The All-in-One Starter Kit for Human iPSC-derived Sensory Neurons
The addition of the new MATURATION MAXIMIZER supplement to the sensory neuron kit gives:
SIGNIFICANTLY INCREASED KEY MARKER EXPRESSION & ACCELERATE NEURONAL MATURATION
An average increase of 30-45% of neurons expressing TRPv1, Nav1.7 and Nav1.8 in week 4 of culture; 90% neurons response to capsaicin on day 22.
FASTER MATURATION, QUICKER RESULTS
An average increase of 30-45% of neurons expressing TRPv1, Nav1.7 and Nav1.8 in week 4 of culture; 90% neurons response to capsaicin on day 22.
FASTER MATURATION, QUICKER RESULTS
An average increase of 30-45% of neurons expressing TRPv1, Nav1.7 and Nav1.8 in week 4 of culture; 90% neurons response to capsaicin on day 22.
FASTER MATURATION, QUICKER RESULTS
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2x 250 mL Striatal Neuron Basal Medium (Store at 4 oC upon receipt)
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2x 7.5 mL Striatal Neuron Medium Supplement (Store at or below -20 oC upon receipt)
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1 vial of Differentiation Supplement A (Store at 4 oC upon receipt)
Our iPSC-derived astrocytes are cryopreserved for convenience, and they are assay-ready within 48 hrs. Once thawed, Axol's astrocytes display all indicative astrocytic markers and will respond to glutamate stimulation, a key functional characteristic within 48-60 hrs. They also express markers showing that Axol's Human iPSC-derived astrocytes are physiologically representative of human primary astrocytes.
Axol's Neuronal Media is designed for optimal growth of normal primary neurons in vitro. For use with ax114667 Primary Cortical Neurons.
Axol’s Cell Recovery Enzyme is exclusively designed for the digestion of the bio-friendly Axol hydrogel enabling recovery of cells, spheroids, organoids or tissue samples intact.
Axol's biocompatible hydrogel is supplied ready to use in a syringe and mimics the extracellular matrix, supporting cell growth and differentiation with consistent results. Tested applications range from: 3D cell culture and organ-on-a-chip models, through to drug release studies and 3D printing.
Sensory Neuron Maintenance Medium for the maintenance of sensory neuron progenitors and derived neurons.
