anti-AMMECR1 antibody

Arigo Biolaboratories

anti-AMMECR1 antibody

23

Western Blot

Research Use Only

Polyclonal

Unconjugated

AMMECR1

AMMECR nuclear protein 1

Alport syndrome mental retardation midface hypoplasia and elliptocytosis chromosomal region protein 1; Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1; AMME syndrome candidate gene 1 protein; AMMERC1; MFHIEN

Rabbit

IgG

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]

Human, Mouse

-20°C

12352203