CD276 Antibodies

Background

CD276 (also known as B7-H3) is a transmembrane glycoprotein belonging to the B7 costimulatory molecule family, which is widely expressed on the surface of various normal tissues and tumor cells. This protein plays a dual role in the immune checkpoint pathway by regulating the immune response activity of T lymphocytes - it can not only suppress excessive immune responses to maintain autoimmune tolerance, but also be utilized by tumor cells to achieve immune escape. Since its first identification by Chapoval et al. in 2001, CD276 has become an important research target in the field of tumor immunotherapy due to its abnormally high expression in malignant tumors such as lung cancer and prostate cancer. Its unique molecular structure and differentiated immunomodulatory functions continuously drive the development of innovative therapies such as immune checkpoint inhibitors and antibody-drug conjugates, providing a key theoretical basis for the study of immune regulatory mechanisms in the tumor microenvironment.

Structure Function Application Advantage Our Products

Structure of CD276

CD276 (B7-H3) is a type I transmembrane glycoprotein. Its molecular weight varies among different species, mainly due to the different degrees of gene splicing and glycosylation modification.

Species Human Mouse Rat Crab-eating macaque
Molecular Weight (kDa) ~60-110 ~55-100 ~58-105 ~62-108
Primary Structural Differences There are two main isomers, 4Ig and 2Ig High homology with human and different glycosylation pattern Extracellular domain highly conserved amino acid sequence The structure closest to human protein

This protein is composed of 316 amino acids (taking human 4Ig-B7-H3 as an example), and its extracellular segment contains immunoglobulin-like domains (IgV and IgC). These domains form stable dimers through disulfide bonds, which form the basis of interaction with ligands. Its intracellular segment is relatively short and lacks known clear signaling motifs. This feature suggests that it may transmit immunosuppressive signals by forming complexes with other membrane proteins. The hydrophobic α -helix in the transmembrane region is responsible for anchoring proteins to the cell membrane. Its complex N-link glycosylation modification not only affects the molecular weight of the protein, but also directly participates in regulating its specificity and affinity for binding to receptors.

Fig. 1:Structure of B7-H3 Protein.Fig. 1 Structure of B7-H3 Protein.1

Key structural properties of CD276:

  • Extracellular immunoglobulin-like domain (IgV-IgC)
  • Homodimer configuration stabilized by disulfide bonds
  • Highly glycosylated immunomodulatory interface

Functions of CD276

The main function of CD276 (B7-H3) is to act as a regulatory molecule in immune responses. However, its specific effects are environmentally dependent and show significant differences under physiological and pathological conditions.

Function Description
Immune co-regulation In the tumor microenvironment, T cell activation and cytokine production are usually inhibited, but costimulatory activity may also be exhibited under specific inflammatory conditions.
Cell adhesion support The extracellular immunoglobulin domain mediates cell-cell interactions and affects the migration and invasion of tumor cells.
Angiogenesis regulation In a variety of solid tumors with high expression, by influencing the promote the formation of the tumor related to vascular endothelial cell function.
Metabolic reprogramming Participating in the metabolic adaptation of the tumor microenvironment through indirect mechanisms may be related to the exhaustion of immune cell function.
Diagnostic markers Its specific high expression pattern on the surface of various malignant tumor cells makes it a potential target for immunotherapy and a diagnostic marker.

The interaction between CD276 and its ligands does not follow the typical affinity saturation model, but rather exhibits complex concentration dependence and microenvironment sensitivity, which reflects its functional plasticity in immune synapses and the complexity of regulation as an immune checkpoint molecule.

Applications of CD276 and CD276 Antibody in Literature

1. Zhou, Wu-Tong, and Wei-Lin Jin. "B7-H3/CD276: an emerging cancer immunotherapy." Frontiers in immunology 12 (2021): 701006. https://doi.org/10.3389/fimmu.2021.701006

The article indicates that CD276 (B7-H3) is an immunomodulatory protein of the B7 family, which is highly expressed in various tumors and participates in the regulation of the tumor microenvironment. It is a potential target for cancer immunotherapy. Multiple therapies based on CD276 have demonstrated good anti-tumor effects and safety in preclinical studies.

