The LightSwitch™ Validated Cholesterol Biosynthesis (SREBP) Pathway Collection is a comprehensive set of sequence-verified, transfection-ready, promoter reporter constructs that can be used to accurately quantify transcriptional activation and repression in response to induction of the cholesterol biosynthesis pathway. These constructs are a subset of the 18,000-member LightSwitch Promoter Reporter GoClone® Collection that were selected based on sequence motif analysis, published information and in-house analysis of each promoter's activity* using our LightSwitch Luciferase Assay.
The SREBP Biomarker Set contains 8 of the highest responding promoters under our chosen test conditions, as well as the promoters of 2 housekeeping genes (Figure 1). The SREBP Profiling Plate contains 88 promoter reporter constructs that showed significant activation or repression in response to induction (See the SREBP Profiling Plate tab below for data and a list of constructs).
Figure 1: Induction ratios for each member of the SREBP Biomarker Set.
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Cholesterol Biosynthesis (SREBP) Pathway
The sterol regulatory element binding proteins (SREBPs) are transcription factors that regulate lipogenesis. The SREBP isoforms, SREBP-1a, SREBP-1c, and SREBP-2, specifically control the expression of genes involved in cholesterol, fatty acid, triglyceride and phospholipid synthesis. SREBP-1c has also been implicated in glucose uptake regulation. Dysregulation of SREBP and the SREBP-regulated pathways is clinically relevant in disorders such as diabetes mellitus, insulin resistance, non-alcoholic fatty liver disease (NAFLD) and obesity. Understanding the mechanisms of how SREBPs are coordinated with other physiological pathways can provide further insight into the roles of SREBP in normal development, and can lead to successful strategies for targeting SREBP pathological research and drug therapies.
The collection of validated LightSwitch SREBP-related promoter reporters enables you to:
- Understand the mechanisms by which SREBP regulated genes are induced or repressed
- Quantify the functional consequences of transcription factor binding – while many other technologies give a qualitative view of transcription factor level, our promoter reporter assays quantify the effects of transcription factor binding
- Confirm data from ChIP, ChIP-chip or ChIP-Seq experiments
- Measure the effect of sequence variants and mutagenesis on promoter function
- Screen for promoter activation or develop activity profiles across the SREBP signaling pathway for many compounds or conditions in parallel
LightSwitch Luciferase Assay System
The LightSwitch Luciferase Assay System is a complete solution for studying transcriptional & post-transcriptional gene regulation in living mammalian cells. It enables you to directly measure the functional activity of promoters and 3´UTRs through use of an engineered luciferase gene (RenSP) and optimized assay & transfection reagents that ensure superior, reproducible results. In addition to Validated Pathway Collections, the LightSwitch System includes collections of over 30,000 cloned human promoter reporter constructs and human 3´UTR reporter constructs, miRNA mimics and inhibitors, as well as collections of synthetic long-range response element constructs and synthetic 3´UTRs target validation constructs that can provide more sensitivity than endogenous sequences.
LightSwitch Promoter Reporter Assays.
Advantages of the LightSwitch Luciferase Assay System
- Quantitative – Novel RenSP luciferase technology allows you to measure promoter activity with industry-leading sensitivity and dynamic range.
- Simple, fast, complete solution – With pre-cloned LightSwitch Reporter vectors and optimized transfection & assay reagents, you can study regulation of your gene today. No cloning, DNA preparation or optimization is needed, and most studies do not require any internal transfection controls.
- Comprehensive and verified – The genome-wide LightSwitch Reporter Collections are sequence-verified, transfection-ready promoter and 3´UTR reporter vectors.
- Functionally insightful – Learn about the actual effects of transcription factor binding to verify computational predictions and supplement microarray or sequencing data.
- Cost-effective – Efficiently screen for activation and/or repression using a multitude of conditions.
The SREBP Biomarker Set contains 5 µg aliquots each of 8 promoter reporter constructs and 2 housekeeping promoter constructs (NO_ANNOTATION & REPIN1) for use as controls. Click on the links below for clone information.
The SREBP Profiling Plate includes 88 promoter reporter constructs and 8 transfection control constructs (4 constructs from housekeeping genes with promoter activities of varying strengths (P1-P4), and 4 constructs with random 1 kb fragments (R1-R4)). To download a plate map with links to clone information, please click here.