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

SMPX Antibody

  • 中文名稱:
    SMPX兔多克隆抗體
  • 貨號:
    CSB-PA887043DSR1HU
  • 規格:
    ¥440
  • 圖片:
    • Immunohistochemistry of paraffin-embedded human kidney tissue using CSB-PA887043DSR1HU at dilution of 1:100
    • Immunohistochemistry of paraffin-embedded human heart tissue using CSB-PA887043DSR1HU at dilution of 1:100
    • Immunofluorescent analysis of HepG2 cells using CSB-PA887043DSR1HU 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) SMPX Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    SMPX
  • 別名:
    1010001C09Rik antibody; Csl antibody; DFNX4 antibody; RP23-60A1.5 antibody; Small muscular protein antibody; SMPX antibody; SMPX_HUMAN antibody; Stretch-responsive skeletal muscle protein antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Small muscular protein (1-88AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    Non-conjugated
  • 克隆類型:
    Polyclonal
  • 抗體亞型:
    IgG
  • 純化方式:
    Antigen Affinity Purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
  • 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:
    Plays a role in the regulatory network through which muscle cells coordinate their structural and functional states during growth, adaptation, and repair.
  • 基因功能參考文獻:
    1. detected a single nucleotide variation in two male controls with normal hearing, SMPX c.55A>G (p.Asn19Asp), which has been annotated as a rare variant in the Single Nucleotide Polymorphism (dbSNP) (rs759552778) and Exome Aggregation Consortium (ExAC) databases. This study has enriched the mutation spectrum of the SMPX gene PMID: 29559740
    2. Results show that SMPX expression is regulated by NOR-1 which binds to SMPX promoter and induces its activity promoting myotube differentiation. PMID: 27181368
    3. We report the first SMPX (DFNX4) mutation in a North American family. Our findings contribute to the existing genotypic and phenotypic spectrum of SMPX associated hearing loss. Furthermore, our data suggest that exome sequencing is promising in the genetic diagnosis of hearing loss PMID: 29287879
    4. A novel frameshift mutation in SMPX. PMID: 28542515
    5. Audiological, medical, and family histories were collected and family members interviewed to compare hearing thresholds and case histories between cases with mutations in SMPX versus POU3F4. PMID: 24687041
    6. SMPX is localized predominantly in repetitive double stripes flanking the Z-disc, and not present in nuclei. PMID: 24936977
    7. Data indicate founder mutation in exon 3 (c.99delC) of SMPX that cosegregates in two Newfoundland families. PMID: 22911656
    8. Demonstrate phenotypic heterogeneity in large family with an X-linked pattern of inherited sensorineural hearing impairment with SMPX mutations. PMID: 21893181
    9. Our study identified mutations in SMPX in patients with X-chromosomal hearing impairment and suggested that the stress response of mechanically challenged inner-ear cells might critically depend on SMPX function. PMID: 21549336
    10. This study identifies SMPX as a gene in which variation is associated with X-linked deafness and illustrates that NGS is instrumental in the efficient identification of disease-causing variants in unexpected genes. PMID: 21549342

    顯示更多

    收起更多

  • 相關疾病:
    Deafness, X-linked, 4 (DFNX4)
  • 蛋白家族:
    SMPX family
  • 組織特異性:
    Preferentially and abundantly expressed in heart and skeletal muscle.
  • 數據庫鏈接:

    HGNC: 11122

    OMIM: 300066

    KEGG: hsa:23676

    STRING: 9606.ENSP00000368808

    UniGene: Hs.734084



主站蜘蛛池模板: 国产精品久久人妻无码网站蜜臀 | 亚洲国产人在线播放首页| 熟女少妇人妻中文字幕| 亚洲人成电影在线播放| 日韩国产精品无码一区二区三区| 综合激情五月综合激情五月激情1| 国产精品久久久久久亚洲色| …日韩人妻无码精品一专区| 五月婷六月婷婷俺也去| 伊人狼人大焦香久久网| 久久久久人妻一区二区三区| 国产乱人伦在线播放| 小宝贝荡货啊用力水湿aⅴ视频 | 午夜亚洲精品久久一区二区| 日韩国产成人无码av毛片| 天堂а√中文最新版地址在线 | 强行糟蹋人妻hd中文字幕| 亚洲 激情 小说 另类 欧美 | 亚洲图片综合图区20p| 少妇人妻精品一区二区三区| 中文字幕一区二区人妻电影 | 亚洲国产成人久久综合电影| 色琪琪丁香婷婷综合久久| 亚洲日韩欧洲乱码av夜夜摸| 久久婷婷五月综合色国产香蕉| 亚洲无人区午夜福利码高清完整版| 2021久久国自产拍精品| 中国女人内谢69xxxx| 中文字幕一二三区波多野结衣| 2018高清国产一区二区三区| 美丽的熟妇中文字幕| 少妇高清精品毛片在线视频| 亚洲乱码中文论理电影| 国产高清自产拍av在线| 国产免国产免‘费| 久久精品国产久精国产果冻传媒| 成人精品v视频在线| 级r片内射在线视频播放| 久久精品99av高久久精品| 国产拍揄自揄精品视频| 揄拍成人国产精品视频|