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  • bsm-62313R5-羟色胺受体7重组兔单抗

    The neurotransmitter, serotonin, is thought to play a role in various cognitive and behavioral functions. The serotonin receptor encoded by this gene belongs to the superfamily of G protein-coupled receptors and the gene is a candidate locus for involvement in autistic disorder and other neuropsychiatric disorders. Three splice variants have been identified which encode proteins that differ in the length of their carboxy terminal ends. [provided by RefSeq, Jul 2008]

    更新时间:2025-03-03
    型号:bsm-62313R
    厂商性质:生产厂家
    浏览量:115
  • bsm-62312R激活素受体2A重组兔单抗

    Members of the transforming growth factor b superfamily bind to a pair of transmembrane proteins, known as receptor types I and II, which contain serine/threonine kinases and associate to form a signaling complex (1). Activin has been shown to bind a heteromeric noncovalent complex, which consists of a type I receptor, ACTR-IA (also designated ACVRI and ALK-2) or ACTR-IB (also designated ALK-4 and SKR2), and a type II receptor, ACTR-IIA (also designated ACVR2A) or ACTR-IIB (also designated

    更新时间:2025-03-03
    型号:bsm-62312R
    厂商性质:生产厂家
    浏览量:75
  • bsm-62311R神经细胞凋亡抑制蛋白重组兔单抗

    Prevents motor-neuron apoptosis induced by a variety of signals. Possible role in the prevention of spinal muscular atrophy that seems to be caused by inappropriate persistence of motor-neuron apoptosis: mutated or deleted forms of NAIP have been found in individuals with severe spinal muscular atrophy.

    更新时间:2025-03-03
    型号:bsm-62311R
    厂商性质:生产厂家
    浏览量:105
  • bsm-62310RCHX10蛋白重组兔单抗

    CHX10 is a 40kDa homeodomain protein of the paired-like class that is essential for development of the mammalian eye. Mutations in CHX10 cause microphthalmia, a cause of congenital blindness in humans, and the ocular retardation (or) phenotype in mice. In the developing mouse retina CHX10 is expressed in retinal progenitors, while in the mature retina, CHX10 expression becomes restricted to bipolar neurons. Concurrent with these expression patterns, the CHX10-/- (or) retina is thin due to a de

    更新时间:2025-03-03
    型号:bsm-62310R
    厂商性质:生产厂家
    浏览量:89
  • bsm-62307R肠型脂肪酸结合蛋白重组兔单抗

    The intracellular fatty acid-binding proteins (FABPs) belong to a multigene family with nearly twenty identified members. FABPs are divided into at least three distinct types, namely the hepatic-, intestinal- and cardiac-type. They form 14-15 kDa proteins and are thought to participate in the uptake, intracellular metabolism and/or transport of long-chain fatty acids. They may also be responsible in the modulation of cell growth and proliferation. Intestinal fatty acid-binding protein 2 gene

    更新时间:2025-03-03
    型号:bsm-62307R
    厂商性质:生产厂家
    浏览量:98
  • bsm-62305RDNA聚合酶γ/DNA pol γ重组兔单抗

    DNA replication, recombination and repair, all of which are necessary for genomic stability, require the presence of exonucleases. In DNA replication, these enzymes are involved in the processing of Okazaki fragments, whereas in DNA repair, they function to excise damaged DNA fragments and correct recombinational mismatches. These exonucleases include the family of DNA polymerases (DNA pol). DNA pol Alpha, Beta, Gamma, and epsilon are involved in DNA replication and repair. DNA pol gamma a

    更新时间:2025-03-03
    型号:bsm-62305R
    厂商性质:生产厂家
    浏览量:91
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