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Creatinine (Cr) Colorimetric Assay Kit (Sarcosine Oxidase Method)– MSE Supplies LLC

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Creatinine (Cr) Colorimetric Assay Kit (Sarcosine Oxidase Method)

SKU: E-BC-K188-M-500

  • $ 71495



Creatinine (Cr) Colorimetric Assay Kit (Sarcosine Oxidase Method)

SKU # E-BC-K188-M
Detection Instrument Microplate reader (510-520 nm, optimum wavelength: 515 nm)
Detection method Colorimetric method


Product Details

Properties

Synonyms Cr
Sample Type Serum, plasma, urine
Sensitivity 3.8 μmol/L
Detection Range 20.45-400 μmol/L
Detection Method Colorimetric method
Assay type Quantitative
Assay time 30 min
Precision Average inter-assay CV: 3.700% | Average intra-assay CV: 1.400%
Other instruments required Micropipettor, Centrifuge, Incubator, Vortex mixer
Other reagents required Normal saline (0.9% NaCl)
Storage 2-8℃
Valid period 12 months


Images

X Zhang et al investigate the usage of H2O2 and O2 for cooperative chemodynamic / starvation cancer therapy. Creatinine (Cr) level in mouse blood was determined using creatinine colorimetric assay kit (E-BC-K188-M).

No significant change of creatinine was observed, the LCFG nanoparticles did not include nephrotoxicity.

 

Dilution of Sample

It is recommended to take 2~3 samples with expected large difference to do pre-experiment before formal experiment and dilute the sample according to the result of the pre-experiment and the detection range (38.2-800 μmol/L).

The recommended dilution factor for different samples is as follows (for reference only):

Sample type Dilution factor
Human urine 20-30
Human serum 1
Rat serum 1
Porcine serum 1

 

Note: The diluent is normal saline (0.9% NaCl).

 

Detection Principle

Creatinine (Cr) can be catalyzed by creatinase and generates creatine. Creatine can be hydrolyzed into sarcosine and urea by creatinase. The sarcosine can be catalyzed by sarcosine oxidase and form glycine, formaldehyde and hydrogen peroxide. The reaction between hydrogen peroxide, 2,4-(6-Tri-iodine-3- hydroxybenzoic acid) and 4-ampyrone can be catalyzed by peroxidase and form pink compound. Creatinine content can be calculated indirectly by measuring the OD value at 515 nm.

 

Kit Components & Storage

Item Component Size 1(48 T) Size 2(96 T) Storage
Reagent 1 Enzyme Solution A 10 mL × 1 vial 20 mL × 1 vial 2-8°C, 12 months, shading light
Reagent 2 Enzyme Solution B 3.5 mL × 1 vial 7 mL × 1 vial 2-8°C, 12 months, shading light
Reagent 3 1 mmol/L Standard Solution 1.5 mL × 1 vial 1.5 mL × 2 vials 2-8°C, 12 months
Microplate 96 wells No requirement
Plate Sealer 2 pieces

 

Note: The reagents must be stored strictly according to the preservation conditions in the above table. The reagents in different kits cannot be mixed with each other. For a small volume of reagents, please centrifuge before use, so as not to obtain sufficient amount of reagents.

 

Technical Data:

Parameter:

Intra-assay Precision

Three human serum samples were assayed in replicates of 20 to determine precision within an assay. (CV = Coefficient of Variation)

Parameters Sample 1 Sample 2 Sample 3
Mean (μmol/L) 88.60 271.00 563.00
%CV 1.7 1.5 1.0


Inter-assay Precision

Three human serum samples were assayed 20 times in duplicate by three operators to determine precision between assays.

Parameters Sample 1 Sample 2 Sample 3
Mean (μmol/L) 88.60 271.00 563.00
%CV 3.2 3.7 4.2

 

Recovery

Take three samples of high concentration, middle concentration and low concentration to test the samples of each concentration for 6 times parallelly to get the average recovery rate of 106%.

Standard 1 Standard 2 Standard 3
Expected Conc. (mmol/L) 0.13 0.22 0.34
Observed Conc. (mmol/L) 0.1 0.2 0.4
Recovery rate (%) 108 106 104

 

Sensitivity

The analytical sensitivity of the assay is 3.8 μmol/L. This was determined by adding two standard deviations to the mean O.D. obtained when the zero standard was assayed 20 times, and calculating the corresponding concentration.

 

Standard Curve

As the OD value of the standard curve may vary according to the conditions of the actual assay performance (e.g. operator, pipetting technique or temperature effects), so the standard curve and data are provided as below for reference only.

Concentration (mmol/L) 0 0.1 0.15 0.2 0.25 0.3 0.35 0.4
Average ΔA 0.001 0.042 0.057 0.078 0.097 0.124 0.144 0.171
Absoluted OD 0.000 0.042 0.056 0.078 0.096 0.123 0.143 0.171