Gel Filtration Media and Columns
Cytiva Superose™ Media Prep Grade Lab Packs
High performance gel filtration media for scaleup to preparative purifications of biomolecules
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Thermo Scientific™ POROS™ GoPure™ 50 D Pre-packed Column, 0.5 x 5 cm, 1 mL
Thermo Scientific™ POROS™ GoPure™ 0.5 cm pre-packed columns are intended for the screening of POROS ion exchange resins or for small scale purification.
Cytiva HiPrep™ Sephacryl™ S-300 HR Columns
Maximum recovery and minimum nonspecific adsorption
Cytiva HiLoad™ 16/600 Superose™ 6 Prep Grade Preparative SEC Column
A prepacked SEC column for high-resolution purification of large biomolecules and protein complexes with sample volumes up to 5 mL
Cytiva Sephadex™ G-25 DNA Grade SF Cleanup Gel
Tested to ensure reproducibly high recovery of DNA (10 bases in length) from small molecules by gel filtration
Cytiva Sephacryl™ S-300 High Resolution Media
Offer good recovery and low nonspecific adsorption. Hydrophilic, rigid allyl dextran/bisacrylamide matrix for fast and reproducible purification of proteins, polysaccharides and other macromolecules. Enable gel filtration at laboratory and industrial scale, and may be purchased in pre-packed columns.
R&D Systems™ Proteome Purify 2 Mouse Serum Protein Immunodepletion Resin
Provides an easy-to-use, high capacity system to reproducibly remove albumin and IgG from mouse serum or plasma
Bioworld SEPAROPOREAGAROSE) 6B
A high gel strength bioagarose matrix for gel filtration and coupling of affinity ligands suitable for analytical and preparative protein purifications. Larger volumes available at more competitive prices(enquie). Specifications: Parti...
Bioworld NAD-SEPAROPOREAGAROSE) 4B
NAD-SEPAROPORE (AGAROSE) 4B, LYOPHILIZED: NAD-Separopore NAD covalently bound to Separoporehas a high affinity for NAD- dependent enzymes and dehydrogenases. NAD Separopore has been used to purify Vibrio cholerae toxin, diptheria toxin ...
Sigma Aldrich Fine Chemicals Biosciences XK 26/40 Column
XK empty columns provide reliable and reproducible separations. The tube material is of borosilicate glass which allows for visual inspection of the media bed. The columns are made of biocompatible materials that exhibit excellent chemical resistance. A broad range of column dimensions makes XK columns suitable for many different purification needs. Column packing can be performed using either a packing reservoir or an extra column tube attached with a packing connector. The QuickLock mechanism of the adapter shaft facilitates rapid and easy movement of the adapter simplifying adjustments of the bed height disassembly and cleaning. The design of the adapter plunger gives a uniform flow which maintains the integrity of the packed bed during operations. An extensive range of spare parts is available facilitating maintenance.
Sigma Aldrich Fine Chemicals Biosciences Sephacryl(R) 200-HR, MW range 5-250 kDa (globular proteins), MW range 1-80 kDa (dextrans) | 65546-95-4 | MFCD00165824 | 100ML
Sephacryl(R) 200-HR, MW range 5-250 kDa (globular proteins), MW range 1-80 kDa (dextrans) | 65546-95-4 | MFCD00165824 | 100ML
Bioworld SEPAROPOREAGAROSE) 6B
A high gel strength bioagarose matrix for gel filtration and coupling of affinity ligands suitable for analytical and preparative protein purifications. Larger volumes available at more competitive prices(enquie). Specifications: Parti...
Sigma Aldrich Fine Chemicals Biosciences SP SephadexR C 25 Cytiva 1
Sephadex(R) ion exchangers are produced by introducing functional groups onto Sephadex a cross-linked Dextran matrix. These groups are attached to glucose units in the matrix by stable ether linkages.
AdipoGen AMPAdePi
Protein. Full-length NAD 5’-nucleotidase Haemophilus influenzae without the signal peptide corresponding to the first 26 aa. Source E. coli. Endotoxin content N/A. Liquid. In 5mM KH2PO4, pH 6.8 containing 100mM TRIS-HCl pH 8.5 and 10mM MgCl2. Purity >98% SDS-PAGE. NadN NAD nucleotidase is a periplasmic enzyme from Haemophilus influenzae, a major pathogen of the respiratory tract in humans that has developed the capability to exploit host NADP for its nicotinamide dinucleotide requirement. NadN plays a central role by degrading NAD into adenosine and NR nicotinamide riboside, NMN to nicotinamide riboside and AMP to adenosine. It shows a broad substrate specificity, recognizing either mono- or di-nucleotide nicotinamides and different adenosine phosphates with a maximal activity on 5-adenosine monophosphate. It can be used as an economically alternative to produce NR nicotinamide riboside. Catalytic activity NAD=AMP NMN=AdeNRPPi
