GTX115945
AMMECR1 antibody
Cannot supply to this region.
- SKU:
- GTX115945
- Additional Names:
- Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 , AMMERC1 , MFHIEN
- Application:
- WB, IF, ICC
- Concentration:
- 1 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human
- Buffer:
- 0.1M Tris, 0.1M Glycine, 20% Glycerol, 0.01% Thimerosal.
- Immunogen:
- Recombinant protein encompassing a sequence within the center region of human AMMECR1. The exact sequence is proprietary.
- Uniprot:
- Q9Y4X0
- Synonyms:
- Alport syndrome mental retardation midface hypoplasia and elliptocytosis chromosomal region protein 1;Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1;AMME syndrome candidate gene 1 protein;AMMERC1;MFHIEN
- Extra Details:
- 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]
- Shipping Conditions:
- Blue Ice