M4880
Magnesium chloride
suitable for insect cell culture, BioReagent, ≥97.0%
Synonym(s):
Magnogene
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
MgCl2
CAS Number:
Molecular Weight:
95.21
NACRES:
NA.75
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
232-094-6
MDL number:
Assay:
≥97.0%
Form:
powder
Solubility:
water: 468.7 g/L at 20 °C
product line
BioReagent
Quality Level
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
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
Still not finding the right product?
Explore all of our products under Magnesium chloride
Storage Class
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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.