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

种属

Human

纯度

>90 %, SDS-PAGE
>90%, SEC-HPLC

标签

rFc Tag

生物活性

未测试

Cat no : Eg3746

Print datasheet

Synonyms

CD158 antigen-like family member J, CD158j, Killer cell immunoglobulin-like receptor 2DS2, Natural killer-associated transcript 5, NK receptor 183 ActI



产品信息

纯度 >90 %, SDS-PAGE
>90%, SEC-HPLC
内毒素 <0.1 EU/μg protein, LAL method
生物活性
Not tested
来源 HEK293-derived Human KIR2DS2 protein His22-His245 (Accession# P43631) with a rabbit IgG Fc tag at the C-terminus.
基因ID 100132285
蛋白编号 P43631
预测分子量 50.9 kDa
SDS-PAGE 55-70 kDa, reducing (R) conditions
组分 Lyophilized from 0.22 μm filtered solution in PBS, pH 7.4. Normally 5% trehalose and 5% mannitol are added as protectants before lyophilization.
复溶 Briefly centrifuge the tube before opening. Reconstitute at 0.1-0.5 mg/mL in sterile water.
储存条件
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.
运输条件 The product is shipped at ambient temperature. Upon receipt, store it immediately at the recommended temperature.

背景信息

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.

参考文献:

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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