Product name: pJAK2(1001–1013)
Sequence: LPQDKE(pY)YKVKEP
Modifications:
phosphorylation of Y(7),
Purity: 95% by HPLC
Counter ion: Trifluoroacetate
Format: Lyophilized powder
Description: SOCS1 antagonist pJAK2(1001-1013) peptide upregulated the expression of the maturation marker (CD83) and costimulatory molecule (CD86) of RNA-electroporated human monocyte-derived mature DCs (mDCs), potentiated the capacity of mDCs to induce T-cell proliferation, stimulated the secretion of proinflammatory cytokines, and enhanced the cytotoxicity of tumor cell antigen-specific CTLs activated by human gastric cancer cell total RNA-electroporated mDCs. Data from Western blot analysis indicate that STAT1 was further activated in pJAK2(1001-1013) peptide-loaded mDCs. These results imply that the SOCS1 antagonist pJAK2(1001-1013) peptide is an effective reagent for the enhancement of antigen-specific antitumor immunity by DCs. pJAK2(1001-1013) is able to bind to the KIR region of SOCS-3, similar to its ability to bind to the KIR region of SOCS-1 (manuscript in preparation). Thus, pJAK2(1001-1013) should be effective as an antagonist of SOCS-3. The implication of this is that SOCS antagonists such as pJAK2(1001-1013) potentially possess broad antiviral activity, which would not be the case for siRNA in terms of specificity and possibly issues of practicality of use as an antiviral drug.
Usage: For Scientific Research Use Only, Not for Human Use.
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