ALX4 Antikörper

Produktnummer ABIN2716017

Produktdetails anti-ALX4 Antikörper

Target: ALX4 (ALX Homeobox 4 (ALX4))

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser ALX4 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Flow Cytometry (FACS)

Produktmerkmale: Homo sapiens ALX homeobox 4 (ALX4)

Aufreinigung: Purified from mouse ascites fluids by affinity chromatography

Immunogen: Full length human recombinant protein of human ALX4(NP_068745) produced in HEK293T cell.

Klon: 2F2

Isotyp: IgG1

Anwendungsinformationen

Applikationshinweise: WB 1:1000, FLOW 1:100,

Kommentare:

The concentration of the product may vary between diferrent lots.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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

Details zu ALX4

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: 44.1 kDa

Gen-ID: 60529

NCBI Accession: NM_021926

HGNC: 60529