Forensics Products & Reviews

Achieve quick, clean, and complete protein digestion

Glycan columns for the analysis of released N-labeled glycans using UPLC and with MaxPeak High Performance Surfaces to reduce non-specific adsorption.

Anion exchange, reverse-phase columns that provide charged-based separations and extra resolution for acidic glycans. With MaxPeak High Performance surfaces that reduce non-specific adsorption.

These columns are been purposefully designed for intact glycoprotein profiling, subunit fragment analysis, and glycopeptide mapping using hydrophilic interaction chromatography (HILIC). 

Designed for reverse-phase separation of amino acids derivatized with AccQ•Tag Ultra reagent. Rapid separation with a superior resolution for HPLC/UHPLC. 

Size-based separations of peptides, proteins, and viral vectors

Markes’ stainless sorbent tubes are available in two sizes: 3.5” x ¼” (industry-standard), and 4.5” x 6mm (DAAMS). Industry-standard tubes are compatible with Markes, PerkinElmer, Shimadzu, Dani, CDS and Gerstel 3.5+ thermal desorption (TD) systems.

Automate entire sample preparation workflow with the new EXTREVA ASE accelerated solvent extractor(ASE). The EXTREVA ASE system combines and automates sample extraction, in-cell cleanup, and evaporation. Faster extraction, with four samples extracted in parallel, increases laboratory throughput and efficiency, and the patented gas-assisted extraction mechanism uses less solvent, helping to advance your sustainability goals.

With new capabilities for multiplexed quantitative proteomics and native protein characterization, the Thermo Scientific Orbitrap ascend tribrid mass spectrometer delivers experimental throughput, versatility, and ease-of-use. 

CPG used to add the non-fluorescent quencher BHQ-1 dye to the 3' end of an oligonucleotide.

CPG for incorporation of unmodified DNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified DNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified RNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified RNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified DNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified RNA base at 3' end of an oligonucleotide.

CPG for incorporation of unmodified RNA base at 3' end of an oligonucleotide.

CPG for the incorporation of a 2'-fluoro modified nucleobase at the 3' end of an oligonucleotide

CPG for the incorporation of a 2'-O-methyl modified ribo- nucleobase at the 3' end of an oligonucleotide.

CPG for the incorporation of an (otherwise unmodified) reverse (5' to 3') nucleobase at the 3' end of an oligonucleotide.

CPG used to incorporate the cyanine-5 dye moiety onto the 3'-end of an oligonucleotide.

A phosphoramidite used for 5'-CAL Fluor Red 610 labelling of oligonucleotides.

CPG for the incorporation of a 2'-O-methyl modified ribo-A nucleobase at the 3' end of an oligonucleotide.

CPG for incorporation of a 2'-O-methyl modified ribo-C nucleobase at the 3' end of an oligonucleotide.

CPG for incorporation of unmodified ribo-G at 3' end of an oligonucleotide.