2. Cheng, Maosheng, et al. "CD276-dependent efferocytosis by tumor-associated macrophages promotes immune evasion in bladder cancer." Nature Communications 15.1 (2024): 2818. https://doi.org/10.1038/s41467-024-46735-5

This study reveals that CD276 is expressed on tumor-associated macrophages (Tams), promoting their cell burial by activating JUN transcription factors, thereby inhibiting T cell infiltration and weakening anti-tumor immunity. Combined blocking of CD276 and PD-1 can significantly inhibit tumor growth, providing a new target for combined immunotherapy.

3. Getu, Ayechew Adera, et al. "New frontiers in immune checkpoint B7-H3 (CD276) research and drug development." Molecular Cancer 22.1 (2023): 43. https://doi.org/10.1186/s12943-023-01751-9

This study reveals that CD276 (B7-H3) is specifically highly expressed in tumors. Besides its immune checkpoint function, it also drives malignant processes such as tumor proliferation, metastasis and metabolic reprogramming. Its significantly different expression pattern from normal tissues makes it a highly potential anti-cancer target. Recent research has made significant progress in both the mechanism of action and drug development.

4. Feng, Yang, et al. "Engineering CD276/B7-H3-targeted antibody-drug conjugates with enhanced cancer-eradicating capability." Cell reports 42.12 (2023). https://doi.org/10.1016/j.celrep.2023.113503

This study reveals that for the CD276 target, researchers have developed a novel antibody-drug conjugate, m276-SL-PBD. This drug, through multiple optimizations, can efficiently eliminate large triple-negative breast cancer tumors at extremely low doses. Its therapeutic index has significantly improved compared to previous generations of drugs, providing a promising targeted solution for the treatment of various solid tumors.

5. Liu, Shengzhuo, et al. "The role of CD276 in cancers." Frontiers in Oncology 11 (2021): 654684. https://doi.org/10.3389/fonc.2021.654684

The article indicates that CD276 (B7-H3) is an abnormally expressed immune checkpoint molecule in malignant tumors, which drives tumor progression by promoting tumor cell proliferation, invasion and migration. Existing evidence indicates that the therapeutic strategy targeting CD276 shows great therapeutic potential in malignant tumors.

Creative Biolabs: CD276 Antibodies for Research

Creative Biolabs specializes in the production of high-quality CD276 antibodies for research and industrial applications. Our portfolio includes monoclonal antibodies tailored for ELISA, Flow Cytometry, Western blot, immunohistochemistry, and other diagnostic methodologies.

  • Custom CD276 Antibody Development: Tailor-made solutions to meet specific research requirements.
  • Bulk Production: Large-scale antibody manufacturing for industry partners.
  • Technical Support: Expert consultation for protocol optimization and troubleshooting.
  • Aliquoting Services: Conveniently sized aliquots for long-term storage and consistent experimental outcomes.

For more details on our CD276 antibodies, custom preparations, or technical support, contact us at email.

Reference

  1. Getu, Ayechew Adera, et al. "New frontiers in immune checkpoint B7-H3 (CD276) research and drug development." Molecular Cancer 22.1 (2023): 43. https://doi.org/10.1186/s12943-023-01751-9
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Anti-CD276 antibodies

