Molecular Biology Reagents

A 100X concentrate that, when diluted to 1X, contains 10 mM Tris, 1 mM EDTA, pH ~8.0.

Biodegradable and readily disposable Low foaming Free rinsing, leaves no residue Tergajet is a nonionic, low foaming phosphate free powdered enzyme cleaner for use in labware washers, manual and ultrasonic cleaning. Its corrosion inhibited formula

Biodegradable and readily disposable Low foaming Free rinsing, leaves no residue Tergajet is a nonionic, low foaming phosphate free powdered enzyme cleaner for use in labware washers, manual and ultrasonic cleaning. Its corrosion inhibited formula

A cell-permeable naphthyridinyl pyrazolo compound that acts as a potent, selective, reversible, and ATP-competitive inhibitor of TGF-&#946 type I receptor (ALK5 IC 50 = 23 nM, 4 nM and 18 nM for ALK5 binding, ALK5 auto-phosphorylation and

A cell-permeable imidazolyl-pyridine compound that acts as a potent, ATP-competitive, reversible, and selective inhibitor of activin receptor-like kinase 4 (IC 50 = 129 nM), 5 ( IC 50 = 47 nM), and 7. It inhibits p38 MAPK&#945 only at much higher

TIE-2/VEGFR-2 kinase-IN-2 is a potent dual VEGFR2 and Tie-2 inhibitor with pIC50 values of 8.61 and 8.56, respectively. TIE-2/VEGFR-2 kinase-IN-2 is an anti-angiogenic agent and can be used for cancer research.

TIE-2/VEGFR-2 kinase-IN-2 is a potent dual VEGFR2 and Tie-2 inhibitor with pIC50 values of 8.61 and 8.56, respectively. TIE-2/VEGFR-2 kinase-IN-2 is an anti-angiogenic agent and can be used for cancer research.

TIE-2/VEGFR-2 kinase-IN-2 is a potent dual VEGFR2 and Tie-2 inhibitor with pIC50 values of 8.61 and 8.56, respectively. TIE-2/VEGFR-2 kinase-IN-2 is an anti-angiogenic agent and can be used for cancer research.

TIP GENOMIC NAT 200UL PAG EXP960

TIP UNIV YEL SRK96

A cell-permeable, non-toxic, 2-phenylaminothiazole derivative that acts as a highly potent, ATP competitive inhibitor of Traf2- and Nck-interacting kinase (TNIK K i = 100 nM, IC 50 = 9 nM). Also shown to inhibit the activity of MLK1 (IC 50 = 18

A cell-permeable, ATP competitive, reversible indolizinoquinoxalin derivative that acts as a specific inhibitor of T-LAK-cell-originated protein kinase (TOPK/PBK)(IC 50 = 2 &#181M). Does not affect the activities of ERK1, JNK1, and p38 MAP kinases.