AMELX Antibody (monoclonal) (M04)

Q99217

WB, E

Variation at the NFATC2 Locus Increases the Risk of Thiazolinedinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study. Bailey SD, et al. Diabetes Care, 2010 Jul 13. PMID 20628086.MMP20 hemopexin domain mutation in amelogenesis imperfecta. Lee SK, et al. J Dent Res, 2010 Jan. PMID 19966041.Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. Talmud PJ, et al. Am J Hum Genet, 2009 Nov. PMID 19913121.Typing of 48 autosomal SNPs and amelogenin with GenPlex SNP genotyping system in forensic genetics. Tomas C, et al. Forensic Sci Int Genet, 2008 Dec. PMID 19083859.Changes in the quaternary structure of amelogenin when adsorbed onto surfaces. Tarasevich BJ, et al. Biopolymers, 2009 Feb. PMID 19025992.

265

Mouse monoclonal antibody raised against a partial recombinant AMELX.

Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (36.63 KDa) .

1:500~1000

WB

Detection limit for recombinant GST tagged AMELX is 0.1 ng/ml as a capture antibody.

NM_001142

Human: ~~ Positive

NP_001133.1; NP_872621.1; NP_872622.1

NP_001133

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. [provided by RefSeq