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2012 Promega catalogue

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Life<br />

Science<br />

Catalog<br />

<strong>2012</strong><br />

Worldwide Contact List<br />

Section<br />

Contents<br />

Table of<br />

Contents<br />

Cell Signaling<br />

280<br />

ViviRen In Vivo Renilla Luciferase<br />

Substrate<br />

Product Size Cat.# Price ($)<br />

ViviRen In Vivo Renilla Luciferase Substrate 0.37 mg P1231 192.00<br />

For Research Use Only. Not for Use in Diagnostic Procedures.<br />

3.7 mg P1232 Pls. Enq.<br />

Description: ViviRen in vivo Renilla Luciferase Substrate is a uniquely<br />

engineered coelenterazine-based compound with protected oxidation sites.<br />

These modifications are designed to minimize substrate degradation and autoluminescence.<br />

It is reported that the ViviRen Substrate demonstrates brighter<br />

output when compared to the native coelenterazine substrate when used in an<br />

in vivo imaging application in a mouse model.<br />

Cat.# P1231 is supplied as a liquid, 60mM in DMSO. Cat.# P1232 is supplied<br />

as a lyophilized solid.<br />

VivoGlo In Vivo Imaging Substrates are provided in cooperation with Xenogen<br />

Corporation and Caliper Life Sciences for use in in vivo bioluminescence<br />

imaging applications.<br />

Features:<br />

• Highest Quality Substrates: Eliminate potential interference in assays<br />

due to the presence of endotoxins.<br />

• Assured Product Integrity: Most products are packaged in amber vials<br />

with septa to ensure product integrity as well as offer ease of dilution and<br />

use for imaging experiments. Product is packaged with fine tolerances to<br />

minimize the need to weigh substrates.<br />

• Flexibility and Convenience: Available in multiple sizes to accommodate<br />

a variety of experimental settings.<br />

Storage Conditions: Store at –20°C.<br />

9540MA<br />

pGL4 in vivo Imaging Vectors<br />

Product Size Cat.# Price ($)<br />

pGL4.50[luc2/CMV/Hygro] Vector 20 µg E1310 545.00<br />

pGL4.51[luc2/CMV/Neo] Vector<br />

For Research Use Only. Not for Use in Diagnostic Procedures.<br />

20 µg E1320 545.00<br />

Description: The pGL4 Luciferase Reporter Vectors are the next generation of<br />

reporter gene vectors optimized for expression in mammalian cells. Numerous<br />

configurations of pGL4 Vectors are available, including those with the synthetic<br />

firefly luc2 (Photinus pyralis) and Renilla hRluc (Renilla reniformis) genes, which<br />

have been codon optimized for more efficient expression in mammalian cells.<br />

Furthermore, both the reporter genes and the vector backbone, including the<br />

ampicillin (Ampr ) gene and mammalian selectable marker genes for hygromycin<br />

(Hygr ), neomycin (Neor ) and puromycin (Puror ), have been engineered to<br />

reduce the number of consensus transcription factor binding sites, reducing<br />

background and the risk of anomalous transcription.<br />

The pGL4 Vector backbone is provided with either the luc2 or hRluc gene and,<br />

in certain vectors, one or both of two Rapid Response Reporter genes. The<br />

proteins encoded by these Rapid Response Luciferase genes respond more<br />

quickly and with greater magnitude to changes in transcriptional activity than<br />

their more stable counterparts. Vectors are available with a minimal promoter<br />

upstream of the lucP reporter gene, useful for cloning in a response element of<br />

choice. Vectors also are available with a minimal promoter plus choice of<br />

response elements or other promoter elements that can be used to study<br />

cellular signaling and other events. These vectors can be used in transient<br />

transfections or to generate a stable cell line. All vectors use a destabilized<br />

luc2P firefly luciferase gene, resulting in low backgrounds and high levels of<br />

induction. Stable cell selection is possible using hygromycin resistance.<br />

Improved Sensitivity and Biological Relevance Due to:<br />

• Increased Reporter Gene Expression: Codon optimization of synthetic<br />

genes for mammalian expression.<br />

• Reduced Background and Risk of Expression Artifacts: Removal of<br />

cryptic DNA regulatory elements and transcription factor binding sites.<br />

• Improved Temporal Response: Rapid Response technology available<br />

using destabilized luciferase genes.<br />

Additional Advantages Include:<br />

• Flexible Detection Options: Choice of either synthetic luc2 (Photinus<br />

pyralis) or hRluc (Renilla reniformis) reporter genes.<br />

• Easy Transition from Transient to Stable Cells: Choice of mammalian<br />

selectable markers.<br />

• Easy Transfer from Vector to Vector: Common multiple cloning site and<br />

a unique SfiI transfer scheme.<br />

Storage Conditions: Store at –20°C.<br />

For complete and up-to-date product information visit: www.promega.com/catalog

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