Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Premade Virus Particles
Ready-to-Use | High Titer | Versatile Applications
Premade AAV, adenovirus, lentivirus particles, safe, stable, in stock.
Virus-Like Particles (VLPs)
Stable | Scalable | Customizable
Advanced VLPs for vaccine development (Chikungunya, Dengue, SARS-CoV-2), gene therapy (AAV1 & AAV9), and drug screening (SSTR2, CCR5).
Oligonucleotide Products
Precise | High Yield | Tailored Solutions
Accelerate your research with cost-effective LncRNA qPCR Array Technology.
RNA Interference Products
Targeted | Potent | High Specificity
Human Druggable Genome siRNA Library enables efficient drug target screening.
Recombinant Drug Target Proteins
Authentic | Versatile | Accelerated
Providing functional, high-purity recombinant proteins—including membrane proteins and nanodiscs—to overcome bottlenecks in drug screening and target validation.
Clones
Validated | Reliable | Comprehensive Collection
Ready-to-use clones for streamlined research and development.
Kits
Complete | Convenient | High Sensitivity
Chromogenic LAL Endotoxin Assay Kit ensures precise, FDA-compliant endotoxin quantification for biosafety testing.
Enzymes
Purified | Stable | Efficient
Powerful Tn5 Transposase for DNA insertion and random library construction.
Aptamers
Highly Specific | Robust | Versatile
Aptamers for key proteins like ACVR1A, Akt, EGFR, and VEGFR.
Adjuvants
Enhancing | Synergistic | Effective
Enhance immune responses with high-purity, potent CpG ODNs.
Laboratory Equipment
Innovative | Reliable | High-Precision
Effortlessly streamline DNA extraction with CB™ Magnetic-Nanoparticle Systems.
Stable Cell Line Generation
Reliable | Scalable | Customizable
Fast proposals, regular updates, and detailed reports; strict quality control, and contamination-free cells; knockout results in 4-6 weeks.
Target-based Drug Discovery Service
Innovative | Comprehensive | Efficient
Target identification, validation, and screening for drug discovery and therapeutic development.
Custom Viral Service
Versatile | High-Yield | Safe
Unbeatable pricing, fully customizable viral packaging services (covering 30,000+ human genes, 200+ mammals, 50+ protein tags).
Custom Antibody Service
Precise | Flexible | Efficient
End-to-end antibody development support, from target to validation, enabling clients to rapidly obtain application-ready antibodies.
Antibody-Drug Conjugation Service
Integrated | Controlled | Translational
Comprehensive solutions covering design, development, and validation to ensure conjugated drugs with consistent quality and clinical potential.
Protein Degrader Service
Efficient | High-Precision | Advanced Therapeutics
Harness the power of protein degraders for precise protein degradation, expanding druggable targets and enhancing therapeutic effectiveness for cutting-edge drug discovery.
Nucleotides Service
Accurate | Flexible | High-Quality
Custom synthesis of oligonucleotides, primers, and probes for gene editing, PCR, and RNA studies.
Custom RNA Service
Custom RNA ServicePrecise | Flexible | GMP-ReadyCustom
RNA design, synthesis, and manufacturing—covering mRNA, saRNA, circRNA, and RNAi. Fast turnaround, rigorous QC, and seamless transition from research to GMP production.
Custom Libraries Construction Service
Comprehensive | High-throughput | Accurate
Custom cDNA, genomic, and mutagenesis libraries for drug discovery, screening, and functional genomics.
Gene Editing Services
Precise | Efficient | Targeted
Gene editing solutions for gene editing, knockouts, knock-ins, and customized genetic modifications. Integrated multi-platform solutions for one-stop CRISPR sgRNA library synthesis and gene screening services
Microbe Genome Editing Service
Precise | Scalable | Customizable
Enhance microbial productivity with advanced genome editing using Rec-mediated recombination and CRISPR/Cas9 technologies.
Biosafety Testing Service
Reliable | Comprehensive | Regulated
Complete biosafety testing solutions for gene therapy, viral vectors, and biologics development.
Plant Genetic Modification Service
Advanced | Sustainable | Tailored
Genetic modification for crop improvement, biotechnology, and plant-based research solutions.
Plant-based Protein Production Service
Efficient | Scalable | Customizable
Plant-based protein expression systems for biopharmaceuticals, enzyme production, and research.
Aptamers Service
Innovative | Fast | Cost-Effective
Revolutionizing drug delivery and diagnostic development with next-generation high-throughput aptamer selection and synthesis technologies.
CGT Biosafety Testing
Comprehensive | Accurate | Regulatory-compliant
Internationally certified evaluation system for biologics, gene therapies, nucleic acid drugs, and vaccines.
Pandemic Detection Solutions
Rapid | Precise | Scalable
Balancing accuracy, accessibility, affordability, and rapid detection to safeguard public health and strengthen global response to infectious diseases.
cGMP Cell Line Development
Reliable | Scalable | Industry-leading
Stable expression over 15 generations with rapid cell line development in just 3 months.
Supports adherent and suspension cell lines, offering MCB, WCB, and PCB establishment.
