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QuantiChrom TM
Magnesium Assay Kit (DIMG-250)
Quantitative Colorimetric
Magnesium Determination at 500 nm
DESCRIPTION
Magnesium (Mg) is one of the
most abundant and essential minerals in mammals.
Magnesium is involved in more than 300
biochemical reactions in the body and plays
important roles in muscle and nerve functions,
heart rhythm, immune system and bone formation.
Magnesium deficiency may lead to nausea,
fatigue, muscle contractions, hypocalcemia and
hypokalemia. Simple, direct and automation-ready
procedures for measuring magnesium concentration
in biological samples are becoming popular in
Research and Drug Discovery. BioAssay Systems'
magnesium assay kit is designed to measure
magnesium directly in biological samples without
any pretreatment. A calmagite dye in the kit
forms a colored complex specifically with
magnesium. The intensity of the color, measured
at 500 nm, is directly proportional to the
magnesium concentration in the sample. The
optimized formulation minimizes interference by
potential substances.
KEY FEATURES
Sensitive and accurate. Use
as little as 5 μL sample. Linear detection range
0.1 mg/dL (41μM) to 3 mg/dL (1.2 mM) Mg2+ in
96-well plate
assay. Simple and
high-throughput.
The procedure involves addition of two reagents
and measuring OD500nm. Can be readily automated
as a highthroughput assay for thousands of
samples per day.
Improved reagent stability and versatility.
The optimized formulation has greatly enhanced
reagent and signal stability. Cuvet or 96-well
plate assay. Low
interference in biological samples.
Assays can be directly performed in serum and
urine samples.
APPLICATIONS
Direct Assays:
Mg2+ in serum, urine and deproteinated samples
(e.g. milk) etc.
Drug Discovery/Pharmacology: effects of drugs on
Mg2+ metabolism. Food and Beverages: Mg2+
determination.
Environment: Mg2+
determination in water and soil.
KIT CONTENTS (250
tests in 96-well plates)
Reagent A: 25 mL Reagent B:
25 mL EDTA Solution: 2 x 1.5 mL Standard: 1 mL
10 mg/dL Mg2+
Storage conditions .
The kit is shipped at room temperature. Store
Reagent and Standard at 4°C. Shelf life of at
least 6 months (see expiry dates on labels).
Precautions :
reagents are for research use only. Normal
precautions for laboratory reagents should be
exercised while using the reagents. Please refer
to Material Safety Data Sheet for detailed
information.
PROCEDURES
Reagent Preparation:
Prepare enough working
reagent by combining equal volumes of Reagent A
and Reagent B. Equilibrate to room temperature
before use. Procedure using 96-well plate:
1. Dilute Standard to 2 mg/dL
by mixing 40 μL 10 mg/dL Standard with 160 μL
distilled water. Transfer 5 μL diluted standard
and samples in duplicate to wells of a clear
bottom plate. Diluted standard can be stored at
4°C for future use.
2. Add 200 μL working reagent
and tap plate to mix thoroughly .
3.
Incubate 2 min at room temperature and read
optical density at 500 nm (OD for
sample and
standard).
4. Add 10
μL EDTA Solution to all
sample wells and tap plate to mix thoroughly.
Incubate 2 min and read OD at 500nm (OD for
blanks).
Procedure using cuvette:
1. Set up test tubes and
transfer 25 μL diluted Standard and samples to
appropriately labeled tubes.
2. Add 1000 μL working
reagent and vortex to mix. Incubate 2 min.
Transfer to cuvet and read OD500nm. Add 50 μL
EDTA solution, mix well, incubate 2 min and read
OD500 nm.
CALCULATION
Magnesium concentration of
the sample is calculated as

ODSAMPLE
and ODBLANK are OD500nm
values of sample before and after the addition
of EDTA. ODMG and ODMGBLANK are OD500nm values
of the standard (2 mg/dL) before and after the
addition of EDTA. Conversions: 1 mg/dL Mg2+
equals 411 μM,
0.001% or 10 ppm.
MATERIALS REQUIRED, BUT NOT
PROVIDED
Pipeting devices and
accessories (e.g. 5 μL ).
Procedure using 96-well plate:
Clear bottom 96-well plates
(e.g. Corning Costar) and plate reader.
Procedure using cuvette:
Cuvets and
spectrophotometer for measuring OD500nm.
GENERAL CONSIDERATIONS
1. EDTA and other Mg2+
chelators interfere with this assay. This assay
can not be applied to plasma samples obtained
with EDTA.
2. Sample pretreatment: for
milk and other lipid/protein-rich samples, mix
equal volumes of sample and 10% trichloroacetic
acid (Sigma Cat# T6399). Incubate 5 min at room
temperature and pellet precipitates for 2 min at
14,000 rpm in a table centrifuge. Assay the
supernatant (dilution factor = 2) using the
above procedure.
EXAMPLES
Samples were assayed in
duplicate using the 96-well plate protocol. The
Mg2+ values (mg/dL) were 1.64 ± 0.04 (rat
serum), 1.77 ± 0.02 (human serum), 2.41 ± 0.5
(goat serum), 2.80 ± 0.14 (Invitrogen fetal
bovine serum).

PUBLICATIONS
[1]. Kim, T. et al (2006). Rapid
production of milligram quantities of proteins
in a batch cell-free protein synthesis system.
J. Biotechnol. 124(2): 373-383.
[2]. Stippler, M. et al (2007).
Serum and cerebrospinal fluid magnesium in
severe traumatic brain injury outcome. J.
Neurotrauma. 24(8): 1347-1354.
[3]. Pratihar, S. et al (2009).
Increased serum magnesium and calcium and their
regulation during hibernation in the Indian
common toad, Duttaphrynus melanostictus .
South Am. J.
Herpetology 4(1): 51-54. |
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