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                                    Alternative name
Mbl ELISA KIT; Mblmbl ELISA KIT; 
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Catalog
E002908
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species
Human
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                                    GeneMBL 
                                
                             
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                                    SpecificityThis assay has high sensitivity and excellent specificity for detection of Anti-MBL. No significant cross-reactivity or interference between Anti-MBL and analogues was observed.
                                
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                                    SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
                                
 
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                                    Sensitivity2.45ng/mL.
                                
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                                Intended UseHuman MBL ELISA Kit allows for the in vitro quantitative determination of MBL  , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
                            
  
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                                    StorageFor 5-7days:Store the whole kit at 4℃
                                        For a Long time :Store the Substrate at 4℃, other reagent should store at -20℃.
                                    
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                                    Product Description 
 specificalIntended Uses: The kit is an enzyme immunoassay for in vitro quantitative measurement of Anti-MBL in human serum, plasma and other biological fluids.
Principle of the Assay||The microtiter plate provided in this kit has been pre-coated with an antigen. Standards or samples are then added to the appropriate microtiter plate wells with a Horseradish Peroxidase (HRP)-conjugated secondary antibody. After TMB substrate solution is added, those wells that contain Anti-MBL will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm +/- 10nm. The concentration of Anti-MBL in the samples is then determined by comparing the O.D. of the samples to the standard curve.
                                 
                                                                                                                                                                                                    
                                                        
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