GMP mRNA Production
Efficient | Scalable | Precise
Scalable mRNA production from milligrams to grams, with personalized process design for sequence optimization, cap selection, and nucleotide modifications, all in one service.
GMP Plasmid Production
High Quality | Scalable | Regulatory-compliant
Our plasmid production services span Non-GMP, GMP-Like, and GMP-Grade levels, with specialized options for linearized plasmids.
GMP Viral Vector Manufacturing
Scalable | High Yield | Quality-driven
Advanced platforms for AAV, adenovirus, lentivirus, and retrovirus production, with strict adherence to GMP guidelines and robust quality control.
AI-Driven Gene Editing and Therapy
Innovative | Precision | Transformative
AI-powered one-click design for customized CRISPR gene editing strategy development.
AI-Antibody Engineering Fusion
Next-Generation | Targeted | Efficient
AI and ML algorithms accelerate antibody screening and predict new structures, unlocking unprecedented possibilities in antibody engineering.
AI-Driven Enzyme Engineering
Smart | Efficient | Tailored
High-throughput enzyme activity testing with proprietary datasets and deep learning models for standardized and precise enzyme engineering design.
AI-Enhanced Small Molecule Screening
Predictive | Efficient | Insightful
Leverage AI to uncover hidden high-potential small molecules, prioritize leads intelligently, and reduce costly trial-and-error in early drug discovery.
AI-Driven Protein Degrader Drug Development
Innovative | Targeted | Accelerated
Use AI-guided design to optimize protein degraders, addressing design complexity and enhancing efficacy while shortening development timelines.
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The CD248 gene, also known as Endosialin, encodes a transmembrane glycoprotein involved in physiological processes such as tissue development, tumor angiogenesis, and inflammation. Being a cell surface glycoprotein, CD248 is important for extracellular matrix (ECM) binding, motility, and tumor angiogenesis. Its expression is intimately related to normal developmental processes and also significantly influences tumor formation as well as several inflammatory disorders. The structure, function, expression, and involvement of the CD248 gene in illnesses will be thoroughly reviewed in this paper.
The CD248 gene is located on the q arm of chromosome 11 in humans and encodes a C-type lectin-like protein. Five extracellular domains—three epidermal growth factor (EGF) repeat sequences, one mucin-like region, then a transmembrane domain and a short cytoplasmic tail define CD248. Using its transmembrane domain, which serves on the cell surface, CD248 binds cells to the extracellular matrix (ECM). Calcium-binding and ECM-binding sites among other functional domains in the protein help CD248 to be involved in cellular motility, tumor angiogenesis, and ECM remodeling.
Figure 1. CD248 protein structure. (Teicher BA, 2019)
Particularly in the tumor microenvironment, CD248 is thought to be quite critical for tumor angiogenesis. Through interactions with ECM elements like collagen and fibronectin, CD248 helps blood vessels around the tumor to develop. Furthermore, the EGF-like domains of the protein imply it could be involved in cell signaling through interactions with other proteins.
The CD248 gene plays a critical role during embryonic development, particularly in the development of lymphoid tissues. Mostly in fibroblasts and perivascular cells, studies have shown that CD248 is abundantly expressed in lymphoid organs including the thymus, lymph nodes, and spleen. CD248 promotes the proliferation and migration of mesenchymal cells, therefore facilitating tissue remodeling and functional repair during the formation of lymphoid tissues. In adults, however, CD248 expression is generally restricted to certain organs, including the normal endometrial stroma and sometimes in fibroblasts.
In cancer research, CD248 is under increasing interest as a possible tumor marker. Early research indicates that most malignant tumors—especially in sarcomas and certain carcinomas—have highly expressed CD248. CD248 promotes the migration and multiplication of endothelial cells in the tumor microenvironment during tumor angiogenesis. CD248 is therefore regarded as a therapeutic target in addition to a molecular marker for tumors. By helping to restrict tumor angiogenesis, targeting CD248 may assist in limiting tumor development and metastases.
Different disorders, including fibrotic diseases and tumor growth, are connected to abnormal expression of the CD248 gene. For example, strongly expressed in synovial tissue of rheumatoid arthritis and psoriatic arthritis, CD248 suggests a possible function in inflammatory reactions and tissue remodeling. In these disorders, CD248 may control the activation of fibroblasts and smooth muscle cells in blood arteries, therefore promoting joint degeneration and ongoing inflammation.
Furthermore, CD248 is quite critical for bone metabolism. Presumably because of higher osteoblast activity, studies have demonstrated that mice devoid of CD248 display notably better mechanical characteristics and bone quality. Therapeutic approaches aiming at CD248 might therefore provide new paths for treating conditions like rheumatoid arthritis.
Given its significant role in tumors and inflammatory diseases, CD248 has become a potential target for cancer immunotherapy and targeted treatment. Future cancer treatments may depend much on developing antibodies or inhibitors aimed at CD248. Furthermore, the function of CD248 as a biomarker is quite important for the diagnosis and prognosis of diseases. For instance, its interactions with Mac-2 BP/90K are a possible prognostic biomarker for lung and breast malignancies.
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