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GlycoFlux™ MSCV-UGP2 Viral Particle installs UGP2 to drive UDP-glucose production for glycogen synthesis and lactose-precursor pathways; MSCV mediates genome-integrating, replication-defective delivery optimized for progenitor targets to create persistent mammalian stable lines.
Product Type
Recombinant MSCV Retrovirus
Target
UGP2
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 enzyme generates UDP-glucose from glucose-1-phosphate and MgUTP, releasing MgPPi. In muscle and liver, UDP-glucose feeds glycogen synthesis; in the mammary gland, it is converted to lactose precursors. Two isoforms arise from alternative splicing.