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Recombinant Cynomolgus/Rhesus Siglec-3/CD33 Fc Protein, CF

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When Recombinant Cynomolgus Monkey/Rhesus Macaque Siglec-3/CD33 Fc Chimera (Catalog # 10885-SL) is immobilized at 1 µg/mL (100 µL/well), Recombinant Human Galectin-3BP/MAC-2BP (2226-GAB) binds with an ED50 of ...read more
2 μg/lane of Recombinant Cynomolgus Monkey/Rhesus Macaque Siglec‑3/CD33 Fc Chimera Protein (Catalog # 10885-SL) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by ...read more

Product Details

Summary
Reactivity Pm-Cm, RMSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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Recombinant Cynomolgus/Rhesus Siglec-3/CD33 Fc Protein, CF Summary

Details of Functionality
Measured by its binding ability in a functional ELISA. When Recombinant Cynomolgus Monkey/Rhesus Macaque Siglec-3/CD33 Fc Chimera (Catalog # 10885-SL) is immobilized at 1 µg/mL (100 µL/well), Recombinant Human Galectin-3BP/MAC-2BP (Catalog # 2226-GAB) binds with an ED50 of 0.15-1.20 µg/mL.
Source
Chinese Hamster Ovary cell line, CHO-derived Siglec-3/CD33 protein
Cynomolgus Monkey/Rhesus Macaque Siglec-3/CD33
(Met16-Gly248)
Accession # XP_045235686.1
IEGRMD Human IgG1
(Pro100-Lys330)
N-terminusC-terminus
Accession #
N-terminal Sequence
Met16
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
<0.10 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
52 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
68-79 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 with Trehalose.
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 Cynomolgus/Rhesus Siglec-3/CD33 Fc Protein, CF

  • CD33 antigen (gp67)
  • CD33 antigen
  • CD33 molecule
  • CD33
  • FLJ00391
  • gp67
  • myeloid cell surface antigen CD33
  • p67
  • sialic acid binding Ig-like lectin 3
  • Sialic acid-binding Ig-like lectin 3
  • Siglec3
  • Siglec-3
  • SIGLEC3gp67

Background

Sialic acid-binding Ig-like lectin 3 (Siglec-3), also known myeloid cell surface antigen CD33 (CD33), is a I-type (Ig-type) lectin belonging to the sialoadhesin subclass of the immunoglobulin superfamily (1). Siglecs are characterized by an N-terminal Ig-like V-type domain, which mediates sialic acid binding, followed by varying numbers of Ig-like C2-type domains in the extracellular domain (ECD). Fourteen human and nine mouse Siglecs have been characterized and are divided into 2 families: CD33 related and evolutionarily conserved (1-3). Mature Siglec-3 consists of an ECD with one Ig-like V-type domain and one Ig-like C2 domain, a single transmembrane and a cytoplasmic tail containing two immunoreceptor tyrosine-based inhibitory motifs (ITIMs) (3). Within the ECD, cynomolgus/rhesus Siglec-3 shares 89% amino acid sequence identity with human Siglec-3. An isoform of Siglec-3 lacking the N-terminal V-type domain, generated by alternative splicing, has been identified in humans (4). Each Siglec family member has a distinct preference for binding the various types of sialylated glycans found on the surface of mammalian cells and they most likely evolved to regulate host immune responses via the recognition of self-glycans (6). Siglec-3 is a disulfide-linked homodimer expressed on neutrophils, monocytes, macrophages and dendritic cells (2). Siglec-3 may be implicated in the regulation of both the innate but also the adaptive immunity and human Siglec-3 continues to be a therapeutic target for the treatment of acute myeloid leukemia and is a high potential risk factor for Alzheimer's (5). Siglec-3's ligands have yet to be classified, however terminal epitope preferences are conserved between Siglec-3 and Siglec-9 when binding to glycans (7). R&D Systems in-house testing indicates that Siglec-3 binds to LGALS3BP, consistent with the demonstrated functional interactions between other members of these protein families (8).
  1. Bhattacherjee, A. et al. (2021) Mol. Neurodegener. 16:19.
  2. Murch, S. et al. (2020) Medical Hypotheses. 144:110168.
  3. Hernandez-Caselles, T. et al. (2019) J. Immunol. Res. 2019:6032141.
  4. Hernández-Caselles, T. et al. (2006) J Leukoc Biol. 79:46
  5. Malik, et al. (2013) J. Neurosci. 33:13320
  6. Paulson, J. et al. (2012) Ann. N. Y. Acad. Sci. 1253:37.
  7. Wang, S. et al. (2021) Front Mol. Biosci. 8:645999.
  8. Laubli, H. et al. (2014) J. Biol. Chem. 289:33481.

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