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ALX4 Antikörper

Der Kaninchen Polyklonal Anti-ALX4-Antikörper wurde für ELISA und IHC validiert. Er ist geeignet, ALX4 in Proben von Human zu detektieren.
Produktnummer ABIN7189784

Kurzübersicht für ALX4 Antikörper (ABIN7189784)

Target

Alle ALX4 Antikörper anzeigen
ALX4 (ALX Homeobox 4 (ALX4))

Reaktivität

  • 35
  • 11
  • 9
  • 6
  • 5
  • 4
  • 4
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 33
  • 3
Kaninchen

Klonalität

  • 33
  • 3
Polyklonal

Konjugat

  • 22
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser ALX4 Antikörper ist unkonjugiert

Applikation

  • 25
  • 14
  • 9
  • 3
  • 1
  • 1
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Kreuzreaktivität

    Human, Maus

    Aufreinigung

    Antigen affinity purification

    Immunogen

    Synthetic peptide of Human ALX4

    Isotyp

    IgG
  • Applikationshinweise

    ELISA:1:1000-1:2000, IHC:1:25-1:100,

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol

    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,-80 °C

    Informationen zur Lagerung

    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target

    ALX4 (ALX Homeobox 4 (ALX4))

    Andere Bezeichnung

    ALX4

    Hintergrund

    Background: This gene encodes a paired-like homeodomain transcription factor expressed in the mesenchyme of developing bones, limbs, hair, teeth, and mammary tissue. Mutations in this gene cause parietal foramina 2 (PFM2), an autosomal dominant disease characterized by deficient ossification of the parietal bones. Mutations in this gene also cause a form of frontonasal dysplasia with alopecia and hypogonadism, suggesting a role for this gene in craniofacial development, mesenchymal-epithelial communication, and hair follicle development. Deletion of a segment of chromosome 11 containing this gene, del(11)(p11p12), causes Potocki-Shaffer syndrome (PSS), a syndrome characterized by craniofacial anomalies, mental retardation, multiple exostoses, and genital abnormalities in males. In mouse, this gene has been shown to use dual translation initiation sites located 16 codons apart.

    Aliases: Alx4 antibody, ALX4_HUMAN antibody, Aristaless like homeobox 4 antibody, CRS5 antibody, FND2 antibody, FPP antibody, homeobox protein aristaless like 4 antibody, Homeobox protein aristaless-like 4 antibody, homeodomain transcription factor ALX4 antibody, KIAA1788 antibody, PFM1 antibody, PFM2 antibody

    UniProt

    Q9H161
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