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rp181294-100μg
Recombinant Human Serpin E1/PAI-1 Protein (C007B-502502)
Price: $594.44List Price: $660.48As a member of the Serpin superfamily of serine protease inhibitors, Serpin E1/PAI 1 is the principal inhibitor of urokinase type plasminogen activator (uPA) and tissue type PA. As important regulators of extracellular matrix remodeling, uPA and PAI -
rp181294-10μg
Recombinant Human Serpin E1/PAI-1 Protein (C007B-502503)
Price: $172.90List Price: $192.12As a member of the Serpin superfamily of serine protease inhibitors, Serpin E1/PAI 1 is the principal inhibitor of urokinase type plasminogen activator (uPA) and tissue type PA. As important regulators of extracellular matrix remodeling, uPA and PAI -
rp181294-1mg
Recombinant Human Serpin E1/PAI-1 Protein (C007B-502504)
Price: $3,272.61List Price: $3,636.23As a member of the Serpin superfamily of serine protease inhibitors, Serpin E1/PAI 1 is the principal inhibitor of urokinase type plasminogen activator (uPA) and tissue type PA. As important regulators of extracellular matrix remodeling, uPA and PAI -
rp181294-50μg
Recombinant Human Serpin E1/PAI-1 Protein (C007B-502505)
Price: $387.63List Price: $430.70As a member of the Serpin superfamily of serine protease inhibitors, Serpin E1/PAI 1 is the principal inhibitor of urokinase type plasminogen activator (uPA) and tissue type PA. As important regulators of extracellular matrix remodeling, uPA and PAI -
66454-1-Ig
Serpin Peptidase Inhibitor, Clade A (Alpha-1 Antiproteinase, Antitrypsin), Member 7
Price: $927.23List Price: $1,030.25The SERPINA7 antibody from Proteintech is a mouse monoclonal antibody to a recombinant protein of human SERPINA7. This antibody recognizes human antigen. The SERPINA7 antibody has been validated for the following applications: ELISA, WB analysis. -
10320-500
SET7/9 (human recombinant)-500 g
Price: $1,391.11List Price: $1,545.68Source: Active recombinant N-terminal His-tagged SET7/9 purified from E. coli Mr: 43. -
A4002-5 mg
SIRT2 inhibitor. It decreases brain atrophy and improves motor function in models of Huntington disease. (C003B-255105)
Price: $241.35List Price: $268.16AK-7 is an inhibitor of sirtuin 2 (SIRT2) sirtuins are considered class III histone deacetylases (HDACs). AK-7 exhibits neuroprotective activity, decreasing brain atrophy and improving motor function and survival in animal models of -
A4002-25 mg
SIRT2 inhibitor. It decreases brain atrophy and improves motor function in models of Huntington disease. (C003B-255715)
Price: $607.61List Price: $675.12AK-7 is an inhibitor of sirtuin 2 (SIRT2) sirtuins are considered class III histone deacetylases (HDACs). AK-7 exhibits neuroprotective activity, decreasing brain atrophy and improving motor function and survival in animal models of -
A4000-5 mg
SIRT2 inhibitor. It prevents hippocampal neurodegeneration in models of Alzheimer disease and induces cell cycle arrest in colon carcinoma cells. (C003B-255026)
Price: $198.12List Price: $220.13AK-1 is an inhibitor of sirtuin 2 (SIRT2) sirtuins are considered class III histone deacetylases (HDACs). AK-1 exhibits neuroprotective and anticancer activities. -
A4000-10 mg
SIRT2 inhibitor. It prevents hippocampal neurodegeneration in models of Alzheimer disease and induces cell cycle arrest in colon carcinoma cells. (C003B-255330)
Price: $322.85List Price: $358.73AK-1 is an inhibitor of sirtuin 2 (SIRT2) sirtuins are considered class III histone deacetylases (HDACs). AK-1 exhibits neuroprotective and anticancer activities. -
A4000-25 mg
SIRT2 inhibitor. It prevents hippocampal neurodegeneration in models of Alzheimer disease and induces cell cycle arrest in colon carcinoma cells. (C003B-255733)
Price: $637.99List Price: $708.87AK-1 is an inhibitor of sirtuin 2 (SIRT2) sirtuins are considered class III histone deacetylases (HDACs). AK-1 exhibits neuroprotective and anticancer activities. -
S413586-25mg
SIS17 (C007B-272499)
Price: $431.58List Price: $479.53InformationSIS17 SIS17 is a mammalian histone deacetylase 11 (HDAC 11) -specific inhibitor with IC50 of 0.83 μM. SIS17 inhibits the demyristoylation of HDAC11 substrate, serine hydroxymethyl transferase 2, without inhibiting other