Large 5 digit LCD display is easy to read Built-in memory recalls last MAX/MIN value stored Autoranging with 0.05% accuracy Contact measurements from 0.
Large 5 digit LCD display is easy to read Built-in memory recalls last MAX/MIN value stored Autoranging with 0.05% accuracy Contact measurements from 0.
Unique display where characters reverse direction depending on measurement mode you are in Large 0.4" (5 digit) LCD display Microprocessor based with quartz crystal oscillator to maintain high accuracy Tachometer memory stores last, max and min
Unique display where characters reverse direction depending on measurement mode you are in Large 0.4" (5 digit) LCD display Microprocessor based with quartz crystal oscillator to maintain high accuracy Tachometer memory stores last, max and min
Large 5 digit LCD display is easy to read Built-in memory recalls last MAX/MIN value stored Autoranging with 0.05% accuracy Contact measurements from 0.
Large 5 digit LCD display is easy to read Built-in memory recalls last MAX/MIN value stored Autoranging with 0.05% accuracy Contact measurements from 0.
TAT TFA (YGRKKRRQRRR) is derived from the transactivator of transcription (TAT) of human immunodeficiency virus (HIV-1) and is a cell-penetrating peptide. TAT can increase the yields and the solubility of heterologous
TAT TFA (YGRKKRRQRRR) is derived from the transactivator of transcription (TAT) of human immunodeficiency virus (HIV-1) and is a cell-penetrating peptide. TAT can increase the yields and the solubility of heterologous
TAT TFA (YGRKKRRQRRR) is derived from the transactivator of transcription (TAT) of human immunodeficiency virus (HIV-1) and is a cell-penetrating peptide. TAT can increase the yields and the solubility of heterologous
TAT TFA (YGRKKRRQRRR) is derived from the transactivator of transcription (TAT) of human immunodeficiency virus (HIV-1) and is a cell-penetrating peptide. TAT can increase the yields and the solubility of heterologous
InformationTA-02 TA-02 is a p38 MAPK inhibitor with IC50 of 20 nM. TA-02 especially inhibits TGFBR-2 .TargetsTGFβRII : p38 MAPK (Cell-free assay) : 20 nM.
InformationTA-02 TA-02 is a p38 MAPK inhibitor with IC50 of 20 nM. TA-02 especially inhibits TGFBR-2 .TargetsTGFβRII : p38 MAPK (Cell-free assay) : 20 nM.
InformationTazemetostat (EPZ-6438) Tazemetostat (EPZ-6438, E7438) is a potent, and selective EZH2 inhibitor with K i and IC50 of 2.5 nM and 11 nM in cell-free assays, exhibiting a 35-fold selectivity versus EZH1 and >:4,500-fold selectivity
InformationTazemetostat (EPZ-6438) Tazemetostat (EPZ-6438, E7438) is a potent, and selective EZH2 inhibitor with K i and IC50 of 2.5 nM and 11 nM in cell-free assays, exhibiting a 35-fold selectivity versus EZH1 and >:4,500-fold selectivity
InformationTazemetostat (EPZ-6438) Tazemetostat (EPZ-6438, E7438) is a potent, and selective EZH2 inhibitor with K i and IC50 of 2.5 nM and 11 nM in cell-free assays, exhibiting a 35-fold selectivity versus EZH1 and >:4,500-fold selectivity
InformationTazemetostat (EPZ-6438) Tazemetostat (EPZ-6438, E7438) is a potent, and selective EZH2 inhibitor with K i and IC50 of 2.5 nM and 11 nM in cell-free assays, exhibiting a 35-fold selectivity versus EZH1 and >:4,500-fold selectivity
InformationTazemetostat (EPZ-6438) Tazemetostat (EPZ-6438, E7438) is a potent, and selective EZH2 inhibitor with K i and IC50 of 2.5 nM and 11 nM in cell-free assays, exhibiting a 35-fold selectivity versus EZH1 and >:4,500-fold selectivity
InformationTazemetostat (EPZ-6438) Tazemetostat (EPZ-6438, E7438) is a potent, and selective EZH2 inhibitor with K i and IC50 of 2.5 nM and 11 nM in cell-free assays, exhibiting a 35-fold selectivity versus EZH1 and >:4,500-fold selectivity
InformationTA-02 TA-02 is a p38 MAPK inhibitor with IC50 of 20 nM. TA-02 especially inhibits TGFBR-2 .TargetsTGFβRII : p38 MAPK (Cell-free assay) : 20 nM.
InformationTA-02 TA-02 is a p38 MAPK inhibitor with IC50 of 20 nM. TA-02 especially inhibits TGFBR-2 .TargetsTGFβRII : p38 MAPK (Cell-free assay) : 20 nM.
InformationTA-02 TA-02 is a p38 MAPK inhibitor with IC50 of 20 nM. TA-02 especially inhibits TGFBR-2 .TargetsTGFβRII : p38 MAPK (Cell-free assay) : 20 nM.
InformationTA-02 TA-02 is a p38 MAPK inhibitor with IC50 of 20 nM. TA-02 especially inhibits TGFBR-2 .TargetsTGFβRII : p38 MAPK (Cell-free assay) : 20 nM.