Iron ( Fe ) Assay Kit LS ( Nitroso-PSAP )
#FE02ME 200 T 38,000 JPY (excluding tax)
・Iron ( Fe ) Assay Kit LS ( Nitroso-PSAP ) can rapidly quantify iron (Fe2+, Fe3+) in biological samples (serum, plasma, urine, etc.) using a microplate reader (96 wells).
・The principle of this assay is a chelation quantification method, not an immunoassay, so it is species-independent.
・No pretreatment is required for serum, plasma, or urine samples.
・Multi-point calibration is not required as calibration is performed using two points along with the standard and blank sample included in the kit.
・The kit does not contain any toxic or hazardous substances, so it is safe to handle and dispose of.
※ When used in combination with our UIBC (Unsaturated Iron Binding Capacity) Assay Kit, the TIBC (total iron binding capacity) can be measured.
※ This product is for research use only. Do not use for diagnostic purposes.
Iron is found in many enzymes as an important constituent element. All iron in blood is bound to transferrin and is transported to erythroblasts and various tissues for synthesis of globin proteins that require iron, such as myoglobin and hemoglobin. Iron is essential for the production of proteins that transport oxygen, and its deficiency can cause iron deficiency anemia, chronic hemorrhagic anemia, and infectious anemia. Increased transferrin and high concentrations of iron are also observed in hepatitis and cirrhosis. Aplastic anemia and pernicious anemia also show increased iron.
This method determines iron concentration by observing the color change in the visible region due to the formation of a chelate complex between nitroso-PSAP and iron.
Iron bound to transport proteins such as transferrin is dissociated by a weak acid or denaturing agent in the reagent to form an iron-ferrozine complex. The iron concentration can be determined by measuring this complex at a wavelength of 750 nm.
◯ Samples that can be directly quantified with this kit
Examples: serum, plasma, urine
The denaturing agent in the kit dissociates iron from protein and causes coloration. No special pretreatment is required.
※ Do not use blood collection tubes containing EDTA which may affect the assay value.
※ When using urine samples, preserve it by adding HCl and adjust the pH to 2~3 when measuring.
◯ Samples that require acid extraction
Examples: cell lysates, tissue homogenates, and other aqueous solutions
By lowering the pH of the sample, iron is dissociated from the protein, and the supernatant is collected and used as the assay sample. However, only the following chemicals can be measured.
・Free iron
・Protein-bound (coordinated) iron (Protein-Fe2+, e.g. transferrin, ferritin, metallothionein)
・Other coordinated iron
※ Lysis buffer containing EDTA should not be used because it may affect the assay value.
※ Organic iron and heme iron should be acid decomposed first.
◯ Samples that require microwave method and decomposition of organic matter with mixed acid.
Examples: Samples containing strong chelating agents such as EDTA, organic iron (-C-Fe-C- single bonded), and iron encapsulating cyclic ligands (Fe-porphyrin, etc.)
It is necessary to measure chemical species that do not dissociate by acid extraction or samples containing interfering substances such as strong iron chelating agents.
※ After decomposition of organic matter by each decomposition method, adjust the pH to 2 to 3, and use a constant volume sample as the assay sample.
(1) Add 15 µl of DIW, standard solution, and assay sample to wells of 96-well plate.
(2) Apply 160 µl of RA to each well.RA 160 µlをwell添加
(3) Incubate the plate at room temperature for 10 minutes.
(4) Add 75 µl of chromogenic solution to each well.
(5) Incubate the plate at room temperature for 5 minutes.
(6) Measure absorbance at the wavelength of 750 nm.
(7) Calculate the iron concentration using the following formula:
Intended use : | Iron (Fe2+, Fe3+) measurement
→ In combination with our UIBC (Unsaturated Iron Binding Capacity) Assay Kit, the TIBC (total iron binding capacity) can be measured. |
Testing sample : | Serum, plasma, urine, saliva, cell lysates, tissue extract, plant extract, hair sample extract, food extract, drinking water, environmental water, mineral water, etc. |
Measurement range : | 10 ~1,000 µg/dL |
Measurement wavelength (maximum wavelength) : | 740~760 nm (750nm) |
Number of measurement: | 200 |
Assay method: | N-PSAP method |
Species specificity: | Any species of organism is acceptable. |
Regulations (Poisonous and Deleterious Substances Control Act) | Not applicable |
Effects of coexisting substances: | Conjugated and unconjugated bilirubin: 30 mg/dL Chyle: 500 FTU Hemoglobin: 0.1 g/dL However, do not use EDTA as it will have an effect. |
Detection devices : | Microplate reader, UV-visible spectrophotometer, colorimeter *The kit does not include 96-well plates or cuvettes. |
(1) Measurement of control serum with this kit
Figure 1: Results of measurement of control serum with known iron concentration.
(2) Measurement of iron concentration in pig liver using this kit
Figure 2: Results of pig liver iron concentration measurement using the ICP-OES method and this kit
Takuya Iwabuchi, Trace metal analysis and its pretreatment technology, Technical Information institute Co., Ltd. (ed.) p192-200 (2015)
Takuya Iwabuchi and Hiroko Suzuki, Development of diagnostic drugs/devices using cutting-edge biomarkers and regulatory compliance, Technical Information institute Co., Ltd. (ed.) (2015)
Hiroko Suzuki, Toru Otsuki, Natsuki Ito, Bunpei Sato, Kazuhiro Koide, Takuya Iwabuchi, A colorimetric assay and a novel probe for biological iron research, Saibou 46(1), 2014.
M. Saito, D. Horiguchi,T. Imamura and K. Kina, Bunseki Kagaku, 30, 635-639 (1981).
In preparation
Our products can be purchased from the following distributors.
Iron Assay kit LS – Nitroso-PSAP Method | Metallo Assay LS
E-mail:sales@funakoshi.co.jp
Tel:+81-3-5684-1615
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