Quick Neuron™ Sensory – mRNA Kit

Quick-Neuron™ Sensory – mRNA Kits enable the differentiation of human pluripotent stem cells into sensory neurons using mRNA-based technology through an optimized and reproducible workflow.

Note: This kit is no longer available for individual sale. We now offer bulk orders and custom differentiation services to support your project needs.

Advantages of iPSC-Derived Sensory Neurons

Rapid Differentiation
~1 week
Optimized & Reproducible
ISO-9001 certified
Highly Pure Population
PRPH+, SCN9A+
No Genetic Footprint
0 modifications

Sensory Neuron Differentiation Kit Protocol

Explore our detailed differentiation protocols, a step-by-step guide designed to simplify and optimize your laboratory procedures using our iPSC-derived cells and differentiation kits. These protocols leverage the latest advancements in iPSC technology to ensure efficient and reproducible results.

Sensory neuron differentiation protocol workflow timeline
Phase contrast images of sensory neuron cell cultures across days 1 to 10 post-differentiation
Sensory neuron morphology is confirmed via phase contrast imagery. Representative images of Quick-Neuron™ Sensory – mRNA Kit cell cultures on days 1-10 post-differentiation (scale bar = 100 μm).

Sensory Neuron Characterization

Characterization of iPSC-derived sensory neurons is crucial to ensure their utility in research. Employing sensory neuron markers, we can confirm the identity and purity of these neurons.

Sensory Neuron Marker Expression

Understanding the role of sensory neuron markers is crucial in neuroscience research. Our comprehensive guide delves into the identification and significance of these markers in iPSC-derived neurons, providing essential information for researchers.

Immunocytochemistry image of Quick-Neuron Sensory cells showing PRPH and BRN3A expression

iPSC-derived sensory neurons express neuronal markers and display typical neurite growth. Immunofluorescent staining of Quick-Neuron™ Sensory – mRNA Kit cell cultures shows typical neurite growth and expression of PRPH and BRN3A on day 10 post-differentiation (scale bar = 100 μm). Staining conditions: Peripherin Rabbit polyclonal antibody (VI3079111) and BRN3A(14A6):sc-8429 mouse (B0521), 1:100, 1:2000. Nuclei were counterstained with Hoechst 33342.

Real-time Quantitative PCR Analysis

Real-time quantitative PCR analysis of expression levels of sensory neuron-associated genes SCN9A, PRPH, ISL1, and BRN3A were examined. The graph shows comparison of gene expression in Quick-Neuron™ – Sensory mRNA Culture on day 10 with gene expression in Human Dorsal Root Ganglion total RNA (TaKaRa, Catalog Number: 636150). The relative gene expression is normalized to phosphoglycerate kinase 1 (PGK1), and then calculated as a fold induction relative to hiPSCs as a control. Error bars show standard deviation.

Real-time quantitative PCR analysis of sensory neuron marker gene expression: SCN9A, PRPH, ISL1, and BRN3A

Product Specifications

Parameters Specifications
Product Name Quick-Neuron™ Sensory – mRNA Kit
Catalog No. SS-mRNA
Product Components QNS-mRNA-P, Component N, Component S1, and Component P
Storage Conditions mRNA should be stored at -80°C. All other components can be stored at -20°C or -80°C.
Cell Type Sensory Neurons
Induction Method Transcription factors delivered by synthetic mRNA
Differentiation At Day 7 Post-Differentiation:
>80% TUBB3+,
>50% PRPH+,
>50% SCN9A+/TUBB3+ (Stain for ISL1, no criteria)
Sterility No growth observed
Mycoplasma No DNA detected
Restricted Use For research use only. Not for use in diagnostic or therapeutic procedures.