OPA3 anticorps (AA 1-100) (AbBy Fluor® 750)
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- Antigène Voir toutes OPA3 Anticorps
- OPA3 (Optic Atrophy 3 (Autosomal Recessive, with Chorea and Spastic Paraplegia) (OPA3))
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Épitope
- AA 1-100
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Reactivité
- Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp OPA3 est conjugé à/à la AbBy Fluor® 750
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Application
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (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
- Top Product
- Discover our top product OPA3 Anticorps primaire
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- Indications d'application
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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
- -20 °C
- Stockage commentaire
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Date de péremption
- 12 months
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- 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
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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
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