H232 isoform human STING (R232H) coding sequence in expression plasmid

STING (stimulator of interferon genes; also known as TMEM173, MITA, MPYS, and ERIS) is essential for the IFN response to microbial or self-DNA, and acts as a direct sensor of cyclic dinucleotides (CDNs).
CDNs are important messengers in bacteria, affecting numerous responses of the prokaryotic cell, but also in mammalian cells, acting as agonists of the innate immune response. Several non-synonymous variants of STING have been described in the human population.

R232H has been identified as a natural variant allele of STING occuring in ∼14% of the human population [1]. H232 contains a single amino acid substitution R232H. The R232H isoform has a diminished response to bacterial and metazoan CDNs when compared to the wild-type allele [1, 2]. R232H has been the most commonly used human STING allele in published structural studies.

This gene is available in pUNO1 expression plasmid selectable with Blasticidin.


Human STING-H232 (pUNO1-hSTING-H232)

   ORF Size: 1139 bp
   Subclone: BspEI - NheI


- 20 µg of lyophilized DNA.
- 4 pouches of E. coli Fast-Media® Blas (2 TB and 2 Agar)
- 1 ml blasticidin at 10 mg/ml


1. Yi G. et al., 2013. Single nucleotide polymorphisms of human STING can affect Innate immune response to cyclic dinucleotides. PLoS One 8(10):e77846.
2. Diner E. et al., 2013. The innate immune DNA sensor cGAS produces a noncanonical cyclic dinucleotide that activates human STING. Cell Rep 3(5):1355-61.



Description H232 isoform human STING (R232H) coding sequence in expression plasmid
Cat. Codepuno1-hsting-h232
Unit Size20 µg
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