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Invitrogen™ AMMECR1 Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA562474

Catalog No. PIPA562474


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Description

Description

Immunogen sequence: ASSSSHCSGE SQCRAGELGL GGAGTRLNGL GGLTGGGSGS GCTLSP Highest antigen sequence identity to the following orthologs: Mouse - 86%, Rat - 88%.

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
Immunohistochemistry (Paraffin)
0.05 mg/mL
PBS with 40% glycerol and 0.02% sodium azide; pH 7.2
Q9Y4X0
AMMECR1
Recombinant protein corresponding to Human AMMECR1. Recombinant protein control fragment (Product #RP-101165).
100 μL
Primary
Human
Antibody
IgG
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