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Promega pCI and pCI-neo Mammalian Expression Vectors DFS Item

Contains the CMV immediate-early enhancer/promoter region and is designed to promote constitutive expression of cloned DNA inserts in mammalian cells.

$748.88 - $750.20

Specifications

Promoter CMV
Storage Buffer TE Buffer (pH 8)
Content And Storage -30°C to -10°C
Quantity 20 μg
For Use With (Application) Promote constitutive expression of cloned DNA inserts in Mammalian cells, can also be used to synthesize transcripts in-vitro using the T7 RNA Polymerase promoter or generate single-stranded DNA in E. coli using the f1 origin of replication
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Products 2
Catalog Number Mfr. No. Vector Price Quantity  
Catalog Number Mfr. No. Vector Price Quantity  
PR-E1731 DFS Item
View Documents Promotion Details
Promega
E1731
pCI vector
Each for $750.20
 
PR-E1841 DFS Item
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Promega
E1841
pCI-neo vector
Each for $748.88
 
Description

Description

pCI Mammalian Expression Vector

  • Designed to promote constitutive expression of cloned DNA inserts in mammalian cells
  • Contains the human cytomegalovirus (CMV) major immediate-early gene enhancer/promoter region†
  • Can be used for both transient and stable expression of genes
  • Note: For stable expression, the pCI Vector must also be transfected with an expression vector containing a selectable gene for mammalian cells
pCI-neo Mammalian Expression Vector
  • Similar to pCI Mammalian Expression Vector
  • Also contains the neomycin phosphotransferase gene, a selectable marker for mammalian cells
  • Can be used for transient expression or for stable expression by selecting transfected cells with the antibiotic G-418
Both Vectors
  • Can also be used to synthesize transcripts in vitro using the T7 RNA polymerase promoter or generate single-stranded DNA in E. coli using the f1 origin of replication

Specifications

Specifications

CMV
-30°C to -10°C
Promote constitutive expression of cloned DNA inserts in Mammalian cells, can also be used to synthesize transcripts in-vitro using the T7 RNA Polymerase promoter or generate single-stranded DNA in E. coli using the f1 origin of replication
TE Buffer (pH 8)
20 μg
SDS
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