Antibody-Binding Proteins and Conjugates
Abcam mFluor™ Red 700 Conjugation Kit, 100UG
mFluor™ Red 700 conjugation / labeling in < 4 hrs with 30 secs hands-on time using mFluor™ Red 700 Conjugation Kit ab312807. 100% antibody recovery.
The product is subject to the following: Abcam Restricted Use Statement
Abcam iFluor Red 750 Conjugation Kit (BSA compatible), 100UG
iFluor Red 750 conjugation / labeling in < 4 hrs with 30 secs hands-on time using iFluor Red 750 Conjugation Kit (BSA compatible) ab312812. 100% antibody recovery.
The product is subject to the following: Abcam Restricted Use Statement
Abcam mFluor™ Violet 510 Conjugation Kit, 100UG
mFluor™ Violet 510 conjugation / labeling in < 4 hrs with 30 secs hands-on time using mFluor™ Violet 510 Conjugation Kit ab312806. 100% antibody recovery.
The product is subject to the following: Abcam Restricted Use Statement
Cayman Chemical CefoxItInsodIum salt 500mg
A potent inhibitor of GSK3B (IC50 22 nM) preventing tau phosphorylation both in vitro and in vivo
Cayman Chemical BucladesInsodIum salt 50mg
A cell permeable inhibitor of kinases that have been mutated by a single base substitution to become analog sensitive (as) as compared to the wild type kinase inhibits v-Src-as1 with an I338G substitution preferentially over v-Src (IC50 4.2 nM versus 28 M respectively) used to elucidate functions of several kinases in both mammalian and yeast systems
Cayman Chemical EtIdronatesodIum salt 500mg
An affinity probe which allows carbaprostacyclin to be detected in complexes with transmembrane receptors and/or nucleic or protein binding partners
Cayman Chemical PIperacIlInsodIum salt 500mg
A potent inhibitor of class I PI3K isoforms (IC50 values of 5 27 7 and 14 nM for PI3Ka B and Y respectively) and mTOR (Ki 17 nM) induces cell cycle arrest or apoptosis in a range of cancer cell lines effective in vivo suppressing the growth of a number of tumor xenografts in mice
Cayman Chemical MItIglInIdecalcIum salt 50mg
An activator of autophagy inhibits mTORC1 signaling by covalently binding to the lysosomal v-ATPase selective for inhibition of mTORC1 over mTORC2 signaling increases lysosome acidification and increases cellular clearance of TDP-43 protein aggregates in a v-ATPase-dependent manner in U2OS osteosarcoma cells inhibits mTORC1 signaling and enhances autophagy in mouse skeletal muscle and heart at 50 mg/kg