SEPN1 anticorps (C-Term)

N° du produit ABIN954715

Cet anticorps Lapin Polyclonal détecte spécifiquement SEPN1 dans WB, IHC (p) et EIA. Il présente une réactivité envers Humain.

Aperçu rapide pour SEPN1 anticorps (C-Term) (ABIN954715)

Antigène: SEPN1 (Selenoprotein N, 1 (SEPN1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SEPN1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Détail du produit anti-SEPN1 anticorps

Épitope: AA 416-445, C-Term

Specificité: Recognizes SEPN1 (C-term).

Purification: Protein A column followed by peptide Affinity purification

Immunogène: KLH conjugated synthetic peptide between 416-445 amino acids from the C-terminal region of Human SEPN1 Genename: SEPN1

Isotype: Ig Fraction

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS with 0.09 % (W/V) Sodium Azide as preservative

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur SEPN1

Antigène: SEPN1 (Selenoprotein N, 1 (SEPN1))

Autre désignation: Selenoprotein N (SEPN1)

Sujet: 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.Synonyms: SELN

ID gène: 57190

NCBI Accession: NP_065184

Pathways: Skeletal Muscle Fiber Development