Phospho-SMAD2 (Ser245/250/255) ELISA Kit

Basic information

Name

Phospho-SMAD2 (Ser245/250/255) ELISA Kit

size

100 assays

Catalog number

K4233-100

Price

1107 €

Extended information

Kit's other name

none

Species reactivity

Human

Storage condition

-20°C

Shipping condition

gel pack

Maximum time can be stored

12 months

Category

ELISA kit

Samples tested

Cell Lysates

Test

ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED

Applications

Quantitative measurement of Phospho-SMAD2 in human cell lysates

Kit's benefits

• Easy, convenient and time-saving method to measure the level of Phospho-SMAD2 (Ser245/250/255)

Properties

E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays

Highlights

• Detection method: Absorbance (450 nm) • Species reactivity: Human • Application: quantitative measurement of Phospho:SMAD2 (Ser245/250/255) in human cell lysates

Contents

• Microplate (Item A) coated with anti-pan SMAD2 antibody • Wash Buffer Concentrate (20x) (Item B) • Assay Diluent (5X) (Item E2) • Detection Antibody SMAD2 (Ser245/250/255) (Item C-1) • HRP-conjugated Anti-rabbit IgG (1000X) (Item D-1) • TMB One-Step Substrate Reagent (Item H) • Stop Solution (Item I) • Cell Lysate Buffer (2X) (Item J) • Positive Control JPMAS001-1 (Item K): lyophilized powder from Jurkat cell lysate

Kit's description

Phospho-SMAD2 (Ser245/250/255) ELISA kit is a very rapid, convenient and sensitive assay kit that can monitor the activation or function of important biological pathways in human, mouse and rat cell lysates. By determining phosphorylated SMAD2 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, mouse and rat phospho-SMAD2. An anti-pan SMAD2 antibody has been coated onto a 96-well plate. Samples are pipetted into the wells and SMAD2 present in a sample is bound to the wells by the immobilized antibody. The wells are washed and rabbit anti-SMAD2 (Ser245/250/255) antibody is used to detect phosphorylated SMAD2. After washing away unbound antibody, HRP-conjugated anti-rabbit IgG 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 SMAD2 (Ser245/250/255) bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.