Mouse Liver Single-Cell Dissociation with Cold Protease v1 (protocols.io.bhpcj5iw)

protocols.io ◽  
2020 ◽  
Author(s):  
Sanjay Subramanian ◽  
Stacey Huppert
PROTEOMICS ◽  
2011 ◽  
Vol 11 (17) ◽  
pp. 3556-3564 ◽  
Author(s):  
Wei Liu ◽  
Yufang Hou ◽  
Huahai Chen ◽  
Handong Wei ◽  
Weiran Lin ◽  
...  

2017 ◽  
Vol 34 (1) ◽  
pp. 293-298 ◽  
Author(s):  
Ursula L. Triantafillu ◽  
Jaron N. Nix ◽  
Yonghyun Kim

iScience ◽  
2021 ◽  
pp. 103233
Author(s):  
Qi Su ◽  
Sun Y. Kim ◽  
Funmi Adewale ◽  
Ye Zhou ◽  
Christina Aldler ◽  
...  

1988 ◽  
Vol 8 (11) ◽  
pp. 4966-4971
Author(s):  
C F Kuo ◽  
K E Paulson ◽  
J E Darnell

In situ hybridization showed that all fetal hepatocytes contain glutamine synthetase (GS) mRNA but that in adult mouse liver, only a single cell layer surrounding the central veins contains GS mRNA. A shift from the fetal to the adult pattern begins within a few days of birth and is complete within 12 days of birth. Since the total GS mRNA and the transcription rate of the single GS gene are similar at birth and in adults, we conclude that there is a generalized reduction in GS transcription for most hepatocytes and a sharp rise in GS transcription for the immediate pericentral cells. This may be a case of positional regulation of specific gene transcription in apparently a single cell lineage.


protocols.io ◽  
2018 ◽  
Author(s):  
James Fletcher ◽  
Rachel Botting ◽  
Emily Stephenson ◽  
Peter Vegh ◽  
Muzlifah Haniffa

2020 ◽  
Author(s):  
Helena García-Castro ◽  
Nathan J Kenny ◽  
Patricia Álvarez-Campos ◽  
Vincent Mason ◽  
Anna Schönauer ◽  
...  

AbstractSingle-cell sequencing technologies are revolutionizing biology, but are limited by the need to dissociate fresh samples that can only be fixed at later stages. We present ACME (ACetic-MEthanol) dissociation, a cell dissociation approach that fixes cells as they are being dissociated. ACME-dissociated cells have high RNA integrity, can be cryopreserved multiple times, can be sorted by Fluorescence-Activated Cell Sorting (FACS) and are permeable, enabling combinatorial single-cell transcriptomic approaches. As a proof of principle, we have performed SPLiT-seq with ACME cells to obtain around ∼34K single cell transcriptomes from two planarian species and identified all previously described cell types in similar proportions. ACME is based on affordable reagents, can be done in most laboratories and even in the field, and thus will accelerate our knowledge of cell types across the tree of life.


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