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D8938

Sigma-Aldrich

KIMBLE Dounce tissue grinder set

2 mL complete

Sinônimo(s):

885300-0002, Dounce, Dounce Homogenizer, Glass Tissue Grinder, KIMBLE Tissue Grinder, KONTES, Pestles, Tissue Grinder, Tubes

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About This Item

Código UNSPSC:
41121800
NACRES:
NB.22

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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Informações legais

KIMBLE is a registered trademark of DWK Life Sciences

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Fang-Yuan Hu et al.
Frontiers in bioengineering and biotechnology, 8, 564057-564057 (2020-10-20)
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
Naomi Habib et al.
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
Naomi Habib et al.
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
Alan Selewa et al.
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
Jonathan M Levy et al.
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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