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pNiFty3-I-SEAP

pNiFty3-I-SEAP Unit size Cat. code Docs Qty Price
pNiFty3 - mIFN-β promoter - ISRE - ZeocinR - SEAP
20 µg
pnf3-sp4
+-
$497.00

pNiFty3-I-SEAP plasmid is composed of three key elements:  the mouse interferon beta minimal promoter, five ISRE transcription factor binding sites and a  SEAP (Secreted alkaline phosphatase) reporter gene.

pNiFty3-I-SEAP plasmid is selectable with Zeocin™ in both E. coli and mammalian cells, and can be used to generate stable clones.

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Specifications

Transcription factor binding sites: ISRE (5x)
Minimal Promoter: mouse IFNβ promoter
Selection: Zeocin™
Reporter Gene: SEAP

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Contents

pNiFty3-I-SEAP plasmid is provided as 20 µg lyophilized DNA with 4 pouches of Fast-Media® (2 TB and 2 Agar), containing Zeocin™.

Products are shipped at room temperature and should be stored at -20°C.

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Description

Minimal promoter

The proximal promoters are shorter than 500 bp and contain transcription factor binding sites. Upon stimulation in 293 cells, their expression level remains undetectable. With the addition of repeated TFBS, the proximal promoters become inducible by the appropriate stimulus and drive the expression of the reporter gene.

IFN-β promoter: the mouse IFN-β minimal promoter comprises several positive regulatory domains that bind different cooperating transcription factors such as NF-kB, IRF3 and IRF7 [1].

Transcription factor binding sites (TFBS)

ISRE binding site: PRRs involved in the antiviral response induce the activation of interferon regulatory factors (IRFs) and the production of type I interferons (IFNs). IFNs trigger the formation of the ISGF3 complex which contains signal transducer and activator of transcription (STAT) 1, STAT2 and IRF9. ISGF3 and IRFs bind to specific nucleotide sequences called interferon-stimulated response elements (ISREs; AGTTTCNNTTTCC) in the promoter of IFN-stimulated genes (ISGs) leading to their activation [2].

Reporter Gene

SEAP reporter gene: Secreted alkaline phosphatase (SEAP) is a reporter widely used to study promoter activity or gene expression. SEAP expression can be rapidly and readily measured in supernatants of transfected cells. SEAP levels can be evaluated qualitatively with the naked eye and quantitatively using SEAP detection media, such as HEK-Blue™ Detection system or the SEAP Reporter Assay.

1. Vodjdani G. et al., 1988. Structure and characterization of a murine chromosomal fragment containing the interferon beta gene. J Mol Biol. 204(2):221-31.
2. Wesoly J. et al., 2007. STAT activation and differential complex formation dictate selectivity of interferon responses. Acta Biochim Pol. 54(1):27-38.

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Details

pNiFty3 map

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