Dystonin, Dst ELISA KIT/ Mouse

Mouse Dystonin, DST ELISA KIT

96 Tests

Operating instruction

FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING!

Synonyms

DST,dystonin; BP240; BPA; BPAG1; CATX-15; CATX15; D6S1101; DMH; HSAN6; MACF2; bullous pemphigoid antigen 1; bullous pemphigoid antigen 1, 230/240kDa; dystonia musculorum protein; hemidesmosomal plaque protein; trabeculin-beta, Microtubule actin cross-linking factor 2

Search name

Mouse DST ELISA KIT ,Mouse dystonin ELISA KIT ,Mouse BP240 ELISA KIT ,Mouse BPA ELISA KIT ,Mouse BPAG1 ELISA KIT ,Mouse CATX-15 ELISA KIT ,Mouse CATX15 ELISA KIT ,Mouse D6S1101 ELISA KIT ,Mouse DMH ELISA KIT ,Mouse HSAN6 ELISA KIT ,Mouse MACF2 ELISA KIT ,Mouse bullous pemphigoid antigen 1 ELISA KIT ,Mouse bullous pemphigoid antigen 1 ELISA KIT ,Mouse 230/240kDa ELISA KIT ,Mouse dystonia musculorum protein ELISA KIT ,Mouse hemidesmosomal plaque protein ELISA KIT ,Mouse trabeculin-beta ELISA KIT ,Mouse  Microtubule actin cross-linking factor 2 ELISA KIT

Intended use

This immunoassay kit allows for the in vitro quantitative determination ofMouse Dystonin concentrations in serum, Plasma,tissue homogenates and Cell culture supernates and Other biological fluids.

Test principle

The microtiter plate provided in this kit has been pre-coated with an antibody specific to Dystonin. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific forDystonin and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain Dystonin, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of Dystonin in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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