The HaloTag® Mammalian Pull-Down Systems (Cat.# G6500, G6504 and G6509) are designed to capture and purify intracellular binary and higher order protein complexes, including transient or weakly interacting partners.
HaloTag® Mammalian Pull-Down System(Cat.# G6504) includes buffers and resin necessary to perform a HaloTag® pull-down.
HaloTag® Mammalian Pull-Down and Labeling System(Cat.# G6500) includes everything in G6504plusthe HaloTag® TMRDirect™ Ligand, which allows correlative cellular localization and real-time imaging studies.
HaloTag® Complete Pull-Down System(Cat.# G6509) includes everything in G6500plusa starter cloning system, Wizard® SV Gel and PCR Clean-Up System, and FuGENE® HD Transfection Reagent.
TheHaloTag® Control Vectorprovides protein expression of the HaloTag® protein in mammalian cells,E. colior in vitro expression systems dependent on human cytomegalovirus (CMV) intermediate early enhancer, T7 or SP6 RNA polymerase promoters. It can be used as a control for any HaloTag® experimental system and can be used for both stable and transient HaloTag® expression in mammalian cells; for stable expression, co-transfection with a vector containing a selectable marker is required.
TheProtease Inhibitor Cocktail, 50X, is a mixture of six different protease inhibitors with different target protease specificities. This product is provided in a freeze-dried format and can be reconstituted using either 100% ethanol or DMSO.
TheMammalian Lysis Bufferis designed for use with HaloTag® Mammalian-based expression systems such as the HaloTag® Mammalian Pull-Down and Labeling Systems (referenced here) as well as the HaloCHIP™ System (Cat.# G9410). Formulation consists of 50mM Tris-HCl, 150mM NaCl, 1% Triton® X-100 and 0.1% sodium deoxycholate (pH 7.5).
Rapid, Efficient and Covalent Capture of Binary and Higher Order Complexes Directly from Lysates:Improved capture of protein partners, including transient interactions.
High Purity and Low Background:Improved accuracy in identification of proteins; covalent attachment allows bait protein to remain behind if desired.
Ability to Fluorescently Label the Same Genetic Fusion:Correlate complex capture with cellular localization.
Compatibility with All Downstream Methods of Analysis:Freedom to identify complexes in variety of applications including mass spectrometry.