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HT Experiment :

Experiment Id  GSE201561 Name  Downstream targeted genes of Satb2 regulate synaptic formation and axonogenesis in developing cerebral cortex [RNA-seq]
Experiment Type  RNA-Seq Study Type  WT vs. Mutant
Source  GEO Curation Date  2023-10-10
description  Special AT-rich sequencebinding protein 2 (SATB2) is essential for the development of cerebral cortex and key molecular node for the establishment of proper neural circuitry and function. Mutations in SATB2 gene lead to SATB2-associated syndrome (SAS), which is characterized by abnormal development of skeleton and central nervus system. We generated Satb2 knockout mouse model through CRISPR-Cas9 technology and performed RNA-seq and ChIP-seq of embryonic cerebral cortex. We conducted RT-qPCR, western blot, immunofluorescence staining, luciferase reporter assay and behavioral analysis for experimental verification. Comparative gene expression profiling analysis of RNA-seq data for E17.5 wildtype and Satb2 knock-out mouse cerebral cortex
  • variables:
  • genotype,
  • bulk RNA-seq

1 Publications

Trail: HTExperiment

5 Samples

Trail: HTExperiment