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Recombinant SMAD2 anticorps

Cet anticorps anti-SMAD2 est un anticorps Human Monoclonal détectant SMAD2 dans ELISA, ICC et PLA. Adapté pour Humain.
N° du produit ABIN7566450

Aperçu rapide pour Recombinant SMAD2 anticorps (ABIN7566450)

Antigène

Voir toutes SMAD2 Anticorps
SMAD2 (SMAD, Mothers Against DPP Homolog 2 (SMAD2))

Type d'anticorp

Recombinant Antibody

Reactivité

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Humain

Hôte

  • 250
  • 18
Human

Clonalité

  • 223
  • 45
Monoclonal

Conjugué

  • 123
  • 19
  • 13
  • 10
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  • 6
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Cet anticorp SMAD2 est non-conjugé

Application

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ELISA, Immunocytochemistry (ICC), Proximity Ligation Assay (PLA)

Clone

PAS4-G7
  • Fonction

    anti-SMAD2 (human), mAb (rec.) (PAS4-G7)

    Attributs du produit

    Recombinant Antibody. Recognizes human SMAD2. Applications: ELISA, ICC, PLA. Clone: PAS4-G7. Isotype: Human IgG1. Formulation: Liquid. In PBS. The TGF-beta signaling pathway regulates key cell fate decisions during embryonic development and in adult homeostasis. This pathway is deregulated in many pathological conditions, including cancer, autoimmunity and fibrotic diseases. TGF-beta functions as a tumor suppressor in early tumors, inhibiting progression through the cell cycle. TGF-beta binds a heterotetrameric cell surface complex composed of type I and II serine/threonine kinase TGF-beta receptors (TGFBRI and TGFBRII). Ligand binding causes receptor phosphorylation and transmission of the signal to a class of intracellular intermediates, the receptor-regulated SMAD proteins. The SMAD family is divided into three subclasses: receptor regulated SMADs, (SMADs 1, 2, 3, 5 and 8), the common partner, (SMAD4) that functions via its interaction to the various SMADs, and the inhibitory SMADs, (SMADs 6 and 7). TGF-beta signaling pathways engage two specific receptor-regulated SMAD proteins, the SMAD2 and SMAD3. The C-terminal MH2 domains of the receptor-regulated SMADs are phosphorylated by the intracellular kinase domain of TGF-beta receptors. The receptor-regulated SMADs then interact with SMAD4 and translocate to the nucleus, where they act as transcriptional regulators. Although TGF-beta signaling engages the above three SMAD proteins, SMAD2, SMAD3 and SMAD4, there is a dominant role of SMAD3 as a mediator of both physiological, homeostatic signaling and of pathophysiological perturbed signaling in all diseases. The SMAD proteins are central nodes in the mechanisms of cross-talk between the TGF-beta pathway and other signaling pathways, including the Notch and Wnt signaling pathways. The SMAD proteins regulate multiple cellular processes, such as cell proliferation, apoptosis and differentiation. SMAD7, also known as Mothers Against Decapentaplegic homolog 7 (MADH7), inhibits selected pathways by binding directly to cell-surface receptors and preventing the activation-induced phosphorylation of other SMAD subunits.

    The TGF-beta signaling pathway regulates key cell fate decisions during embryonic development and in adult homeostasis. This pathway is deregulated in many pathological conditions, including cancer, autoimmunity and fibrotic diseases. TGF-beta functions as a tumor suppressor in early tumors, inhibiting progression through the cell cycle. TGF-beta binds a heterotetrameric cell surface complex composed of type I and II serine/threonine kinase TGF-beta receptors (TGFBRI and TGFBRII). Ligand binding causes receptor phosphorylation and transmission of the signal to a class of intracellular intermediates, the receptor-regulated SMAD proteins. The SMAD family is divided into three subclasses: receptor regulated SMADs, (SMADs 1, 2, 3, 5 and 8), the common partner, (SMAD4) that functions via its interaction to the various SMADs, and the inhibitory SMADs, (SMADs 6 and 7). TGF-beta signaling pathways engage two specific receptor-regulated SMAD proteins, the SMAD2 and SMAD3. The C-terminal MH2 domains of the receptor-regulated SMADs are phosphorylated by the intracellular kinase domain of TGF-beta receptors. The receptor-regulated SMADs then interact with SMAD4 and translocate to the nucleus, where they act as transcriptional regulators. Although TGF-beta signaling engages the above three SMAD proteins, SMAD2, SMAD3 and SMAD4, there is a dominant role of SMAD3 as a mediator of both physiological, homeostatic signaling and of pathophysiological perturbed signaling in all diseases. The SMAD proteins are central nodes in the mechanisms of cross-talk between the TGF-beta pathway and other signaling pathways, including the Notch and Wnt signaling pathways. The SMAD proteins regulate multiple cellular processes, such as cell proliferation, apoptosis and differentiation. SMAD7, also known as Mothers Against Decapentaplegic homolog 7 (MADH7), inhibits selected pathways by binding directly to cell-surface receptors and preventing the activation-induced phosphorylation of other SMAD subunits.

    Purification

    Puified

    Pureté

    >95 % (SDS-PAGE)

    Immunogène

    Synthetic human SMAD2 peptide (aa234-254).

    Isotype

    IgG1
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    In PBS.

    Conseil sur la manipulation

    After opening, prepare aliquots and store at -20 °C.Avoid freeze/thaw cycles.Please handle under sterile conditions to avoid contamination.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Stable for at least 1 year after receipt when stored at -20°C.

    Stable for at least 1 week when stored at +4°C.

  • Antigène

    SMAD2 (SMAD, Mothers Against DPP Homolog 2 (SMAD2))

    Autre désignation

    SMAD2

    UniProt

    Q15796

    Pathways

    Cycle Cellulaire, Hormone Transport, Chromatin Binding, Protein targeting to Nucleus
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