| Cat.No. | Name | Information |
|---|---|---|
| M52658 | Cathepsin L-IN-3 | Cathepsin L-IN-3 is a tripeptide-sized cathepsin L inhibitor. |
| M52657 | Cathepsin L-IN-4 | Cathepsin L-IN-4 is an inhibitor of cathepsin L with IC50 at nanomolar concentrations. |
| M52656 | Z-FG-NHO-BzOME | Z-FG-NHO-BzOME is a cysteine protease inhibitor that selectively inhibits cathepsin B, cathepsin L, cathepsin S, and papain. |
| M52655 | Z-Arg-Arg-AMC | Z-Arg-Arg-AMC is a selective substrate of cathepsin B. |
| M52654 | Z-Arg-Arg-pNA | Z-Arg-Arg-pNA is a substrate for cathepsin B and can be used to detect this enzyme activity. |
| M52653 | Arg-Arg-AMC | Arg-Arg-AMC is a highly selective substrate of Cathepsin B. |
| M52652 | Cathepsin G | Cathepsin G acts as a potent agonist of human platelet activation leading to their aggregation., and can be used for screening of relevant inhibitors. |
| M52651 | Z-FG-NHO-Bz | Z-FG-NHO-Bz is a selective cathepsin inhibitor. |
| M52650 | Z-DEVD-CMK | Z-DEVD-CMK is an irreversible inhibitor of most of the cathepsins in vitro. |
| M52649 | RKLLW-NH2 | RKLLW-NH2 is a Cathepsin L inhibitor. |
| M52648 | Z-FF-FMK | Z-FF-FMK is a selective cathepsin-L inhibitor. |
| M52647 | Cytochrome P450 reductase | Cytochrome P450 reductase is a NADPH-cytochrome reductase. |
| M52646 | Diprotin B | Diprotin B is a dipeptidyl aminopeptidase IV (DPP IV) inhibitor. |
| M52645 | IYPTNGYTR | IYPTNGYTR, a deamidation-sensitive signature peptide, is a deamidation product of Trastuzumab. |
| M52644 | Amlodipine aspartic acid impurity | Amlodipine aspartic acid impurity is the impurity of Amlodipine aspartic acid. |
| M52643 | S-Phenylmercapturic acid | S-Phenylmercapturic acid, a metabolite of benzene, can be used as a biomarker, identified by GC, HPLC (UV or fluorescence detection), GC-MS, LC-MS/MS or immunoassay. |
| M52642 | FTISADTSK | FTISADTSK is an endogenous stable signature peptide from Trastuzumab monitored by selected reaction monitoring (SRM). |
| M52641 | TRAF6 peptide | TRAF6 peptide is a specific TRAF6-p62 inhibitor. |
| M52640 | Ala-Ala-Pro-Val-chloromethylketone | Ala-Ala-Pro-Val-chloromethylketone is an irreversible human neutrophil elastase (NE) inhibitor for use in the study of chronic inflammatory airway diseases. |
| M52639 | MeOSuc-Ala-Ala-Pro-Met-AMC | MeOSuc-Ala-Ala-Pro-Met-AMC is a peptide substrate of elastases and chymotrypsin-like serine peptidases. |
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