OPA3 Antikörper (AA 1-100) (AbBy Fluor® 680)
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- Target Alle OPA3 Antikörper anzeigen
- OPA3 (Optic Atrophy 3 (Autosomal Recessive, with Chorea and Spastic Paraplegia) (OPA3))
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Bindungsspezifität
- AA 1-100
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Reaktivität
- Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser OPA3 Antikörper ist konjugiert mit AbBy Fluor® 680
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Applikation
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Kreuzreaktivität
- Maus
- Homologie
- Human,Dog,Cow,Sheep,Horse
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human OPA3
- Isotyp
- IgG
- Top Product
- Discover our top product OPA3 Primärantikörper
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- Applikationshinweise
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Haltbarkeit
- 12 months
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- Target
- OPA3 (Optic Atrophy 3 (Autosomal Recessive, with Chorea and Spastic Paraplegia) (OPA3))
- Andere Bezeichnung
- OPA3 (OPA3 Produkte)
- Synonyme
- D630048P19Rik antikoerper, Gm1425 antikoerper, Gm472 antikoerper, MGA3 antikoerper, optic atrophy 3 antikoerper, OPA3, outer mitochondrial membrane lipid metabolism regulator antikoerper, opa3 antikoerper, Opa3 antikoerper, OPA3 antikoerper
- Hintergrund
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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).
- Gen-ID
- 80207
- UniProt
- Q9H6K4
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