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Merck

M2933

Sigma-Aldrich

MES hydrate

BioPerformance Certified, suitable for cell culture, ≥99.5%

Szinonimák:

2-Morpholineethanesulfonic acid hydrate, 2-(N-Morpholino)ethanesulfonic acid hydrate, 4-Morpholineethanesulfonic acid

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

Tapasztalati képlet (Hill-képlet):
C6H13NO4S · xH2O
CAS-szám:
Molekulatömeg:
195.24 (anhydrous basis)
MDL-szám:
UNSPSC kód:
12161700
eCl@ss:
32129211
PubChem Substance ID:
NACRES:
NA.25

Minőségi szint

grade

BioPerformance Certified
for molecular biology

Teszt

≥99.5%

form

crystalline powder

tárolási körülmény

dry at room temperature

technika/technikák

cell culture | mammalian: suitable
immunofluorescence: suitable
nucleic acid detection: suitable

szennyeződések

endotoxin and Total Aerobic Microbial Count, tested

szín

white

hasznos pH-tartomány

5.5-6.7

pKa 

6.1

oldhatóság

water: 335.3 g/L at 20 °C

alkalmasság

suitable for component for culture media
suitable for molecular biology

alkalmazás(ok)

agriculture
diagnostic assay manufacturing
life science and biopharma
sample preparation

idegen aktivitás

DNase, RNase, protease, none detected

SMILES string

O.OS(=O)(=O)CCN1CCOCC1

InChI

1S/C6H13NO4S.H2O/c8-12(9,10)6-3-7-1-4-11-5-2-7;/h1-6H2,(H,8,9,10);1H2

Nemzetközi kémiai azonosító kulcs

MIIIXQJBDGSIKL-UHFFFAOYSA-N

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Általános leírás

MES hydrate buffer (2-(N-morpholino)ethanesulfonic acid monohydrate) is a versatile zwitterionic biological buffer widely utilized in molecular biology and cell culture applications. With a pKa of 6.1, it′s the ideal choice for buffering solutions at physiological pH, ensuring precise and reliable results. This buffer′s high water solubility and minimal metal ion binding make it a top choice for various applications, including molecular biology tasks such as DNA and RNA extraction, PCR, and gel electrophoresis. It′s also a key player in cell culture, offering a less toxic alternative to Tris and phosphate buffers.

Beyond these applications, MES hydrate buffer is widely used in regulating pH in plant culture media, reagent solutions, and physiological experiments. It′s the preferred choice for studying the effects of pH on enzymatic reactions and investigating the interactions of proteins and other biomolecules with metal ions. As a Good′s buffer, MES hydrate meets stringent criteria of having a midrange pKa, maximum water solubility, minimal solubility in other solvents, minimal salt effects, stability across different temperatures, chemical and enzymatic stability, minimal absorption in the visible and UV spectral range, and ease of synthesis. Furthermore, it does not form complexes with most metal ions, ensuring reliable outcomes in applications involving metal ions.

Alkalmazás

MES Hydrate has been used:
  • To suspend cells before autophagic induction studies
  • In the preparation of Murashige and Skoog growth medium for the growth of Arabidopsis thaliana seedlings
  • In the conjugation of hybridization probes to beads before PCR amplification
  • To treat fibroblast-derived matrix before conjugation with heparin for use as a vascular endothelial growth factor delivery platform
  • as a wash buffer in a study about molecular biology
  • as a component of culture media

Tulajdonságok és előnyök

  • Suitable for Molecular Biology and Cell Culture
  • Can be used as a Buffer component, for Electrophoresis and Protein separation
  • Tested for Endotoxins and Total Aerobic Microbial Count
  • Free from DNase, NICKase, RNase, and Protease
  • Tested to confirm low levels of heavy metal contamination, ensuring suitability for various applications
  • Effective Buffering from pH 5.5-6.7 (25 °C) with a pKa of 6.1 (25 °C)
  • Highly soluble in water
  • Minimal metal ion binding
  • Less toxic to cells than other buffers such as Tris and phosphate
  • Stable in a wide pH range
  • Low UV absorptivity
  • Minimal reactivity

Elkészítési megjegyzés

A buffer using MES can be prepared by titrating with NaOH to the desired pH. Alternatively, stock solutions of MES and MES sodium salt can be mixed to attain the desired pH. Standard mixing tables using stock solutions to prepare buffers of a given pH have been published. MES is not recommended for buffering at pH 7.4; other buffers should be considered.

Tárolás és stabilitás

Solutions are stable at 2-8°C for months. Sterilize by filtration through 0.2uM filters. Autoclaving is not recommended for any sulfonic acid buffer. If buffers must be nuclease-free, treat the water first, and then add the buffer after autoclaving. When MES solutions are autoclaved, they turn yellow (although pH does not change measurably). The identity of the yellow breakdown product is unknown.

Egyéb megjegyzések

For additional information on our range of Biochemicals, please complete this form.

összehasonlítható termékek

Tárolási osztály kódja

11 - Combustible Solids

WGK

WGK 1

Lobbanási pont (F)

Not applicable

Lobbanási pont (C)

Not applicable

Egyéni védőeszköz

Eyeshields, Gloves


Analitikai tanúsítványok (COA)

Analitikai tanúsítványok (COA) keresése a termék sarzs-/tételszámának megadásával. A sarzs- és tételszámok a termék címkéjén találhatók, a „Lot” vagy „Batch” szavak után.

Már rendelkezik ezzel a termékkel?

Az Ön által nemrégiben megvásárolt termékekre vonatkozó dokumentumokat a Dokumentumtárban találja.

Dokumentumtár megtekintése

Dawson, R.M.C. et al.
Data for Biochemical Research, 410-410 (1987)
Protocol: An improved high-throughput method for generating tissue samples in 96-well format for plant genotyping (Ice-Cap 2.0).
Plant methods, 3 (1), 8-8 (2007)
Multiplex assay for subtyping avian influenza A viruses by cDNA hybridization and adapter-mediated amplification.
Applied Microbiology and Biotechnology, 100 (20), 8809-8818 (2016)
Autophagic or necrotic cell death in the absence of caspase and bcl-2 family members.
Lam, David, et al.
Biochemical and biophysical research communications, 363 (3), 536-541 (2007)
Fibroblast-derived matrix (FDM) as a novel vascular endothelial growth factor delivery platform.
Du, Ping, et al.
J. Controlled Release, 194, 122-129 (2014)

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