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Recombinant Human KIR2DS2 protein (rFc Tag) (HPLC verified)

Species

Human

Purity

>90 %, SDS-PAGE
>90%, SEC-HPLC

Tag

rFc Tag

Activity

not tested

Cat no : Eg3746



Product Information

Purity >90 %, SDS-PAGE
>90%, SEC-HPLC
Endotoxin <0.1 EU/μg protein, LAL method
Activity
Not tested
Expression HEK293-derived Human KIR2DS2 protein His22-His245 (Accession# P43631) with a rabbit IgG Fc tag at the C-terminus.
GeneID 100132285
Accession P43631
PredictedSize 50.9 kDa
SDS-PAGE 55-70 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.
  • Until expiry date, -20℃ to -80℃ as lyophilized proteins.
  • 3 months, -20℃ to -80℃ under sterile conditions after reconstitution.
Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the recommended temperature.

Background

KIR2DS2 is associated with reduced post-transplant recurrence and improved prognosis in solid tumors of hematologic malignancies and is an attractive target for NK-based therapeutic strategies. Furthermore, KIR2DS2 is associated with increased activation of anti-glioblastoma cells and improved clinical responses in breast, colorectal, non-small cell lung and hepatocellular carcinomas. (PMID: 35768150) Currently KIR2DS2 has been shown to directly recognize viral deconjugating peptides in the context of HLA-C and is protective against chronic hepatitis C virus infection. The high sequence homology between KIR2DS2 and inhibitory KIRs (KIR2DL2 and KIR2DL3) has made it difficult to develop an antibody that specifically detects KIR2DS2.

References:

1. Blunt MD, et al. J Immunol. 2022;209(2):379-390. 2. Graham LV, et al. Front Oncol. 2024;14:1404051. 3. Blunt MD, et al. HLA. 2019;93(1):32-35.

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