Recombinant Human KIR3DL3 protein (rFc Tag)
Species
Human
Purity
>90 %, SDS-PAGE
Tag
rFc Tag
Activity
not tested
Cat no : Eg4358
Validation Data Gallery
Product Information
| Purity | >90 %, SDS-PAGE |
| Endotoxin | <0.1 EU/μg protein, LAL method |
| Activity |
Not tested |
| Expression | HEK293-derived Human KIR3DL3 protein Gln26-Leu322 (Accession# Q8N743) with a rabbit IgG Fc tag at the C-terminus. |
| GeneID | 115653 |
| Accession | Q8N743 |
| PredictedSize | 58.3 kDa |
| SDS-PAGE | 60-70 kDa, reducing (R) conditions |
| Formulation | Lyophilized from 0.22 μm filtered solution in PBS, pH 7.4. Normally 5% trehalose and 5% mannitol are added as protectants before lyophilization. |
| Reconstitution | Briefly centrifuge the tube before opening. Reconstitute at 0.1-0.5 mg/mL in sterile water. |
| Storage Conditions |
It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
|
| Shipping | The product is shipped at ambient temperature. Upon receipt, store it immediately at the recommended temperature. |
Background
KIR3DL3, a member of the killer cell immunoglobulin-like receptor (KIR) family, is an inhibitory receptor primarily expressed on natural killer (NK) cells and a subset of CD8+ T cells. It plays a role in immune regulation by recognizing specific HLA class I molecules, contributing to the balance between immune activation and inhibition. Recent research has identified KIR3DL3 as an inhibitory receptor for HHLA2, a B7 family ligand, suggesting its involvement in immune checkpoint pathways. KIR3DL3's interaction with HHLA2 can recruit SHP-1 and SHP-2 to attenuate signaling pathways such as Vav1, ERK1/2, AKT, and NF-κB, thereby inhibiting CD8+ T and NK cell functions. It is expressed on immune cells infiltrating HHLA2+ tumors from the human kidney, lung, gallbladder, and stomach, suggesting its potential as a therapeutic target for cancer.
References:
1.Trundley AE. et al. (2006). Immunogenetics. 57(12):904-916. 2.Wei Y. et al. (2021). Sci Immunol. 6(61):eabf9792. 3.Campbell KS. (2021). Cancer Immunol Res. 9(2):128. 4.Li Y. et al. (2023). J Adv Res. 47:137-150.
