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Abnova
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Product may be used with Western Blot (Transfected lysate).
The Isotype of this product is composed of an IgG Mixture.
Immunogen sequence: MAAGCCGVKK QKLSSSPPSG SGGGGGASSS SHCSGESQCR AGELGLGGAG TRLNGLGGLT GGGSGSGCTL SPPQGCGGGG GGIALSPPPS CGVGTLLSTP AAATSSSPSS SSAASSSSPG SRKMVVSAEM CCFCFDVLYC HLYGYQQPRT PRFTNEPYAL KDSRFPPMTR DELPRLFCSV SLLTNFEDVC DYLDWEVGVH GIRIEFINEK GSKRTATYLP EVAKEQGWDH IQTIDSLLRK GGYKAPITNE FRKTIKLTRY RSEKMTLSYA EYLAHRQHHH FQNGIGHPLP PYNHYS
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Alport syndrome mental retardation midface hypoplasia and elliptocytosis chromosomal region protein 1; AMME syndrome candidate gene 1 protein; Nuclear protein AMMECR1
基因别名: AMMECR1; AMMERC1
UniProt ID: (Human) Q9Y4X0
Entrez Gene ID: (Human) 9949