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DTNA anticorps (AA 240-480)

Cet anticorps anti-DTNA est un anticorps Lapin Polyclonal détectant DTNA dans WB. Adapté pour Humain.
N° du produit ABIN6139849

Aperçu rapide pour DTNA anticorps (AA 240-480) (ABIN6139849)

Antigène

Voir toutes DTNA Anticorps
DTNA (Dystrobrevin alpha (DTNA))

Reactivité

  • 16
  • 13
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 15
  • 7
Lapin

Clonalité

  • 18
  • 4
Polyclonal

Conjugué

  • 17
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp DTNA est non-conjugé

Application

  • 21
  • 14
  • 9
  • 8
  • 5
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 8
    • 5
    • 2
    • 2
    • 1
    • 1
    AA 240-480

    Séquence

    PVECSYCHSE SMMGFRYRCQ QCHNYQLCQD CFWRGHAGGS HSNQHQMKEY TSWKSPAKKL TNALSKSLSC ASSREPLHPM FPDQPEKPLN LAHIVDTWPP RPVTSMNDTL FSHSVPSSGS PFITRSSPPK DSEVEQNKLL ARAAPAFLKG KGIQYSLNVA DRLADEHVLI GLYVNMLRNN PSCMLESSNR LDEEHRLIAR YAARLAAESS SSQPPQQRSA PDISFTIDAN KQQRQLIAEL E

     Réactivité croisée

    Humain, Souris

    Attributs du produit

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein containing a sequence corresponding to amino acids 240-480 of human DTNA (NP_001381.2).

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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. Avoid freeze / thaw cycles.
  • Antigène

    DTNA (Dystrobrevin alpha (DTNA))

    Autre désignation

    DTNA

    Sujet

    The protein encoded by this gene belongs to the dystrobrevin subfamily of the dystrophin family. This protein is a component of the dystrophin-associated protein complex (DPC), which consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and alpha- and beta-dystrobrevin. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene.,DTNA,D18S892E,DRP3,DTN,DTN-A,LVNC1,Signal Transduction,Cell Biology & Developmental Biology,Cell Adhesion,Tight Junctions,Cytoskeleton,Neuroscience,Cell Type Marker,Neuron marker,Synapse marker,DTNA

    Poids moléculaire

    22 kDa/36 kDa/41-44 kDa/50 kDa/58-83 kDa

    ID gène

    1837

    UniProt

    Q9Y4J8
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