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Are you currently facing challenges in identifying novel BC biomarkers, understanding drug resistance mechanisms, or developing targeted therapies? Our cutting-edge Glycosylation Analysis Service helps you accelerate critical discoveries, unravel complex disease biology, and pinpoint new therapeutic targets through advanced mass spectrometry, chromatography, and bioinformatics. Creative Biolabs' BC related glycosylation analysis service offers unparalleled precision in characterizing the glycans and glycosylation patterns crucial for understanding BC initiation, progression, and therapeutic response. Our service provides detailed insights into altered glycosylation, which can serve as novel biomarkers for diagnosis, prognosis, and predicting sensitivity to treatment. We deliver comprehensive profiles of N-linked and O-linked glycans, quantitative comparisons between samples, and identification of specific glycosylation sites on proteins of interest. These deliverables empower researchers to uncover mechanisms of disease, identify new drug targets, and develop more effective diagnostic and prognostic tools.
Creative Biolabs offers comprehensive glycosylation analysis services utilizing state-of-the-art mass spectrometry platforms coupled with advanced separation techniques. Our approach is highly customizable to meet your specific research needs, whether it's broad glycan profiling or targeted site-specific glycopeptide mapping. We leverage enzymatic and chemical methods for glycan release, ensuring compatibility with diverse sample types, and employ sophisticated data analysis pipelines for accurate quantification and biological interpretation. Our detailed analysis process involves:
Isolation of proteins/glycoproteins from your samples, followed by enzymatic (e.g., PNGase F for N-glycans, O-glycosidase for O-glycans) or chemical release of glycans.
Enhancing detection capabilities by labeling released glycans with fluorescent tags or chemical derivatizing agents.
Employing advanced chromatographic methods (e.g., reverse-phase liquid chromatography) to separate complex mixtures of glycans.
Utilizing high-accuracy mass spectrometers capable of detecting and quantifying even low-abundance glycans, providing both molecular weight and structural information through fragmentation.
Applying proprietary and public databases, algorithms, and statistical tools to identify glycan structures, quantify their relative and absolute abundances, and perform comparative analyses between different sample groups.
Creative Biolabs offers a range of glycosylation analysis services tailored for BC research:
Comprehensive identification and quantification of N-linked glycans from total cellular proteins or specific glycoprotein fractions. This is critical for understanding changes in cell surface receptors, secreted proteins, and their roles in signaling and immune recognition.
Detailed analysis of O-linked glycans, which are often found on mucins and play crucial roles in cell adhesion, growth factor signaling, and immune modulation.
Precise determination of which amino acid residues (asparagine for N-glycans, serine/threonine for O-glycans) are glycosylated on your target proteins, providing a deeper understanding of functional implications.
Using label-free or labeled methods to accurately quantify changes in glycan abundance between healthy and cancerous tissue samples.
A targeted approach to identify unique glycan signatures that can serve as diagnostic, prognostic, or predictive biomarkers for various breast cancer pathologies and responses to therapies.
To further support your comprehensive BC research endeavors, Creative Biolabs also offers a suite of complementary services:
Creative Biolabs is your trusted partner in advancing BC research and therapeutic development. We provide various cancer glycosylation analysis services (e.g., Prostate Cancer, Colorectal Cancer, Ovarian Cancer, Pancreatic Cancer, etc.), combined with our extensive suite of complementary offerings, which provides a powerful platform to accelerate your discoveries from fundamental biology to clinical application. We are committed to empowering our clients with the precision data needed to combat these complex diseases effectively. Please contact us to inquire about more details.
A1: Yes, Creative Biolabs utilizes state-of-the-art mass spectrometry platforms and optimized sample preparation protocols to achieve exceptional sensitivity. This allows for the detection and quantification of even low-abundance glycan biomarkers in complex biological matrices such as serum or tissue lysates, crucial for discovery and validation.
A2: Absolutely. Our quantitative glycosylation analysis services are designed to perform comparative studies across various BC subtypes or disease stages. By identifying differentially expressed glycans, we can help you uncover subtype-specific glycosylation signatures that may aid in more precise patient stratification and personalized treatment strategies.
A3: Proper sample handling is critical for accurate results. We recommend rapid freezing of tissue and fluid samples, avoiding repeated freeze-thaw cycles, and storing them at -80°C. For specific guidelines tailored to your sample type, our technical support team provides detailed instructions upon project initiation to ensure sample integrity and optimal analytical outcomes.
Detailed Reporting and Quick Turnaround
"Using Creative Biolabs' glycosylation analysis service in our research has significantly improved our understanding of how altered glycosylation on membrane proteins contributes to BC cell invasiveness. The quantitative data provided was highly precise and directly led us to focus on specific glycoforms that we now believe are key drivers. The detailed reporting and quick turnaround were invaluable." - Dr. C. Dav***s.
Superior Resolution and Sensitivity
"Our previous attempts at comprehensive glycan profiling were costly and time-consuming, yielding inconsistent results. Creative Biolabs' platform provided superior resolution and sensitivity, enabling us to pinpoint critical glycosylation alterations linked to acquired resistance to anti-estrogen therapies. The technical team also provided crucial insights into potential precautions during sample handling for optimal results, a level of guidance we hadn't received elsewhere." - Prof. P. Wils***n.