STEMdiff™ Sensory Neuron Maturation Kit

Maturation kit for generation of functional sensory neurons from human iPS cell-derived sensory neuronal precursor cells
概要

Maturation kit for generation of functional sensory neurons from human iPS cell-derived sensory neuronal precursor cells

Advantages
⦁ Reduce animal usage by eliminating costly dorsal root ganglia explant workflows
⦁ Mature and maintain sensory neurons seamlessly following STEMdiff™ Sensory Neuron Differentiation Kit
⦁ Streamline PSC-derived sensory neuron generation with a simple, easy-to-use media format
⦁ Obtain physiologically relevant results with integrated BrainPhys™ media supporting neuronal activity and maturation
Components
  • BrainPhys™ Neuronal Medium, 100 mL (Catalog #05797)
  • STEMdiff™ Sensory Neuron Maturation Supplement, 25 mL
Subtype
专业培养基
Cell Type
PSC衍生神经细胞, 神经元
Species
Application
免疫细胞化学, 分化, 功能检测, 细胞培养, 表型, 表征
Brand
BrainPhys, STEMdiff
Area of Interest
疾病模型, 神经科学, 药物发现和毒性测试
Formulation
无血清


技术资料

Scientific Resources


数据及文献

Product Applications

This product is designed for use in the following research area(s) as part of the highlighted workflow stage(s). Explore these workflows to learn more about the other products we offer to support each research area.

Data and Publications

数据

Experimental Protocol for STEMdiff™ Sensory Neuron Differentiation and Maturation Kits

Figure 1. Schematic for the STEMdiff™ Sensory Neuron Culture System Protocol

Sensory neurons can be generated in 7 days from sensory neuron precursors after 6 days in STEMdiff™ Sensory Neuron Differentiation Medium. For the differentiation of sensory neuron precursors from hPSC-derived neural crest cells, see the PIS.

Figure 2. STEMdiff™ Sensory Neuron Kits Promote Differentiation Across Multiple Embryonic Stem and Induced Pluripotent Stem Cell Lines

NCCs generated from hPSCs in mTeSR™ Plus using the STEMdiff™ Neural Crest Differentiation Kit were differentiated and matured to sensory neurons using the STEMdiff™ Sensory Neuron Differentiation and Maturation Kits. (A) Sensory neurons were generated after hPSC-derived NCCs were cultured with the STEMdiff™ Sensory Neuron Differentiation Kit for 6 days and then the STEMdiff™ Sensory Neuron Maturation Kit for 6 days. The resulting cultures contain a population of cells expressing sensory neuron markers peripherin (green) and BRN3A (red) along with (B) neuronal marker class III β-tubulin (TUJ1, red). (C) Midbrain neuron controls generated with STEMdiff™ Midbrain Neuron Differentiation and Maturation Kits do not have detectable peripherin (green) or BRN3A (red) expression, although they express (D) neuronal marker class III β-tubulin (TUJ1, red). Nuclei are labeled with DAPI (blue). Human ES and iPS cell lines were maintained in either mTeSR™1, TeSR™-E8™, or mTeSR™ Plus and differentiated with STEMdiff™ Neural Crest Differentiation Kit, followed by STEMdiff™ Sensory Neuron Differentiation and Maturation Kits. The percentage expression of (E) BRN3A+ and (F) TUJ1+ cells in the resulting cultures was quantified. This differentiation generated BRN3A+ sensory neurons (25.3% ± 6.9%, mean ± SEM; n=7 cell lines, 3 - 23 replicates per condition) that expressed neuronal marker class III β-tubulin (TUJ1; 90.3% ± 4.1%, mean ± SEM; n=4 cell lines, 3 - 12 replicates per condition). Numbers are % positive over total DAPI in a tiled image. NCCs = neural crest cells; hPSCs = human pluripotent stem cells; ES = embryonic stem; iPS = induced pluripotent stem


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