ABCG8 analysis is essential for evaluating the efficacy and safety of new cholesterol-lowering drugs by measuring their impact on sterol transport. This data is critical for dose optimization and minimizing potential adverse effects in patients.
At Creative Biolabs, we provide an integrated suite of biomarker assays, which are indispensable for validating targets, predicting therapeutic efficacy, and ensuring safety. Our comprehensive portfolio, along with our scientific and regulatory expertise, fully supports your program from start to finish. Find the ABCG8 analysis service that fits your needs.
Located on chromosome 2p21, the ABCG8 gene has 13 exons that encode 673 amino acid residues. As a member of the ATP-binding cassette (ABC) transporter superfamily, ABCG8 plays a pivotal role in the regulation of intestinal plant sterol absorption by actively exporting plant sterols back into the intestinal lumen. This process is a critical frontline defense against the over-absorption of phytosterols.
Fig.1 Structure and SNP of ABCG5/G8.1
The ABCG5/ABCG8 transporters are functional heterodimers that are co-expressed in both the canalicular membrane of the hepatocyte and the apical membrane of the enterocytes. They work in concert to export cholesterol and phytosterols, thereby excluding them from systemic circulation. The formation of this heterodimer is an absolute necessity to direct the complex from the endoplasmic reticulum to the apical membrane, ensuring proper function. Mutations in either of these half-transporters can lead to defective biliary sterol transport and result in the rare human disease known as sitosterolemia.
Creative Biolabs offers a range of sophisticated services to provide a complete overview of the ABCG8 pathway, from genetic variations to protein function and localization. We provide the highest quality and most specific data to guide your critical decisions in drug development and diagnostics. Our team has validated our in-house developed anti-ABCG8 antibodies using multiple techniques, including Western blotting, ELISA, IHC, ICC, and IF with known positive and negative samples to ensure specificity and high affinity.
Our popular services targeting ABCG8 include, but are not limited to, the following key areas:
We identify pathogenic mutations and single nucleotide polymorphisms (SNPs) within the ABCG8 gene, providing insight into an individual's genetic predisposition and therapeutic response.
Our assays are designed to precisely identify and localize ABCG8 protein expression in specific tissues and cellular compartments, which is crucial for understanding its functional role.
We assess the critical interaction between ABCG8 and ABCG5, as well as with other potential binding partners or compounds, to help elucidate complex signaling pathways.
Our cell-based models provide in vitro quantification of ABCG8 transport activity, measuring sterol efflux and uptake to determine the efficacy of your compounds.
Our streamlined service workflow is designed for efficiency and collaboration. The process is clear and transparent from start to finish.
Our streamlined process begins with a dedicated consultation where our experts discuss your specific research goals and project requirements in detail, ensuring a customized approach tailored to your ABCG8 analysis needs.
You will provide the necessary starting materials, which can include purified proteins, established cell lines, or fresh or frozen tissue samples. We'll provide clear, detailed guidelines to ensure proper handling and transport, guaranteeing the integrity of your samples upon arrival.
Our expert team performs the specified ABCG8 analysis using our proprietary, validated methodologies and state-of-the-art equipment. This step is executed with precision to ensure reliable and reproducible data.
We maintain open and proactive communication throughout the project. You will receive regular updates on the progress of your analysis, and our team is always available to answer any questions you may have.
The project concludes with the delivery of a comprehensive, meticulously prepared report. This document includes a detailed breakdown of the analytical results, a clear summary of our findings, and a discussion of their implications for your research program.
ABCG8 analysis is essential for evaluating the efficacy and safety of new cholesterol-lowering drugs by measuring their impact on sterol transport. This data is critical for dose optimization and minimizing potential adverse effects in patients.
Research into ABCG8 polymorphisms provides valuable insights into the genetic risk factors for diabetes, cardiovascular diseases, and other metabolic syndromes. Understanding the link between sterol metabolism and these conditions can inform therapeutic strategies.
ABCG8 is increasingly being studied in the context of digestive cancers. Our analysis services can help elucidate its precise role in tumorigenesis and its potential as a therapeutic target, opening new avenues for cancer research.
Our services support the identification of genetic markers associated with sitosterolemia and other lipid disorders. This is vital for developing new diagnostic tools and enabling early, proactive intervention for at-risk individuals.
Customers frequently face issues with antibody specificity, low expression levels, and the complexity of analyzing a heterodimeric protein. We address these by using our validated, high-affinity antibodies, employing sensitive detection methods, and providing expert consultation to design a robust experimental strategy.
Our functional assays utilize advanced cell-based models that closely mimic in vivo conditions, allowing for accurate quantification of sterol efflux and uptake. We provide a highly controlled environment and precise measurement tools to ensure your data is both accurate and biologically meaningful, offering a superior alternative to standard methods.
We offer a high-throughput compound screening service to identify activators or inhibitors of the ABCG8 pathway. Our platform rapidly screens compound libraries and provides detailed dose-response data, essential for identifying promising candidates and optimizing therapeutic potential early in the discovery process.
Our genetic services support clinical research by identifying SNPs and pathogenic mutations in the ABCG8 gene linked to sitosterolemia and other metabolic disorders. This information can be used to develop diagnostic tests for patient stratification and to predict an individual's response to therapy.
Yes, our services are designed to evaluate the co-localization and critical interaction between ABCG5 and ABCG8. We utilize advanced techniques like co-immunoprecipitation and immunofluorescence, which provide visual and quantitative data on their co-expression and dimerization.
Our highly sensitive and validated methods are well-suited for analyzing ABCG8 expression in rare or difficult-to-obtain tissue samples. We provide specialized protocols for sample handling, and our expertise ensures we extract the maximum high-quality data from your valuable specimens.
If you are interested in our analysis services or need a tailored solution, please feel free to contact us for more information.
Reference
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