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NK2 Homeobox 5 Antikörper (AA 82-111)

Der Kaninchen Polyklonal Anti-NK2 Homeobox 5-Antikörper wurde für WB validiert. Er ist geeignet, NK2 Homeobox 5 in Proben von Human und Maus zu detektieren.
Produktnummer ABIN1538648

Kurzübersicht für NK2 Homeobox 5 Antikörper (AA 82-111) (ABIN1538648)

Target

Alle NK2 Homeobox 5 (NKX2-5) Antikörper anzeigen
NK2 Homeobox 5 (NKX2-5)

Reaktivität

  • 41
  • 19
  • 7
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Maus

Wirt

  • 42
  • 8
  • 1
Kaninchen

Klonalität

  • 44
  • 7
Polyklonal

Konjugat

  • 41
  • 3
  • 2
  • 2
  • 2
  • 1
Dieser NK2 Homeobox 5 Antikörper ist unkonjugiert

Applikation

  • 43
  • 29
  • 8
  • 6
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)

Klon

RB36777
  • Bindungsspezifität

    • 6
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 82-111

    Aufreinigung

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This NKX2-5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 82-111 amino acids from the Central region of human NKX2-5.

    Isotyp

    Ig Fraction
  • Applikationshinweise

    WB: 1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    Informationen zur Lagerung

    NKX2-5 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Haltbarkeit

    6 months
  • Target

    NK2 Homeobox 5 (NKX2-5)

    Andere Bezeichnung

    NKX2-5

    Hintergrund

    This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants.

    Molekulargewicht

    34918

    Gen-ID

    1482

    NCBI Accession

    NP_001159647, NP_001159648, NP_004378

    UniProt

    P52952

    Pathways

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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