ALX4 anticorps

N° du produit ABIN2716017

Détail du produit anti-ALX4 anticorps

Antigène: ALX4 (ALX Homeobox 4 (ALX4))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp ALX4 est non-conjugé

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

Attributs du produit: Homo sapiens ALX homeobox 4 (ALX4)

Purification: Purified from mouse ascites fluids by affinity chromatography

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

Clone: 2F2

Isotype: IgG1

Information d'application

Indications d'application: WB 1:1000, FLOW 1:100,

Commentaires:

The concentration of the product may vary between diferrent lots.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5-1.0 mg/mL

Buffer: PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.

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

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: 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.

Poids moléculaire: 44.1 kDa

ID gène: 60529

NCBI Accession: NM_021926

HGNC: 60529