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Invitrogen™ SEPN1 Polyclonal Antibody
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Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA550752

Catalog No. PA550752


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Description

Description

The antibody detects endogenous levels of total SEPN1 protein.

SEPN1 is a selenoprotein, which contains a selenocysteine (Sec) residue at its active site. Mutations in SEPN1 gene cause the classical phenotype of multiminicore disease and congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome. This gene encodes a selenoprotein, which contains a selenocysteine (Sec) residue at its active site. The selenocysteine is encoded by the UGA codon that normally signals translation termination. The 3' UTR of selenoprotein genes have a common stem-loop structure, the sec insertion sequence (SECIS), that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. Mutations in this gene cause the classical phenotype of multiminicore disease and congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

SEPN1
Polyclonal
Unconjugated
SELENON
1110019I12Rik; AI414492; cb686; CFTD; FLJ24021; MDRS1; RSMD1; RSS; selenon; Selenoprotein N; selenoprotein N, 1; SELN; SePN; sepn1; wu:fb06g01; wu:fb73d02; wu:fv41b08; zgc:101091
Rabbit
Antigen Affinity Chromatography
RUO
57190
-20°C
Liquid
Immunohistochemistry (Paraffin)
0.5 mg/mL
PBS with 40% glycerol and 0.05% sodium azide; pH 7.4
Q9NZV5
SELENON
Synthetic peptide corresponding to a region derived from internal residues of human selenoprotein N, 1.
100 μL
Primary
Human
Antibody
IgG
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