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Adeno-X™ Expression System 1

 
 
 
 
 

Certificates of Analysis

 
If you do not see the Certificate of Analysis for your specific lot, please follow this link.
 

The Adeno-X Expression System 1 uses a ligation-based method to generate adenoviral vectors for high-level protein expression in a wide variety of mammalian host cells. This Adeno-X expression system offers several major advantages over standard transfection and other adenoviral systems:

  • High protein expression levels. Recombinant adenovirus containing your gene of interest infects target cells with multiple copies and high efficiency, cells transiently express the protein of interest at very high levels.
  • Efficient infection of many mammalian cell types. Adenovirus efficiently infects a majority of human and many nonhuman cell types including mouse, rat, dog, chicken, rabbit, sheep, pig, and nonhuman primates (2–11). Adenovirus infects both dividing and nondividing cells.
  • Optimized protocol for fast results. Instead of homologous recombination, this protocol uses an efficient, ligation-based method with pre-linearized, ready-to-ligate Adeno-X System 1 Viral DNA (Figure 1). Our protocol has been optimized so that recombinant adenovirus can be generated faster than with other methods (Figure 2). The system also provides a convenient shuttle vector, pShuttle2, and a unique double digestion buffer that saves time during cloning.
  • Simple cloning procedures. With our optimized ligation-based approach, the Adeno-X System 1 eliminates nonrecombinant adenovirus and produces recombinant adenovirus much more rapidly and reliably than conventional homologous recombination approaches (Table I), without having to switch bacterial strains.

Adeno-X Method

To produce recombinant adenovirus, insert your gene of interest into the multiple cloning site of the pShuttle2 vector’s expression cassette. Then, transfer the cassette into the ligation-ready Adeno-X Viral DNA using the two extremely rare restriction enzyme sites, PI-Sce I and I-Ceu I. Subsequent digestion with Swa I removes self-ligated or nonrecombinant adenoviral DNA. Transform E. coli strain with the ligation mixture and identify recombinant clones by restriction enzyme digests. Then transfect a low-passage HEK 293 cell line with linearized recombinant adenoviral DNA and harvest recombinant adenovirus several days later.

The Adeno-X Expression System 1 includes predigested, ready-to-use Adeno-X System 1 Viral DNA, pShuttle2 Vector, pShuttle-lacZ Control Vector, PI-Sce I, I-Ceu I, Double Digestion Buffer, BSA, a User Manual, and a Vector Information Packet. The predigested Adeno-X System 1 Viral DNA (linear) is also sold separately. To supplement the Adeno-X System 1, we offer the Adeno-X™ Accessory Kit, which includes the restriction enzymes, Double Digestion Buffer, and BSA.

Clontech also offers Knockout Adenovirual RNAi System for delivery of shRNA as well as the Adeno-X Rapid Titer Kit, the Adeno-X System 2, the Adeno-X Purification Kit, and Adeno-X Marker Viruses.

 
 
 
 

Figure 1. The Adeno-X Expression System 1. The Swa I site is located between I-Ceu I and PI-Sce I in the circular, nonlinearized Adeno-X vector.

 
 

Figure 2. Adeno-X Expression System 1—available in constitutive and Tet-inducible formats—lets you produce recombinant adenovirus in a fraction of the time of other adenoviral systems.

 
 

 
 
 
 

References

1. Mizuguchi, H. & Kay, M. A. (1998) Hum. Gene Ther. 9:2577–2583.
2. Lee, J., et al. (1996) J. Thor. Cardiovas. Surg. 111:246–252.
3. Stratford-Perricaudet, L. D., et al. (1990) Hum. Gene Ther. 1:241–256.
4. Mastrangeli, A., et al. (1993) J. Clin. Invest. 91:225–234.
5. Fang, B., et al. (1996) Gene Ther. 3:217–222.
6. Fisher, S. A. & Watanabe, M. (1996) Cardiovas. Res. 31:86–95.
7. Bout, A., et al. (1994) Hum. Gene Ther. 5:3–10.
8. Riew, K. D., et al. (1998) Calcif. Tissue Intl. 63(4):357–360.
9. Holzinger, A., et al. (1995) Pediatr. Res. 38:844–850.
10. French, B. A., et al. (1994) Circulation 90:2402–2413.
11. Donahue, J. K., et al. (1998) Gene Ther. 5:630–634.

Components

Adeno-X Expression System 1
Adeno-X System 1 Viral DNA (PI-Sce I/I-Ceu I digested)
pShuttle2 Vector
pShuttle-lacZ Control Vector
Adeno-X Forward PCR Primer
Adeno-X Reverse PCR Primer
PI-Sce I
I-Ceu I
BSA
Double Digestion Buffer
User Manual (PT3414-1)
Protocol-at-a-Glance (PT3507-2)
Vector Information Packet (PT3416-5)

Adeno-X Accessory Kit
PI-Sce I
I-Ceu I
Double Digestion Buffer
BSA

Storage Conditions

–20°C