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GlycoFlux™ MSCV-PHKG1 Viral Particle provides durable expression of the catalytic γ subunit PHKG1, supporting skeletal-muscle-like control of glycogen breakdown. Ideal for contractile models; quantify γ-subunit-driven PhK activity, phosphorylase activation, and exercise-mimetic energy flux.
Product Type
Recombinant MSCV Retrovirus
Target
PHKG1
Species
Human
Promotor
MSCV 5' LTR promoter
Packaging System
Retrovirus
Packaging Cell
HEK293T
Application
This MSCV vector is a common retroviral vector system used to achieve high-efficiency, stable gene delivery into target cells, such as hematopoietic stem cells. It ensures long-term, sustained expression by stably integrating the gene into the host cell's genome.
Shipping
Dispatched on dry ice with temperature held at or below -80°C.
Storage
Store at -80°C to preserve titer and stability.
Handling Notes
Store at -80°C and avoid repeated freeze-thaw cycles to preserve viral titer. For safety, handle materials in a biological safety cabinet while wearing appropriate PPE (lab coat, gloves, and eye protection).
Product Disclaimer
These products are for research use only and not for diagnostic or clinical use. The user assumes full responsibility for all safety protocols and compliance with relevant regulations. While we are committed to quality, Creative Biolabs makes no guarantee as to the performance of these products in a specific application.
Quality Control
Titer Assay
qPCR
Mycoplasma Test
Negative
Sterility
Sterility testing confirmed no microbial contamination.
Transduction Evaluation
Creative Biolabs offers, upon request, in vitro and in vivo transduction assays to verify lentiviral targeting and to quantify transgene expression and functional output.
Insert Identity Confirmation
All Creative Biolabs retroviral vectors undergo PCR-based verification of proviral integration. Cells are transduced across a dilution series of the retroviral preparation; after several days, genomic DNA is isolated, and a defined region of the expected insert is PCR-amplified to confirm correct identity and integration.
The encoded protein is a serine/threonine kinase with a single kinase domain and two calmodulin-binding regions. It serves as the catalytic element of the phosphorylase kinase holoenzyme, a 16-part complex critical for glycogen breakdown. Pseudogenes appear on 7q11.21 and 11p11.12, and multiple mRNA variants exist.