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

  1. Home
  2. 抗體
  3. 多克隆抗體
  4. CLN5 Antibody

CLN5 Antibody

  • 中文名稱：
    CLN5兔多克隆抗體
  • 貨號：
    CSB-PA005567LA01HU
  • 規(guī)格：
    ￥440
  • 圖片：
    • IHC image of CSB-PA005567LA01HU diluted at 1:300 and staining in paraffin-embedded human prostate tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
    • IHC image of CSB-PA005567LA01HU diluted at 1:300 and staining in paraffin-embedded human colon cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
    • Immunofluorescence staining of 293T cells with CSB-PA005567LA01HU at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).
  • 其他：

產(chǎn)品詳情

  • 產(chǎn)品名稱：
    Rabbit anti-Homo sapiens (Human) CLN5 Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    CLN5
  • 別名：
    Ceroid lipofuscinosis neuronal 5 antibody; Ceroid-lipofuscinosis neuronal protein 5 antibody; CLN5 antibody; CLN5_HUMAN antibody; NCL antibody; Protein CLN5 antibody
  • 宿主：
    Rabbit
  • 反應(yīng)種屬：
    Human
  • 免疫原：
    Recombinant Human Ceroid-lipofuscinosis neuronal protein 5 protein (42-181AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標(biāo)記方式：
    Non-conjugated

    本頁面中的產(chǎn)品，CLN5 Antibody (CSB-PA005567LA01HU)，的標(biāo)記方式是Non-conjugated。對于CLN5 Antibody，我們還提供其他標(biāo)記。見下表：

    可提供標(biāo)記
    標(biāo)記方式 貨號 產(chǎn)品名稱 應(yīng)用
    HRP CSB-PA005567LB01HU CLN5 Antibody, HRP conjugated ELISA
    FITC CSB-PA005567LC01HU CLN5 Antibody, FITC conjugated
    Biotin CSB-PA005567LD01HU CLN5 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(chǎn)品提供形式：
    Liquid
  • 應(yīng)用范圍：
    ELISA, IHC, IF
  • 推薦稀釋比：
    Application Recommended Dilution
    IHC 1:200-1:500
    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(chǎn)品評價

靶點詳情

  • 功能：
    Plays a role in influencing the retrograde trafficking of lysosomal sorting receptors SORT1 and IGF2R from the endosomes to the trans-Golgi network by controlling the recruitment of retromer complex to the endosomal membrane. Regulates the localization and activation of RAB7A which is required to recruit the retromer complex to the endosomal membrane.
  • 基因功能參考文獻：
    1. Genotype-phenotype correlation between CNL5 gene mutations and CNL5 disease symptoms. PMID: 28542837
    2. We conclude that, whereas sleep homeostasis is present in CLN5(-/-) sheep, underlying CLN5(-/-) disease processes prevent its full expression, even at early stages. PMID: 27488642
    3. findings support CLN5 hypomorphic mutations cause autosomal recessive cerebellar ataxia, confirming other reports showing CLN mutations are associated with adult-onset neurodegenerative disorders PMID: 25359263
    4. Two forms of CLN5, derived from the C-terminal proteolytic processing, are present in most cells and tissues. PMID: 26342652
    5. There are functional differences in various N-glycosylation sites of CLN5 which affect folding, trafficking, and lysosomal function of CLN5. PMID: 24058541
    6. a role for CLN5 in controlling the itinerary of the lysosomal sorting receptors by regulating retromer recruitment at the endosome PMID: 22431521
    7. This study highlights a close interaction between CLN5/CLN8 proteins, and their role in sphingolipid metabolism. Our findings suggest that CLN5p/CLN8p most likely are positive modulators of CerS1 and/or CerS2. PMID: 23160995
    8. analysis of mutations in neuronal ceroid lipofuscinosis protein CLN5 PMID: 20052765
    9. CLN5 mutations are 1) more common in patients with neuronal ceroid lipofuscinosis (NCL) than previously reported, 2) found in patients of broad ethnic diversity, and 3) can be identified in patients with disease onset in adult and juvenile epochs PMID: 20157158
    10. Study found that CLN5 interacts with several other NCL proteins namely, CLN1/PPT1, CLN2/TPP1, CLN3, CLN6 and CLN8. PMID: 19941651
    11. biosynthesis and intracellular localization of this protein PMID: 11971870
    12. A novel missense mutation in CLN5 was found in a Colombian family with juvenile-onset neuronal ceroid lipofuscinosis: c. 1627G>A causing Arg112His. PMID: 15728307
    13. The CLN5/mRNA expression level reduced to 45% supports the existence of one mRNA non-producing allele, further noticeable at the protein level. PMID: 16814585
    14. Reports two sibs harbouring a novel mutation (p.Tyr258Asp) in the CLN5 gene and displaying behaviour disturbances and mental deterioration, rather than epilepsy, as the dominant disease manifestation at onset. PMID: 17607606
    15. In cultures of brain microvascular endothelial cells, VEGF-A specifically down-regulated CLN-5 and OCLN protein and mRNA PMID: 19174516
    16. Double immunofluorescence microscopy showed that while the wild-type CLN5 protein is localized in lysosomes, both mutant CLN5 proteins are retained in the endoplasmic reticulum rather than reaching the lysosome. PMID: 19309691

    顯示更多

    收起更多

  • 相關(guān)疾病：
    Ceroid lipofuscinosis, neuronal, 5 (CLN5)
  • 亞細(xì)胞定位：
    [Ceroid-lipofuscinosis neuronal protein 5, secreted form]: Lysosome.; [Ceroid-lipofuscinosis neuronal protein 5]: Membrane; Single-pass type II membrane protein.
  • 蛋白家族：
    CLN5 family
  • 組織特異性：
    Ubiquitous.
  • 數(shù)據(jù)庫鏈接：

    HGNC: 2076

    OMIM: 256731

    KEGG: hsa:1203

    STRING: 9606.ENSP00000366673

    UniGene: Hs.30213



主站蜘蛛池模板： 中文字幕乱码人妻二区三区| 亚洲丁香婷婷久久一区二区| 成在线人永久免费视频播放| 四虎影视久久久免费观看| 日本理论片午午伦夜理片2021| 尹人香蕉99久久综合网站| 国产ww久久久久久久久久| 国产综合久久久久| 国产av高清无亚洲| 少妇人妻综合久久中文| 国产内射老熟女aaaa| 人人妻人人爽人人做夜欢视频| 少妇白浆呻吟爽| 无码av喷白浆在线播放| 国产精品久久久久久久久久久免费看 | 热99re久久精品天堂| 亚洲欧美成人中文日韩电影网站| 97精品国产97久久久久久免费| 欧美人与动牲交zooz乌克兰| 国产成人92精品午夜福利| 成·人免费午夜视频香蕉| 久久精品国产欧美日韩| 精品爆乳一区二区三区无码av| 天天综合网久久综合免费人成| 精品免费国产一区二区三区四区介绍| 亚洲男人av香蕉爽爽爽爽| 无码国产午夜福利片在线观看| 成人无码视频在线观看网址| 天天爽夜夜爽人人爽曰| 国产精品国产三级国产a| 欧美亚洲另类 丝袜综合网| 男人靠女人的免费视频| 亚洲一区精品二人人爽久久| 国产白浆喷水在线视频| 无码啪啪熟妇人妻区 | 亚洲人精品亚洲人成在线| 99re8这里有精品热视频免费| 国产精品一区二区av麻豆| 丰满少妇aaaaaa爰片毛片| 亚洲成a人片在线观看无码| 亚洲午夜无码毛片av久久京东热|