Human Programmed cell death protein 1,PDCD1 ELISA Kit

Starting at: $696.00

  • Model: ELA-E0515h
  • 20 Units in Stock
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Human Programmed cell death protein 1, PDCD1 ELISA Kit

96 Tests

Operating instruction

 

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

 

Synonyms

PDCD1,CD279; PD-1; PD1; SLEB2; hPD-1; hPD-l; hSLE1; programmed cell death protein 1; protein PD-1; systemic lupus erythematosus susceptibility 2; programmed cell death 1, Programmed cell death protein 1,Protein PD-1,mPD-1,

 

Search name

Human PDCD1 ELISA KIT ,Human CD279 ELISA KIT ,Human PD-1 ELISA KIT ,Human PD1 ELISA KIT ,Human SLEB2 ELISA KIT ,Human hPD-1 ELISA KIT ,Human hPD-l ELISA KIT ,Human hSLE1 ELISA KIT ,Human programmed cell death protein 1 ELISA KIT ,Human protein PD-1 ELISA KIT ,Human systemic lupus erythematosus susceptibility 2 ELISA KIT ,Human programmed cell death 1 ELISA KIT ,Human  Programmed cell death protein 1 ELISA KIT ,Human Protein PD-1 ELISA KIT ,Human mPD-1 ELISA KIT

 

Intended use

This immunoassay kit allows for the in vitro quantitative determination of human programmed cell death protein 1,hPD-1 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 hPD-1. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for hPD-1 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 hPD-1, 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 hPD-1 in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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