General description SRM 8599_cert SRM 8599 _SDS Other Notes Example analytes are listed below as a reference. Please download a current certificate at nist.
General description SRM 8599_cert SRM 8599 _SDS Other Notes Example analytes are listed below as a reference. Please download a current certificate at nist.
General description SRM 8599_cert SRM 8599 _SDS Other Notes Reference/Informational value is provided for the following analytes. Uranium (U), Rhenium (Re), Osmium ( 187 Os) See certificate for values and more details at nist.
General description SRM 8599_cert SRM 8599 _SDS Other Notes Reference/Informational value is provided for the following analytes. Uranium (U), Rhenium (Re), Osmium ( 187 Os) See certificate for values and more details at nist.
Application SB-366791 has been used as a transient receptor potential cation channel subfamily V member 1 (TRPV1) antagonist: to infer the in vitro and in vivo pharmacology of
Application SB-366791 has been used as a transient receptor potential cation channel subfamily V member 1 (TRPV1) antagonist: to infer the in vitro and in vivo pharmacology of
Application SB-366791 has been used as a transient receptor potential cation channel subfamily V member 1 (TRPV1) antagonist: to infer the in vitro and in vivo pharmacology of
Application SB-366791 has been used as a transient receptor potential cation channel subfamily V member 1 (TRPV1) antagonist: to infer the in vitro and in vivo pharmacology of
Application SKF-96365 has been used as : a nonselective transient receptor potential 6 (TRPC6) blocker in human podocytes an antagonist of store-operated Ca 2+ influx in neurons an inhibitor for transient receptor potential 3 (TRPC3) in
Application SKF-96365 has been used as : a nonselective transient receptor potential 6 (TRPC6) blocker in human podocytes an antagonist of store-operated Ca 2+ influx in neurons an inhibitor for transient receptor potential 3 (TRPC3) in
General description Membrane Preparations for Vesicular Transport Assays (VT) are suitable for general drug-efflux transporter interaction studies. Both substrate and inhibitor interactions can be assessed using vesicles.
General description Membrane Preparations for Vesicular Transport Assays (VT) are suitable for general drug-efflux transporter interaction studies. Both substrate and inhibitor interactions can be assessed using vesicles.
Biochem/physiol Actions Sk052-145-2 is a potent and selective inhibitor of bacterial Lipoprotein signal peptidase (Lsp). Sk052-145-2 potently inhibits growth of E.
Biochem/physiol Actions Sk052-145-2 is a potent and selective inhibitor of bacterial Lipoprotein signal peptidase (Lsp). Sk052-145-2 potently inhibits growth of E.
Biochem/physiol Actions Sk052-145-2 is a potent and selective inhibitor of bacterial Lipoprotein signal peptidase (Lsp). Sk052-145-2 potently inhibits growth of E.
Biochem/physiol Actions Sk052-145-2 is a potent and selective inhibitor of bacterial Lipoprotein signal peptidase (Lsp). Sk052-145-2 potently inhibits growth of E.
Biochem/physiol Actions SK33, a trifluoromethylated enobosarm analog, is a cell and brain penetrant, tissue selective and highly potent anti-androgen that reduces androgen receptor (AR) transcriptional activity. SK33 induces cell cycle arrest at
Biochem/physiol Actions SK33, a trifluoromethylated enobosarm analog, is a cell and brain penetrant, tissue selective and highly potent anti-androgen that reduces androgen receptor (AR) transcriptional activity. SK33 induces cell cycle arrest at