HSE Luciferase Reporter Lentivirus (Heat Shock Response)

Catalog #
78669
$875 *
Size: 500 µl x 2
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Description

The HSE (Heat Shock Response) Luciferase Reporter Lentiviruses are replication incompetent, HIV-based, VSV-G pseudotyped lentiviral particles ready to transduce most mammalian cells, including primary and non-dividing cells. These viruses transduce cells with the firefly luciferase gene driven by multiple copies of the heat shock response element (HSE) located upstream of the minimal TATA promoter. The lentiviruses also transduce a puromycin selection gene (Figure 1).  After transduction, the heat shock response in the target cells can be monitored by measuring luciferase activity.

Figure 1. Schematic of the lenti-vector used to generate the HSE luciferase reporter lentivirus.

Product Info
Storage and Usage
Citations
Supplied As
Two vials (500 µl x 2) of lentivirus at a titer >107 TU/ml. The titer will vary with each lot; the exact value is provided with each shipment.
Materials Required But Not Supplied
Name Ordering Information
HeLa Cells ATCC #CCL-2
Thaw Medium 1 BPS Bioscience #60187
17-Allylaminogeldanamycin (17-AAG) Sigma #A8476
96-well tissue culture, clear-bottom, white plate Corning #3610
One-Step™ Luciferase Assay System BPS Bioscience #60690
Luminometer  

 

Formulation

The lentiviruses were produced in HEK293T cells in medium containing 90% DMEM + 10% FBS. Virus particles can be packaged in custom formulations by special request, for an additional fee.    

Background

The Heat Shock Response (HSR) is crucial for cells to adapt to stressful conditions. In the presence of high temperatures, oxidative stress or heavy metals, several proteins can unfold and become unable to perform their normal functions. This in turn can result in cell damage and/or death. To maintain proteins with the proper structure the expression of Heat Shock Proteins (HSP) is induced. Expression of HSPs is regulated by the transcription factor Heat Shock Factor 1 (HSF1). When cellular stress occurs HSF1 undergoes a confirmation change and moves to the nucleus, where it can bind to Heat Shock Elements (HSE) and lead to transcription of the HSP mRNA. Dysfunction in the HSR can lead to pathologies such as neurodegenerative diseases and cancer. Targeting HSE may prove beneficial in the treatment of pathologies linked to defective HSR.