ALX4 anticorps

N° du produit ABIN7189784

Détail du produit anti-ALX4 anticorps

Antigène: ALX4 (ALX Homeobox 4 (ALX4))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALX4 est non-conjugé

Application: ELISA, Immunohistochemistry (IHC)

Réactivité croisée: Humain, Souris

Purification: Antigen affinity purification

Immunogène: Synthetic peptide of Human ALX4

Isotype: IgG

Information d'application

Indications d'application: ELISA:1:1000-1:2000, IHC:1:25-1:100,

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: -20 °C, 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 (ALX4 Produits)

Synonymes: anticorps im:7142878, anticorps zgc:162606, anticorps alx4, anticorps FND2, anticorps lst, anticorps ALX homeobox 4b, anticorps ALX homeobox 4a, anticorps ALX homeobox 4, anticorps aristaless-like homeobox 4, anticorps alx4b, anticorps alx4a, anticorps ALX4, anticorps 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