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

MIP Antibody

  • 中文名稱:
    MIP兔多克隆抗體
  • 貨號:
    CSB-PA000910
  • 規格:
    ¥1090
  • 圖片:
    • Western Blot analysis of HT29 cells using AQP0 Polyclonal Antibody
  • 其他:

產品詳情

  • Uniprot No.:
  • 基因名:
    MIP
  • 別名:
    MIP; AQP0; Lens fiber major intrinsic protein; Aquaporin-0; MIP26; MP26
  • 宿主:
    Rabbit
  • 反應種屬:
    Human,Mouse,Rat
  • 免疫原:
    Synthesized peptide derived from the Internal region of Human AQP0.
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    Non-conjugated
  • 抗體亞型:
    IgG
  • 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.
  • 保存緩沖液:
    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 產品提供形式:
    Liquid
  • 應用范圍:
    WB, IHC, ELISA
  • 推薦稀釋比:
    Application Recommended Dilution
    WB 1:500-1:2000
    IHC 1:100-1:300
    ELISA 1:5000
  • 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:
    Water channel. Channel activity is down-regulated by CALM when cytoplasmic Ca(2+) levels are increased. May be responsible for regulating the osmolarity of the lens. Interactions between homotetramers from adjoining membranes may stabilize cell junctions in the eye lens core. Plays a role in cell-to-cell adhesion and facilitates gap junction coupling.
  • 基因功能參考文獻:
    1. Study presented genetic and functional evidence for a novel major intrinsic protein mutation of G212R, which leads to congenital progressive cortical punctate with or without Y suture. PMID: 28059152
    2. In summary, whole-exome sequencing identifies a novel heterozygous missense variant (c.402G > T) in rarely reported cataract gene of MIP in an unconsanguineous marriage of three-generation Chinese family with congenital cataracts. PMID: 28836894
    3. The data evidence a broad lipidation profile of AQP0 that is both species and site independent, suggesting a chemical-based ester aminolysis mechanism to explain such modifications. PMID: 27378310
    4. A novel MIP frame-shift mutation in familial congenital nuclear cataract patient PMID: 27456987
    5. defects in AQP-0 permeability may be a cause for presbyopia. PMID: 26615967
    6. the p.D150H mutation is a novel disease-causing mutation in MIP, which leads to congenital progressive cortical punctate cataract by impairing the trafficking mechanism of AQP0. PMID: 25946197
    7. Authors identified a novel nonsense mutation in MIP (c.657 C>G; p.Y219*) (major intrinsic protein gene) that segregates with congenital posterior polar cataract in a Chinese family. PMID: 25803033
    8. Functional evidence linking the new MIP mutation of G215D to autosomal dominant congenital cataracts. PMID: 25033405
    9. A novel donor splice-site mutation (c.606+1G>A) in the MIP gene causes congenital cataract in a Chinese family. PMID: 24319327
    10. the first nonsense mutation of MIP identified in autosomal dominant congenital cataracts PMID: 24405844
    11. Mutation of this conserved glycine residue leads to improper trafficking of AQP0-G165D and loss of water channel function. PMID: 23116563
    12. Aquaporin 0 R233K mutation did not affect the expression, location and trafficking of the protein but did influence the interaction between AQP0 and CaM. PMID: 22662182
    13. Direct tissue analysis led to the detection of aging-related AQP0 modifications including carbamylation, acetylation, and oleoylation. PMID: 22036630
    14. Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese. PMID: 21921980
    15. Cerulean cataract has been mapped to chromosome 12q13 and associated with a novel initiation codon mutation in MIP. PMID: 21850180
    16. A novel mutation in the MIP gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family. PMID: 21647270
    17. analysis of a novel disease-causing mutation p.R187C in MIP in a Chinese cataract family PMID: 21245956
    18. AQP-0 gene expression was 3.4-fold higher in rat retinas. AQP-0 was predominantly expressed in the bipolar cells of the non-diabetic rat retinas, whereas it was also expressed in the retinal nerve fibers of diabetic rat retinas PMID: 21232536
    19. This is the first report of activation of a cryptic splice site in the 3' UTR in the human MIP gene. PMID: 21139677
    20. This study has identified a novel MIP mutation, p.V107I in a Chinese family with congenital cataracts. PMID: 20361015
    21. In human, multiple aquaporins are expressed in developing teeth and in selected orofacial tissues. PMID: 12522663
    22. Analysis of C-terminal peptides of AQP0 from normal lenses of donors aged 34 to 38 reveals a remarkably similar pattern and distribution of truncation products, suggesting specific temporal mechanisms for post-translational modification of AQP0. PMID: 15274640
    23. Expression of hMafF or MIP alone did not alter basal reporter transcription activity, whereas co-expression of hMafF and MIP activated transcription efficiently. PMID: 16549056
    24. We identified a novel single base pair deletion in the MIP gene and conclude that it is a pathogenic sequence alteration. PMID: 16564824
    25. First dominant cataract mutation in MIP that is located outside the phylogenetically conserved transmembrane domain. PMID: 17893667
    26. The structure of aquaporin-0 (AQP0) has recently been determined by electron crystallography of two-dimensional crystals and by X-ray crystallography of three-dimensional crystals--REVIEW PMID: 17932686
    27. Arginine in this domain plays a crucial role in the function of the carboxyl-end of this protein and provides a helpful clue to further studies on completely understanding the physiological significance of MIP and its role in the formation of cataract. PMID: 17960133
    28. presence of measurable interactions between MIP26 and all crystallins, with the extent of interactions decreasing from alphaA- and alphaB-crystallin to betaB2- and gammaC-crystallin. PMID: 18004741
    29. To map the disease locus for a congenital cataract family, and detect the disease-causing gene. PMID: 18247294
    30. deletion mutation in AQP0 resulted in the localization of the mutant protein in the ER without trafficking to the plasma membrane, and cytotoxicity due to the accumulation of the mutant protein PMID: 18501347
    31. This is the first report on an acceptor splice-site mutation in human genes associated with dominant congenital cataract. PMID: 19137077
    32. Only in the presence of both MIP and hMafF could the nUS2-pLacZi reporter in yeast genome be activated. PMID: 19723544
    33. this is the first report validating the possible structural role of intact AQP0 as a cell-to-cell adhesion protein, using an in vitro expression system. PMID: 19857466

