Protein Purification Reagents and Kits
Hampton Research HR2-930-B5/Grid Screen MPD #B5, 185 ml - 0.1 M Tris pH 8.0, 20% (+/-)-2-Methyl-2,4-pentanediol
HR2-930-B5/Grid Screen MPD #B5, 185 ml - 0.1 M Tris pH 8.0, 20% (+/-)-2-Methyl-2,4-pentanediol. Please note items from this supplier are non-returnable.
Hampton Research HR2-930-C5/Grid Screen MPD #C5, 185 ml - 0.1 M Tris pH 8.0, 40% (+/-)-2-Methyl-2,4-pentanediol
HR2-930-C5/Grid Screen MPD #C5, 185 ml - 0.1 M Tris pH 8.0, 40% (+/-)-2-Methyl-2,4-pentanediol. Please note items from this supplier are non-returnable.
Hampton Research PEG/ION SCREEN NO28 185ML
HR2-922-28/PEG/Ion Screen #28 (C4), 185 ml - 0.2 M Calcium acetate hydrate, 20% w/v Polyethylene glycol 3,350. Please note items from this supplier are non-returnable.
Hampton Research HR2-432/Proti-Ace 2 - 3 aliquots of 6 unique protease Pepsin, Thermolysin, Bromelain and Actinase E) and 6 aliquots of Proti-Ace Dilution Buffer
HR2-432/Proti-Ace 2 - 3 aliquots of 6 unique proteases (Proteinase K, Clostripain (Endoproteinase-Arg-C), Pepsin, Thermolysin, Bromelain and Actinase E) and 6 aliquots of Proti-Ace Dilution Buffer. Please note items from this supplier are non-returnable.
Biotium Fura-2, AM Ester, 10x100ug
Fura-2, AM ester is an intracellular fluorescent calcium indicator, and the preferred dye for ratiometric imaging microscopy. The membrane-permeant AM ester can be loaded into cells via incubation, but due to limited water solubility, a mild detergent Pluronic F-127 is often used to facilitate cell loading. Fura-2, AM ester itself does not bind Ca2, but intracellular esterases readily hydrolyze it to Fura-2. Upon calcium binding, the excitation maximum of Fura-2 undergoes a blue-shift from 363 nm (no Ca2) to 335 nm (high Ca2) while the emission maximum is relatively unchanged. Measure by flow cytometry, fluorescence microscopy, or certain fluoresence microplate readers. Properties: Light yellow solid soluble in DMSO; Store at -20°C, protect from light, especially in solution; Kd: 145 nM (22°C, pH 7.2 buffer); Ex/Em = 363/512 nm, e = 27,000 M-1cm-1 (no Ca2); Ex/Em 335/505 nm, e = 35,000 M-1cm-1 (high Ca2); C44H47N3O24; MW: 1001.9; [108964-32-5].
Sartorius Octet AAVX Biosensors, Rapid AAV Capsid Quantitation, Label-Free Measurement, 5 Trays
The Sartorius Octet AAVX Biosensors provide a rapid and label-free solution for quantifying Adeno-Associated Virus (AAV) capsids using Bio-Layer Interferometry (BLI). Designed for efficiency, these biosensors allow measurement in both crude and purified samples, featuring a regeneration capability up to 20 cycles. This streamlined approach enhances process development and quality control in biopharmaceutical applications, making it superior over traditional ELISA methods.
Tosoh Bioscience LLC TSKGEL CN-80TS 4.6X150
Column, Reversed Phase Chromatography; Tosoh TSKgel CN-80Ts; Media: Silica; Particle: 5 micrometer; Pore Size: 80 angstrom; 4.6mm I.D. x 15cm Length; Stainless Steel - Standard
Genscript Corporation MonoRab Anti-DYKDDDDK Magnet
GenScript MonoRab sup TM /sup Anti-DYKDDDDK Magnetic Beads are super paramagnetic beads with diameter of 70 m covalently coated with a rabbit monoclonal anti-DYKDDDDK antibody The beads are supplied as 50% slurry in TBS with 50% glycerol and 0 02% sodium azide The MonoRab sup TM /sup Anti-DYKDDDDK Magnetic Beads have a binding capacity of 1 5 mg DYKDDDDK-tagged protein (Size 50KDa) per 1 ml settled beads The beads can be re-used for at least 5 times Based on our new rabbit monoclonal antibody technology (MonoRab sup TM /sup ) this beads offers high binding capacity high purity and withstand stringent washing steps especially with buffers containing high concentration of salt The beads are resistant to up to 2 M NaCl and to buffers with pH as low as 2 5
Active Motif Nuclear Complex Co-IP Kit
Active Motif's Nuclear Complex Co-IP Kit simplifies co-immunoprecipitation of nuclear protein complexes by providing high-quality reagents for both nuclear extract preparation and immunoprecipitation. The kit's extraction process maintains protein complexes contained in the nucleus, specifically those previously bound to DNA, while the stringency of the Co-IP reagents can be easily adjusted so you can better study protein/protein interactions of varying strength.