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AMELY encodes a member of the amelogenin family of extracellular matrix proteins. Additionally we are shipping AMELY Kits (12) and AMELY Proteins (4) and many more products for this protein.
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demonstrate the presence of copy number variations in regions containing 9 of the 13 CODIS(Combined DNA Index System) short tandem repeat(STR (show STATH Antibodies)) and AMELX (show AMELX Antibodies)/Y loci
252 confirmed and unrelated father/son pairs from the Moroccan population were examined using 17 Y-STR (show STATH Antibodies) markers of the AmpFISTR Yfiler kit. A total of 15 single repeat mutations between fathers and sons were observed as mutational events.
Results of haplogroup prediction showed that seven AMELY dropouts combined with variant Y-STR (show STATH Antibodies) deletions can be classified as the J2 subdivision, suggesting that some of these Y chromosomes might descend from a common ancestor.
Multigene deletions encompassing AMELY on short arm of chromosome Y.
The combined frequency of the AMELY null allele in Singapore and Malaysia populations is 2.7%, 0.6% in Indian and Malay ethnic groups respectively. It is absent among 541 Chinese screened.
This gene encodes a member of the amelogenin family of extracellular matrix proteins. Amelogenins are involved in biomineralization during tooth enamel development. Mutations in a related gene on chromosome X cause X-linked amelogenesis imperfecta.
amelogenin (Y chromosome)
, amelogenin, Y isoform
, Y-linked amelogenin
, class II amelogenin
, amelogenin, Y-linked
, Amelogenin, Y isoform