在线日韩日本国产亚洲丨少妇伦子伦情品无吗丨欧美性猛交xxxx免费看蜜桃丨精品人妻系列无码一区二区三区丨亚洲精品无码不卡在线播放

Your Good Partner in Biology Research

LCA5 Antibody, FITC conjugated

  • 中文名稱:
    LCA5兔多克隆抗體, FITC偶聯
  • 貨號:
    CSB-PA769789LC01HU
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) LCA5 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    LCA5
  • 別名:
    LCA5 antibody; C6orf152Lebercilin antibody; Leber congenital amaurosis 5 protein antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Lebercilin protein (101-400AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    FITC
  • 克隆類型:
    Polyclonal
  • 抗體亞型:
    IgG
  • 純化方式:
    >95%, Protein G purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
  • 產品提供形式:
    Liquid
  • 儲存條件:
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 貨期:
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
  • 用途:
    For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

  • 功能:
    Involved in intraflagellar protein (IFT) transport in photoreceptor cilia.
  • 基因功能參考文獻:
    1. The authors report novel biallelic LCA5 mutations, Ala212Pro and Tyr441Cys, as causing cone dystrophy. PMID: 27067258
    2. Identification of novel LCA5 mutations in patients with Leber congenital amaurosis and retinitis pigmentosa. PMID: 23946133
    3. This work reveals a higher frequency of LCA5 mutations in a Spanish Leber congenital amaurosis cohort than in other populations. PMID: 24144451
    4. A novel LCA5 mutation is present in a Pakistani family with Leber congenital amaurosis and cataracts. PMID: 21850168
    5. Macular coloboma-type LCA shows genetic heterogeneity and it is not possible to establish a phenotype-genotype correlation with LCA5 and macular coloboma. PMID: 16082399
    6. The LCA5 gene on chromosome 6q14 encodes the ciliary protein lebercilin associated with Leber congenital amaurosis type 5. PMID: 17546029
    7. Data report the identification of three novel LCA5 mutations (3/3 homozygous) in three families confirming the modest implication of this gene in this series (3/179; 1.7%). PMID: 18000884
    8. This is the second report of LCA5 mutations causing Leber congenital amaurosis. PMID: 18334959
    9. This result shows that mutation in LCA5 is likely to be a rare genetic cause in Koreans PMID: 19172513
    10. Leber congenital amaurosis 2 patients with LCA5 mutation had evidence of retained photoreceptors mainly in the central retina; retinal remodeling was present in pericentral regions PMID: 19503738
    11. OFD1 is mutated in X-linked Joubert syndrome and interacts with LCA5-encoded lebercilin PMID: 19800048

    顯示更多

    收起更多

  • 相關疾病:
    Leber congenital amaurosis 5 (LCA5)
  • 亞細胞定位:
    Cytoplasm, cytoskeleton. Cytoplasm, cytoskeleton, cilium axoneme. Cytoplasm, cytoskeleton, cilium basal body. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cell projection, cilium.
  • 蛋白家族:
    LCA5 family
  • 組織特異性:
    Widely expressed.
  • 數據庫鏈接:

    HGNC: 31923

    OMIM: 604537

    KEGG: hsa:167691

    STRING: 9606.ENSP00000358861

    UniGene: Hs.21945



主站蜘蛛池模板: 少妇高潮太爽了在线视频| 成人亚洲欧美日韩在线观看| 日韩精品电影综合区亚洲| 精品久久久无码中文字幕| 久久久国产精品消防器材| 野外少妇被弄到喷水在线观看| 无码精品人妻一区二区三区av| 综合 欧美 小说 另类 图| 狠狠色狠狠色综合网| 久久精品人妻一区二区蜜桃| 18禁成年免费无码国产| 菠萝菠萝蜜午夜视频在线播放观看| 最新中文乱码字字幕在线| 久久www免费人成一看片| 人与动人物xxxx毛片人与狍 | 国产女人高潮叫床视频| 国产69精品久久久久乱码免费| 免费无码作爱视频| 国产午夜福利久久精品| 一边添奶一边添p好爽视频| 久久综合给合久久狠狠狠88| 国产日韩在线观看不卡顿| 亚洲夂夂婷婷色拍ww47| 国产手机在线国内精品| 色偷偷人人澡久久超碰97| 波多野结衣初尝黑人| 另类内射国产在线| 粉嫩虎白女毛片人体| 国产亚洲日韩在线a不卡| 国产女人好紧好爽| 中文字幕久久综合伊人| 亚洲伊人成无码综合影院| 精品人妻无码一区二区色欲产成人 | 中文在线а√在线天堂中文| 天天摸天天做天天添欧美| 国产亚洲精品字幕在线观看| 法国白嫩大屁股xxxx| 120秒试看无码体验区| 露脸叫床粗话东北少妇| 2018国产精华国产精品| 啪啪后入内射日韩|