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Dental enamel forms the outer cap of teeth and is the hardest substance found in vertebrates. Additionally we are shipping Enamelin Antibodies (22) and Enamelin Proteins (2) and many more products for this protein.
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Among the variants shared with modern humans, two are ancestral (common with apes) and one is the derived enamelin major variant, T648I (rs7671281), associated with a thinner enamel and specific to the Homo lineage.
The study revealed the strong association between rs12640848 marker of ENAM gene and caries susceptibility in primary teeth in children from Poland.
Overrepresentation of the G allele of the enamelin marker was seen in the erosion group compared to the unaffected group.
Screening of ENAM and LAMB3 (show LAMB3 ELISA Kits) genes was performed by direct sequencing of genomic DNA from blood samples.
findings provide useful information for the implication of ENAM gene polymorphism in autosomal-dominant/-recessive amelogenesis imperfecta.
Whole-exome sequencing identified 2 novel heterozygous nonsense mutations in the ENAM gene (c.454G>T p.Glu152* in family 1, c.358C>T p.Gln120* in family 2) in the probands. Affected individuals were heterozygous for the mutation in each family.
2 exonic SNPs, both changing an amino acid in protein region encoded by exon 10 (p.I648T and p.R763Q), increased caries susceptibility 2.66-fold. findings support ENAM as gene candidate for caries susceptibility.
Associations between TFIP11 (show TFIP11 ELISA Kits) (p=0.02), ENAM (p=0.00001), and AMELX (show AMELX ELISA Kits) (p=0.01) could be seen with caries independent of having MIH or genomic DNA copies of Streptococcus mutans detected by real time PCR in the Brazilian sample.
Mutations in FAM83H (show FAM83H ELISA Kits) and ENAM and related phenotypes were observed in Chinese families with amelogenesis imperfecta.
hypocalcified amelogenesis imperfecta, Witkop type III, was unrelated to previously described mutations in the ENAM or MMP-20 genes
Data suggest that a specific quantity of enamelin is critical for normal enamel formation.
enamelin genotype, which affects enamel integrity, and food hardness influence bodyweight gain in postnatal and young adult mice
The enamelin mutation was associated with earlier forming enamel defects.The study supported the critical involvement of amelogenin (show AMELX ELISA Kits) and enamelin in enamel mineralization.
enamelin acts as an adhesion molecule (show NCAM1 ELISA Kits) and is involved in ameloblast cell differentiation during the early stages of tooth development
The results suggested that Wnt (show WNT2 ELISA Kits)/beta-catenin (show CTNNB1 ELISA Kits) signaling could function in enamelin gene expression by direct interaction through two conserved LEF1 (show LEF1 ELISA Kits) responsive elements on the enamelin gene in ameloblast-like cells.
the amelogenesis imperfecta phenotype is linked to a C > T transition in exon 8 of the enamelin gene
enamelin is essential for proper enamel matrix organization and mineralization
new insights into regulatory mechanisms governing enamelin expression
This study provides new insights into the molecular control of Enam cell- and stage-specific expression.
Mice lacking expression of the AmelX (show AMELX ELISA Kits), Enam and Mmp20 (show MMP20 ELISA Kits) genes have been generated.
Results demonstrate that the 32 kDa enamelin has a direct interaction with amelogenin (show AMELX ELISA Kits) in vitro.
Dental enamel forms the outer cap of teeth and is the hardest substance found in vertebrates. This gene encodes the largest protein in the enamel matrix of developing teeth. The protein is involved in the mineralization and structural organization of enamel. Defects in this gene result in amelogenesis imperfect type 1C.
, amelogenesis imperfecta 2, hypocalcification (autosomal dominant)