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SOD1 anticorps (AA 14-148)

L’anticorps Souris Monoclonal anti-SOD1 a été validé pour WB et IHC (f). Il convient pour détecter SOD1 dans des échantillons de Humain.
N° du produit ABIN7126948

Aperçu rapide pour SOD1 anticorps (AA 14-148) (ABIN7126948)

Antigène

Voir toutes SOD1 Anticorps
SOD1 (Superoxide Dismutase 1, Soluble (SOD1))

Reactivité

  • 182
  • 103
  • 93
  • 39
  • 26
  • 16
  • 14
  • 14
  • 14
  • 12
  • 10
  • 9
  • 9
  • 9
  • 9
  • 9
  • 5
  • 4
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 195
  • 41
  • 7
  • 4
  • 2
  • 2
  • 1
Souris

Clonalité

  • 199
  • 52
Monoclonal

Conjugué

  • 107
  • 31
  • 23
  • 13
  • 9
  • 9
  • 7
  • 7
  • 7
  • 7
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SOD1 est non-conjugé

Application

  • 215
  • 125
  • 121
  • 61
  • 60
  • 52
  • 31
  • 18
  • 15
  • 14
  • 13
  • 7
  • 6
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Formalin-fixed Sections) (IHC (f))
  • Épitope

    • 34
    • 23
    • 16
    • 16
    • 8
    • 8
    • 7
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 14-148

    Specificité

    Cu-Zn superoxide dismutase-1 (SOD-1) is a well-characterized cytosolic scavenger of oxygen free radicals that requires copper and zinc binding to potentiate its enzymatic activity. Enzymatically, SOD-1 facilitates the dismutation of oxygen radicals to hydrogen peroxide and also catalyzes pro-oxidant reactions, which include the peroxidase activity and hydroxyl radical generating activity. SOD-1 is ubiquitously expressed in somatic cells and functions as a homodimer. Defects in the gene encoding SOD-1 have been implicated in the progression of neurological diseases, including amyotrophic lateral sclerosis (ALS), a neurodegenerative disease characterized by the loss of spinal motor neurons, Down syndrome and Alzheimer s disease. In familial ALS, several mutations in SOD-1 predominate, resulting in the loss of zinc binding, the loss of scavenging activity of SOD-1, and correlate with an increase in neurotoxicity and motor neuron death.

    Réactivité croisée (Details)

    Human.

    Purification

    1.0mg/ml of Ab purified from Bioreactor by Protein A/G.

    Immunogène

    Recombinant fragment (around aa14-148) of human SOD1 (exact sequence is proprietary)

    Isotype

    IgG1
  • Indications d'application

    Known_Application: Western Blot (1-2 μg/mL), ,Immunohistochemistry (Formalin-fixed) (1-2 μg/mL for 30 minutes at RT),(Staining of formalin-fixed tissues requires heating tissue sections in 10 mM Tris with 1 mM EDTA, pH 9.0, for 45 min at 95 °C followed by cooling at RT for 20 minutes),Optimal dilution for a specific application should be determined.

    Positive_Control: LNCaP, JEG-3 or Jurkat cells. Human breast or ovarian carcinoma.

    Restrictions

    For Research Use only
  • Concentration

    1.0 mg/mL

    Buffer

    Prepared in 10 mM PBS, WITHOUT BSA and Azide.

    Agent conservateur

    Azide free

    Stock

    -20 °C,-80 °C

    Stockage commentaire

    Antibody without azide - store at -20 to -80 °C. Antibody is stable for 24 months. Non-hazardous.

    Date de péremption

    24 months
  • Antigène

    SOD1 (Superoxide Dismutase 1, Soluble (SOD1))

    Autre désignation

    SOD1

    Sujet

    Amyotrophic lateral sclerosis 1 (ALS1), Cu/Zn SOD, Cu/Zn Superoxide Dismutase, Epididymis Secretory Protein Li 44, Indophenoloxidase A (IPOA), Superoxide Dismutase [Cu-Zn], Superoxide Dismutase 1 (SOD1),Superoxide Dismutase 1 (SOD1) (Antioxidant Enzyme)
    Cellular localisation: Cytoplasm

    Poids moléculaire

    16kDa

    ID gène

    6647, 443914

    UniProt

    P00441

    Pathways

    Sensory Perception of Sound, Transition Metal Ion Homeostasis
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