Cytochrome b5 Polyclonal Antibody (E-AB-11133)
For research use only.
Verified Samples |
Verified Samples in WB: Human kidney cancer, Mouse liver, Human bladder carcinoma Verified Samples in IHC: Human thyroid cancer, Human cervical cancer |
Dilution | WB 1:200-1:1000, IHC 1:50-1:200 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human, Mouse, Rat |
Applications | WB, IHC |
Clonality | Polyclonal |
Immunogen | Recombinant protein of human CYB5A |
Abbre | Cytochrome b5 |
Synonyms | CYB 5, CYB 5A, CYB5, Cyb5a, Cytochrome b 5, Cytochrome b5, Cytochrome b5 (microsomal), Cytochrome b5 type A, Cytochrome b5 type A (microsomal), MCB 5, MCB5, Microsomal cytochrome b5, Microsomal cytochrome b5 type A, Type 1 cyt b5 |
Swissprot | |
Calculated MW | 15 kDa |
Cellular Localization | Cytoplasm and Endoplasmic reticulum membrane. Microsome membrane. |
Concentration | 0.4 mg/mL |
Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
Purification Method | Affinity purification |
Research Areas | Cancer, Metabolism, Signal Transduction |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
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. |
Other Clones
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Other Formats
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Unconjugated
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