Active Recombinant Human EFNB3 protein, Fc/His-Tagged, Biotinylated

Cat.No. : EFNB3-713H
Product Overview : Biotinylated Recombinant Human EFNB3 protein(Q15768)(Leu28-Ser224), fused with C-terminal Fc and His Tag, was expressed in Insect Cells.
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Species : Human
Source : Insect Cells
Tag : Fc&His
Protein Length : Leu28-Ser224
Form : Lyophilized from a 0.2 μm filtered solution in PBS with BSA as a carrier protein.
Bio-activity : Measured by its binding ability in a functional ELISA. Immobilized recombinant mouse EphB3 Fc Chimera at 2 μg/mL (100 μL/well) can bind biotinylated Recombinant Human Ephrin‑B3 Fc Chimera with a linear range of 1.3-80 ng/mL.
Molecular Mass : 49.2 kDa (monomer)
Purity : >95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Storage : Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70 °C as supplied.
1 month, 2 to 8 °C under sterile conditions after reconstitution.
3 months, -20 to -70 °C under sterile conditions after reconstitution.
Reconstitution : Reconstitute at 100 μg/mL with sterile PBS.
Gene Name EFNB3 ephrin-B3 [ Homo sapiens ]
Official Symbol EFNB3
Synonyms EFNB3; ephrin-B3; EPLG8; LERK 8; Ephrin B3; eph-related receptor tyrosine kinase ligand 8; EPH-related receptor transmembrane ligand ELK-L3; EFL6; LERK8
Gene ID 1949
mRNA Refseq NM_001406
Protein Refseq NP_001397
MIM 602297
UniProt ID Q15768

Case 1: Prydz K, et al. Biochem Biophys Res Commun. 2018

Ephrin-B3 binds secretory/cell-associated proteoglycans (e.g., CD44, agrin) via a 20/45 kDa protein complex, modulating extracellular matrix interactions in cancer metastasis. CD44 variants regulate binding affinity, suggesting therapeutic targets for oral squamous carcinoma and Eph receptor signaling dysregulation.

Fig1. Ephrin-B3-binding proteoglycans.

Fig2. Heparin blocks ephrin-B3 binding to H367 cells.

Case 2: Holen HL, et al. Scand J Immunol. 2011

Ephrin-B3 binds B lymphocytes via a heparin-sensitive, Arg-188-dependent non-Eph receptor, selectively driving memory B-cell migration—a novel mechanism for modulating immune responses and leukocyte trafficking in autoimmune or lymphoma therapies.

Fig1. Detection of cell surface proteins binding ephrin-B3.

Fig2. Ephrin-B3 enhances migration of memory CD19+ B cells.

1. Therapeutic Potential of Recombinant EFNB3 Protein in Neuroprotection and Oncology Recombinant ephrin-B3 (EFNB3) protein, a critical Eph receptor ligand, demonstrates dual therapeutic utility in neuroprotection and cancer therapy. In neurodegenerative contexts, EFNB3 mitigates glutamate excitotoxicity by restoring astrocytic EAAT1/2 function, counteracting HIV Tat-induced neuronal damage. In oncology, it suppresses glioma and lung adenocarcinoma progression by inhibiting Eph receptor-driven PI3K/AKT and ERK pathways, reducing tumor migration and metastasis. 2. Mechanistic Insights and Preclinical Applications Preclinical studies reveal EFNB3’s ability to modulate EphA4 signaling, enhancing glutamate uptake in astrocyte-neuron co-cultures and improving neuronal survival in neuroHIV models. In cancer, EFNB3 destabilizes focal adhesions and downregulates MMP-2/9, impairing invasion. Rodent glioma models show EFNB3 overexpression reduces tumor volume by 40% and prolongs survival, while synergizing with immune checkpoint inhibitors to enhance T-cell infiltration. 3. Delivery Challenges and Future Innovations Current limitations include poor CNS bioavailability and transient activity. Emerging solutions include engineered exosomes for blood-brain barrier penetration and CRISPR-activation systems for sustained EFNB3 expression. Combining EFNB3 with antiretroviral therapies or CAR-T cells could address neurocognitive disorders and therapy-resistant cancers, positioning it as a versatile candidate for precision medicine.

Fig1. Model of the mechanism of guidance and migration of SC after CNS demyelination. (Beatriz Garcia-Diaz, 2019)

Not For Human Consumption!

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