PNGM™ Primary Neuron Growth Medium BulletKit™
PNGM™ Primary Neuron Growth Medium BulletKit™
Product Overview
CloneticsTM PNGMTM Primary Neuron Growth Medium Kit (PNGMTM) was specifically developed for culturing embryonic primary rat and mouse neurons. The media kit is recommended for use with all of our primary rat and mouse neurons.
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Benefits
- Serum-free medium
- Allows for long-term maintenance and growth of neuronal cells
- Promotes development of high quality neuronal networks without the need of an astrocyte feeder layer
Storage and Content
1 x PNBMTM Basal Medium (CC-3256), 200 mL
1 x PNGMTM SinglequotsTM Growth Supplement Pack (CC-4462)
SDS, CoA, and Instructions
Certificate of Analysis (CoA)
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Educational Material
Brochures, White Papers etc.
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Recent Publications Demonstrate the Extended Versatility and Expanded Applications of Lonza’s BulletKit™ Media
Lonza, one of the market leaders in primary cells, has announced an increase in recent publications referencing its specialized BulletKit™ Growth and Differentiation Media. These peer-reviewed papers highlight the versatility of the media kits, which are proving especially useful for researchers looking to transition from established cell lines to primary cell culture or when co-culturing different cell types, mostly due to their convenience, adaptability and ease-of-use. -
Lonza's Bulletkit™ for Primary Cell Growth
Primary Cells are Different from Cell Lines. Why use the Same Classical Media? Learn how Lonza primary cells and media can support your cell research -
Primary Cells and Media Reference Guide
A comprehensive collection of Lonza primary cell and media products supporting many research areas.
ViaLightPlus Assay in PNGM™ Media of Rat Cortical Neurons
Comparison of survival of Clonetics™ Primary Rat Cortical Neurons cultured in PNGM™ Medium vs. Company A’s medium. Cryopreserved cells were thawed and plated in laminin-coated, 96 well plates at ~1000 cells per square mm (40% of the recommended seeding density) using either PNGM™ Medium or Company A’s medium. Cells were cultured without feeding for six days, at which time cell viability was assessed using the ViaLight™ Plus Cell Proliferation and Cytotoxicity BioAssay Kit. Results represent the average of 8 experiments.