ALX4 Antibody (Center)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| FC, WB, E |
---|---|
Primary Accession | Q9H161 |
Other Accession | O35137, Q4LAL6, NP_068745.2 |
Reactivity | Human |
Predicted | Bovine, Mouse |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 44241 Da |
Antigen Region | 249-275 aa |
Gene ID | 60529 |
---|---|
Other Names | Homeobox protein aristaless-like 4, ALX4, KIAA1788 |
Target/Specificity | This ALX4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 249-275 amino acids from the Central region of human ALX4. |
Dilution | WB~~1:1000 FC~~1:10~50 |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | ALX4 Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | ALX4 |
---|---|
Synonyms | KIAA1788 |
Function | Transcription factor involved in skull and limb development. Plays an essential role in craniofacial development, skin and hair follicle development. |
Cellular Location | Nucleus {ECO:0000255|PROSITE-ProRule:PRU00108, ECO:0000255|PROSITE-ProRule:PRU00138, ECO:0000269|PubMed:19692347} |
Tissue Location | Expression is likely to be restricted to bone. Found in parietal bone |
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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. [provided by RefSeq].
References
Jugessur, A., et al. PLoS ONE 5 (7), E11493 (2010) :
Tanzer, M., et al. PLoS ONE 5 (2), E9061 (2010) :
Kayserili, H., et al. Hum. Mol. Genet. 18(22):4357-4366(2009)
Chang, H., et al. J. Clin. Pathol. 62(10):908-914(2009)
Drenos, F., et al. Hum. Mol. Genet. 18(12):2305-2316(2009)
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