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48795

Sigma-Aldrich

Manganese(II) chloride 0.1 M solution

Synonym(s):

Manganese(II) chloride solution, Additive Screening Solution 26/Kit-No 78374

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About This Item

Linear Formula:
MnCl2
CAS Number:
7773-01-5
Molecular Weight:
125.84
MDL number:
MFCD00011114
UNSPSC Code:
12352200
PubChem Substance ID:
57651164
NACRES:
NA.32

Quality Level

100

density

1.01 g/mL at 20 °C

storage temp.

2-8°C

SMILES string

Cl[Mn]Cl

InChI

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

InChI key

GLFNIEUTAYBVOC-UHFFFAOYSA-L

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Application

Manganese(II) chloride 0.1 M solution has been used:
  • as a component of reprogramming media for culturing mouse neonatal tail-tip fibroblasts
  • in the mutagenesis of WT clone by error-prone polymerase chain reaction (PCR)
  • as a standard in isothermal titration calorimetry and differential scanning calorimetry

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Hazard Classifications

Eye Irrit. 2

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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Robert W Siegel
Methods in molecular biology (Clifton, N.J.), 504, 351-383 (2009-01-23)
Many biosensors depend on molecular recognition reagents to achieve highly sensitive and specific detection levels of an analyte of interest. Although new and improved detection platforms continue to be developed, improvements in the affinity and specificity of the molecular recognition
Alexey Gribenko et al.
Journal of molecular biology, 425(18), 3429-3445 (2013-07-06)
MntC is a metal-binding protein component of the Mn²⁺-specific mntABC transporter from the pathogen Staphylococcus aureus. The protein is expressed during the early stages of infection and was proven to be effective at reducing both S. aureus and Staphylococcus epidermidis
Xiaowen Wang et al.
Scientific reports, 6, 23017-23017 (2016-03-16)
We have recently shown that a combination of microRNAs, miR combo, can directly reprogram cardiac fibroblasts into functional cardiomyocytes in vitro and in vivo. However, direct reprogramming strategies are inefficient and slow. Moving towards the eventual goal of clinical application
Barry J Bowman et al.
Eukaryotic cell, 11(11), 1362-1370 (2012-09-18)
The pmr gene is predicted to encode a Ca(2+)-ATPase in the secretory pathway. We examined two strains of Neurospora crassa that lacked PMR: the Δpmr strain, in which pmr was completely deleted, and pmr(RIP), in which the gene was extensively
Anne Bertrand et al.
NeuroImage, 64, 693-702 (2012-09-11)
The impairment of axonal transport by overexpression or hyperphosphorylation of tau is well documented for in vitro conditions; however, only a few studies on this phenomenon have been conducted in vivo, using invasive procedures, and with contradictory results. Here we
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