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  • bs-23441R-BF555BF555標(biāo)記的蛋白激酶C亞性D型抗體

    Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and the second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC family members also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play distinct roles

    更新時(shí)間:2025-03-05
    型號(hào):bs-23441R-BF555
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:49
  • bs-4609R-PEPE標(biāo)記的內(nèi)皮糖蛋白抗體

    This gene encodes a homodimeric transmembrane protein which is a major glycoprotein of the vascular endothelium. This protein is a component of the transforming growth factor beta receptor complex and it binds to the beta1 and beta3 peptides with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. This gene may also be involved in preeclampsia and several types o

    更新時(shí)間:2025-03-05
    型號(hào):bs-4609R-PE
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:47
  • bs-4609R-FITCFITC標(biāo)記的內(nèi)皮糖蛋白抗體

    This gene encodes a homodimeric transmembrane protein which is a major glycoprotein of the vascular endothelium. This protein is a component of the transforming growth factor beta receptor complex and it binds to the beta1 and beta3 peptides with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. This gene may also be involved in preeclampsia and several types o

    更新時(shí)間:2025-03-05
    型號(hào):bs-4609R-FITC
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:51
  • bs-4511R-HRPHRP標(biāo)記的微管蛋白β tubulin/Tubulin β(內(nèi)參)抗體

    This gene encodes a beta tubulin protein. This protein forms a dimer with alpha tubulin and acts as a structural component of microtubules. Mutations in this gene cause cortical dysplasia, complex, with other brain malformations 6. Alternative splicing results in multiple splice variants. There are multiple pseudogenes for this gene on chromosomes 1, 6, 7, 8, 9, and 13. [provided by RefSeq, Jun 2014]

    更新時(shí)間:2025-03-05
    型號(hào):bs-4511R-HRP
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:45
  • bs-10421R-HRPHRP標(biāo)記的磷酸化Nemo樣激酶抗體

    Nemo-like kinase (NLK) plays a role in cell fate determination and is required for differentiation of bone marrow stromal cells. It acts downstream of MAP3K7 and HIPK2 to negatively regulate the canonical Wnt/beta-catenin signaling pathway and the phosphorylation and destruction of the MYB transcription factor. It may suppress a wide range of transcription factors by phosphorylation of the coactivator, CREBBP. (referenced from swissprot)

    更新時(shí)間:2025-03-05
    型號(hào):bs-10421R-HRP
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:53
  • bs-0586R-HRPHRP標(biāo)記的血管假性血友病因子/血管性血友病因子抗體

    Von Willebrand Factor (VWF) was previously known as Factor VIII related antigen. VWF is synthesized exclusively by endothelial cells and megakaryocytes, and stored in the intracellular granules or constitutively secreted into plasma. This glycoprotein functions as both an antihemophilic factor carrier and a platelet vessel wall mediator in the blood coagulation system. Important in the maintenance of homeostasis, it participates in platelet vessel wall interactions by forming a noncovalent c

    更新時(shí)間:2025-03-05
    型號(hào):bs-0586R-HRP
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:45
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