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Merck
CN

D8938

KIMBLE Dounce组织研磨套装

2 mL complete

别名:

Dounce匀浆器, KIMBLE组织研磨器

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NACRES:
NB.22
UNSPSC Code:
41121800
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产品名称

KIMBLE Dounce组织研磨套装, 2 mL complete

material

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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Features and Benefits

  • 3.3硼硅玻璃制成
  • 主要用于匀浆后细胞核依然保持完整的细胞工作。
  • 全玻璃结构
  • 每套配有两根研磨杵
  • 松研磨杵用于初步研磨
  • 紧研磨杵用于最终匀浆
  • 部件可更换

Legal Information

KIMBLE is a registered trademark of DWK Life Sciences

历史批次信息供参考:

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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
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
Nur Jury et al.
Clinical epigenetics, 12(1), 32-32 (2020-02-20)
Hexanucleotide repeat expansions of the G4C2 motif in a non-coding region of the C9ORF72 gene are the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Tissues from C9ALS/FTD patients and from mouse models of ALS
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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