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G1372246-1mg
G3-VC-PAB-DMEA-Duocarmycin DM
Price: $4,675.21List Price: $5,194.68G3-VC-PAB-DMEA-Duocarmycin DM (Compound LD-1) is a duocarmycin-based linker molecule that can be used for ADC preparation -
J67325-AC
Kasugamycin, 50mg/ml in dist water, 25ml
Price: $726.00List Price: $806.67Kasugamycin, 50mg/ml in dist water, 25ml -
M767887-1mg
MA-PEG4-VC-PAB-DMEA-duocarmycin DM
Price: $1,216.09List Price: $1,351.22MA-PEG4-VC-PAB-DMEA-duocarmycin DM is a part of the antibody conjugated active molecule ADC (drug linker conjugate for ADC), which is composed of DNA groove alkylating agent Duocarmycin DM and linker MA-PEG4-vc-PAB-DMEA. -
APrEST75279-100
PrEST Antigen PDCL phosducin-like, 100ul UN 1687 6.1 PG2 (C003B-499187)
Price: $657.25List Price: $730.28PrEST Antigen PDCL phosducin-like, 100ul UN 1687 6.1 PG2 -
APrEST75280-100
PrEST Antigen PDCL phosducin-like, 100ul UN 1687 6.1 PG2 (C003B-499188)
Price: $657.25List Price: $730.28PrEST Antigen PDCL phosducin-like, 100ul UN 1687 6.1 PG2 -
APrEST84229-100
PrEST Antigen PDCL2 phosducin-like 2, 100ul UN 1687 6.1 PG2
Price: $657.25List Price: $730.28PrEST Antigen PDCL2 phosducin-like 2, 100ul UN 1687 6.1 PG2 -
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19202-5
Tulathromycin A-5 mg
Price: $187.75List Price: $208.62A macrolide antibiotic that inhibits bacterial protein synthesis (IC<sub>50</sub> = 0.26 µM) by targeting the 50S ribosomal subunit effective against M. -
13604-10
WYE-354-10 mg
Price: $432.93List Price: $481.03A selective, potent, and cell-permeable inhibitor of mTOR (IC<sub>50</sub> = 4.3 nM) which blocks signaling through both mTORC1 and mTORC2 induces G1 cell cycle arrest in both rapamycin-sensitive and rapamycin-resistant cancer cell lines and -
13604-25
WYE-354-25 mg
Price: $953.63List Price: $1,059.59A selective, potent, and cell-permeable inhibitor of mTOR (IC<sub>50</sub> = 4.3 nM) which blocks signaling through both mTORC1 and mTORC2 induces G1 cell cycle arrest in both rapamycin-sensitive and rapamycin-resistant cancer cell lines and -
13604-5
WYE-354-5 mg
Price: $237.75List Price: $264.17A selective, potent, and cell-permeable inhibitor of mTOR (IC<sub>50</sub> = 4.3 nM) which blocks signaling through both mTORC1 and mTORC2 induces G1 cell cycle arrest in both rapamycin-sensitive and rapamycin-resistant cancer cell lines and