AMMECR1 Antibody (C-term) Blocking Peptide
€363.00
In stock
SKU
AC-BP19068b
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 deletionsyndrome, the AMME complex (Alport syndrome, mental retardation,midface hypoplasia, and elliptocytosis). Alternatively splicedtranscript variants encoding different isoforms have been found forthis gene.
Other Names:
AMME syndrome candidate gene 1 protein, AMMECR1
Gene Name: AMMECR1
Gene ID: 9949
Primary Accession: Q9Y4X0
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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 deletionsyndrome, the AMME complex (Alport syndrome, mental retardation,midface hypoplasia, and elliptocytosis). Alternatively splicedtranscript variants encoding different isoforms have been found forthis gene.
Other Names:
AMME syndrome candidate gene 1 protein, AMMECR1
Gene Name: AMMECR1
Gene ID: 9949
Primary Accession: Q9Y4X0
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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