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FUNDC2 Antikörper

Der Kaninchen Polyklonal Anti-FUNDC2-Antikörper wurde für ELISA und IHC validiert. Er ist geeignet, FUNDC2 in Proben von Human zu detektieren.
Produktnummer ABIN7246850

Kurzübersicht für FUNDC2 Antikörper (ABIN7246850)

Target

Alle FUNDC2 Antikörper anzeigen
FUNDC2 (FUN14 Domain Containing 2 (FUNDC2))

Reaktivität

  • 15
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 14
  • 3
Kaninchen

Klonalität

  • 15
  • 2
Polyklonal

Konjugat

  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser FUNDC2 Antikörper ist unkonjugiert

Applikation

  • 10
  • 4
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Antigen affinity purification

    Immunogen

    Fusion protein of human FUNDC2

    Isotyp

    IgG
  • Applikationshinweise

    IHC 1:50-1:300, ELISA 1:5000-1:10000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.72 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    FUNDC2 (FUN14 Domain Containing 2 (FUNDC2))

    Andere Bezeichnung

    FUNDC2

    Hintergrund

    FUNDC2 (FUN14 domain-containing protein 2), also known as HCC-3 (cervical cancer proto-oncogene 3 protein), HCBP6 (hepatitis C virus core-binding protein 6) or DC44, is a 189 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC2 maps to human chromosome Xq28. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

    UniProt

    Q9BWH2
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