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  1. Alles ansehen
  2. Polyclonal

GTX115945

AMMECR1 antibody

Eine Lieferung in diese Region ist nicht möglich.

SKU:
GTX115945
Zusätzliche Namen:
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 , AMMERC1 , MFHIEN
Anwendung:
WB, IF, ICC
Konzentration:
1 mg/ml
Physischer Zustand:
Liquid
Spezies-Reaktivität:
Human
Aufreinigung:
Affinity Purified
Lagerbedingungen:
-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.
Hersteller:
Genetex
Host:
Rabbit
Reaktivitäten:
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
Synonyme:
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
Weitere 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]
Versandbedingungen:
Blue Ice