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SMAD1 Kit ELISA

Ce kit ELISA Colorimetric est conçu pour la mesure quantitative de Humain SMAD1.
N° du produit ABIN2747895

Aperçu rapide pour SMAD1 Kit ELISA (ABIN2747895)

Antigène

Voir toutes SMAD1 Kits ELISA
SMAD1 (SMAD, Mothers Against DPP Homolog 1 (SMAD1))

Épitope

pSer463, pSer465, total

Reactivité

  • 9
  • 7
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Méthode de détection

Colorimetric

Type de méthode

Sandwich ELISA

Application

ELISA

Type d'échantillon

Cell Lysate, Tissue Lysate
  • Fonction

    Human Phospho-SMAD1 (SER463/465) and Total SMAD1 Kit. This assay semi-quantitatively measures phophorylated SMAD1 (Ser463/465) and Total SMAD1 in lysate samples.

    Analytical Method

    Semi-Quantitative

    Specificité

    The antibody pair provided in this kit recognizes human SMAD1 phosphorylated at site Serine-463/465 and Total SMAD1.

    Attributs du produit

    • Simultaneously measure Phosphorylated protein and pan protein in one experiment (for normalization purpose)
    • Screen numerous different cell lysates without performing a Western Blot analysis
    • Minimal hands-on time, convenient, and non-radioactive material

    Ingrédients

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

    Matériel non inclus

    • Distilled or deionized water
    • 100 mL and 1 liter graduated cylinders
    • Tubes to prepare sample dilutions
    • Protease and Phosphatase inhibitors
    • Precision pipettes to deliver 2 μL to 1 mL volumes
    • Adjustable 1-25 mL pipettes for reagent preparation
    • Benchtop rocker or shaker
    • Microplate reader capable of measuring absorbance at 450 nm
  • Volume d'échantillon

    100 μL

    Plaque

    Pre-coated

    Protocole

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

    Procédure de l'essai

    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 1X 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.

    Restrictions

    For Research Use only
  • Stock

    -20 °C

    Stockage commentaire

    Upon receipt, the kit should be stored at -20 °C. Please use within 6 months from the date of shipment. After initial use, Wash Buffer Concentrate (Item B), Assay Diluent (Item E), TMB One-Step Substrate Reagent (Item H), HRP-Streptavidin (Item G), Stop Solution (Item I) and Cell Lysate Buffer (Item J) should be stored at 4 °C to avoid repeated freeze-thaw cycles. Return unused wells to the pouch containing desiccant pack, reseal along entire edge and store at -20 °C. Reconstituted Positive Control (Item K) should be stored at -70 °C.

    Date de péremption

    6 months
  • Antigène Voir toutes SMAD1 Kits ELISA

    SMAD1 (SMAD, Mothers Against DPP Homolog 1 (SMAD1))

    Autre désignation

    SMAD1

    Sujet

    Mothers against decapentaplegic homolog 1 (SMAD1) phosphorylated at Serine-463/465 and Total SMAD1

    ID gène

    4086

    UniProt

    Q15797

    Pathways

    Stem Cell Maintenance, Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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