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

MFSD8 Antibody

  • 中文名稱:
    MFSD8兔多克隆抗體
  • 貨號:
    CSB-PA844087LA01HU
  • 規格:
    ¥440
  • 圖片:
    • Immunohistochemistry of paraffin-embedded human adrenal gland tissue using CSB-PA844087LA01HU at dilution of 1:100
    • Immunofluorescent analysis of HepG2 cells using CSB-PA844087LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) MFSD8 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    MFSD8
  • 別名:
    Ceroid-lipofuscinosis neuronal protein 7 antibody; CLN7 antibody; Major facilitator superfamily domain-containing protein 8 antibody; MFSD8 antibody; MFSD8_HUMAN antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Major facilitator superfamily domain-containing protein 8 protein (1-40AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    Non-conjugated

    本頁面中的產品,MFSD8 Antibody (CSB-PA844087LA01HU),的標記方式是Non-conjugated。對于MFSD8 Antibody,我們還提供其他標記。見下表:

    可提供標記
    標記方式 貨號 產品名稱 應用
    HRP CSB-PA844087LB01HU MFSD8 Antibody, HRP conjugated ELISA
    FITC CSB-PA844087LC01HU MFSD8 Antibody, FITC conjugated
    Biotin CSB-PA844087LD01HU MFSD8 Antibody, Biotin conjugated ELISA
  • 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
  • 應用范圍:
    ELISA, IHC, IF
  • 推薦稀釋比:
    Application Recommended Dilution
    IHC 1:20-1:200
    IF 1:50-1:200
  • 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:
    May be a carrier that transport small solutes by using chemiosmotic ion gradients.
  • 基因功能參考文獻:
    1. This study highlights a hierarchy of MFSD8 variant severity, predicting three consequences of mutation: (1) nonsyndromic localized maculopathy, (2) nonsyndromic widespread retinopathy, or (3) syndromic neurological disease. PMID: 28586915
    2. MFSD8 genetic testing should also be considered in patients with Rett like phenotype at onset and negative MECP2 mutation PMID: 25439737
    3. A mutation in MFSD8, c.472G>A (p.Gly158Ser), segregates with the disease phenotype in variant late infantile neuronal ceroid lipofuscinosis. PMID: 25270050
    4. In this study, we identified variants in MFSD8 as a novel cause of nonsyndromic autosomal recessive macular dystrophy with central cone involvement. PMID: 25227500
    5. This study showed that Gene disruption of Mfsd8 provides animal model for CLN7 disease. PMID: 24423645
    6. Expression and lysosomal targeting of CLN7 are reported. PMID: 20826447
    7. MFSD8 gene is involved in late-infantile-onset neuronal ceroid lipofuscinose;it was mapped to chromosome 4q28.1-q28.2. PMID: 17564970
    8. Results describe a novel mutation in the MFSD8 gene, responsible for neuronal ceroid lipofuscinoses, in a consanguineous Egyptian family PMID: 18850119
    9. Study contributes to a better molecular characterization of Italian NCL cases, and will facilitate medical genetic counseling in such families. PMID: 19177532
    10. CLN7/MFSD8 defects are not restricted to the Turkish population, as initially anticipated, but are a relatively common cause of NCL in different populations. PMID: 19201763
    11. Data show that neuronal ceroid lipofuscinosis in a Saudi family is due to a homozygous novel mutation in the most recently described NCL gene (MFSD8). PMID: 19277732

    顯示更多

    收起更多

  • 相關疾病:
    Ceroid lipofuscinosis, neuronal, 7 (CLN7); Macular dystrophy with central cone involvement (CCMD)
  • 亞細胞定位:
    Lysosome membrane; Multi-pass membrane protein. Note=Sorting to lysosomes involves tyrosine- and/or dileucine-based motifs.
  • 蛋白家族:
    Major facilitator superfamily
  • 組織特異性:
    Expressed at very low levels in all tissues tested.
  • 數據庫鏈接:

    HGNC: 28486

    OMIM: 610951

    KEGG: hsa:256471

    STRING: 9606.ENSP00000296468

    UniGene: Hs.480701



主站蜘蛛池模板: 久久亚洲一区二区三区舞蹈| 无码av大香线蕉伊人久久| 99久久精品日本一区二区免费| 欧美18精品久久久无码午夜福利| 国产少妇高潮在线观看| 日韩人妻少妇一区二区| 亚洲国产精品久久一线不卡| 精品丝袜人妻久久久久久| 亚洲精品久久yy5099| 无码一区二区三区av在线播放 | 女性高爱潮视频| 手机在线看片| 国产99青草视频在线播放视 | 久久久久久人妻一区二区三区| 欧美色欧美亚洲高清在线观看| 免费午夜理论不卡| 午夜天堂一区人妻| 成熟丰满熟妇高潮xxxxx视频 | 无码办公室丝袜ol中文字幕| 精品少妇ay一区二区三区| 日本熟妇浓密毛毛多| 肉体裸交137日本大胆摄影| 亚洲日韩欧洲乱码av夜夜摸| 久久人妻无码中文字幕| 中文字幕一区二区精品区| 伊人色合天天久久综合网| 2018国产大陆天天弄| 久久www免费人成人片| 亚洲精品久久久久国产剧8| 日日摸日日碰人妻无码| 国产精品一国产精品| 国产又爽又黄又刺激的视频| 久久久久麻豆v国产精华液好用吗 99久久人妻精品免费一区 | 精品无码一区二区三区不卡| 欧美综合自拍亚洲图久青草| 婷婷综合缴情亚洲狠狠小说| 髙清国产性猛交xxxand| 精品麻豆国产色欲色欲色欲www| 亚洲精品自产拍在线观看亚瑟| 日韩精品一区二区午夜成人版| 偷看农村女人做爰毛片色|