AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1
Motor Neuron Disease
Amyotrophic Lateral Sclerosis hiPSC samples expanded and characterized in-house
Age: 37 YR
The cell line submitted to the Repository was recovered and expanded. The expanded line was evaluated for viability surface antigen expression and alkaline phosphatase activity. Pluripotency was assessed via embryoid body (EB) formation. Steady-state mRNA
Storage and Shipping
Liquid nitrogen. Dry ice.
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