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Status |
Public on Mar 05, 2020 |
Title |
Raptor is required for β-cell metabolic coupling and repressing an α cell program before onset of hyperglycemia |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
Raptor deficient mice showed diabetic phenotype, to dissect the effect of hyperglycemia, we isolated euglycemic 2-week-old β cells to perform microarray. To determine the influence of Raptor deficiency on β cells independent of hyperglycemia, we hace employed whole transcriptome expression profiling as a discovery platform to identify differentially expressed genes compared with wild type controls. We isolated mice islets, then disgested them into single cells by 0.25% EDTA, and sorted for GFP by FACS.
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Overall design |
Raptor regulated gene expression in β cells from knockout mice was measured at 2 weeks after birth. Age-matched wild type mice were set as controls.
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Contributor(s) |
Wang Q, Ning G |
Citation(s) |
32439909 |
Submission date |
Nov 12, 2019 |
Last update date |
Jun 01, 2020 |
Contact name |
Qinglei Yin |
E-mail(s) |
yinqinglei128@163.com
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Organization name |
Ruijin Hospital Affiliated to Shanghai Jiaotong University School of Medicine
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Street address |
Ruijin Second Road No.197
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City |
Shanghai |
ZIP/Postal code |
200025 |
Country |
China |
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Platforms (1) |
GPL23038 |
[Clariom_S_Mouse] Affymetrix Clariom S Assay, Mouse (Includes Pico Assay) |
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Samples (7)
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Relations |
BioProject |
PRJNA588976 |