-
Alternative name
SCAN domain-containing protein 3 ELISA KIT; Transposon-derived Buster4 transposase-like protein ELISA KIT; Zinc finger BED domain-containing protein 9ZBED9 ELISA KIT; Buster4 ELISA KIT; KIAA1925 ELISA KIT; SCAND3 ELISA KIT; ZNF305P2 ELISA KIT; ZNF452 ELISA KIT
-
Catalog
E034267
-
species
Human
-
GeneSCAND3
-
SpecificityThis assay has high sensitivity and excellent specificity for detection of SCAN Domain Containing Protein 3 (SCAND3).
No significant cross-reactivity or interference between SCAN Domain Containing Protein 3 (SCAND3) and analogues was observed.
-
SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
-
SensitivityTypically less than 0.059ng/mL.
-
Intended UseHuman SCAND3 ELISA Kit allows for the in vitro quantitative determination of SCAND3 , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
-
StorageFor 5-7days:Store the whole kit at 4℃
For a Long time :Store the Substrate at 4℃, other reagent should store at -20℃.
-
Product Description
specificalPrinciple of the Assay: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to SCAN Domain Containing Protein 3 (SCAND3). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to SCAN Domain Containing Protein 3 (SCAND3). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain SCAN Domain Containing Protein 3 (SCAND3), biotin-conjugated antibody and enzyme-conjugated Avidin 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 SCAN Domain Containing Protein 3 (SCAND3) in the samples is then determined by comparing the O.D. of the samples to the standard curve.
-