Phospho-LSD1 (S112) and Total LSD1 ELISA Kit

Blue ice

Cell Lysates
Tissue Lysates

Colorimetric

96-well Microplate

Pre-Coated 96-well Strip Microplate
Wash Buffer
Anti-Phospho Antibody
Anti-Pan Antibody
HRP-Conjugated Secondary Antibody
Streptavidin-Conjugated HRPli id="">
Assay Diluent
TMB One-Step Substrate
Stop Solution
Lysis Buffer
Positive Control Sample

Prepare all reagents and samples as instructed in the manual.
Add 100 µl of sample or positive control to each well.
Incubate 2.5 h at RT or O/N at 4°C.
Add 100 µl of prepared primary antibody to each well.
Incubate 1 h at RT.
Add 100 µl of prepared 1
X HRP-Streptavidin to each well.
Incubate 1 h at RT.
Add 100 µl of TMB One-Step Substrate Reagent to each well.
Incubate 30 min at RT.
Add 50 µl of Stop Solution to each well.
Read at 450 nm immediately.

Lysine-specific histone demethylase 1A (EC 1.-.-.-) (BRAF35-HDAC complex protein BHC110) (Flavin-containing amine oxidase domain-containing protein 2)

The antibody pair provided in this kit recognizes human and mouse LSD1 phosphorylated at Serine-112 and total LSD1.

RayBio® Phospho-LSD1 (S112) and Total LSD1 ELISA kit is a very rapid, convenient and sensitive assay kit that can monitor the activation or function of important biological pathways in human cell lysates. By determining phosphorylated LSD1 protein in your experimental model system, you can verify pathway activation in your cell lysates. You can simultaneously measure numerous different cell lysates without spending excess time and effort in performing a Western Blotting analysis.This Sandwich ELISA kit is an in vitro enzyme-linked immunosorbent assay for the measurement of human phospho-LSD1 and total LSD1. An anti-pan LSD1 antibody has been coated onto a 96-well plate. Samples are pipetted into the wells and LSD1 present in a sample is bound to the wells by the immobilized antibody. The wells are washed and biotinylated anti-LSD1 (S112) antibody is used to detect phosphorylated LSD1 or biotinylated anti-LSD1 antibody is used to detect pan LSD1. After washing away unbound antibody, HRP-conjugated Streptavidin is pipetted to the wells. The wells are again washed, a TMB substrate solution is added to the wells and color develops in proportion to the amount of LSD1 (S112) or pan LSD1 bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.

Jurkat cells were treated with Calyculin A and Pervanadate. Cell lysates were analyzed using this phosphoELISA and Western Blot.