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CYB5A antibody

CYB5A Reactivity: Human, Mouse, Rat WB, IHC, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7261351
  • Target See all CYB5A Antibodies
    CYB5A (Cytochrome B5 Type A (Microsomal) (CYB5A))
    Reactivity
    Human, Mouse, Rat
    Host
    • 35
    • 6
    Rabbit
    Clonality
    • 36
    • 4
    Polyclonal
    Conjugate
    • 17
    • 5
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CYB5A antibody is un-conjugated
    Application
    • 30
    • 27
    • 19
    • 8
    • 7
    • 2
    • 2
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human CYB5A (NP_683725.1).
    Isotype
    IgG
    Top Product
    Discover our top product CYB5A Primary Antibody
  • Application Notes
    WB 1:500-1:2000 IHC 1:50-1:200 IF 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    CYB5A (Cytochrome B5 Type A (Microsomal) (CYB5A))
    Alternative Name
    CYB5A (CYB5A Products)
    Synonyms
    CYB5 antibody, MCB5 antibody, Cyb5 antibody, cyb5 antibody, zgc:64123 antibody, wu:fb44a11 antibody, MGC80327 antibody, 0610009N12Rik antibody, Cyb5a antibody, CYB5A antibody, cytochrome b5 type A antibody, cytochrome b5 type A (microsomal) antibody, cytochrome b5 type A (microsomal) L homeolog antibody, cytochrome b5 antibody, CYB5A antibody, Cyb5a antibody, cyb5a antibody, cyb5a.L antibody, LOC100328915 antibody, LOC100735904 antibody
    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.
    Molecular Weight

    Observed_MW: 17 kDa

    Calculated_MW: 11 kDa/14 kDa/15 kDa

    Gene ID
    1528
    UniProt
    P00167
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