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Expression of NMDA Receptor Channel Subunit Proteins Using Baculovirus and Herpesvirus Vectors

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Foreign gene transfer and expression in the cells are among the most important techniques for determining the characteristics and function of cloned genes. Glutamate receptor genes have been expressed by RNA injection of Xenopus oocytes or transfection of mammalian cells, such as HEK, CHO, and COS cells, and bacterial Escherichia coli cells. Viral vectors, such as baculovirus (Autographa californica nuclear polyhedrosis virus, AcNPV) or herpesvirus (herpes simplex virus-1, HSV-1), have been also used because of high efficiency of gene transfer. Existing viral clones expressing recombinant glutamate receptor proteins (1 25 ) are summarized in Table 1 .
Table 1  Summary of Viral Vectors Expressing Glutamate Receptor Proteins

Viral vector, mouseGluR/ratGluR

Reference

Baculovirus vector

 

α1

1–5

α2/GluRB

3,6–9

(α4)/GluRD

9–11

(β2)/GluR6

12–14

ζ1/NMDAR1

15–17

ε1

18 and this study

ε2

18 and this study

δ2

18 and this study

mGluR1 (rat)

13

Herpesvirus vector

 

(α1)/GluR1

19

(β2)/GluR6

20–22

ζ1

This study

Adenovirus vector

 

(a1)/GluR1

23

(a2)/GluR2

23

(ζ1)/NMDAR1 (antisense)

24

Adenoassociated virus vector

 

(ζ1)/NMDAR1 (antisense)

25

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