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serpinb 6

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    TargetMol | Recombinant_Protein
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    TargetMol | Antibody_Products
  • TargetMolTargetMol对比
    Serpin B6 Protein, Human, Recombinant (E. coli, His)
    SERPINB6, Serpin B6, PTI, Placental Thrombin Inhibitor, PI-6, PI6, Peptidase Inhibitor 6, Cytoplasmic Antiproteinase, CAP
    TMPJ-00243
    Serpin B6 belongs to the serpin family. Serpin B6 localizes to the cytoplasm. Serpin B6 is expressed in many tissues, abundantly by mast cells in different tissues and mastocytoma lesions. Serpin B6 may be involved in the regulation of serine proteinases present in the brain or extravasated from the blood. In addition, Serpin B6 may play an important role in the inner ear in the protection against leakage of lysosomal content during stress and loss of this protection results in cell death and sensorineural hearing loss.
    • ¥ 1170
    5日内发货
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  • TargetMolTargetMol对比
    Serpin B6 Protein, Human, Recombinant (His)
    SPI3, serpin peptidase inhibitor, clade B (ovalbumin), member 6, Serpin B6, RP1-90J20.6, PTI, PI-6, PI6, MSTP057, MGC111370, DKFZp686I04222, DFNB91, CAP
    TMPY-02242
    SerpinB6, also known as Cytoplasmic antiproteinase, Peptidase inhibitor 6, Placental thrombin inhibitor, SERPINB6 and PI-6, is a cytoplasm protein that belongs to the serpin family and Ov-serpin subfamily. SerpinB6 PI-6 is an inhibitor of cathepsin G, kallikrein-8 and thrombin. It may play an important role in the inner ear in the protection against leakage of lysosomal content during stress and loss of this protection results in cell death and sensorineural hearing loss. SerpinB6 PI-6 is expressed in keratinocytes (at protein level). It is also found in placenta, cardiac muscle, lung, liver, kidney and pancreas. SerpinB6 PI-6 is expressed in the inner ear hair cells. It's expressed abundantly by normal mast cells in different tissues and by mast cells in mastocytoma lesions. SerpinB6 PI-6 may be involved in the regulation of serine proteinases present in the brain or extravasated from the blood. Defects in SerpinB6 are the cause of deafness autosomal recessive type 91 which is a form of non-syndromic deafness characterized by progressive and age-dependent sensorineural hearing loss. Vestibular function is normal.
    • ¥ 3820
    5日内发货
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