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MORPHOLINOETHANE SULFONIC ACID MONOHYDRATE Mes Buffer

MORPHOLINOETHANE SULFONIC ACID MONOHYDRATE Mes Buffer
SKU
RXSOL-60-6605-013
Supply Location::
Locations
[MORPHOLINOETHANE SULFONIC ACID MONOHYDRATE Mes Buffer] manufacturers, suppliers, exporters in Mumbai, Gandhidham, Kolkata, Varanasi, Visakhapatnam, Chennai, Fujairah, Dubai, Canada BC, Barka, Sohar, Muscat, Oman.
Lab chemicals manufacturers, suppliers, exporters in India, UAE Middle East, Barka, Sohar, Muscat, Oman, Canada.
 
[MORPHOLINOETHANE SULFONIC ACID MONOHYDRATE Mes Buffer] is available in small packing as well as in bulk. Buy premium quality [MORPHOLINOETHANE SULFONIC ACID MONOHYDRATE Mes Buffer] and other lab chemicals from one of the most trusted brands.

MUSCAT CHEMICAL TAG::
Category

MES is the common name for the compound 2-(N-morpholino)ethanesulfonic acid. Its chemical structure contains a morpholine ring. It has a molecular weight of 195.2 and the chemical formula is C6H13NO4S. 

Note

The accurate and quantitative detection of microRNAs (miRNAs) as next-generation, reliable biomarkers will provide vital information for cancer research and treatment. However, their unique, intrinsic features pose quite a challenge for miRNA profiling, especially for multiplexed detection. Thus, there is a strong and an ever-growing need to develop an accurate, simple, sensitive and specific miRNA sensing method.

Morpholineethanesulfonic acid (MES) is one of the good′s buffers, and the most extensively application is biological buffers. MES is a zwitterionic N-substituted aminosulfonic acid with a morpholinic ring and it does not form complexes with the majority of the metals used in environmental and biological studies. It is easily soluble in water and has minimum lipid solubility, making it impermeable to membranes. MES has been also used as a component of the elution buffer used to elute plasma from α2-macroglobulin affinity column. It has been used as an activation buffer during antibody conjugation to microparticles and it has been used in the functionalization of microchannels during the creation of microfluidic-integrated surface plasmon resonance (SPR) platform for pathogen detection.

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