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Target: CD276
Host: Rat
Antibody Isotype: IgG1, κ
Specificity: Mouse
Clone: AG18
Application*: B, F, In Vivo
In Vivo Assay Functional Assay
Target: CD276
Host: Human
Antibody Isotype: IgG1
Specificity: Human, Monkey
Clone: 5F9
Application*: E, F
Target: CD276
Host: Mouse
Antibody Isotype: IgG
Specificity: Human
Clone: CBT293
Application*: WB, P, IF, F, E
Target: CD276
Host: Mouse
Antibody Isotype: IgG1
Specificity: Human
Clone: CBT4390
Application*: IH, F
Target: CD276
Host: Rat
Antibody Isotype: IgG1, κ
Specificity: Mouse
Clone: MJ18
Application*: F, in vivo
In Vivo Assay
Target: CD276
Host: Mouse
Antibody Isotype: IgG1, κ
Specificity: Human
Clone: CBFYC-1198
Application*: E, WB
Target: CD276
Host: Mouse
Antibody Isotype: IgG1, κ
Specificity: Human
Clone: CBFYC-1197
Application*: E, IF
Target: CD276
Host: Mouse
Antibody Isotype: IgG1, κ
Specificity: Human
Clone: 7C10
Application*: E, IF, WB
Target: CD276
Host: Mouse
Antibody Isotype: IgG2b
Specificity: Human
Clone: C2107
Application*: F, IF, E
Target: CD276
Host: Mouse
Antibody Isotype: IgG2b, κ
Specificity: Human, Mouse, Rat, Dog, Cattle
Clone: CBYY-1722
Application*: WB, IP, E, IF
Target: CD276
Host: Mouse
Antibody Isotype: IgG1, κ
Specificity: Human, Mouse, Rat
Clone: CBYY-1660
Application*: WB, IP, E, IF
Target: CD276
Host: Rabbit
Antibody Isotype: IgG
Specificity: Mouse
Clone: CBYY-0975
Application*: E
Target: CD276
Host: Mouse
Antibody Isotype: IgG2a, κ
Specificity: Human, Mouse, Rat
Clone: CBYY-0973
Application*: WB, IP, E, IF, P
Target: CD276
Host: Mouse
Antibody Isotype: IgG2b, κ
Specificity: Human, Mouse, Rat, Dog, Cattle
Clone: CBYY-0972
Application*: WB, IP, E, IF
Target: CD276
Host: Mouse
Antibody Isotype: IgG1, κ
Specificity: Human, Mouse, Rat, Dog, Cattle
Clone: CBYY-0971
Application*: WB, IP, E, IF
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Submit A Review Fig.3 Signaling pathways in cancers. (Creative Biolabs Authorized) Fig.4 Protocols troubleshootings & guides. (Creative Biolabs Authorized) Submit A Review Fig.3 Signaling pathways in cancers. (Creative Biolabs Authorized) Fig.4 Protocols troubleshootings & guides. (Creative Biolabs Authorized)
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(P): Predicted
* Abbreviations
  • AActivation
  • AGAgonist
  • APApoptosis
  • BBlocking
  • BABioassay
  • BIBioimaging
  • CImmunohistochemistry-Frozen Sections
  • CIChromatin Immunoprecipitation
  • CTCytotoxicity
  • CSCostimulation
  • DDepletion
  • DBDot Blot
  • EELISA
  • ECELISA(Cap)
  • EDELISA(Det)
  • ESELISpot
  • EMElectron Microscopy
  • FFlow Cytometry
  • FNFunction Assay
  • GSGel Supershift
  • IInhibition
  • IAEnzyme Immunoassay
  • ICImmunocytochemistry
  • IDImmunodiffusion
  • IEImmunoelectrophoresis
  • IFImmunofluorescence
  • IGImmunochromatography
  • IHImmunohistochemistry
  • IMImmunomicroscopy
  • IOImmunoassay
  • IPImmunoprecipitation
  • ISIntracellular Staining for Flow Cytometry
  • LALuminex Assay
  • LFLateral Flow Immunoassay
  • MMicroarray
  • MCMass Cytometry/CyTOF
  • MDMeDIP
  • MSElectrophoretic Mobility Shift Assay
  • NNeutralization
  • PImmunohistologyp-Paraffin Sections
  • PAPeptide Array
  • PEPeptide ELISA
  • PLProximity Ligation Assay
  • RRadioimmunoassay
  • SStimulation
  • SESandwich ELISA
  • SHIn situ hybridization
  • TCTissue Culture
  • WBWestern Blot
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