Innate Immunity
Products Related to Innate Immunity(566)
- GC52346IDR 1002 (trifluoroacetate salt)Purity: >95.00%
A synthetic cationic innate defense regulator peptide
- GC52363Citrullinated Histone H3 (R2 + R8 + R17) (2-22)-biotin Peptide
A biotinylated and citrullinated histone H3 peptide
- GC52367Citrullinated Vimentin (G146R) (R144 + R146) (139-159)-biotin PeptidePurity: >99.00%
A biotinylated and citrullinated mutant vimentin peptide
- GC52370Citrullinated Vimentin (R144) (139-159)-biotin PeptidePurity: >98.00%
A biotinylated and citrullinated vimentin peptide
- GC52371Vimentin (G146R) (139-159)-biotin PeptidePurity: >98.00%
A biotinylated mutant vimentin peptide
- GC52384NFAT Inhibitor (cell-permeable) (trifluoroacetate salt)Purity: >95.00%
A cell-permeable form of NFAT inhibitor
- GC52457WRW4 (trifluoroacetate salt)Purity: >98.00%
WRW4 (trifluoroacetate salt) is a selective antagonist of formyl peptide receptor 2 (FPR2, formerly known as FPRL1), which is a synthetic C-terminal amidated hexapeptide, its IC 50 value for inhibiting the binding of WKYMVm to FPRL2 is 0.23 μM.
- GC52499Abz-Ala-Pro-Glu-Glu-Ile-Met-Arg-Arg-Gln-EDDnp (trifluoroacetate salt)Purity: >95.00%
A sensitive substrate for neutrophil elastase
- GC60622BAY 2416964CAS: 2242464-44-2Purity: >98.00%
BAY 2416964 is a potent and orally active inhibitor targeting aryl hydrocarbon receptor (AhR) with IC 50 value of 341nM.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC52343 | 113-O12B | 2803699-72-9 | >98.00% | |
An ionizable cationic lipidoid | ||||
| GC52346 | IDR 1002 (trifluoroacetate salt) | - | >95.00% | |
A synthetic cationic innate defense regulator peptide | ||||
| GC52363 | Citrullinated Histone H3 (R2 + R8 + R17) (2-22)-biotin Peptide | - | - | |
A biotinylated and citrullinated histone H3 peptide | ||||
| GC52364 | Vimentin (139-159)-biotin Peptide | - | >98.00% | |
A biotinylated vimentin peptide | ||||
| GC52367 | Citrullinated Vimentin (G146R) (R144 + R146) (139-159)-biotin Peptide | - | >99.00% | |
A biotinylated and citrullinated mutant vimentin peptide | ||||
| GC52370 | Citrullinated Vimentin (R144) (139-159)-biotin Peptide | - | >98.00% | |
A biotinylated and citrullinated vimentin peptide | ||||
| GC52371 | Vimentin (G146R) (139-159)-biotin Peptide | - | >98.00% | |
A biotinylated mutant vimentin peptide | ||||
| GC52384 | NFAT Inhibitor (cell-permeable) (trifluoroacetate salt) | - | >95.00% | |
A cell-permeable form of NFAT inhibitor | ||||
| GC52394 | LC10 | - | >98.00% | |
A lipidoid derivative of lithocholic acid | ||||
| GC52406 | AMPR-22 (trifluoroacetate salt) | - | >95.00% | |
An antimicrobial peptide | ||||
| GC52412 | TT-232 (trifluoroacetate salt) | - | >98.00% | |
A synthetic peptide derivative of somatostatin | ||||
| GC52424 | Bradykinin Fragment (1-5) (trifluoroacetate salt) | - | >98.00% | |
A metabolite of bradykinin | ||||
| GC52457 | WRW4 (trifluoroacetate salt) | - | >98.00% | |
WRW4 (trifluoroacetate salt) is a selective antagonist of formyl peptide receptor 2 (FPR2, formerly known as FPRL1), which is a synthetic C-terminal amidated hexapeptide, its IC 50 value for inhibiting the binding of WKYMVm to FPRL2 is 0.23 μM. | ||||
| GC52496 | Sulfatide (bovine) (sodium salt) | - | >95.00% | |
A mixture of isolated bovine sulfatides | ||||
| GC52499 | Abz-Ala-Pro-Glu-Glu-Ile-Met-Arg-Arg-Gln-EDDnp (trifluoroacetate salt) | - | >95.00% | |
A sensitive substrate for neutrophil elastase | ||||
| GC52505 | Ganglioside GT1b (bovine) (sodium salt) | - | >98.00% | |
A sphingolipid | ||||
| GC52516 | Erbstatin | 100827-28-9 | >90.00% | |
A tyrosine kinase inhibitor | ||||
| GC56074 | DSG-PEG 2000 | 308805-39-2 | >99.00% | |
| GC60183 | GSK2245035 | 1207629-49-9 | >99.50% | |
A TLR7 agonist | ||||
| GC60622 | BAY 2416964 | 2242464-44-2 | >98.00% | |
BAY 2416964 is a potent and orally active inhibitor targeting aryl hydrocarbon receptor (AhR) with IC 50 value of 341nM. | ||||
| GC61286 | SP-8356 | 1454885-45-0 | >99.00% | |
| GC61293 | SR-717 | 2375421-09-1 | >99.50% | |
SR-717 is a non-nucleotide STING agonist. SR-717 activates STING in ISG-THP1 (WT) and ISG-THP1 cGAS KO (cGAS KO) cells (EC 50 =2.1μM, 2.2μM). | ||||
| GC61367 | VAF347 | 574759-62-9 | >99.50% | |
VAF347 is a cell permeable and highly affinity aryl hydrocarbon receptor (AhR) agonist and induces AhR signaling. | ||||
| GC61843 | Mofezolac | 78967-07-4 | >98.50% | |
Mofezolac, a non-steroidal anti-inflammatory drug (NSAID), is a selective, reversible and orally active COX-1 inhibitor with an IC50 of 1.44 nM. | ||||
