Anti-AMMECR1 Aptamer SELEX Service(Cat#: CTApt-1298)

This is an aptamer development services to screening aptamers binds to the AMMECR1 with an affinity of 1nM~1μM.

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Certificate of Analysis Lookup

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Lot Number

TOP
Summary

Specifications
Target Category Protein
Target AMMECR1
Alternative Names AMMECR Nuclear Protein 1; Alport Syndrome, Mental Retardation, Midface Hypoplasia And Elliptocytosis Chromosomal Region Gene 1; AMME Syndrome Candidate Gene 1 Protein; Alport Syndrome Mental Retardation Midface Hypoplasia And Elliptocytosis Chromosomal Region Protein 1; AMMERC1; AMMECR1; MFHIEN
Gene ID 9949
UniProt ID Q9Y4X0
Target Overview 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.
Chemical Modification N/A
Type DNA
Length 20-80 nt
Affinity (Kd) 1nM~1μM
Binding Conditions/Buffer PBS; buffer system with Serum; other
For Research Use Only. Not for Diagnostic or Therapeutic Applications.
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