| Description : |
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, Oct 2009] |
| Source : |
Wheat Germ |
| Species : |
Human |
| Tag : |
GST |
| Molecular Mass : |
45.3 kDa |
| AA Sequence : |
MNAETCVSYCESPAAAMDAYYSPVS QSREGSSPFRAFPGGDKFGTTFLSA AAKAQGFGDAKSRARYGAGQQDLAT PLESGAGARGSFNKFQPQPSTPQPQ PPPQPQPQQQQPQPQPPAQPHLYLQ RGACKTPPDGSLKLQEGSSGHSAAL QVPCYAKESSLGEPELPPDSDTVGM DSSYLSVKEAGVKGPQDRASSDLPS PLEKADSESNKGKKRRNRTTFTSYQ LEELEKVFQKTHYPDVYAREQLAMR TDLTEARVQVWFQNRRAKWRKRERF GQMQQVRTHFSTAYELPLLTRAENY AQIQNPSWLGNNGAASPVPACVVPC DPVPACMSPHAHPPGSGASSVTDFL SVSGAGSHVGQTHMGSLFGAASLSP GLNGYELNGEPDRKTSSIAALRMKA KEHSAAISWAT |
| Applications : |
Enzyme-linked Immunoabsorbent Assay; Western Blot (Recombinant protein); Antibody Production; Protein Array |
| Notes : |
Best use within three months from the date of receipt of this protein. |
| Storage : |
Store at -80 centigrade. Aliquot to avoid repeated freezing and thawing. |
| Storage Buffer : |
50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer. |
