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17477-10A synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1 phosphorylated by Cdk5 with a Km value of 5 µM.
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17477-5A synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1 phosphorylated by Cdk5 with a Km value of 5 µM.
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17477-500A synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1 phosphorylated by Cdk5 with a Km value of 5 µM.
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17767-10An uncompetitive inhibitor of Epac1 activity toward its effector Rap1 in vitro (IC<sub>50</sub> = 23 µM) and in cells has no effect on PKA activity.
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17767-5An uncompetitive inhibitor of Epac1 activity toward its effector Rap1 in vitro (IC<sub>50</sub> = 23 µM) and in cells has no effect on PKA activity.
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17767-50An uncompetitive inhibitor of Epac1 activity toward its effector Rap1 in vitro (IC<sub>50</sub> = 23 µM) and in cells has no effect on PKA activity.
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C0476-1 mg
Thomas Scientific
Cecropin B-thanatin conjugate that inhibits microbial growth (C08-0489-325)
Price: $503.66List Price: $559.62This peptide is a derivative of the N-terminal end of cecropin B and the C-terminal end of thanatin that exhibits antimicrobial peptide (AMP) activity. Grade: &ge95% -
C0476-2 mg
Thomas Scientific
Cecropin B-thanatin conjugate that inhibits microbial growth (C08-0489-620)
Price: $794.97List Price: $883.30This peptide is a derivative of the N-terminal end of cecropin B and the C-terminal end of thanatin that exhibits antimicrobial peptide (AMP) activity. Grade: &ge95% -
C0476-5 mg
Thomas Scientific
Cecropin B-thanatin conjugate that inhibits microbial growth (C08-0489-807)
Price: $1,408.86List Price: $1,565.40This peptide is a derivative of the N-terminal end of cecropin B and the C-terminal end of thanatin that exhibits antimicrobial peptide (AMP) activity. Grade: &ge95% -
11495-10A potent inhibitor of VEGFR1, 2, and 3 (IC50s = 5, 1, and 3 nM, respectively) also potently inhibits a variety of other receptor and non-receptor tyrosine kinases blocks tubule formation by HUVECs in vitro and prevents angiogenesis as well as
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11495-25A potent inhibitor of VEGFR1, 2, and 3 (IC50s = 5, 1, and 3 nM, respectively) also potently inhibits a variety of other receptor and non-receptor tyrosine kinases blocks tubule formation by HUVECs in vitro and prevents angiogenesis as well as
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11495-5A potent inhibitor of VEGFR1, 2, and 3 (IC50s = 5, 1, and 3 nM, respectively) also potently inhibits a variety of other receptor and non-receptor tyrosine kinases blocks tubule formation by HUVECs in vitro and prevents angiogenesis as well as