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C217

Recombinant Human Cytochrome b5/MCB5/CYB5A

10ug

1200

1080

现货

国产

C217

Recombinant Human Cytochrome b5/MCB5/CYB5A

50ug

3520

3168

现货

国产

C217

Recombinant Human Cytochrome b5/MCB5/CYB5A

500ug

12320

11088

现货

国产

C217

Recombinant Human Cytochrome b5/MCB5/CYB5A

1mg

17600

15840

现货

国产

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  • Catalog# C217
    Source E.coli
    Description Recombinant Human Cytochrome b5/CYB5A is produced by our E. coli expression system. The target protein is expressed with sequence (Ala2-Asp134) of Human CYB5A fused with a His tag at the N-terminus.
    Names Cytochrome b5, Microsomal Cytochrome b5 Type A, MCB5, CYB5A, CYB5
    Accession # P00167
    Formulation Lyophilized from a 0.2 μm filtered solution of 20mM PB, 150mM NaCl, 0.1mM EDTA, pH 7.25
    Shipping The product is shipped at ambient temperature.
    Reconstitution Always centrifuge tubes before opening. Do not mix by vortex or pipetting.
    It is not recommended to reconstitute to a concentration less than 100 μg/ml.
    Dissolve the lyophilized protein in 1X PBS.
    Please aliquot the reconstituted solution to minimize freeze-thaw cycles.
    Storage Lyophilized protein should be stored at < -20°C, though stable at room temperature for 3 weeks.
    Reconstituted protein solution can be stored at 4-7°C for 2-7 days.
    Aliquots of reconstituted samples are stable at < -20°C for 3 months.
    Purity Greater than 95% as determined by reducing SDS-PAGE.
    Endotoxin Less than 0.1 ng/μg (1 IEU/μg).
    Amino Acid Sequence
    MGSSHHHHHHSSGLVPRGSHMAEQSDEAVKYYTLEEIQKHNHSKSTWLILHHKVYDLTKFLEEHP GGEEVLREQAGGDATENFEDVGHSTDAREMSKTFIIGELHPDDRPKLNKPPETLITTIDSSSSWW TNWVIPAISAVAVALMYRLYMAED
    Background Cytochrome b5 (CYB5A) is a membrane bound hemoprotein which function as an electron carrier for several membrane bound oxygenases. CYB5A contains one cytochrome b5 heme-binding domain and has two isoforms produced by alternative splicing. Isoform 1 is a sngle-pass membrane protein. Isoform 2 is located in cytoplasm. The defects in CYB5A can result in type IV hereditary methemoglobinemia.