catalog number :
MBS722033
products type :
ELISA Kit
products full name :
Rat Bone Alkaline Phosphatase ELISA Kit
products short name :
Bone Alkaline Phosphatase
other names :
bap; BAP; BAP; Bap
products gene name :
BALP
other gene names :
bap; Dsecap; Dsec_GM10423; GM10423
uniprot entry name :
B2ZIB7_DROSE
specificity :
This assay has high sensitivity and excellent specificity for detection of BALP. No significant cross-reactivity or interference between BALP and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between BALP and all the analogues, therefore, cross reaction may still exist in some cases.
storage stability :
Store all reagents at 2-8 degree C.
other info1 :
Samples: Serum, plasma, cell culture supernatants, body fluid and tissue homogenate. Assay Type: Sandwich. Sensitivity: 1.0 U/L.
products description :
Intended Uses This BALP ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Rat BALP. This ELISA kit for research use only, not for therapeutic or diagnostic applications!. Principle of the Assay: BALP ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for BALP. Standards or samples are then added to the microtiter plate wells and BALP if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of BALP present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for BALP are added to each well to "sandwichâ the BALP immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain BALP and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The BALP concentration in each sample is interpolated from this standard curve.
ncbi acc num :
EDW55325.1
ncbi mol weight :
42,112 Da