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C627

Recombinant Human Cyclophilin B/PPIB

10ug

640

576

现货

国产

C627

Recombinant Human Cyclophilin B/PPIB

50ug

2000

1800

现货

国产

C627

Recombinant Human Cyclophilin B/PPIB

500ug

12320

11088

现货

国产

C627

Recombinant Human Cyclophilin B/PPIB

1mg

17600

15840

现货

国产

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  • Catalog# C627
    Source HEK293
    Description Recombinant Human Cyclophilin B/CYPB is produced with our mammalian expression system in human cells. The target protein is expressed with sequence (Asp34-Glu216) of Human CYPB fused with a polyhistidine tag at the C-terminus.
    Names Peptidyl-Prolyl Cis-Trans Isomerase B, PPIase B, CYP-S1, Cyclophilin B, Rotamase B, S-Cyclophilin, SCYLP, PPIB, CYPB
    Accession # P23284
    Formulation Supplied as a 0.2 μm filtered solution of 10mM Tris-HCl, 150mM NaCl, 10% Glycerol, pH 7.4
    Shipping The product is shipped on dry ice/ice packs.
    Storage Store at < -20°C, stable for 6 months after receipt.
    Please minimize freeze-thaw cycles.
    Purity Greater than 95% as determined by SEC-HPLC and reducing SDS-PAGE.
    Endotoxin Less than 0.1 ng/μg (1 IEU/μg).
    Amino Acid Sequence
    DEKKKGPKVTVKVYFDLRIGDEDVGRVIFGLFGKTVPKTVDNFVALATGEKGFGYKNSKFHRVIK DFMIQGGDFTRGDGTGGKSIYGERFPDENFKLKHYGPGWVSMANAGKDTNGSQFFITTVKTAWLD GKHVVFGKVLEGMEVVRKVESTKTDSRDKPLKDVIIADCGKIEVEKPFAIAKEVDHHHHHH
    Background Cyclophilin B is a member of the cyclophilin-type PPIase family and PPIase B subfamily which contains one PPIase cyclophilin-type domain. Cyclophilin B is a cyclosporin A binding protein that can be secreted in response to inflammatory stimuli. Cyclophilin B interaction with prolactin potentiated prolactin-induced proliferation, cell growth, and the nuclear retrotransport of prolactin. The intranuclear prolactin/cyclophilin B complex acts as a transcriptional inducer by interacting directly with Stat5, resulting in the removal of the Stat-repressor protein inhibitor of activated Stat 3 (PIAS3), thereby enhancing Stat5 DNA-binding activity and prolactin-induced, Stat5-mediated gene expression. Defects in PPIB are the cause of osteogenesis imperfecta type 9 (OI9).