CD73, His-Tag (Human) Recombinant

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Catalog #
71184
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Description

Recombinant human CD73 (also known as NT5E, 5'-nucleotidase), encompassing amino acids 27-547. This construct contains a C-terminal His tag (6xHis). The protein was affinity purified.

Synonyms
5'- nucleotidase, Ecto-5'-nucleotidase, CD73, CD73 Protein, 5'-NT, 5'-nucleotidase, NT, eN, NT5, NTE, eNT, E5NT, CALJA, Ecto-5'-nucleotidase
Product Info
Storage and Usage
Citations
Species
Human
Construct
CD73 (27-547-His)
Host Species/Expression System
HEK293
Purity

≥90%

Format
Aqueous buffer solution
Formulation
40 mM Tris-HCl, pH 8.0, 110 mM NaCl, 2.2 mM KCl, and 20% glycerol
MW
59 kDa + glycans
Amino Acids
27-547
Glycosylation
This protein runs at a higher MW by SDS-PAGE due to glycosylation.
Specific Activity

≥20 pmol/min/µg

Genbank #
NM_002526
UniProt #
P21589
Tag(s)
C-terminal His-Tag
Background

CD73, or cluster of differentiation 73, is an enzyme which hydrolyzes AMP to adenosine. Increased concentrations of adenosine in the microenvironment has an immunosuppressive effect and promotes tumor cell growth.

Adenosine can enhance tumor growth via two mechanisms – 1) binding of adenosine to A2A and A2B receptors expressed on tumor cells directly promotes tumor cell proliferation and 2) binding of adenosine to A2A and A2B receptors on immune cells such as also  inhibits the activity of pro-inflammatory, anti-tumor immune cells like CD4+ T Cells, CTLs, dendritic cells, NK cells, while and activating immunosuppressant cells like Tregs, MDSCs and TAMs.

Development of inhibitory antibodies and small molecules against CD73 could serve as a new therapeutic strategy in the treatment of cancer. In preclinical models have provided proof of concept for this hypothesis as Inhibition of CD73 in mouse models has resulted in anti-tumor effects, providing proof of concept for this hypothesis.

CD73/CD39 Immunotherapy

References

1. Deaglio, S. et al., J. Exp. Med. 2007; 204(6): 1257-1265.
2. Thompson, L.F., et al., J. Exp. Med. 2004; 200(11): 1395-1405.