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  • bs-20601R-PEPE標(biāo)記的一氧化氮合成酶-2(誘導(dǎo)型)抗體

    Nitric oxide (NO) is an inorganic, gaseous free radical that carries a variety of messages between cells. Vasorelaxation, neurotransmission and cytotoxicity can all be potentiated through cellular response to NO. NO production is mediated by members of the nitric oxide synthase (NOS) family. NOS catalyzes the oxidization of L-arginine to produce L-citrulline and NO. Two constitutive isoforms, brain or neuronal NOS (b or nNOS, type I) & endothelial cell NOS (eNOS, type III), and one i

    更新時間:2025-03-07
    型號:bs-20601R-PE
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:201
  • bs-2358R-PEPE標(biāo)記的肝細(xì)胞核因子3抗體

    This gene encodes a member of the forkhead class of DNA-binding proteins. These hepatocyte nuclear factors are transcriptional activators for liver-specific genes such as albumin and transthyretin, and they also interact with chromatin. Similar family members in mice have roles in the regulation of metabolism and in the differentiation of the pancreas and liver. This gene has been linked to sporadic cases of maturity-onset diabetes of the young. Transcript variants encoding different isofor

    更新時間:2025-03-07
    型號:bs-2358R-PE
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:239
  • bs-2358R-FITCFITC標(biāo)記的肝細(xì)胞核因子3抗體

    This gene encodes a member of the forkhead class of DNA-binding proteins. These hepatocyte nuclear factors are transcriptional activators for liver-specific genes such as albumin and transthyretin, and they also interact with chromatin. Similar family members in mice have roles in the regulation of metabolism and in the differentiation of the pancreas and liver. This gene has been linked to sporadic cases of maturity-onset diabetes of the young. Transcript variants encoding different isofor

    更新時間:2025-03-07
    型號:bs-2358R-FITC
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:271
  • bs-6895R-HRPHRP標(biāo)記的纖維蛋白原γ鏈抗體

    Fibrinogen has a double function: yielding monomers that polymerize into fibrin and acting as a cofactor in platelet aggregation.$nInvolvement in disease: Defects in FGG are a cause of thrombophilia.$nDefects in FGG are a cause of congenital afibrinogenemia (CAFBN). It is a rare autosomal recessive disorder characterized by complete absence of detectable fibrinogen.

    更新時間:2025-03-07
    型號:bs-6895R-HRP
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:196
  • bs-20395R-HRPHRP標(biāo)記的血栓調(diào)節(jié)蛋白抗體

    Thrombomodulin, TM is cell surface glycoprotein; plays an important role in the protein C anticoagulant pathway. It located in a vein, artery and capillary endothelial cells on the surface of plasma membrane protein. It is generally believed: TM vascular endothelial injury is an important parameter is the thrombin receptor, known in a variety of normal human tissues, can also be expressed in many tumors, TM may be similar to the E-cadherin,and is a lectin Like activity of a new class of member

    更新時間:2025-03-07
    型號:bs-20395R-HRP
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:241
  • bs-11716R-BioBiotin標(biāo)記的cereblon蛋白抗體

    CRBN is a 442 amino acid protein which is highly concentrated in human brain tissue. CRBN functions are thought to be related to energy metabolism, learning and memory. Localized to the cytoplasm, CRBN acts as a protease in mitochondria and is thought to regulate the assembly of KCNT1, as well as the surface expression of KCNT1 in brain regions known to affect memory and learning, such as the hippocampus. The gene encoding CRBN belongs to a family of ATP-dependent lon proteases that play a r

    更新時間:2025-03-07
    型號:bs-11716R-Bio
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:208
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