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Siglec-7/CD328 Fc Chimera Protein, Human

Siglec-7/CD328 Fc Chimera Protein, Human

Catalog Number: UA010910 Reactivity: Human Conjugation: Unconjugated Brand: UA BIOSCIENCE
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Regular price $364 USD
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Product Details

Product Specification


Species Human
Synonyms CDw328, AIRM-1, Adhesion inhibitory receptor molecule 1, D-siglec, QA79 membrane protein, CD328, siglec-7
Accession Q9Y286-1
Amino Acid Sequence Gln19-Leu353, with C-hIgG Fc
Expression System HEK293
Molecular Weight 75-95kDa (Reducing)
Purity >95% by SDS-PAGE
Endotoxin <0.1EU/μg
Conjugation Unconjugated
Physical Appearance Lyophilized Powder
Storage Buffer PBS, 5% trehalose, pH7.4
Reconstitution Reconstitute at 0.1-1 mg/ml according to the size in ultrapure water after rapid centrifugation.
Stability & Storage · 12 months from date of receipt, lyophilized powder stored at -20 to -80℃.
· 3 months, -20 to -80℃ under sterile conditions after reconstitution.
· 1 week, 2 to 8℃ under sterile conditions after reconstitution.
· Please avoid repeated freeze-thaw cycles.
Reference

Crocker, P.R. et al. (1998) Glycobiology 8:v. Crocker, P.R. and A. Varki (2001) Trends Immunol. 22:337. Crocker, P.R. and A. Varki (2001) Immunology 103:137. Angata, T. et al. (2002) J. Biol. Chem. 277:24466.

Background

Siglecs (sialic acid binding Ig-like lectins) are I-type (Ig-type) lectins belonging to the Ig superfamily. They are sialoadhesin/CD169/Siglec-1, CD22/Siglec-2, CD33/Siglec-3, Myelin-Associated Glycoprotein (MAG/Siglec-4a) and Siglecs 5 to 11. To date, no Siglec has been shown to recognized any cell surface ligand other than sialic acids, suggesting that interactions with glycans containing this carbohydrate are important in mediating the biological functions of Siglecs. The sialic acid recognition site may be masked by cis interactions with sialic acids on the same cell surface.  In the immune response, may act as an inhibitory receptor upon ligand induced tyrosine phosphorylation by recruiting cytoplasmic phosphatase(s) via their SH2 domain(s) that block signal transduction through dephosphorylation of signaling molecules. Mediates inhibition of natural killer cells cytotoxicity. May play a role in hemopoiesis. Inhibits differentiation of CD34+ cell precursors towards myelomonocytic cell lineage and proliferation of leukemic myeloid cells.

Picture

SDS-PAGE

2μg (R: reducing condition, N: non-reducing condition).

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