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Merck
CN

D8938

Sigma-Aldrich

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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UNSPSC代码:
41121800
NACRES:
NB.22
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物料

glass

特点

autoclavable

制造商/商品名称

Kimble® 885300-0002

杵A空隙

0.0030-0.0050 in.

杵B空隙

0.0005-0.0025 in.

工作体积 × 长度

2 mL × 60 mm

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特点和优势

  • 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

法律信息

KIMBLE is a registered trademark of DWK Life Sciences

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
Benjamin C Reiner et al.
G3 (Bethesda, Md.), 10(5), 1647-1655 (2020-03-07)
Long interspersed element-1 retrotransposons (LINE-1 or L1) are ∼6 kb mobile DNA elements implicated in the origins of many Mendelian and complex diseases. The actively retrotransposing L1s are mostly limited to the L1 human specific (L1Hs) transcriptional active (Ta) subfamily.
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

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