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SOD1 anticorps

Cet anticorps anti-SOD1 est un anticorps Lapin Polyclonal détectant SOD1 dans WB, IHC (p) et IF (p). Adapté pour Humain, Souris, Rat et Boeuf (Vache). Ce Primary Antibody a été cité dans 1 publication.
N° du produit ABIN737346

Aperçu rapide pour SOD1 anticorps (ABIN737346)

Antigène

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

Reactivité

  • 182
  • 102
  • 92
  • 38
  • 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, Souris, Rat, Boeuf (Vache)

Hôte

  • 194
  • 42
  • 7
  • 4
  • 2
  • 2
  • 1
Lapin

Clonalité

  • 198
  • 53
Polyclonal

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
  • 14
  • 13
  • 13
  • 7
  • 6
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  •  Réactivité croisée

    Boeuf (Vache), Humain, Souris, Rat

    Purification

    Purified by Protein A.

    Immunogène

    KLH conjugated synthetic peptide derived from mouse SOD1

    Isotype

    IgG
  • Indications d'application

    WB(1:100-500)
    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % 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.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C for 12 months.

    Date de péremption

    12 months
  • Li, He, Zhang, Miao: "Differential proteome and gene expression reveal response to carbon ion irradiation in pubertal mice testes." dans: Toxicology letters, Vol. 225, Issue 3, pp. 433-44, (2014) (PubMed).

  • Antigène

    SOD1 (Superoxide Dismutase 1, Soluble (SOD1))

    Autre désignation

    SOD1

    Sujet

    Synonyms: Superoxide Dismutase 1, ALS 1, ALS, ALS1, Amyotrophic lateral sclerosis 1 adult, Amyotrophic lateral sclerosis 1, Cu/Zn SOD, Cu/Zn superoxide dismutase, Homodimer, Indophenoloxidase A, IPOA, Mn superoxide dismutase, SOD 1, SOD, SOD soluble, SOD1, SOD2, SODC, Soluble indophenoloxidase A, Superoxide dismutase 1, Superoxide dismutase 1 soluble, Superoxide dismutase Cu Zn, Superoxide dismutase cystolic, SODC_HUMAN, Superoxide dismutase [Cu-Zn], hSod1, Ipo1, SODC, Ipo-1, Sod-1, CuZnSOD, Cu/Zn-SOD, MGC107553, B430204E11Rik, superoxide-dimutase-1.

    Background: SOD1 encoded by this gene binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body. The encoded isozyme is a soluble cytoplasmic protein, acting as a homodimer to convert naturally-occuring but harmful superoxide radicals to molecular oxygen and hydrogen peroxide. The other isozyme is a mitochondrial protein. Mutations in this gene have been implicated as causes of familial amyotrophic lateral sclerosis. Rare transcript variants have been reported for this gene. Mutations in the copper/ zinc superoxide dismutase (SOD1) gene are associated with 15- 20 % of the familial forms of motoneuron disease. This 153 amino acid metalloenzyme is expressed in virtually all cells of all organisms above bacteria and is highly conserved across species, although some minor variations do occur. The incorporation of the mutated form of the SOD1 human gene into a transgenic mouse leads to the onset of the disease that closely resembles the human condition. These animals become weak at about 2-4 months of age and rapidly lose function, which results in death 4- 6 weeks later.

    Poids moléculaire

    17kDa

    ID gène

    20655

    Pathways

    Sensory Perception of Sound, Transition Metal Ion Homeostasis
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