AMMECR1 Proteine
(Alport Syndrome, Mental Retardation, Midface Hypoplasia and Elliptocytosis Chromosomal Region Gene 1 (AMMECR1))
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, Jan 2010].
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AMMECR1
Spezies: Human
Wirt: Wheat germ
Recombinant
ELISA, WB, AA, AP
1 image
custom-made
AMMECR1
Spezies: Maus
Wirt: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
custom-made
AMMECR1
Spezies: Human
Wirt: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
AMMECR1
Spezies: Human
Wirt: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliase für AMMECR1 Proteine
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 L homeolog (ammecr1.L) ProteineAlport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (AMMECR1) Proteine
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (Ammecr1) Proteine
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (ammecr1) Proteine
6230420G18Rik Proteine
AMMECR1 Proteine
Ammecr1 Proteine
ammerc1 Proteine
AMMERC1 Proteine
MGC84095 Proteine
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