SIS3 HCl Universal

SIS3 HCl UniversalSIS3, a novel specific inhibitor of Smad3, inhibits TGF ? and activin signaling by suppressing Smad3 phosphorylation without affecting the MAPK p38, ERK, or PI3 kinase signaling pathways.

no inhibition on the GTPases Ras and RhoA

Felodipine is a selective L-type Ca2+ channel blocker with IC50 of 0

Corning 96 Well Clear Round Bottom TC-Treated Microplate

2-Methoxy-1

BX912 is a potent and specific PDK1 inhibitor with IC50 of 12 nM

with putative activity against several bacteria

EGFR L858R

1395-25SS or 1395-25TS)

All XA 4Y PLUS analytical balances are complaint with 21 CFR part 11 regulations and with provisions of EU GMP part 4

Chenodeoxycholic Acid is a naturally occurring human bile acid

2 adrenergic agonist with an ED50 of 0

used to achieve prompt suppression of inflammation