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EndoSafe mRNA Transfection Kit

The purpose of the EndoSafe mRNA Transfection Kit is to transfect RNA into a variety of cell types with the least amount of cellular damage possible. By delivering the RNA straight to the cytoplasm for expression, RNA delivery overcomes the effects of transcriptional control. mRNAs can be delivered using the EndoSafe mRNA Transfection Kit. It has several uses, including investigations on short-term protein expression, viral production and replication studies.
EndoSafe mRNA Reagent and mRNA TurboMix are the two components of the mRNA transfection kit. The transfection efficiency is highest when serum is present, and this kit is compatible with serum. It also has minimal toxicity to the target cells, preventing cell death during transfection.
No. Size Price Qty Status
C15053-K01 0.5 mL*1 $720.00 Inquiry
C15053-K02 0.5 mL*2 $1,160.00 Inquiry
The price does not include shipping fee and tax. Order Request Quote
Intended Use:
The EndoSafe mRNA transfection kit is typically intended for introducing exogenous mRNA molecules into cells for various purposes, such as gene expression studies, protein production, or gene therapy research. The kit's reagents efficiently transport mRNA into target cells with minimal toxicity, ensuring high transfection efficiency. Researchers often use mRNA transfection kits in molecular biology and biotechnology experiments to manipulate gene expression levels in cells temporarily without altering the genome permanently.

Package & Component:
 
Reagents Form C15053-K01 C15053-K02
EndoSafe mRNA Reagent Liquid 0.5 mL*1 0.5 mL*2
mRNA TurboMix Liquid 0.5 mL*1 0.5 mL*2






Storage & Stability:
This product is stable after storage at:
• -20°C or -80°C for 12 months under sterile conditions from date of receipt.
• 2-8°C for 6 months under sterile conditions from date of receipt.
Avoid repeated freeze/thaw cycles.

Shipping Conditions:
Blue ice


This test compares the transfection efficiency of Croyez Endosafe mRNA transfection kit with Competitor’s transfection reagents in HEK 293T cells. Cells were transfected with mNeonGreen mRNA, and fluorescence images were captured 24 hours post-transfection to evaluate protein expression. The comparison was conducted using various mRNA concentrations and corresponding reagent volumes.
 
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