• Target：
• AMMR1

• Gene Name：
• AMMECR1

• Protein Name：
• AMMR1

• Human Gene Id：
• 9949

• Human Swiss Prot No：
• Q9Y4X0

• Mouse Gene Id：
• 56068

• Mouse Swiss Prot No：
• Q9JHT5

• Immunogen：
• Synthesized peptide derived from human AMMR1 AA range: 12-62

• Specificity：
• This antibody detects endogenous levels of AMMR1 at Human/Mouse

• Formulation：
• Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

• Source：
• Polyclonal, Rabbit,IgG

• Dilution：
• WB 1：500-2000

• Purification：
• The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

• Concentration：
• 1 mg/ml

• Storage Stability：
• -15°C to -25°C/1 year(Do not lower than -25°C)

• Molecular Weight(Da)：
• 37kD

• 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, Jan 2010],

• Function：
• disease:Defects in AMMECR1 may be a cause of AMME complex [MIM:300194]; also known as Alport syndrome with mental retardation, midface hypoplasia and elliptocytosis. The AMME complex is a contiguous gene deletion syndrome.,similarity:Contains 1 AMMECR1 domain.,

• Subcellular Location：
• Nucleus .

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