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Determination of Protein Concentration Using Bradford Microplate Protein Quantification Assay

مجله بیماری و تشخیص، دوره: 4، شماره: 1
Year: 1394
COI: JR_IEJM-4-1_003
Language: EnglishView: 181
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Rouhollah Valipour Nouroozi - Parasitology Department, Medical school, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IR Iran
Moulood Valipour Noroozi - Student Research Committee, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IR Iran
Masoumeh Ahmadzadeh - School of Health, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IR Iran


Background: Bradford protein assay is popular due to its ease of performance and relative sensitivity. Many researchers and laboratories in Iranuse standard assay of Bradford by cuvette. No commercial kit was available for Bradford microplate assay in Iran. Meanwhile, importedBradford commercial kits are very expensive and have a long delivery time in Iran. Till now no study or document on Bradford microplateprotein quantification assay was reported in Iran, so this study aimed to design and carried out this assay.Methods: In the current study, antigen B of hydatid cyst fluid was used as sample and the assay was performed in microplate wells. Theabsorbance values were measured at 595 nm and standard curve was generated by Microsoft Office Excel software. The protein concentrationof sample was calculated using the equation of the standard curve.Results: Average protein concentration of the sample was 1175 μg/ml. The total time needed for reading of absorbance was two minutesapproximately.Conclusion: Bradford microplate protein assay is a fast and suitable method. This method could be replacing the time consuming method withcuvette. In addition, if this assay produces as a low price kit it could have many benefits for students and laboratories that need to determineprotein concentration by Bradford assay.


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Valipour Nouroozi, Rouhollah and Valipour Noroozi, Moulood and Ahmadzadeh, Masoumeh,1394,Determination of Protein Concentration Using Bradford Microplate Protein Quantification Assay,

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