Human Tsukushin,TSKU ELISA KIT

Starting at: $696.00

  • Model: ELI-29058h
  • 20 Units in Stock
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Human Tsukushin, TSKU ELISA KIT

96 Tests

Operating instructions

 

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

 

Synonyms

TSKU,tsukushi,Tsukushin, small leucine rich proteoglycan; tsukushi small leucine rich proteoglycan homolog; tsukushi homolog; E2IG4; LRRC54; TSK; E2-induced gene 4 protein; leucine rich repeat containing 54; leucine-rich repeat-containing protein 54,

 

Search name

Human TSKU ELISA KIT ,Human tsukushi ELISA KIT ,Human Tsukushin ELISA KIT ,Human  small leucine rich proteoglycan ELISA KIT ,Human tsukushi small leucine rich proteoglycan homolog ELISA KIT ,Human tsukushi homolog ELISA KIT ,Human E2IG4 ELISA KIT ,Human LRRC54 ELISA KIT ,Human TSK ELISA KIT ,Human E2-induced gene 4 protein ELISA KIT ,Human leucine rich repeat containing 54 ELISA KIT ,Human leucine-rich repeat-containing protein 54 ELISA KIT

 

Intended use

This immunoassay kit allows for the in vitro quantitative determination of Human Tsukushin concentrations in serum, plasma, tissue homogenates, cell culture supernates, and other biological fluids.

 

Test principle

The ELISA is based on the competitive binding enzyme immunoassaytechnique. The microtiter plate provided in this kit has been pre-coated with an antibody specific toTsukushi, During the reaction,Tsukushiin the sample or standard competes with a fixed amount of biotin-labeledTsukushi for sites on a pre-coated Monoclonal antibody specific to Tsukushi. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Thena TMB substrate solution is added to each well. 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 Tsukushi in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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