|Western Blot (WB)||1:500-1:3000|
|Tested Species reactivity||Human|
|Host / Isotype||Rabbit / IgG|
|Immunogen||Recombinant protein fragment corresponding to a region within amino acids 107 and 285 of Human AMMECR1|
|Purification||Antigen affinity chromatography|
|Storage buffer||0.1M tris glycine, pH 7, with 20% glycerol|
|Storage conditions||-20° C, Avoid Freeze/Thaw Cycles|
PA5-30555 targets AMMECR1 in IF and WB applications and shows reactivity with Human samples.
The PA5-30555 immunogen is recombinant protein fragment corresponding to a region within amino acids 107 and 285 of Human 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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Alport syndrome mental retardation midface hypoplasia and elliptocytosis chromosomal region protein 1; AMME syndrome candidate gene 1 protein; AMMERC1
Gene Aliases: AMMECR1; AMMERC1
UniProt ID: (Human) Q9Y4X0
Entrez Gene ID: (Human) 9949
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