for understanding its biological functions. A variety of abnormalities in terms of morphology and function are
Nature neuroscience, 23(6), 701-706 (2020-04-29)
The role of non-neuronal cells in Alzheimer's disease progression has not been fully elucidated. Using single-nucleus RNA sequencing, we identified a population of disease-associated astrocytes in an Alzheimer's disease mouse model. These disease-associated astrocytes appeared at early disease stages and
Nature methods, 14(10), 955-958 (2017-08-29)
Single-nucleus RNA sequencing (sNuc-seq) profiles RNA from tissues that are preserved or cannot be dissociated, but it does not provide high throughput. Here, we develop DroNc-seq: massively parallel sNuc-seq with droplet technology. We profile 39,111 nuclei from mouse and human
Scientific reports, 10(1), 1535-1535 (2020-02-01)
A comprehensive reference map of all cell types in the human body is necessary for improving our understanding of fundamental biological processes and in diagnosing and treating disease. High-throughput single-cell RNA sequencing techniques have emerged as powerful tools to identify
Nature biomedical engineering, 4(1), 97-110 (2020-01-16)
The success of base editors for the study and treatment of genetic diseases depends on the ability to deliver them in vivo to the relevant cell types. Delivery via adeno-associated viruses (AAVs) is limited by AAV packaging capacity, which precludes
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