Trans 293 Kit ​Pro

The upgraded Trans 293 Kit Pro includes 3 components: CD 293 01 basal medium, ALLY 293 feed medium, and 293 PEI Plus transfection reagent, all of which are chemically defined and free of serum, animal-origin components, or hydrolysates. The kit is well suited for high density suspension culture and is experimentally proven to deliver high transfection efficiency and protein yield for multiple HEK293 cell lines.

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Product Catalog

Product Catalog No. Form Package Size Description User Guide Inquiry and Trial
Trans 293 Kit Pro 33007 Liquid 1000 mL
100 mL
5 mL
Basal medium/
Feed/
Transfection reagents
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Case Studies

Case 1: Expression of 7 Proteins in HEK293 Cells

Trans 293 Kit Pro delivered markedly higher expression for all 7 proteins, with several molecules showing more than a twofold increase, underscoring its excellent perfor-mance on the transient transfection of difficult-to-express proteins.

Figure 1. Transient expression of 7 difficult-to-express proteins in HEK293 cells: Trans 293 Kit Pro versus control


Case 2: Monoclonal Antibody (mAb) Titer in High-Expression Process

Trans 293 Kit Pro consistently achieved higher titers over a 7-day culture period. At Day 7, mAb titer almost reached 2 g/L, representing a 45% increase over the control.

Figure 2. Transient mAb expression in a high-express-ing HEK293 culture: Trans 293 Kit Pro versus control

Case 3: Transient mAb Expression Across Different Processes in HEK293F Culture

A comparative transient-expression study of an antibody in HEK293F cells was performed under the following four process conditions:
▪ Single feeding on Day 1
▪ Dual feeding on Day 1 and Day 4
▪ Centrifugation before transfection + single feeding on Day 1
▪Centrifugation before transfection + dual feeding on Day 1 and Day 4

Figure 3. Transient mAb expression across different processes: Trans 293 Kit Pro versus control.


Trans 293 Kit Pro consistently delivered higher titers than the control, with more than 29% improvement on Day 7. No significant differ-ence was observed between single and dual feeding during the first five days, indicating that a simplified single-feed strategy can maintain expression performance while reducing process complexity.

With optimized feeding strategy and pre-transfection centrifugation, titer on Day 7 exceeded 2 g/L—110% higher than the control—sug-gesting robust expression performance and broad process adaptability.