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

STH Antibody, Biotin conjugated

  • 中文名稱:
    STH兔多克隆抗體, Biotin偶聯
  • 貨號:
    CSB-PA022827LD01HU
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) STH Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    STH
  • 別名:
    STH antibody; Saitohin antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Saitohin protein (1-128AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    Biotin
  • 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
  • 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

  • 基因功能參考文獻:
    1. Saitohin Q7R polymorphism is associated with late-onset Alzheimer's disease susceptibility among caucasian populations. (Meta-analysis) PMID: 28211174
    2. Results showed a significant interaction effect of COMT and STH polymorphisms on cognitive performances, strengthening the involvement of STH in cognitive impairments, especially in the domains commonly impaired in schizophrenia PMID: 25283873
    3. The rs6203857 polymorphism of the saitohin gene is a genetic risk factor for Parkinson's disease. PMID: 25168738
    4. results of this meta-analysis suggested that MAPT_238bp/STH Q7R polymorphisms might modulate the risk of Parkinson's disease susceptibility PMID: 25305495
    5. These results suggest a possible contribution of STH gene products on the heterogeneity of core frontal executive functions deterioration in schizophrenia PMID: 22187337
    6. Single polymorphisms within the saitohin gene were associated with increased cognitive impairment and functional dependence persons with moderate-to-advanced Alzheimer disease. PMID: 21934306
    7. effect of Saitohin on Abl-mediated phosphorylation appears to be allele-specific, providing evidence for a new cellular function for STH PMID: 21769920
    8. STH polymorphisms play a possibly shared role with those of serotinin transporter 5-HTTLPR gene as a susceptibility factor for Alzheimer's disease and frontotemperal lobar dementia. PMID: 20852909
    9. Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) PMID: 20852909
    10. a gene within an intron of the tau gene; Q7R polymorphism appears to be over-represented in the homozygous state in late onset Alzheimer's disease subjects PMID: 12032355
    11. The saitohin Q allele, a novel determinant of tau H1 haplotypes, may represent a causative factor involved in the determinism of several tauopathies, e.g., frontotemporal dementia. PMID: 12447938
    12. At the STH gene only a common polymorphic change was found. PMID: 12826737
    13. Increased risk of Alzheimer's disease associated with the STH RR genotype is limited to late-onset Alzheimer's disease. PMID: 12826738
    14. The R allele of STH is associated with the H2 haplotype of tau; no correlation is found between R allele frequency and Alzheimer's or Parkinson's disease. PMID: 12932819
    15. Saitohin interacts with peroxiredoxin 6, a unique member of that family that is bifunctional and the levels of which increase in Pick disease. PMID: 16186110
    16. We found no evidence that could support a major pathogenic role of STH and TAU haplotype in AD, FTD or PD. PMID: 16909000
    17. Q allele of STH gene is over-represented in a tested group of patients with Huntington disease and might be considered a risk factor for HD like diseases. PMID: 18300012
    18. Homozygous Q/Q of STH Q7R polymorphism was the only one genotype found in either LOAD group or controls. No R allele was detected in LOAD and control groups. PMID: 18396294
    19. The Saitohin Q7R polymorphism is unlikely to contribute significantly to Alzheimer's disease susceptibility of the Han population in south China. PMID: 18850062
    20. Observational study of gene-disease association. (HuGE Navigator) PMID: 18850062
    21. Observational study of gene-disease association. (HuGE Navigator) PMID: 18509094
    22. Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) PMID: 18396294
    23. Observational study of genotype prevalence. (HuGE Navigator) PMID: 18300012
    24. Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) PMID: 18307033
    25. Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) PMID: 15136700
    26. Observational study of gene-disease association. (HuGE Navigator) PMID: 16603077
    27. Observational study of gene-disease association. (HuGE Navigator) PMID: 16909000

    顯示更多

    收起更多

  • 亞細胞定位:
    Cytoplasm. Nucleus.
  • 組織特異性:
    Highest expression in placenta, muscle, fetal brain, and adult brain, with lower expression in heart, kidney, stomach, testis, and adrenal gland. In the central nervous system, highest expression is in temporal lobe, hypothalamus, medulla and spinal cord,
  • 數據庫鏈接:

    HGNC: 18839

    OMIM: 607067

    KEGG: hsa:246744

    STRING: 9606.ENSP00000443168

    UniGene: Hs.661831



主站蜘蛛池模板: 亚洲熟妇av午夜无码不卡| 亚洲精品色播一区二区| 人妻老妇乱子伦精品无码专区| 麻豆人妻无码性色av专区| 国产高清在线精品一区免费| 日本成熟少妇喷浆视频| 日本乱理伦片在线观看中文| 国产精品自在在线午夜免费| 亚洲美女又黄又爽在线观看| 无码人妻精品一区二区蜜桃网站| 亚洲精品第一国产综合境外资源| 无码国产片观看| 伦埋琪琪久久影院三级| 亚洲精品久久无码av片| 国产suv精品一区二区883| 孕妇怀孕高潮潮喷视频孕妇| 久久久99精品成人片中文字幕 | 少妇人妻陈艳和黑人教练| 精品无码久久久久久久动漫| 国产精品白丝喷水在线观看| 性欧美牲交在线视频| 亚洲国产精品无码久久久蜜芽| 天堂…中文在线最新版在线| 久久99精品久久久久婷婷| 国产第一页浮力影院入口| 亚洲国产美女久久久久| 思思久久99热只有频精品66| 中文字幕乱码人妻二区三区| 亚洲妇女行蜜桃av网网站| 日本丰满老妇bbw| 内射少妇一区27p| 精品无人区一区二区三区| 国产亚洲欧美日韩精品一区二区| 亚洲aⅴ天堂av天堂无码app | 国产如狼似虎富婆找强壮黑人| 国产美女精品视频线免费播放软件| 欧美成人一区二免费视频软件| yyyy11111少妇无码影院| 欧美国产日韩亚洲中文| 亚洲精品中国国产嫩草影院美女| 99久久国产露脸国语对白|