General SB(Stercobilin) ELISA Kit

General SB(Stercobilin) ELISA Kit

SB-366791
20-abx076632
  • EUR 376.80
  • EUR 1028.40
  • 10 mg
  • 50 mg

SB 216763
A8240-10 10 mg
EUR 142.8
Description: SB-216763 is a Potent and selective inhibitor of glycogen synthase kinase-3 (GSK-3) with IC50 of 34.3 nM. It competes with ATP and potently inhibits the activity against both GSK-3? and GSK-3?.

SB 216763
A8240-50 50 mg
EUR 338.4
Description: SB-216763 is a Potent and selective inhibitor of glycogen synthase kinase-3 (GSK-3) with IC50 of 34.3 nM. It competes with ATP and potently inhibits the activity against both GSK-3? and GSK-3?.

SB 415286
A8241-10 10 mg
EUR 184.8
Description: SB-415286 is a potent and selective cell permeable inhibitor of glycogen synthase kinase-3 (GSK-3) with Ki of 31 nM. It shows similar potency against GSK-3 and GSK3? [1].

SB 415286
A8241-5.1 10 mM (in 1mL DMSO)
EUR 212.4
Description: SB-415286 is a potent and selective cell permeable inhibitor of glycogen synthase kinase-3 (GSK-3) with Ki of 31 nM. It shows similar potency against GSK-3 and GSK3? [1].

SB 415286
A8241-50 50 mg
EUR 518.4
Description: SB-415286 is a potent and selective cell permeable inhibitor of glycogen synthase kinase-3 (GSK-3) with Ki of 31 nM. It shows similar potency against GSK-3 and GSK3? [1].

SB 431542
A8249-10 10 mg
EUR 166.8
Description: SB431542 is a selective ATP-competitive inhibitor of ALK5 (activin receptor-like kinase 5) with an IC50 value of 94 nM [1].SB431542 showed most potent efficacy among the series of hits screened out.

SB 431542
A8249-5.1 10 mM (in 1mL DMSO)
EUR 199.2
Description: SB431542 is a selective ATP-competitive inhibitor of ALK5 (activin receptor-like kinase 5) with an IC50 value of 94 nM [1].SB431542 showed most potent efficacy among the series of hits screened out.

SB 431542
A8249-50 50 mg
EUR 517.2
Description: SB431542 is a selective ATP-competitive inhibitor of ALK5 (activin receptor-like kinase 5) with an IC50 value of 94 nM [1].SB431542 showed most potent efficacy among the series of hits screened out.

SB 431542
A8249-S Evaluation Sample
EUR 97.2
Description: SB431542 is a selective ATP-competitive inhibitor of ALK5 (activin receptor-like kinase 5) with an IC50 value of 94 nM [1].SB431542 showed most potent efficacy among the series of hits screened out.

SB 203580
A8254-100 100 mg
EUR 262.8
Description: SB203580, also called 4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl) 1Himidazole [6], is a specific pyridinyl imidazole inhibitor of p38-MAPK (Mitogen-activated Protein Kinase) signaling pathway [1] [3].

SB 203580
A8254-25 25 mg
EUR 146.4
Description: SB203580, also called 4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl) 1Himidazole [6], is a specific pyridinyl imidazole inhibitor of p38-MAPK (Mitogen-activated Protein Kinase) signaling pathway [1] [3].

SB 203580
A8254-250 250 mg
EUR 452.4
Description: SB203580, also called 4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl) 1Himidazole [6], is a specific pyridinyl imidazole inhibitor of p38-MAPK (Mitogen-activated Protein Kinase) signaling pathway [1] [3].

SB 203580
A8254-5.1 10 mM (in 1mL DMSO)
EUR 135.6
Description: SB203580, also called 4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl) 1Himidazole [6], is a specific pyridinyl imidazole inhibitor of p38-MAPK (Mitogen-activated Protein Kinase) signaling pathway [1] [3].

SB 203580
A8254-50 50 mg
EUR 176.4
Description: SB203580, also called 4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl) 1Himidazole [6], is a specific pyridinyl imidazole inhibitor of p38-MAPK (Mitogen-activated Protein Kinase) signaling pathway [1] [3].

SB 203580
A8254-S Evaluation Sample
EUR 97.2
Description: SB203580, also called 4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl) 1Himidazole [6], is a specific pyridinyl imidazole inhibitor of p38-MAPK (Mitogen-activated Protein Kinase) signaling pathway [1] [3].

SB 239063
A3792-25 25 mg
EUR 544.8
Description: SB239063 is a potent and selective p38 MAPK inhibitor with an IC50 of 44 nM against p38? MAPK while exihibited no activity against the ?- and ?-kinase isoforms [1].

SB 239063
A3792-5 5 mg
EUR 196.8
Description: SB239063 is a potent and selective p38 MAPK inhibitor with an IC50 of 44 nM against p38? MAPK while exihibited no activity against the ?- and ?-kinase isoforms [1].

SB 239063
A3792-5.1 10 mM (in 1mL DMSO)
EUR 228
Description: SB239063 is a potent and selective p38 MAPK inhibitor with an IC50 of 44 nM against p38? MAPK while exihibited no activity against the ?- and ?-kinase isoforms [1].

SB-222200
A3795-10 10 mg
EUR 240
Description: SB 222200 is a selective and potent antagonist of NK-3 receptor [1].Neurokinin-3 (NK-3) receptor is a member of the G-protein-coupled superfamily and functions as a receptor for tachykinin.

SB-222200
A3795-5.1 10 mM (in 1mL DMSO)
EUR 258
Description: SB 222200 is a selective and potent antagonist of NK-3 receptor [1].Neurokinin-3 (NK-3) receptor is a member of the G-protein-coupled superfamily and functions as a receptor for tachykinin.

SB-222200
A3795-50 50 mg
EUR 841.2
Description: SB 222200 is a selective and potent antagonist of NK-3 receptor [1].Neurokinin-3 (NK-3) receptor is a member of the G-protein-coupled superfamily and functions as a receptor for tachykinin.

SB-674042
A3800-10 10 mg
EUR 350.4
Description: SB-674042 is a specific, high-affinity OX1 selective antagonist.

SB-674042
A3800-25 25 mg
EUR 717.6
Description: SB-674042 is a specific, high-affinity OX1 selective antagonist.

General SB(Stercobilin) ELISA Kit