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NACRES:
NB.22
UNSPSC Code:
41121800
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Laissez-nous vous aidermaterial
glass
feature
autoclavable
manufacturer/tradename
Kimble® 885300-0002
pestle A clearance
0.0030-0.0050 in.
pestle B clearance
0.0005-0.0025 in.
working volume × L
2 mL × 60 mm
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Catégories apparentées
Features and Benefits
- Manufactured from borosilicate glass 3.3
- Designed primarily for cellular work where the nucleus remains intact after homogenization.
- All-glass construction
- Two pestles are supplied with each complete unit
- Large clearance pestle is used for the initial sample reduction
- Small clearance pestle is used to form the final homogenate
- Replacement components are available and completely interchangeable
Legal Information
KIMBLE is a registered trademark of DWK Life Sciences
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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
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 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
Sripriya Ravindra Kumar et al.
Nature methods, 17(5), 541-550 (2020-04-22)
Recombinant adeno-associated viruses (rAAVs) are efficient gene delivery vectors via intravenous delivery; however, natural serotypes display a finite set of tropisms. To expand their utility, we evolved AAV capsids to efficiently transduce specific cell types in adult mouse brains. Building
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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