Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Sequence of this protein is as follows: PVIPQQPMMP VPGQHSMTPI QHHQPNLPPP AQQPYQPQPV QPQPHQPMQP QPPVHPMQPL PPQPPLPPMF PMQPLPPMLP DLTLEAWPST DKTKREEVD
This gene encodes a member of the amelogenin family of extracellular matrix proteins. Amelogenins are involved in biomineralization during tooth enamel development. Mutations in this gene cause X-linked amelogenesis imperfecta. Alternative splicing results in multiple transcript variants encoding different isoforms.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: amelogenesis imperfecta 1; amelogenin (amelogenesis imperfecta 1, X-linked); amelogenin (X chromosome, amelogenesis imperfecta 1); Amelogenin, X isoform
Gene Aliases: AI1E; AIH1; ALGN; AMELX; AMG; AMGL; AMGX
UniProt ID: (Human) Q99217
Entrez Gene ID: (Human) 265
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Learn moreGet expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.
Contact tech support