3-Acetylindole is a substituted indole and a reactant in the first step of multiple biological synthesis applications. Indoles, especially 3-acetylindole derivatives, possess a wide variety of biological activities. Many biological molecules, from Antibacterial agents against Staphylococcus to anti-HIV synthesis agents like N-arylsulfonyl-3-acetylindoles, use 3-acetylindole as a starting reagent. They can react with aromatic aldehydes to produce chalcones, which are intermediates for biologically active heterocyclic compounds. 3-Acetylindole is also the reactant for the synthesis of inhibitors that are used with hepatitis protease and nuclear factor kappa-light-chain enhancer of B cells (NF-κB).

3-Indoxyl caprylate is a reagent used in chemical synthesis.

3-Indoxyl phosphate bis (2-amino-2-methyl- 1,3-propanediol) saltY™-phosphate bis(2-amino-2-methyl-1,3-propanediol) salt Y™-phos • 2 AMPD

3-Indoxyl-3-acetate is a chromogenic substrate used to differentiate between esterases of various microorganism species.

3-Iodo-L-tyrosine is a tyrosine hydroxylase inhibitor.

3-O-Methyl-D-glucopyranoside is a glucose that is not metabolized, giving it the ability to study glucose transport capacity in diabetic rats. It has been used as an intermediate in the synthesis of surfactants, resins, emulsifiers and thickening agents.

The 3xERRE-luciferase plasmid is designed to study the activity of the Estrogen-Related Receptor (ERR) signaling pathway, specifically its role in transcriptional regulation. This plasmid contains three copies of the Estrogen-Related Receptor Response Element (ERRE), which is a DNA sequence recognized by the estrogen-related receptor (ERR) family of transcription factors. ERK/MAPK regulates ERRgamma expression, transcriptional activity, and receptor-mediated Tamoxifen resistance in ER+ breast cancer.

The 3xERRE-luciferase plasmid is a synthetic plasmid obtained from a third party and its sequence has been confirmed at GoldBio

Agarose is a very inert polysaccharide that forms hydrophilic and high gel strength gels at low concentrations.Agarose beads are microspheres of agarose gels with different particle diameters and concentrations. Small spherical particles of agarose act as a porous gel to filter or separate a mixture of molecules according to their individual sizes. Due to its chemical structure (easy to activate), the agarose beads may be prepared to bind biomolecules in a reversible or irreversible manner. Plain agarose beads are used in gel filtration chromatography (or molecular exclusion chromatography) as well as for activating beads for biomolecule purification or immobilization.Plain agarose beads can also be used for activating processes, generating active groups inside its pores capable of reversible or irreversible biomolecule bonds. Due to the bead’s large internal surface and to its composition (inert polysaccharide), agarose is an ideal medium for the preparation of activated beads.

Agarose is a very inert polysaccharide that forms hydrophilic and high gel strength gels at low concentrations.Agarose beads are microspheres of agarose gels with different particle diameters and concentrations. Small spherical particles of agarose act as a porous gel to filter or separate a mixture of molecules according to their individual sizes. Due to its chemical structure (easy to activate), the agarose beads may be prepared to bind biomolecules in a reversible or irreversible manner.Cross-linked agarose beads are used in gel filtration chromatography (or molecular exclusion chromatography) as well as for activating beads for biomolecule purification or immobilization.Cross-linked agarose beads can also be used for activating processes, generating active groups inside its pores capable of reversible or irreversible biomolecule bonds. Due to the bead’s large internal surface and to its composition (inert polysaccharide), agarose is an ideal medium for the preparation of activated beads.

This matrix is a highly cross-linked 4% agarose bead with a bead size of 50-150 µm. It is a gel filtration resin developed for industrial-scale separation of large molecules and virus particles utilizing higher pressure and flow rates rather than low pressure standard beads.

This matrix is not preactivated. For preactivated resins, look for Glyoxal Agarose Beads or Protein G.