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Invitrogen™ AMMECR1 Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA530555

Catalog No. PIPA530555


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Description

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.
TRUSTED_SUSTAINABILITY
Specifications

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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