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

ALX4 Antikörper

ALX4 Reaktivität: Human, Maus, Ratte WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7260673
  • Target Alle ALX4 Antikörper anzeigen
    ALX4 (ALX Homeobox 4 (ALX4))
    Reaktivität
    • 38
    • 10
    • 7
    • 6
    • 5
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    Human, Maus, Ratte
    Wirt
    • 36
    • 4
    Kaninchen
    Klonalität
    • 36
    • 4
    Polyklonal
    Konjugat
    • 21
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser ALX4 Antikörper ist unkonjugiert
    Applikation
    • 28
    • 18
    • 13
    • 4
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human ALX4 (NP_068745.2).
    Isotyp
    IgG
    Top Product
    Discover our top product ALX4 Primärantikörper
  • Applikationshinweise
    WB 1:500-1:2000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    ALX4 (ALX Homeobox 4 (ALX4))
    Andere Bezeichnung
    ALX4 (ALX4 Produkte)
    Synonyme
    im:7142878 antikoerper, zgc:162606 antikoerper, alx4 antikoerper, FND2 antikoerper, lst antikoerper, ALX homeobox 4b antikoerper, ALX homeobox 4a antikoerper, ALX homeobox 4 antikoerper, aristaless-like homeobox 4 antikoerper, alx4b antikoerper, alx4a antikoerper, ALX4 antikoerper, Alx4 antikoerper
    Hintergrund
    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.
    Molekulargewicht

    Observed_MW: 44 kDa

    Calculated_MW: 44 kDa

    Gen-ID
    60529
    UniProt
    Q9H161
Sie sind hier:
Kundenservice