OPA3 antibody (AA 1-100) (Biotin)
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- Target See all OPA3 Antibodies
- OPA3 (Optic Atrophy 3 (Autosomal Recessive, with Chorea and Spastic Paraplegia) (OPA3))
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Binding Specificity
- AA 1-100
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Reactivity
- Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This OPA3 antibody is conjugated to Biotin
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Application
- Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Cross-Reactivity
- Mouse
- Predicted Reactivity
- Human,Dog,Cow,Sheep,Horse
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human OPA3
- Isotype
- IgG
- Top Product
- Discover our top product OPA3 Primary Antibody
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- Application Notes
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IHC-P 1:200-400
IHC-F 1:100-500 - 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.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C for 12 months.
- Expiry Date
- 12 months
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- Target
- OPA3 (Optic Atrophy 3 (Autosomal Recessive, with Chorea and Spastic Paraplegia) (OPA3))
- Alternative Name
- OPA3 (OPA3 Products)
- Synonyms
- D630048P19Rik antibody, Gm1425 antibody, Gm472 antibody, MGA3 antibody, optic atrophy 3 antibody, OPA3, outer mitochondrial membrane lipid metabolism regulator antibody, opa3 antibody, Opa3 antibody, OPA3 antibody
- Background
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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).
- Gene ID
- 80207
- UniProt
- Q9H6K4
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