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Merck
CN

63052

Magnesium acetate solution

BioUltra, Molecular Biology, ~1 M in H2O

Synonym(s):

Magnesium acetate anhydrous, Mg(OAc)2

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About This Item

Linear Formula:
(CH3COO)2Mg
CAS Number:
142-72-3
Molecular Weight:
142.39
UNSPSC Code:
12161700
NACRES:
NA.25
PubChem Substance ID:
329759766
MDL number:
MFCD00003539
Beilstein/REAXYS Number:
3692530

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InChI

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

SMILES string

CC(=O)O[Mg]OC(C)=O

InChI key

UEGPKNKPLBYCNK-UHFFFAOYSA-L

grade

Molecular Biology

product line

BioUltra

form

liquid

concentration

~1 M in H2O

impurities

DNases, none detected, RNases, none detected, insoluble matter, passes filter test, phosphatases, none detected, proteases, none detected

refractive index

n20/D 1.358

pH

5.0-7.0 (25 °C)

cation traces

Al: ≤5 mg/kg, Ba: ≤1 mg/kg, Bi: ≤1 mg/kg, Ca: ≤5 mg/kg, Cd: ≤1 mg/kg, Co: ≤1 mg/kg, Cr: ≤1 mg/kg, Cu: ≤5 mg/kg, Fe: ≤1 mg/kg, K: ≤20 mg/kg, Li: ≤1 mg/kg, Mn: ≤5 mg/kg, Mo: ≤1 mg/kg, Na: ≤20 mg/kg, Ni: ≤2 mg/kg, Pb: ≤1 mg/kg, Sr: ≤1 mg/kg, Zn: ≤1 mg/kg

λ

neat

UV absorption

λ: 260 nm Amax: 0.04, λ: 280 nm Amax: 0.02

Quality Level

200

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Application

Magnesium acetate is used in molecular biology applications such as batch in vitro transcription of RNA and the crystallization of transcription factor:DNA complexes and proteins via the sitting-drop vapor-diffusion method.
Magnesium acetate solution has been used:
  • to supplement Midkin fused to the biotin ligase BioID2 (MK-BioID2) conditioned medium for in-tube biotinylation assay
  • as a component of lysis buffer and amplified RNA (aRNA) fragmentation buffer to perform aRNA fragmentation
  • as a component of lysis buffer and DamID buffer for sequencing zygote samples

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM9646
BCCL3788
BCCJ9123
BCCH2942
BCCH5826

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Roberto Stella et al.
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The illegal use of pharmacologically active compounds for growth promotion in food-producing species poses risks for consumer health and animal welfare. Surveillance relies on the quantification of drug residues in animal fluids or tissues, but the efficacy can be negatively
Navneet Bung et al.
Scientific reports, 8(1), 9599-9599 (2018-06-27)
AMPK is considered as a potential high value target for metabolic disorders. Here, we present the molecular modeling, in vitro and in vivo characterization of Activator-3, 2-[2-(4-(trifluoromethyl)phenylamino)thiazol-4-yl]acetic acid, an AMP mimetic and a potent pan-AMPK activator. Activator-3 and AMP likely
Quentin M Dudley et al.
ACS synthetic biology, 5(12), 1578-1588 (2016-08-02)
Cell-free metabolic engineering (CFME) is advancing a powerful paradigm for accelerating the design and synthesis of biosynthetic pathways. However, as most cell-free biomolecule synthesis systems to date use purified enzymes, energy and cofactor balance can be limiting. To address this
Hina Akhter et al.
Comparative biochemistry and physiology. Part A, Molecular & integrative physiology, 203, 144-151 (2016-10-28)
The larvae of the mosquito, Aedes aegypti normally inhabit freshwater (FW) where they face dilution of body fluids by osmotic influx of water. In response, the physiological actions of the anal papillae result in ion uptake while the Malpighian tubules
Lena Haffo et al.
Scientific reports, 8(1), 12671-12671 (2018-08-25)
The tumor suppressor p53 is commonly inactivated in human tumors, allowing evasion of p53-dependent apoptosis and tumor progression. The small molecule APR-246 (PRIMA-1Met) can reactive mutant p53 in tumor cells and trigger cell death by apoptosis. The thioredoxin (Trx) and
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