Blood Phosphorus Content Assay Kit (Visible Spectrophotometers)
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Blood Phosphorus Content Assay Kit (Visible Spectrophotometers)

Cat.No: BBITK-HMM-0001 Datasheet

Specification Quantities

60T/50S:
- +
Product Details Related Products
Product Name Blood Phosphorus Content Assay Kit (Visible Spectrophotometers)
Catalog No. BBITK-HMM-0001
Description Blood phosphorus mainly refers to inorganic phosphorus existing in the blood in the form of inorganic phosphorus salts. The concentrations of calcium and phosphorus in plasma have a significant influence on the formation of bone salts and bone calcification, etc. The relative stability of their contents depends on the relative balance of the absorption and excretion of calcium and phosphorus, and the two metabolizations of calcification and decalcification. Blood phosphorus content can be used as one of the detection indicators for various diseases and has important applications in the field of medical detection.
Testing Equipment Visible Spectrophotometers
Matching 1 mL glass cuvette (d=10 mm)
Number of Testable Samples 50 Samples
Estimated Measurement Time 3 h (50 Samples)
Storage Store at 4°C away from light
Self-contained Reagents H2SO4,MW=98.078,CAS: 7664-93-9
Detection Principle After the serum sample is processed to remove the organic phosphorus, the inorganic phosphorus can react with ammonium molybdate to generate phosphomolybdic acid, which is reduced by ferrous sulfate to generate blue compounds, and the product has a characteristic absorption peak at 660 nm, which can be quantitatively detected by the change of absorbance value of the blood phosphorus content.
Detection Methods Molybdenum Blue Method
Detection Wavelength 660 nm
Signal Response Incremental
Standard Phosphorus
Reference Standards y=0.838x+0.0039 (R2=0.9999)
Standard Linear Range 0.0625-1.5 mmol/L
Detection Limit 0.02 mmol/L
Note The measurement should be completed as soon as possible after blood collection to avoid hemolysis; if the A-measurement is greater than 1.0, it is recommended that the sample to be tested be diluted appropriately with Reagent I and then measured; if the A-measurement is less than 0.05, it is recommended that the ratio of serum and Reagent I be changed appropriately in the process of extraction and then measured, for example, 100 μL of serum should be added to 900 μL of Reagent I, and the calculations should be modified accordingly.
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