Human FLOT2(Flotillin 2) EIA Kit

Catalog no.

E-EL-H0388-96T

Size

96Test

Price

492 EUR

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Target Name

FLOT2

Target Species

Human

UNIProt ID

Q14254

Type

Sandwich

Sensitivity

0.38ng/mL

Detection Type

Colormetric

Detection Range

0.63~40ng/mL

Target Synonym

ECS-1, ECS1, ESA, ESA1, M17S1

Tested Sample Types

Serum, Plasma, Cell supernatant

Product Name

Human FLOT2(Flotillin 2) EIA Kit

Description

This ELISA test kit or EIA Enzyme immuno assay is an enzyme linked immuno assay supplied as coated 96 well plates with antigen or antibody and needs to be stored at +4°C.

Properties

MeSH E05 478 566 350 170 Enzyme-Linked Immunosorbent Assay,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

This EIA kit uses the Sandwich-EIA principle. The micro EIA plate provided in this kit has been pre-coated with an antibody specific to Human FLOT2. Standards or samples are added to the micro EIA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Human FLOT2 and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Human FLOT2, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Human FLOT2. You can calculate the concentration of Human FLOT2 in the samples by comparing the OD of the samples to the standard curve.