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ATM anticorps (pSer1981)

L’anticorps anti-ATM Polyclonal Mouton est utilisé pour la détection de ATM dans des échantillons de Humain. Il a été validé pour WB et EIA.
N° du produit ABIN401482
1.147,69 €
Plus frais de livraison 40,00 € et TVA
0.1 mg
Destination: France
Envoi sous 17 jours ouvrables

Aperçu rapide pour ATM anticorps (pSer1981) (ABIN401482)

Antigène

Voir toutes ATM Anticorps
ATM (Ataxia Telangiectasia Mutated (ATM))

Reactivité

  • 195
  • 83
  • 35
  • 3
  • 1
  • 1
Humain

Hôte

  • 163
  • 27
  • 5
  • 1
Mouton

Clonalité

  • 121
  • 75
Polyclonal

Conjugué

  • 91
  • 11
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 5
  • 5
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
Cet anticorp ATM est non-conjugé

Application

  • 114
  • 71
  • 65
  • 52
  • 50
  • 47
  • 41
  • 39
  • 28
  • 25
  • 8
  • 7
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Épitope

    • 44
    • 16
    • 15
    • 13
    • 7
    • 7
    • 7
    • 7
    • 7
    • 6
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    pSer1981

    Specificité

    This antibody is directed against ATM.

    Purification

    Affinity chromatography

    Immunogène

    Synthetic peptide corresponding to a region near serine 1981 of human ATM conjugated to KLH using maleimide

    Isotype

    IgG
  • Indications d'application

    ELISA: 1/2,000 - 1/10,000. Western Blot: 1/500 - 1/2,000.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.0 mg/mL (by UV absorbance at 280 nm)

    Buffer

    0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2 containing 0.01 % (w/v) Sodium Azide

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    -20 °C
  • Antigène

    ATM (Ataxia Telangiectasia Mutated (ATM))

    Autre désignation

    ATM

    Sujet

    ATM, the gene mutated in the hereditary disease ataxia-telangiectasia, codes for a protein kinase that acts as a master regulator of cellular responses to DNA double-strand breaks. ATM is normally inactive and the question of how it is activated in the event of DNA damage (due to ionizing radiation (IR) for instance) is central to understanding its function. ATM protein is present in undamaged cells as an inactive dimer. Low doses of ionizing radiation, which induce only a few DNA breaks, activate at least half of the total ATM protein present, possibly in response to changes in chromatin structure. The ATM gene encodes a 370- kDa protein that belongs to the phosphoinositide 3-kinase (PI(3)K) superfamily, but phosphorylates proteins rather than lipids. The 350-amino-acid kinase domain at the carboxy terminus of this large protein is the only segment of ATM with an assigned function. Exposure of cells to IR triggers ATM kinase activity and this function is required for arrests in G1, S and G2 phases of the cell cycle. Several substrates of the ATM kinase participate in these IR-induced cell-cycle arrests. These include p53, Mdm2 and Chk2 in the G1 checkpoint, Nbs1, Brca1, FancD2 and SMC1 in the transient IR-induced S-phase arrest, and Brca1 and hRad17 in the G2/M checkpoint. This antibody is similar to the rabbit host antibody discussed by Bakkenist, C. J. & Kastan, M. B. in Nature 421, 499-506 (2003).Synonyms: A-T mutated, ATDC, Ataxia telangiectasia mutated, Serine-protein kinase ATM, TEL1, TELO1

    ID gène

    472

    NCBI Accession

    NP_000042

    UniProt

    Q13315

    Pathways

    Signalisation p53, Apoptose, Réparation de l'ADN, Inositol Metabolic Process, Positive Regulation of Response to DNA Damage Stimulus
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