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ALPL anticorps (Center)

Cet anticorps Lapin Polyclonal détecte spécifiquement ALPL dans WB, IHC et IHC (p). Il présente une réactivité envers Humain, Souris et Mouton et a été mentionné dans 1 publication.
N° du produit ABIN2854870

Aperçu rapide pour ALPL anticorps (Center) (ABIN2854870)

Antigène

Voir toutes ALPL Anticorps
ALPL (Alkaline Phosphatase, Liver/bone/kidney (ALPL))

Reactivité

  • 86
  • 52
  • 20
  • 7
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Mouton

Hôte

  • 86
  • 22
  • 1
  • 1
Lapin

Clonalité

  • 85
  • 25
Polyclonal

Conjugué

  • 66
  • 9
  • 7
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ALPL est non-conjugé

Application

  • 76
  • 39
  • 35
  • 18
  • 17
  • 14
  • 13
  • 13
  • 13
  • 12
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Épitope

    • 16
    • 9
    • 8
    • 8
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Center

     Réactivité croisée

    Souris, Chat, Chien, Rat (Rattus), Boeuf (Vache)

    Réactivité croisée (Details)

    Mouse (91 %), Cat (90 %), Dog (89 %), Rat (91 %), Bovine (89 %)

    Attributs du produit

    Rabbit polyclonal antibody to alkaline phosphatase (liver/bone/kidney) (alkaline phosphatase, liver/bone/kidney)
    Alkaline Phosphatase (Tissue Non-Specific) antibody

    Purification

    Purified by antigen-affinity chromatography.

    Immunogène

    Recombinant protein encompassing a sequence within the center region of human Alkaline Phosphatase (Tissue Non-Specific). The exact sequence is proprietary.

    Isotype

    IgG
  • Indications d'application

    Suggested dilution Reference Immunohistochemistry Assay-dependent dilution IHC (Formalin-fixed paraffin-embedded sections) 1:100-1:1000* Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceImmunohistochemistryAssay-dependent dilution IHC (Formalin-fixed paraffin-embedded sections)1:100-1:1000* Western blot1:500-1:3000*

    Commentaires

    Positive Control: HeLa , HepG2 , Molt-4 , Raji

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.48 mg/mL

    Buffer

    0.1M Tris, 0.1M Glycine, 10 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.

    Agent conservateur

    Thimerosal (Merthiolate)

    Précaution d'utilisation

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Agustina, Asyifa, Aziz, Hernowo: "The Role of Osteocalcin and Alkaline Phosphatase Immunohistochemistry in Osteosarcoma Diagnosis." dans: Pathology research international, Vol. 2018, pp. 6346409, (2018) (PubMed).

  • Antigène

    ALPL (Alkaline Phosphatase, Liver/bone/kidney (ALPL))

    Autre désignation

    Alkaline Phosphatase (Liver/bone/kidney)

    Sujet

    There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The first three are located together on chromosome 2, while the tissue non-specific form is located on chromosome 1. The product of this gene is a membrane bound glycosylated enzyme that is not expressed in any particular tissue and is, therefore, referred to as the tissue-nonspecific form of the enzyme. The exact physiological function of the alkaline phosphatases is not known. A proposed function of this form of the enzyme is matrix mineralization, however, mice that lack a functional form of this enzyme show normal skeletal development. This enzyme has been linked directly to hypophosphatasia, a disorder that is characterized by hypercalcemia and includes skeletal defects. The character of this disorder can vary, however, depending on the specific mutation since this determines age of onset and severity of symptoms. Alternatively spliced transcript variants, which encode the same protein, have been identified for this gene.

    Cellular Localization: Cell membrane, Lipid-anchor , GPI-anchor

    Poids moléculaire

    57 kDa

    ID gène

    249
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