M1028
Magnesium chloride solution
for molecular biology, 1.00 M±0.01 M
Synonym(s):
MgCl2, dichloromangesium, magnesium chloride
About This Item
Recommended Products
grade
for molecular biology
Quality Level
sterility
non-sterile; 0.2 μm filtered
form
liquid
concentration
1.00 M±0.01 M
technique(s)
DNA sequencing: suitable
impurities
DNAse, none detected
NICKase, none detected
Protease, none detected
RNAse, none detected
solubility
water: soluble
density
1.080 g/cm3
cation traces
heavy metals (as Pb): ≤5 ppm
suitability
suitable for electrophoresis
suitable for molecular biology
application(s)
cell analysis
foreign activity
DNase, RNase, NICKase and protease, none detected
SMILES string
Cl[Mg]Cl
InChI
1S/2ClH.Mg/h2*1H;/q;;+2/p-2
InChI key
TWRXJAOTZQYOKJ-UHFFFAOYSA-L
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General description
Application
- to prepare buffer to lyse cells for immunoprecipitation
- as a supplement in Krebs-Henseleit buffer in chronic high-fat diet studies of aged mice.
- in embedding 3-dimensional mtgase hydrogels in invitro studies of osteocyte differentitaion and interconnected cellular networks.
- It has been used to protect the liver from oxidative damage.
- to prepare serum-free medium for electrophysiological studies of rat brain slice cultures.
Features and Benefits
- Available as a Ready-to-use solution which reduces the need for preparation time.
- Heavy metals (as Pb): ≤5 ppm
- Free from DNase, RNase, NICKase and protease
Components
Other Notes
comparable product
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Protocols
This procedure may be used for Mutanolysin products.
Measure hexokinase activity using a continuous spectrophotometric rate-determination assay at 340 nm, catalyzing D-hexose sugar phosphorylation using ATP.
Enzymatic assay of lipase type XIII from Pseudomonas sp. using a coupled enzyme system of glycerol kinase and glycerophosphate oxidase (EC 3.1.1.3)
To measure glucose-6-phosphate dehydrogenase activity, beta-nicotinamide adenine dinucleotide phosphate is used in a spectrophotometric rate determination assay at 340 nm.
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