Mol In Tszaujvaros

Lab Reagents

Human IgG antibody Laboratories manufactures the mol in tszaujvaros reagents distributed by Genprice. The Mol In Tszaujvaros reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact Molecular Innovations. Other Mol products are available in stock. Specificity: Mol Category: In Group: Tszaujvaros

Tszaujvaros information

Tak-285, dual Inhibitor of Her2/EGFR Tyr kinase (IC50=17 nM; mol wt 547; >98%)

SM-101130-5 5 mg
EUR 416.4

Arry-380, Oral, potent Inhibitor of Her2/Erbb2 Tyr kinase (IC50=8 nM; mol wt 869; >98%)

SM-101120-25 25 mg
EUR 1074

Arry-380, Oral, potent Inhibitor of Her2/Erbb2 Tyr kinase (IC50=8 nM; mol wt 869; >98%)

SM-101120-5 5 mg
EUR 416.4

Inhibitor of EGFR/HER family (Her1, Her2, Her3 or Pan Her-inhibitor) (BMS-59926/AC480, Mol wt 567.01, >99%)

SM-101010-5 5 mg
EUR 270

Inhibitor of EGFR/HER family (Her1, Her2, Her3 or Pan Her-inhibitor) (BMS-59926/AC480, Mol wt 567.01, >99%)

SM-101010-50 50 mg
EUR 1220.4

Alkaline phosphatase (AP), calf intestine, Mol Biol grade (3000-6000 u/mg) (free Free of endonuclease, exonuclease and RNase activities)

ALP16-N-1 1 mg
EUR 242.4

Alkaline phosphatase (AP), calf intestine, Mol Biol grade (3000-6000 u/mg) (free Free of endonuclease, exonuclease and RNase activities)

ALP16-N-10 10 mg
EUR 708

Inhibitor of EGFR/HDAC/Her2 (CUDC-101; 7-((4-((3-ethynylphenyl)amino)-7-methoxyquinazolin-6-yl)oxy)-N-hydroxyheptanamide, Mol wt 434.49, >99%)

SM-101020-10 10 mg
EUR 196.8

Inhibitor of EGFR/HDAC/Her2 (CUDC-101; 7-((4-((3-ethynylphenyl)amino)-7-methoxyquinazolin-6-yl)oxy)-N-hydroxyheptanamide, Mol wt 434.49, >99%)

SM-101020-50 50 mg
EUR 634.8

?-Gliadin (57?89) [Ac-LQL QPF PQP ELP YPQ PQL PYP QPQ LPY PQP QPF-NH2; mol wt 3953.5), 33-aa, deamidated antigen for celiac disease

SP-89924-1 1 mg
EUR 343.2

Cell permeable Inhibitor of EGFR2/FGFR/PDGFr/JAK1/Her2 ((E)-4-((4-)1H-1,2,3-Triazol-1-yl)butyl)phenoxy)methyl)-2-(4-trifluoromethyl)oxazole, mol wt 468; >98%)

SM-101050-10 10 mg
EUR 196.8

Cell permeable Inhibitor of EGFR2/FGFR/PDGFr/JAK1/Her2 ((E)-4-((4-)1H-1,2,3-Triazol-1-yl)butyl)phenoxy)methyl)-2-(4-trifluoromethyl)oxazole, mol wt 468; >98%)

SM-101050-100 100 mg
EUR 927.6

JNK-IN-8

2729-100 Ask for price

JNK-IN-8

2729-25
EUR 836.4

JNK-IN-8

2729-5
EUR 261.6

BMX-IN-1

A3260-10 10 mg
EUR 477.6
Description: BMX-IN-1 is a highly selective and irreversible inhibitor of BMX kinase [1].BMX, also known as ETK, is a member of Tec family and plays an important role in regulating ischemia-mediated arteriogenesis and lymphangiogenesis

BMX-IN-1

A3260-100 100 mg
EUR 2008.8
Description: BMX-IN-1 is a highly selective and irreversible inhibitor of BMX kinase [1].BMX, also known as ETK, is a member of Tec family and plays an important role in regulating ischemia-mediated arteriogenesis and lymphangiogenesis