This nuclear receptor assay system utilizes proprietary non-human cells engineered to provide constitutive, high-level expression of the human retinoid X receptor beta (NR2B2), a ligand-dependent transcription factor commonly referred to as RXRB or
This nuclear receptor assay system utilizes proprietary non-human cells engineered to provide constitutive, high-level expression of the human retinoid X receptor beta (NR2B2), a ligand-dependent transcription factor commonly referred to as RXRB or
An updated version of our popular atomic model sets that are suitable for constructing complex organic and inorganic molecules. The teacher set contains 100 atom centers and 86 bonds.
An updated version of our popular atomic model sets that are suitable for constructing complex organic and inorganic molecules. The teacher set contains 100 atom centers and 86 bonds.
This nuclear receptor assay system utilizes proprietary non-human cells engineered to provide constitutive, high-level expression of the human retinoid X receptor beta (NR2B2), a ligand-dependent transcription factor commonly referred to as RXRB or
This nuclear receptor assay system utilizes proprietary non-human cells engineered to provide constitutive, high-level expression of the human retinoid X receptor beta (NR2B2), a ligand-dependent transcription factor commonly referred to as RXRB or
This nuclear receptor assay system utilizes proprietary non-human mammalian cells engineered to provide constitutive, high-level expression of human liver X receptor beta (NR1H2), a ligand-dependent transcription factor commonly referred to as
This nuclear receptor assay system utilizes proprietary non-human mammalian cells engineered to provide constitutive, high-level expression of human liver X receptor beta (NR1H2), a ligand-dependent transcription factor commonly referred to as
Remove both proteins and phospholipids from biological samples in one easy, high-efficiency procedure. Avoid signal suppression by removing interfering phospholipids from the sample matrix.
Remove both proteins and phospholipids from biological samples in one easy, high-efficiency procedure. Avoid signal suppression by removing interfering phospholipids from the sample matrix.