OPA3 anticorps (AA 1-100)

N° du produit ABIN6989915

Détail du produit anti-OPA3 anticorps

Antigène: OPA3 (Optic Atrophy 3 (Autosomal Recessive, with Chorea and Spastic Paraplegia) (OPA3))

Épitope: AA 1-100

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp OPA3 est non-conjugé

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunocytochemistry (ICC), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Réactivité croisée: Souris

Homologie: Human,Dog,Cow,Sheep,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human OPA3

Isotype: IgG

Information d'application

Indications d'application: IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur OPA3

Antigène: OPA3 (Optic Atrophy 3 (Autosomal Recessive, with Chorea and Spastic Paraplegia) (OPA3))

Autre désignation: OPA3 (OPA3 Produits)

Synonymes: anticorps D630048P19Rik, anticorps Gm1425, anticorps Gm472, anticorps MGA3, anticorps optic atrophy 3, anticorps OPA3, outer mitochondrial membrane lipid metabolism regulator, anticorps opa3, anticorps Opa3, anticorps OPA3

Sujet:

Synonyms: FLJ22187, FLJ25932, Iraqi Jewish optic atrophy plus (3 methylglutaconicaciduria type 3), MGA3, MGC75494, OPA 3, OPA3 protein, Optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia), Optic atrophy 3 (Iraqi Jewish 'optic atrophy plus'), Optic atrophy 3, Optic atrophy 3 protein.

Background: OPA3 may play some role in mitochondrial processes. Defects in OPA3 are the cause of 3-methylglutaconic aciduria type 3 (MGA3), also known as optic atrophy plus syndrome, and of optic atrophy type 3 (OPA3), also known as autosomal dominant optic atrophy and cataract (ADOAC).

ID gène: 80207

UniProt: Q9H6K4