ALX4 anticorps

N° du produit ABIN7189784

L’anticorps Lapin Polyclonal anti-ALX4 a été validé pour ELISA et IHC. Il convient pour détecter ALX4 dans des échantillons de Humain.

Aperçu rapide pour ALX4 anticorps (ABIN7189784)

Antigène: ALX4 (ALX Homeobox 4 (ALX4))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALX4 est non-conjugé

Application: ELISA, Immunohistochemistry (IHC)

Détail du produit anti-ALX4 anticorps

Fonction: ALX4 Antibody

Réactivité croisée: Souris

Purification: Antigen affinity purification

Immunogène: Synthetic peptide of Human ALX4

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer:  pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C,-80 °C

Stockage commentaire: Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Détails sur ALX4

Antigène: ALX4 (ALX Homeobox 4 (ALX4))

Autre désignation: ALX4

Sujet:

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