|Full Name||Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1|
|Product Description||Rabbit Polyclonal antibody to AMMECR1 (Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1)|
|Background||The exact function of this gene is not known, however, submicroscopic deletion of the X chromosome including this gene, COL4A5, and FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq]|
|Synonyms||AMMERC1 antibody, AMMECR1 antibody, AMME syndrome candidate gene 1 protein antibody, "Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 antibody"|
|Immunogen||Recombinant protein encompassing a sequence within the center region of human AMMECR1. The exact sequence is proprietary.|
|Predicted Cross Reactivity species Predicted cross-reactivity:|
Predicted cross-reactivity is based on sequence homology, with greater than 80% immunogen sequence identity considered positive.
Please note that we are only able to guarantee products to work in applications and species in which they have been tested.
|Predict Reactivity Note||Mouse (98%), Zebrafish (94%)|