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Merck

M4880

Magnesium chloride

suitable for insect cell culture, BioReagent, ≥97.0%

Sinónimos:

Magnogene

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About This Item

Fórmula lineal:
MgCl2
Número CAS:
7786-30-3
Peso molecular:
95.21
NACRES:
NA.75
PubChem Substance ID:
24896955
UNSPSC Code:
12352302
EC Number:
232-094-6
MDL number:
MFCD00011106
assay:
≥97.0%
form:
powder
solubility:
water: 468.7 g/L at 20 °C

Nombre del producto

Magnesium chloride, suitable for insect cell culture, BioReagent, ≥97.0%

InChI key

TWRXJAOTZQYOKJ-UHFFFAOYSA-L

InChI

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

SMILES string

Cl[Mg]Cl

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.)

Quality Level

300

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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

Clase de almacenamiento

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
0000520121
0000520121
0000505297
0000505297
0000507413

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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
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
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
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
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