ELISA Kit for Induced Myeloid Leukemia Cell Differentiation Protein Mcl-1 (MCL1)

Format

48T, 96T, 96T×5, 96T×10, 96T×100

Detection range

0.156-10ng/mL

Application

Enzyme-linked immunosorbent assay for Antigen Detection.

Organism species

Mus musculus (Mouse)

Sensitivity

The minimum detectable dose of this kit is typically less than 0.063ng/mL

Sample type

Serum, plasma, tissue homogenates and other biological fluids

Assay length

3h

Method

Double-antibody Sandwich

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 Induced Myeloid Leukemia Cell Differentiation Protein Mcl-1 (MCL1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Induced Myeloid Leukemia Cell Differentiation Protein Mcl-1 (MCL1). 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 Induced Myeloid Leukemia Cell Differentiation Protein Mcl-1 (MCL1), 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 Induced Myeloid Leukemia Cell Differentiation Protein Mcl-1 (MCL1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Alternative Names

EAT; MCL1L; MCL1S; BCL2L3; TM; Myeloid Cell Leukemia Sequence 1, Bcl2 Related; Bcl-2-like protein 3; Bcl-2-related protein EAT/mcl1; mcl1/EAT

Item Name

Induced Myeloid Leukemia Cell Differentiation Protein Mcl-1

Research Area

Tumor immunity;

Reference