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Invitrogen™ AMMECR1 Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA530555
Description
Recommended positive controls: 293T, A431, Raji. Predicted reactivity: Mouse (100%), Zebrafish (95%). Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
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.
Specifications
AMMECR1 | |
Polyclonal | |
Unconjugated | |
AMMECR1 | |
6230420G18Rik; Alport syndrome mental retardation midface hypoplasia and elliptocytosis chromosomal region protein 1; Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1; Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 homolog; AMME syndrome candidate gene 1 protein; AMME syndrome candidate gene 1 protein homolog; Ammecr1; AMMERC1 | |
Rabbit | |
Antigen affinity chromatography | |
RUO | |
9949 | |
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
Liquid |
Western Blot, Immunocytochemistry | |
1 mg/mL | |
0.1M tris glycine with 20% glycerol and 0.01% thimerosal; pH 7 | |
Q9Y4X0 | |
AMMECR1 | |
Recombinant protein fragment corresponding to a region within amino acids 107 and 285 of Human AMMECR1. | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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