PRODUCT DESCRIPTION
Conjugation :
UnconjugateHost :
RabbitClonality :
Polyclonal AntibodyGene symbol :
ALX4Immunogen :
A synthetic peptide of human ALX4Synonym :
CRS5;FND2Isotype :
IgGGene ID :
60529Clone No :
Swiss Port :
Q9H161Molecular weight :
44kDaPurification :
Affinity purificationReactivity :
Human MouseApplication :
WBRecommended dilution :
WB 1:200-1000.Subcellular location :
Storage :
Store at -20°C. Avoid freeze / thaw cycles.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.RELATED PRODUCTS
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REFERENCE LIBRARY
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