Sigma货号D8938-1SET组织研磨套装KIMBLE

Sigma货号D8938-1SET组织研磨套装KIMBLE Dounce上海睿安生物13611631389

属性

物料:glass

特点:autoclavable

manufacturer/tradename: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:2ml╳60mm

说明

一般描述:主要为细胞工作设计，在匀浆后细胞核保持完整。全玻璃结构。每一套配有两根研杵。大间隙研杵用于初始样本降解。小间隙研杵用于最终匀浆。

法律信息:KIMBLE is a registered trademark of DWK Life Sciences.

同行评审论文(部分文献)

Disease-associated astrocytes in Alzheimer's disease and aging.
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
Cell Development Deficiency and Gene Expression Dysregulation of Trisomy 21 Retina Revealed by Single-Nucleus RNA Sequencing.
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
Restriction Enzyme Based Enriched L1Hs Sequencing (REBELseq): A Scalable Technique for Detection of Ta Subfamily L1Hs in the Human Genome.
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.
Massively parallel single-nucleus RNA-seq with DroNc-seq.
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
Cytosine and adenine base editing of the brain, liver, retina, heart and skeletal muscle of mice via adeno-associated viruses.
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