    顯示更多

    收起更多

  • 相關疾病:
    Cataract 15, multiple types (CTRCT15)
  • 亞細胞定位:
    Cell membrane; Multi-pass membrane protein. Cell junction, gap junction.
  • 蛋白家族:
    MIP/aquaporin (TC 1.A.8) family
  • 組織特異性:
    Expressed in the cortex and nucleus of the retina lens (at protein level). Major component of lens fiber gap junctions.
  • 數據庫鏈接:

    HGNC: 7103

    OMIM: 154050

    KEGG: hsa:4284

    STRING: 9606.ENSP00000257979

    UniGene: Hs.574026



主站蜘蛛池模板: 亚洲经典国产精华液单品榜| 国产手机在线精品| 欧美人妻aⅴ中文字幕| 精品久久久久久无码中文字幕一区| 亚洲国产一区二区三区在观看| 久热中文字幕无码视频| 国产精品夜色一区二区三区| 狠狠综合久久久久尤物丿| 国产精品色无码av在线观看| 国产成人欧美日韩在线电影| 久久久国产乱子伦精品| 久久综合九色综合网站| 欧美亚洲精品中文字幕乱码 | 在线日产精品一区| 亚洲成av人片在线观看一区二区三区| 最新亚洲人成无码网站| 999久久久国产精品消防器材| 精品国产一区二区三区四区精华液| 黑人与人妻无码中字视频| 真人与拘做受免费视频一| 欧美激情性做爰免费视频 | 新香蕉少妇视频网站| 精品国产偷窥一区二区| 国产亚洲日本精品成人专区| 天堂网www最新版官网| av无码av天天av天天爽| 久久五月精品中文字幕| 国产成人精品午夜福利在线播放| 人人爽久久久噜人人看| 日韩精品射精管理在线观看| 亚洲三区在线观看无套内射| 国产 高潮 抽搐 正在播放| 亚洲最大无码中文字幕网站| 国产精品视频一区二区噜噜 | 7m精品福利视频导航| 亚洲综合无码无在线观看| 免费做爰猛烈吃奶摸视频在线观看 | 色妞ww精品视频7777| 国产嫖妓一区二区三区无码| 极品国产主播粉嫩在线| 久久久久久无码av成人影院|