Recombinant Human Neuropilin 2 protein (rFc Tag)(HPLC verified)

Species

Human

Purity

>90 %, SDS-PAGE
>90 %, SEC-HPLC

Tag

rFc Tag

Activity

not tested

Cat no : Eg3125



Product Information

Purity >90 %, SDS-PAGE
>90 %, SEC-HPLC
Endotoxin <0.1 EU/μg protein, LAL method
Activity
Not tested
Expression HEK293-derived Human Neuropilin 2 protein Arg21-Pro864 (Accession# O60462-1) with a rabbit IgG Fc tag at the C-terminus.
GeneID 8828
Accession O60462-1
PredictedSize 121.1 kDa
SDS-PAGE 120-140 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

NRP2 (Neuropilin-2) is a type I transmembrane glycoprotein belonging to the neuropilin family. It acts as a multifunctional receptor that binds to a variety of ligands, including vascular endothelial growth factor (VEGF) and signaling proteins (e.g., Sema3C and Sema3F), and plays important roles in neurodevelopment, angiogenesis, and immunomodulation. NRP2 is a cell surface molecule that is widely present in pancreatic cancer cells and is upregulated in various malignant tumors, such as hepatocellular carcinoma, gastric carcinoma, thyroid carcinoma and prostate cancer. It plays a crucial role in tumor cell growth, migration, invasion and angiogenesis, and monoclonal antibodies against NRP2 have been proposed as a potential strategy for pancreatic cancer treatment.

References:

1. Zhao Z, et al. Adv Sci (Weinh). 2023;10(30):e2303872. 2. Luo S, et al. FASEB J. 2022;36(2):e22079. 3. Kang Y, et al. Am J Transl Res. 2021;13(8):8938-8951. 4. Schulz A, et al. Front Oncol. 2020;9:1461. 5. Luo X, et al. Cell Biosci. 2020;10:113.