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Recombinant Mouse ASGR2 Fc Chimera Protein, CF

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Immobilized Recombinant Mouse ASGR2 Fc Chimera (10447-AS) binds human plasma von Willebrand Factor with an ED50 of 0.05-0.6 μg/mL.
2 μg/lane of Recombinant Mouse ASGR2 Fc Chimera (Catalog # 10447-AS) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Blue staining, showing bands at kDa.

Product Details

Summary
Reactivity MuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

Order Details

Recombinant Mouse ASGR2 Fc Chimera Protein, CF Summary

Details of Functionality
Measured by its binding ability in a functional ELISA. Immobilized Recombinant Mouse ASGR2 Fc Chimera (Catalog # 10447-AS) binds Human plasma von Willebrand Factor with an ED50 of 0.05‑0.6 μg/mL.
Source
Chinese Hamster Ovary cell line, CHO-derived mouse ASGR2 protein
MDPMouse IgG2A
(Glu98-Lys330)
IEGR Mouse ASGR2
(Ser79-His301)
Accession # P24721.1
N-terminusC-terminus
Accession #
N-terminal Sequence
Met
Structure / Form
Disulfide-linked homodimer
Protein/Peptide Type
Recombinant Proteins
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<1.0 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
53 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
62-81 kDa, under reducing conditions

Packaging, Storage & Formulations

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.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS.
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 500 μg/mL in PBS.

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Mouse ASGR2 Fc Chimera Protein, CF

  • ASGPR 2
  • ASGP-R 2
  • ASGPR2
  • ASGP-R2
  • ASGR2
  • asialoglycoprotein receptor 2
  • CLEC4H2
  • CLEC4H2FLJ60040
  • C-type lectin domain family 4 member H2
  • HBxAg-binding protein
  • HBXBP
  • Hepatic lectin H2
  • HL-2

Background

Asialoglycoprotein receptor 2 (ASGR2), also known as hepatic lectin 2 (HL-2), is an approximately 38 kDa member of the C-type lectin receptor family (1). ASGR2 is a single-pass type II transmembrane protein that plays a role in the endocytosis of desialylated glycoproteins, hepatic thrombopoietin production, and gastrointestinal malignancies (2, 3). ASGR2 is closely related to ASGR1 which is about 2 kDa smaller and is encoded by distinct but closely linked genes. Variations in ASGR2 structure due to alternative splicing have been reported (4-6). Mature ASGR2 consists of a cytoplasmic domain, transmembrane segment and an extracellular domain (ECD). Within the ECD, mouse ASGR2 shares 67% and 83% aa sequence identity with human and rat ASGR2, respectively. Both ASGR2 and ASGR1 compose the asialoglycoprotein receptor (ASGPR) which mediates removal of potentially hazardous glycoconjugates from blood in health and disease (7). ASGPR, also known as the Ashwell receptor, can modulate von Willebrand factor (vWF) and platelet homeostasis in part via clearance of platelets that are first desialylated during sepsis caused by pathogens including S. pneumoniae. The ASGR1 chain of the Ashwell receptor participates in plasma vWF clearance independently of sialylation and sepsis, ASGR2 colocalization with plasma vWF was increased in ASGR1 deficient mice (8). In addition, ASGR2 expression was shown to be associated with malignant phenotypes in gastric cancer and may represent a specific biomarker for recurrence of some gastric cancers (9).
  1. Ishibashi, S. et al. (1994) J. Biol. Chem. 269:27803.
  2. Grozovsky, R. et al. (2015) Nat Med. 1:47.
  3. Tanaka, H. et al. (2018) Mol. Cancer Res. 16:1420.
  4. Drickamer, K. et al. (1984) J. Biol. Chem. 259:770.
  5. Halberg, D.F. et al. (1987) J. Biol. Chem. 262:9828.
  6. Paietta, E. et al. (1992) J. Biol. Chem. 267:11078.
  7. Harris R.L. et al. (2012) Mol Biol Int. 2012:283974.
  8. Grewal, P. et al. (2008) Nature Medicine. 14:6.
  9. Tanaka H. et al. (2018) Mol Cancer Res. 16:1420.

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