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  • bs-11511R巴爾得-別德爾綜合征相關(guān)蛋白9抗體

    BBS9 is an 887 amino acid protein that localizes to both the cytoplasm and the centrosome and exists as six alternatively spliced isoforms. Expressed in a wide variety of tissues, including liver, lung, heart, brain and skeletal muscle, BBS9 functions as a component of the multi-protein BBSome complex which is required for ciliogenesis and is regulated by GDP/GTP exchange factors. Defects in the gene encoding BBS9 are associated with the pathogenesis of Bardet-Biedl syndrome type 9 (BBS9),

    更新時間:2025-02-26
    型號:bs-11511R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:93
  • bs-11501RGDNF家族受體α3抗體 GFR α3

    Glial cell line-derived neurotrophic factor (GDNF) and the related neurotrophic factor neurturin (NTN) are potent survival factors for central and peripheral neurons. GDNF is a glycosylated, disulfide-bonded homodimer that is distantly related to the TGF Beta superfamily of growth factors. Three receptors for these factors, GFR Alpha-1 (also designated GDNFR-Alpha, RETL1 or TrnR-1), GFR Alpha-2 (also designated GDNFR-Beta, RETL2, NTNR-Alpha or TrnR-2) and GFR Alpha-3 have been identified. Th

    更新時間:2025-02-26
    型號:bs-11501R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:91
  • bs-3249R磷酸化絲氨酸/蘇氨酸蛋白激酶抗體

    This gene, which encodes a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterized by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterized. [provided

    更新時間:2025-02-26
    型號:bs-3249R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:142
  • bs-3248R磷酸化絲氨酸/蘇氨酸蛋白激酶抗體

    This gene, which encodes a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterized by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterized. [provided

    更新時間:2025-02-26
    型號:bs-3248R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:162
  • bs-3247R磷酸化單絲氨酸蛋白激酶1/2抗體

    LIMK1 is a protein kinase which regulates actin filament dynamics. Phosphorylates and inactivates the actin binding/depolymerizing factor cofilin, thereby stabilizing the actin cytoskeleton. LIMK1 may be involved in brain development; it is highly expressed in both adult and fetal nervous system. Detected ubiquitously throughout the different regions of adult brain, with highest levels in the cerebral cortex. Expressed to a lesser extent in heart and skeletal muscle.

    更新時間:2025-02-26
    型號:bs-3247R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:102
  • bs-2904R腫瘤抑制基因LATS1抗體

    This gene encodes a serine/threonine protein kinase belonging to the LATS tumor suppressor family. The protein localizes to centrosomes during interphase, and early and late metaphase. It interacts with the centrosomal proteins aurora-A and ajuba and is required for accumulation of gamma-tubulin and spindle formation at the onset of mitosis. It also interacts with a negative regulator of p53 and may function in a positive feedback loop with p53 that responds to cytoskeleton damage. Additi

    更新時間:2025-02-26
    型號:bs-2904R
    廠商性質(zhì):生產(chǎn)廠家
    瀏覽量:108
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