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Sigma-Aldrich

Magnesiumchlorid -Lösung

BioUltra, for molecular biology, ~0.025 M in H2O

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About This Item

Lineare Formel:
MgCl2
CAS-Nummer:
7786-30-3
Molekulargewicht:
95.21
MDL-Nummer:
MFCD00011106
UNSPSC-Code:
12352302
PubChem Substanz-ID:
329759763
NACRES:
NA.26

Qualität

for molecular biology

Qualitätsniveau

100

Produktlinie

BioUltra

Konzentration

~0.025 M in H2O

Verunreinigungen

DNases, none detected
 RNases, none detected
 insoluble matter, passes filter test
 phosphatases, none detected
 proteases, none detected
≤0.0002% total nitrogen (N)

pH-Wert

5.0-7.0 (25 °C)

Anionenspuren

phosphate (PO43-): ≤5 mg/kg
sulfate (SO42-): ≤20 mg/kg

Kationenspuren

Al: ≤1 mg/kg
As: ≤0.1 mg/kg
Ba: ≤1 mg/kg
Bi: ≤1 mg/kg
Ca: ≤10 mg/kg
Cd: ≤1 mg/kg
Co: ≤1 mg/kg
Cr: ≤1 mg/kg
Cu: ≤1 mg/kg
Fe: ≤1 mg/kg
K: ≤500 mg/kg
Li: ≤1 mg/kg
Mn: ≤1 mg/kg
Mo: ≤1 mg/kg
Na: ≤1000 mg/kg
Ni: ≤1 mg/kg
Pb: ≤1 mg/kg
Sr: ≤1 mg/kg
Zn: ≤1 mg/kg

λ

neat

UV-Absorption

λ: 260 nm Amax: 0.03
λ: 280 nm Amax: 0.03

SMILES String

Cl[Mg]Cl

InChI

1S/2ClH.Mg/h2*1H;/q;;+2/p-2

InChIKey

TWRXJAOTZQYOKJ-UHFFFAOYSA-L

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Verpackung

Packung mit 10 x 1 mL Amplullen

Lagerklassenschlüssel

10 - Combustible liquids

WGK

nwg

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves

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Analysenzertifikate (COA)

Lot/Batch Number
BCCG6475
BCBT8379
BCBN7545V
BCBL5374V
BCBF1190

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Elaine T Lim et al.
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Exome sequencing studies in complex diseases are challenged by the allelic heterogeneity, large number and modest effect sizes of associated variants on disease risk and the presence of large numbers of neutral variants, even in phenotypically relevant genes. Isolated populations
Hideyuki Arita et al.
Brain tumor pathology, 32(1), 22-30 (2014-04-22)
Assessment of the mutational status of the isocitrate dehydrogenase 1/2 (IDH1/2) gene has become an integral part of the standard diagnostic procedure and, therefore, needs to be accurate. This may, however, be compromised by various factors including the method of
Stephen Q Wong et al.
Oncotarget, 6(2), 1115-1127 (2014-12-30)
Melanoma is often caused by mutations due to exposure to ultraviolet radiation. This study reports a recurrent somatic C > T change causing a P131L mutation in the RQCD1 (Required for Cell Differentiation1 Homolog) gene identified through whole exome sequencing
Manal A Farg et al.
Human molecular genetics, 23(13), 3579-3595 (2014-02-20)
Intronic expansion of a hexanucleotide GGGGCC repeat in the chromosome 9 open reading frame 72 (C9ORF72) gene is the major cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia. However, the cellular function of the C9ORF72 protein remains unknown.
Susanne Hellmuth et al.
The EMBO journal, 33(10), 1134-1147 (2014-05-02)
The universal triggering event of eukaryotic chromosome segregation is cleavage of centromeric cohesin by separase. Prior to anaphase, most separase is kept inactive by association with securin. Protein phosphatase 2A (PP2A) constitutes another binding partner of human separase, but the
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