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14-629
JAK3 Protein, active, 10 µg
Price: $989.14List Price: $1,099.05N-terminal His6-tagged, recombinant, human JAK3 amino acids 781-end Product Source: expressed by baculovirus in Sf21 cells Application Research Category Inflammation & Immunology Biochem/physiol Actions Protein Target: JAK3 Target Sub-Family: -
30001
JC-1 Mitochondrial Membrane Potential Detection Kit, 100 Ass
Price: $528.32List Price: $587.02JC-1 Mitochondrial Membrane Potential Detection Kit is used to measure mitochondrial membrane potential changes in cells. -
N6100038
Jet Assembly for for NPD Detector
Price: $603.06List Price: $670.07The PerkinElmer jet assembly is designed to use with NPD detector in the gas chromatography technology. -
J413666-100mg​JND3229 JND3229 is a potent reversible inhibitor of EGFR C797S with an IC50 value of 5.8 nM. JND3229 also potently suppresses EGFR L858R/T790M and EGFR WT with IC50 values of 30.5 nM and 6.8 nM, respectively.
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J413666-10mg​JND3229 JND3229 is a potent reversible inhibitor of EGFR C797S with an IC50 value of 5.8 nM. JND3229 also potently suppresses EGFR L858R/T790M and EGFR WT with IC50 values of 30.5 nM and 6.8 nM, respectively.
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J413666-50mg​JND3229 JND3229 is a potent reversible inhibitor of EGFR C797S with an IC50 value of 5.8 nM. JND3229 also potently suppresses EGFR L858R/T790M and EGFR WT with IC50 values of 30.5 nM and 6.8 nM, respectively.
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J4649-1MG
JNJ-10198409
Price: $440.82List Price: $489.80Biochem/physiol Actions JNJ-10198409 is a potent ATP-competitive inhibitor of Platelet-Derived Growth Factor receptor tyrosine kinase (PDGF-RTK) with both antiangiogenic and a direct tumor cell antiproliferative activity. It is selective for -
J171811-10mgJNJ-39758979 is a selective, orally active, and high-affinity histamine H4 receptor antagonist with Kis of 12.5, 5.3, and 25 nM for human, mouse, and monkey histamine H4 receptor, respectively. JNJ-39758979 functionally antagonizes histamine-induced
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J171811-1mgJNJ-39758979 is a selective, orally active, and high-affinity histamine H4 receptor antagonist with Kis of 12.5, 5.3, and 25 nM for human, mouse, and monkey histamine H4 receptor, respectively. JNJ-39758979 functionally antagonizes histamine-induced
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J171811-25mgJNJ-39758979 is a selective, orally active, and high-affinity histamine H4 receptor antagonist with Kis of 12.5, 5.3, and 25 nM for human, mouse, and monkey histamine H4 receptor, respectively. JNJ-39758979 functionally antagonizes histamine-induced
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J171811-50mgJNJ-39758979 is a selective, orally active, and high-affinity histamine H4 receptor antagonist with Kis of 12.5, 5.3, and 25 nM for human, mouse, and monkey histamine H4 receptor, respectively. JNJ-39758979 functionally antagonizes histamine-induced
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J171811-5mgJNJ-39758979 is a selective, orally active, and high-affinity histamine H4 receptor antagonist with Kis of 12.5, 5.3, and 25 nM for human, mouse, and monkey histamine H4 receptor, respectively. JNJ-39758979 functionally antagonizes histamine-induced