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

CLDN19 Antibody

  • 中文名稱:
    CLDN19兔多克隆抗體
  • 貨號:
    CSB-PA202194
  • 規格:
    ¥2024
  • 圖片:
    • Western blot analysis of extracts fromHepG2 cells and Jurkat cells, using CLDN19 antibody.
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) CLDN19 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    CLDN19
  • 別名:
    CLDN19; Claudin-19
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Synthesized peptide derived from internal of Human CLDN19.
  • 免疫原種屬:
    Homo sapiens (Human)
  • 克隆類型:
    Polyclonal
  • 純化方式:
    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 產品提供形式:
    Liquid
  • 應用范圍:
    ELISA,WB
  • 推薦稀釋比:
    Application Recommended Dilution
    WB 1:500-1:3000
  • Protocols:
  • 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:
    Plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity.
  • 基因功能參考文獻:
    1. permeability barriers and affected cell morphology, proliferation, migration, AKT signaling, and gene expression. When claudins are exogenously expressed, ARPE-19 more closely model native RPE. PMID: 27593915
    2. CLDN19 genetic mutation is responsible for familial magnesium deficiency with hypercalciuria and nephrocalcinosis. PMID: 25410674
    3. analysis of a novel mutation c.241C>T in exon 2 of CLDN19 in a Chinese patient PMID: 25555744
    4. Claudin-19, the most abundant claudin in myelin, exhibited no binding to ZO2 protein. PMID: 25712527
    5. patients with CLDN19 mutations have a high risk of progression to chronic renal disease PMID: 23301036
    6. Case Reports: novel CLDN19 mutation in familial hypomagnesemia with hypercalciuria and nephrocalcinosis. PMID: 23538362
    7. The risk of end-stage renal disease in patients with CLDN19 mutations was two times the risk of patients with CLDN16 mutations. Ocular abnormalities were observed only in patients with CLDN19 mutations. PMID: 22422540
    8. In a patient with consanguineous parents, history of disturbed organization and development of the retina, a diagnosis of Familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by claudin-19 mutation should be considered. PMID: 22734304
    9. Ocular manifestations and exercise intolerance mimicking mild to moderate periodic paralysis are two symptoms that may occur in patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis and may indicate CLDN19 mutations. PMID: 21030577
    10. The identification of CLDN19 mutations in patients with chronic renal failure and severe visual impairment supports the fundamental role of claudin-19 for normal renal tubular function and undisturbed organization and development of the retina. PMID: 17033971

    顯示更多

    收起更多

  • 相關疾?。?/div>
    Hypomagnesemia 5 (HOMG5)
  • 亞細胞定位:
    Cell junction, tight junction. Cell membrane; Multi-pass membrane protein.
  • 蛋白家族:
    Claudin family
  • 數據庫鏈接:

    HGNC: 2040

    OMIM: 248190

    KEGG: hsa:149461

    STRING: 9606.ENSP00000296387

    UniGene: Hs.496270



主站蜘蛛池模板: 久久五月丁香激情综合| 婷婷亚洲久悠悠色悠在线播放| 羞羞视频在线观看| 男人猛戳女人30分钟视频大全| 国产台湾无码av片在线观看| 中文字幕精品久久久久人妻红杏1 久久久精品日本一区二区三区 | 老熟女 露脸 嗷嗷叫| 国产午夜精品一区二区三区老| 婷婷色怡春院| 激情综合色五月丁香六月欧美| 日本妇人成熟免费| 麻豆自媒体 一区 二区| 欲女熟妇国产一区二区| 日韩免费视频| 狠狠躁日日躁夜夜躁2022麻豆| 午夜福利不卡在线视频| 国产成人综合久久精品| 久久国产精品二国产精品| 在线观看黄a∨免费无毒网站| 色情无码www视频无码区澳门| 国产女女做受ⅹxx高潮| 老熟妇性老熟妇性色| 极品熟妇大蝴蝶20p| 国产av国内精品jk制服| 成 人 a v免费视频在线观看| av无码久久久久不卡网站蜜桃 | 国产午夜精品无码一区二区| 国产精品秘入口18禁麻豆免会员| 大香线蕉伊人精品超碰| 亚洲精品综合一区二区| 国产亚州精品女人久久久久久| 欧美xxxxx高潮喷水麻豆| 欧美日韩在手机线旡码可下载| 初尝黑人嗷嗷叫中文字幕| 色多多性虎精品无码av| 曰本极品少妇videossexhd| 成人网站www污污污网站| 国产欧美高清在线观看| 亚洲精品国产精品制服丝袜| 女人被狂躁高潮啊的视频在线看| 成人性生交大片免费看中文|