FH antibody (AA 411-510) (Alexa Fluor 680)
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- Target See all FH Antibodies
- FH (Fumarate Hydratase (FH))
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Binding Specificity
- AA 411-510
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This FH antibody is conjugated to Alexa Fluor 680
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Application
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Predicted Reactivity
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human Fumarate hydratase (447-496aa)
- Isotype
- IgG
- Top Product
- Discover our top product FH Primary Antibody
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- Application Notes
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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.
- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Expiry Date
- 12 months
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- Target
- FH (Fumarate Hydratase (FH))
- Alternative Name
- Fumarate hydratase/FH (FH Products)
- Synonyms
- FH antibody, DDBDRAFT_0205237 antibody, DDBDRAFT_0231397 antibody, DDBDRAFT_0231400 antibody, DDB_0205237 antibody, DDB_0231397 antibody, DDB_0231400 antibody, HLRCC antibody, LRCC antibody, MCL antibody, MCUL1 antibody, Fh1 antibody, im:7152785 antibody, ns:zf-e152 antibody, zf-e152 antibody, zgc:66253 antibody, zgc:77498 antibody, Fh antibody, Fh-1 antibody, fumarate hydratase antibody, fumarate hydratase 1 antibody, FH antibody, fumH antibody, Fh antibody, fh antibody, Fh1 antibody
- Background
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Synonyms: mitochondrial, FH, Fumarase, Fumarate hydratase, Fumarate hydratase mitochondrial, FUMH_HUMAN, HLRCC, LRCC, MCL, MCUL 1, MCUL1, Multiple hereditary cutaneous leiomyomata.
Background: Defects in FH are the cause of fumarase deficiency (FHD)also known as fumaricaciduria. FHD is characterized by progressive encephalopathy, developmental delay, hypotonia, cerebral atrophy and lactic and pyruvic acidemia.
- Gene ID
- 2271
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