pFUSE-CHIg-hG1e6
Product | Unit size | Cat. code | Docs. | Qty. | Price | |
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pFUSE-CHIg-hG1e6 Human IgG1 |
Show product |
20 µg |
pfuse-hchg1e6
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pFUSEss-CHIg-hG1e6 Human IgG1 with IL2ss |
Show product |
20 µg |
pfusess-hchg1e6
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pFUSE-CHIg general plasmid map
Human IgG1 heavy chain constant region with increased binding to FcRn
pFUSE-CHIg-hG1e6 is a cloning plasmid that expresses the human IgG1 heavy chain constant region with P257I + Q311I mutations. It contains a multiple cloning site upstream of the constant region to enable cloning of the heavy chain (CH) variable region. This plasmid is designed for antibody generation when co-transfected into mammalian cells with the light chain variable region cloned into pFUSE-CLIg.
pFUSEss-CHIg-hG1e6 additionally features the IL2 signal sequence to allow the secretion of recombinant antibodies generated using fragment antigen-binding (Fab) or single-chain variable fragment (scFv) fragments selected from phage display libraries that lack a signal sequence.
Key features of pFUSE-CHIg-hG1e6
- Encodes the human IgG1e6 CH constant region (P257I + Q311I mutations)
- Long-lasting expression due to the composite hEF1-HTLV promoter
- Selectable with Zeocin™ in both bacterial and mammalian cells
- Available with or without the IL-2 signal sequence
Reference:
1. Datta-Mannan A. et al., 2007. Humanized IgG1 Variants with Differential Binding Properties to the Neonatal Fc Receptor: Relationship to Pharmacokinetics in Mice and Primates. Drug Metab. Dispos. 35: 86 - 94.
Back to the topSpecifications
• pFUSE-CHIg-hG1e6 features the constant region of the human IgG1 heavy chain with P257I / Q311I mutations
• pFUSEss-CHIg-hG1e6 features the constant region of the human IgG1 heavy chain with P257I / Q311I mutations and the IL2 signal sequence
Characteristics of P257I / Q311I mutations:
- Increased binding to FcRn
- Unchanged half-life
Both plasmids are selectable with Zeocin™.
Back to the toppFUSE Contents
- 20 µg of lyophilized DNA
- 1 ml of Zeocin® (100 mg/ml)
Product is shipped at room temperature
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