S2404

Sigma-Aldrich

Sodium acetate buffer solution

BioXtra, pH 7.0±0.05 (25 °C), for molecular biology, 3 M, non-sterile; 0.2 μm filtered

CAS Number:
Beilstein/REAXYS Number:
3786729
MDL number:
PubChem Substance ID:
NACRES:
NA.52
Pricing and availability is not currently available.

Quality Level

grade

for molecular biology

sterility

non-sterile; 0.2 μm filtered

product line

BioXtra

form

liquid

concentration

3 M

pH

7.0±0.05 (25 °C)

suitability

suitable for DNA precipitation

storage temp.

2-8°C

SMILES string

[Na+].CC(O)=O.CC([O-])=O

InChI

1S/2C2H4O2.Na/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+1/p-1

InChI key

BHZOKUMUHVTPBX-UHFFFAOYSA-M

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General description

Sigma′s Sodium Acetate Buffer is a 3M solution prepared with 18 megaohm water and filter-sterilized.

Application

Sodium acetate buffer solution has been used for the precipitation of DNA. It has also been used as a component of supporting electrolyte for electrochemical sensor.
Sodium acetate buffer solution is suitable for elution of proteins and for use in general molecular biology applications.

RIDADR

NONH for all modes of transport

WGK Germany

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis
Certificate of Origin
Application of sensitive electrochemical sensing system for detecting bromate from disinfection process in desalination plant
Lee YG and Jang A
Desalination, 423, 135-140 (2017)
Buket Onel et al.
Methods in molecular biology (Clifton, N.J.), 2035, 201-222 (2019-08-25)
DNA G-quadruplexes are globular nucleic acid secondary structures which occur throughout the human genome under physiological conditions. There is accumulating evidence supporting G-quadruplex involvement in a number of important aspects of genome functions, including transcription, replication, and genomic stability, and...
Sambrook, J., and Russell, D.W.
Molecular Cloning: A Laboratory Manual, A1-A1 (2001)
Jaspreet Kaur et al.
Antimicrobial agents and chemotherapy, 55(2), 659-666 (2010-12-01)
In this study we utilized the concept of rational drug design to identify novel compounds with optimal selectivity, efficacy and safety, which would bind to the target enzyme pteridine reductase 1 (PTR1) in Leishmania parasites. Twelve compounds afforded from Baylis-Hillman...
Jaspreet Kaur et al.
The Journal of antimicrobial chemotherapy, 65(8), 1742-1748 (2010-06-04)
Using the pteridine reductase (PTR1) enzyme of Leishmania as the target, the objective of our study was to find a drug candidate that can enter the clinical development process after being evaluated for safety and efficacy in animals. Monastrol (R)...

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