Cytochrome b5 (CYTB5) (AA 9-80) antibody (Biotin)
Quick Overview for Cytochrome b5 (CYTB5) (AA 9-80) antibody (Biotin) (ABIN709903)
Target
See all Cytochrome b5 (CYTB5) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 9-80
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Cross-Reactivity
- Mouse
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Predicted Reactivity
- Human,Rat,Dog,Cow,Sheep,Pig
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Purification
- Purified by Protein A.
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Immunogen
- KLH conjugated synthetic peptide derived from human Cytochrome b5
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Isotype
- IgG
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Application Notes
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 -
Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 μg/μL
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Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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Preservative
- ProClin
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Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Store at -20°C for 12 months.
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Expiry Date
- 12 months
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- Cytochrome b5 (CYTB5)
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Alternative Name
- Cytochrome b5
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Background
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Synonyms: CYB 5, CYB 5A, CYB5, CYB5_HUMAN, CYB5A, Cytochrome b 5, Cytochrome b5 microsomal, Cytochrome b5, Cytochrome b5 type A microsomal, Cytochrome b5 type A, MCB 5, MCB5, Microsomal cytochrome b5, Microsomal cytochrome b5 type A, Type 1 cyt b5, CYB5A.
Background: The protein encoded by this gene is a membrane-bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin, which is required for stearyl-CoA-desaturase activity. Defects in this gene are a cause of type IV hereditary methemoglobinemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]
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Gene ID
- 1528
Target
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