Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

DTNA Antikörper

Dieses Maus Monoklonal-Antikörper erkennt spezifisch DTNA in WB, IF und FACS. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN2719779

Kurzübersicht für DTNA Antikörper (ABIN2719779)

Target

Alle DTNA Antikörper anzeigen
DTNA (Dystrobrevin alpha (DTNA))

Reaktivität

  • 17
  • 13
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 16
  • 7
Maus

Klonalität

  • 19
  • 4
Monoklonal

Konjugat

  • 18
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser DTNA Antikörper ist unkonjugiert

Applikation

  • 22
  • 14
  • 9
  • 8
  • 5
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)

Klon

1A2
  • Produktmerkmale

    Homo sapiens dystrobrevin, alpha (DTNA), transcript variant 5

    Aufreinigung

    Purified from mouse ascites fluids by affinity chromatography

    Immunogen

    Full length human recombinant protein of human DTNA (NP_116761) produced in HEK293T cell.

    Isotyp

    IgG2a
  • Applikationshinweise

    WB 1:2000, IF 1:100, FLOW 1:100

    Kommentare

    The concentration of the product may vary between diferrent lots.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.5-1.0 mg/mL

    Buffer

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C
  • Target

    DTNA (Dystrobrevin alpha (DTNA))

    Andere Bezeichnung

    DTNA

    Hintergrund

    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.

    Molekulargewicht

    58.7 kDa

    Gen-ID

    1837

    NCBI Accession

    NM_032979

    HGNC

    1837
Sie sind hier:
Chat with us!