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: 成人污污污www网站免费| 欧美肥熟妇xxxxx| 亚洲一区波多野结衣在线| 亚洲性av网站| 无码国产成人午夜电影在线观看| 天天弄天天模| 粉嫩被粗大进进出出视频| 亚洲中文字幕久久精品无码va| 高清乱码一区二区三区| 曰本av中文字幕一区二区 | 午夜三级a三级三点在线观看| 毛多水多www偷窥小便| 在线观看的网站| 99久久免费国产精品| 上海少妇高潮狂叫喷水了| 免费看成人啪啪| 成人亚洲精品久久久久| 久久国产欧美成人av| 久久久日韩精品一区二区三区| 久9re热视频这里只有精品| 日产精品卡二卡三卡四卡乱码视频 | 亚洲综合色无码| 国产对白老熟女正在播放| 国产高潮抽搐喷水高清| 爆乳喷奶水无码正在播放| 第九色区av天堂| 亚洲最大成人网色| 亚洲最大激情中文字幕| 久久久无码精品亚洲日韩按摩| 国产成人无码视频一区二区三区| 国产精品亚洲а∨天堂免下载| 国产传媒精品1区2区3区| 国产小呦泬泬99精品| 国产极品白嫩精品| 精品国产一区二区三区av色诱 | 99久久久无码国产精品古装| 美女被啪到深处抽搐视频| 日本中文字幕乱码免费| 欧美顶级metart裸体全部自慰| 无遮无挡爽爽免费视频| 亚洲色大成网站www久久九九|