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Merck
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M4880

Sigma-Aldrich

Magnesium chloride

BioReagent, suitable for insect cell culture, ≥97.0%

Sinónimos:

Magnogene

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About This Item

Fórmula lineal:
MgCl2
Número de CAS:
7786-30-3
Peso molecular:
95.21
EC Number:
232-094-6
MDL number:
MFCD00011106
UNSPSC Code:
12352302
PubChem Substance ID:
24896955
NACRES:
NA.75

product line

BioReagent

assay

≥97.0%

form

powder

technique(s)

cell culture | insect: suitable

mp

714 °C (lit.)

solubility

water: 468.7 g/L at 20 °C

density

2.32 g/mL at 25 °C (lit.)

SMILES string

Cl[Mg]Cl

InChI

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

InChI key

TWRXJAOTZQYOKJ-UHFFFAOYSA-L

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Application

Magnesium chloride has been used:
  • as a metal cofactor supplement in the terminal deoxynucleotidyl transferase (TdT) reaction
  • as a component of Tris assay buffer to prepare substrate stocks for /-N-Acyl lysine substrate screening
  • as a component of low-calcium differentiation medium for keratinocyte differentiation

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Elaine T Lim et al.
PLoS genetics, 10(7), e1004494-e1004494 (2014-08-01)
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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Protocolos

Determination of Water Content in Magnesium chloride Using Karl Fischer Titration

Summary application report for analysis of moisture in Magnesium chloride

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