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Class A(Rhodopsin)
The human GPCR family is classified into subclasses A (rhodopsin-like), B (secretin and adhesion), C (glutamate), and F (Frizzled) based on their amino acid sequences. Class A GPCRs, a family of rhodopsin-like receptors consisting of 719 members, are further divided into several subclasses: amines, peptides, proteins, lipids, melatonin, nucleotides, steroids, saccharocarboxylic acids, sensory receptors, and orphan receptors. Indications for Class A GPCRs include pain relief, allergies, cardiovascular diseases, hypertension, and cancer.
Class B1(Secretin)
Class B GPCRs are divided into two subfamilies: B1 secretin receptors and B2 adhesion receptors. Members of the secretin receptor subfamily have large extracellular domains and bind to vasoactive intestinal peptide (VIP), pituitary adenylate cyclase-activating peptide (PACAP), corticotropin-releasing factor (CRF), parathyroid hormone (PTH), growth hormone-releasing hormone (GHRH), calcitonin gene-related peptide (CGRP), glucagon, and glucagon-like peptide (GLP). The adhesion receptor subfamily has nine subclasses and possesses unique N-terminal motifs, such as epidermal growth factor, cadherin, and immunoglobulin domains.
Class C(Glutamate)
Class C glutamate receptors contain 22 receptors, divided into 5 subfamilies, including 1 calcium-sensitive receptor (CaSR), 2 GABA type B receptors (GABAB1 and GABAB2), 3 taste 1 receptors (TS1R1-3), 8 metabolic glutamate receptors (mGluR1-8), and 8 orphan GPCRs.
Combination
CLP1R, GCGR, and GIPR are crucial drug targets for treating metabolic diseases. CLP1R is involved in regulating insulin secretion; GCGR plays a key role in glucose homeostasis and is a major target for diabetes drug development; GIPR mediates incretin effects and influences energy metabolism. Our company offers high-quality drug-target cells for these receptors, supporting high-throughput screening and activity validation to accelerate drug discovery for metabolic disorders.
Orphan and other 7TM
GPR55, GPR75, MRGPRB2, and other orphan or understudied 7-Transmembrane (7TM) receptors represent the "frontier" of novel drug discovery. They play crucial roles in key physiological and pathological processes such as neurobiology, metabolism, and immunity, offering vast untapped therapeutic potential.
Parental Cell
GPCRs (G protein-coupled receptors) are important proteins in cell signaling, with a topological conformation of seven transmembrane receptors. When an extracellular ligand acts on this receptor, the intracellular portion of the receptor binds to the G protein, activating the G protein and initiating different signal transduction pathways, leading to various biological effects.
Combination
Our platform provides engineered cellular models covering multi-pathway combinations including PD-1, CTLA4, TIGIT, LAG3, 41BB, OX40, and SIRPα/CD47. Utilizing dual-reporter systems and antigen-presenting cell platforms, these models enable simultaneous evaluation of immune checkpoint synergy, antibody efficacy, and immune cell activation, offering physiologically relevant in vitro tools for developing combination immunotherapy.
Fc Effector
Designed for precise evaluation of key biological activities in antibody therapeutics. Our platform delivers standardized ADCC/ADCP reporter cells, comprehensively covering core mechanisms such as antibody-dependent cellular cytotoxicity and phagocytosis. These tools provide reliable solutions for antibody optimization and potency assessment.
T Cell Activation
These engineered cellular models assess T cell activation through key signaling pathways. NFAT and NFκB reporter lines measure early transcriptional activity, while IL-2 secretion assays quantify functional cytokine output. Ideal for screening immunomodulators, bispecific antibodies, and CAR-T candidates, they deliver reliable, quantitative data for immunotherapy development.
Co-Stimulatory
Our platform provides reliable cellular tools for evaluating agonists targeting key co-stimulatory pathways. Available models include OX40, 4-1BB, GITR, CD27, HVEM/LIGHT, CD28, and BTLA, engineered with reporter systems to quantify pathway-specific activation. These standardized assays enable robust potency and efficacy assessment, accelerating the development of next-generation immunostimulatory therapeutics.
Co-Inhibitory
Our platform provides comprehensive in vitro testing solutions for key co-inhibitory pathways, covering core targets including PD-1/PD-L1&L2, TIGIT/CD155, CTLA4, and LAG3, along with their common combinations. Utilizing standardized reporter cells and binding assays, we support activity evaluation, mechanism investigation, and drug screening for both single-target and dual immune checkpoint inhibitors, facilitating efficient development in cancer immunotherapy.
Immune Checkpoint
We provide engineered cellular models targeting novel immune checkpoint molecules, including BDCA2, CD24, and VSIG4. These standardized reporter systems enable efficient evaluation of target activation/inhibition activity, supporting the screening and mechanistic study of immunomodulators. They offer reliable tools for drug development in cancer immunotherapy and autoimmune diseases.
STING
We offer specialized cellular tools for studying the Stimulator of Interferon Genes (STING) pathway, a critical target in cancer immunotherapy and antiviral research. Our assays enable precise evaluation of STING agonist activity, cyclic dinucleotide sensing, and downstream interferon response, supporting the development of novel immunotherapeutics.
Cytokine&Growth Factor
Our comprehensive testing platform offers validated cellular assays for a wide range of cytokines and growth factors, including BCMA, TGFβ, EGF, CSF1R, and key interleukins (e.g., IL2, IL4/13, IL6). We also support pathways such as IFN signaling, RANKL, VEGF, Wnt, and TSLP. These ready-to-use, standardized assays enable sensitive and quantitative evaluation of ligand activity, receptor engagement, and pathway modulation to accelerate drug discovery and development.
TAA
We offer standardized cellular models covering a broad range of tumor-associated antigens (TAAs), including key targets such as 5T4, B7H3, CD123, CD19, CD20, CD22, CD30, CD33, and CD38. This platform supports in vitro activity evaluation and screening for antibody drugs, CAR-T therapies, and bispecific antibodies, providing efficient and reliable detection tools for cancer immunotherapy development.
TLR
We provide engineered reporter cells covering key innate immune receptors, including TLR2, TLR3, TLR4, TLR5, TLR7, TLR8, and TLR9. This platform enables efficient detection of ligand-induced activation, supporting agonist/antagonist screening, vaccine adjuvant evaluation, and innate immune pathway research. It serves as a standardized tool for drug discovery in infectious diseases, oncology, and autoimmune disorders.
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