Human VMAT2(Vesicular Monoamine Transporter 2) ELISA Kit

 

Human VMAT2(Vesicular Monoamine Transporter 2) ELISA Kit

Size

96T

Catalog no.

ELK4439

Price

608 EUR

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Assay length

3h

Standard

10ng/mL

Assay Type

Sandwich

Sensitivity

0.055ng/mL

Detection range

0.156-10ng/mL

Research Area

Signal transduction;

Test

ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED

Alternative Names

SLC18A2; SVMT; SVAT; Solute Carrier Family 18 Member 2,Vesicular Monoamine; Monoamine transporter; Synaptic vesicular amine transporter

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 Vesicular Monoamine Transporter 2 (VMAT2). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Vesicular Monoamine Transporter 2 (VMAT2). 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 Vesicular Monoamine Transporter 2 (VMAT2), 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 Vesicular Monoamine Transporter 2 (VMAT2) in the samples is then determined by comparing the O.D. of the samples to the standard curve.