Human SELE(Selectin, Endothelium) ELISA Kit

 

Human SELE(Selectin, Endothelium) ELISA Kit

Size

96T

Catalog no.

ELK1013

Price

526 EUR

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Assay length

3h

Sensitivity

16pg/mL

Assay Type

Sandwich

Standard

2500pg/mL

Detection range

39-2500pg/mL

Test

ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED

Research Area

Signal transduction;CD & Adhesion molecule;Tumor immunity;Infection immunity;

Alternative Names

CD62E; CD62-E; E-Selectin; ELAM; ELAM1; ESEL; SEL-E; E-LAM; E-LAM1; E-SEL; LECAM2; Endothelial Leukocyte Adhesion Molecule 1; CD62 Antigen-Like Family Member E

Properties

E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,Human proteins, cDNA and human recombinants are used in human reactive ELISA kits and to produce anti-human mono and polyclonal antibodies. Modern humans (Homo sapiens, primarily ssp. Homo sapiens sapiens). Depending on the epitopes used human ELISA kits can be cross reactive to many other species. Mainly analyzed are human serum, plasma, urine, saliva, human cell culture supernatants and biological samples.

Test principle

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 Selectin, Endothelium (SELE). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Selectin, Endothelium (SELE). 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 Selectin, Endothelium (SELE), 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 Selectin, Endothelium (SELE) in the samples is then determined by comparing the O.D. of the samples to the standard curve.