DBCO-C6-acid

DBCO-C6-Acid is an analog of DBCO-Acid with an extended 6-carbon atom spacer arm. The extended 6-carbon atom spacer arm improves its derivatization efficiency and the

TD5 Table Top Low Speed Centrifuge 

Features:  1.Microprocessor control, digital display, touch panel, parameters in running can be edited and change to display other running parameter and RCF. 2.Brushless frequency motor

Tetra(3-methoxy-N-(prop-2-ynyl)propanamide) Methane

Tetra(3-methoxy-N-(prop-2-ynyl)propanamide) Methane is a 4-branched molecule with propargyl groups that can be linked to azide-containing biomolecules via Click Chemistry. Reagent grade, for research purpose. Please

Human Herpes Virus 2 (HHV2)

Description Nucleic acid testing (NAT) is the method of choice for detection and quantification of a wide range of micro organisms. Primerdesign manufactures and supplies

Bis-propargyl-PEG6

Bis-propargyl-PEG6 has two propargyl groups which can participate in Click Chemistry reactions to yield a stable triazole linkage with azide compounds; copper is needed as

OT-2 Tips, 1000µL

Opentrons OT-2 Tips, 1000µL. Optimized for volumes 100µL to 1000µL Clear Tips, Polypropylene. These tips are DNAse/RNAse, pyrogen and protease free – they are sterilized

IVD3182 HiPure Circulating DNA Kit

Introduction Free-circulating nucleic acids, such as tumor-specific extracellular DNA fragments and mRNAs in the blood or fetal nucleic acids in maternal blood, are present in

Cerillo Canopy Wireless Accessory Package

Cerillo’s Canopy Wireless Accessory Package includes the Canopy wireless device which enables wireless plate reader monitoring. It also comes with a companion software for retrieving,

Alkyne-ethyl-PEG1-t-Butyl ester

Alkyne-ethyl-PEG1-t-Butyl ester has an alkyne group and a t-butyl protected carboxyl group. The alkyne reacts with azide compounds or biomolecules via copper catalyzed Click Chemistry

Propargyl-PEG13-acid

Propargyl-PEG13-acid consists of an alkyne group and a carboxylic acid. The carboxylic acid reacts with amine groups to form amide bonds in the presence of