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TAZ anticorps (Tafazzin) (C-Term) Primary Antibody

TAZ Reactivité: Humain IHC (p) Hôte: Lapin Polyclonal
N° du produit ABIN2854556
$509.08
Plus shipping costs $45.00
100 μL
local_shipping Destination: Etats-Unis
Envoi sous 3 à 4 jours ouvrables
  • Antigène
    Épitope
    C-Term
    Reactivité
    Humain
    Hôte
    Lapin
    Clonalité
    Polyclonal
    Conjugué
    Cet anticorp TAZ est non-conjugé
    Application
    Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
     Réactivité croisée
    Souris, Rat (Rattus), Lapin, Macaque rhésus, Chimpanzé
    Réactivité croisée (Details)
    Mouse (91 %), Rat (91 %), Rabbit (100 %), Rhesus Monkey (100 %), Chimpanzee (100 %)
    Attributs du produit
    Rabbit Polyclonal antibody to TAZ (tafazzin)
    TAZ antibody [C2C3], C-term
    Purification
    Purified by antigen-affinity chromatography.
    Immunogène
    Carrier-protein conjugated synthetic peptide encompassing a sequence within the C-terminus region of human TAZ. The exact sequence is proprietary.
    Isotype
    IgG
  • Indications d'application
    Suggested dilution Reference IHC (Formalin-fixed paraffin-embedded sections) 1:100-1:1000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceIHC (Formalin-fixed paraffin-embedded sections)1:100-1:1000*
    Commentaires

    Positive Control: Synthetic peptide: 1:8,000

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    1XPBS, 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.
  • Antigène
    Autre désignation
    TAZ (TAZ Antibody Extrait)
    Sujet
    This gene encodes a protein that is expressed at high levels in cardiac and skeletal muscle. Mutations in this gene have been associated with a number of clinical disorders including Barth syndrome, dilated cardiomyopathy (DCM), hypertrophic DCM, endocardial fibroelastosis, and left ventricular noncompaction (LVNC). Multiple transcript variants encoding different isoforms have been described. A long form and a short form of each of these isoforms is produced, the short form lacks a hydrophobic leader sequence and may exist as a cytoplasmic protein rather than being membrane-bound. Other alternatively spliced transcripts have been described but the full-length nature of all these transcripts is not known.

    Cellular Localization: Isoform 1: Membrane, Single-pass membrane protein , Isoform 2: Cytoplasm , Isoform 3: Membrane, Single-pass membrane protein , Isoform 4: Membrane, Single-pass membrane protein , Isoform 5: Membrane, Single-pass membrane protein , Isoform 6: Cytoplasm , I
    Poids moléculaire
    33 kDa
    ID gène
    6901
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