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

PLS3 Antibody, Biotin conjugated

  • 中文名稱:
    PLS3兔多克隆抗體, Biotin偶聯
  • 貨號:
    CSB-PA018206LD01HU
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) PLS3 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    PLS3
  • 別名:
    BMND18 antibody; Plastin 3 (T isoform) antibody; Plastin 3 antibody; Plastin-3 antibody; PLS3 antibody; PLST_HUMAN antibody; T fimbrin antibody; T-plastin antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Plastin-3 protein (310-455AA)
  • 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

  • 功能:
    Actin-bundling protein found in intestinal microvilli, hair cell stereocilia, and fibroblast filopodia. May play a role in the regulation of bone development.
  • 基因功能參考文獻:
    1. PLS3 deletions lead to severe childhood-onset osteoporosis resulting from defective bone matrix mineralization. PMID: 28777485
    2. PLS3 sequencing in childhood-onset primary osteoporosis identifies two novel disease-causing variants. PMID: 28748388
    3. T-plastin mediates the hypoxia-induced membrane trafficking PMID: 28218996
    4. PLS3 mutation plays a role in low turnover osteoporosis pathophysiology. PMID: 28379384
    5. Patients with PLS3 mutation-related osteoporosis respond to teriparatide treatment. PMID: 27732335
    6. We show that genes of the classical apoptosis pathway are involved in the smn-1-mediated neuronal death, and that this phenotype can be rescued by the expression of human SMN1, indicating a functional conservation between the two orthologs. Finally, we determined that Plastin3/plst-1 genetically interacts with smn-1 to prevent degeneration, and that treatment with valproic acid is able to rescue the degenerative phenotype PMID: 27260405
    7. PLS3 expression does not always modify SMA phenotype PMID: 27279027
    8. findings emphasize the power of genetic modifiers, PLS3 and CORO1C, to unravel the cellular pathomechanisms underlying spinal muscular atrophy (SMA)--and the power of combinatorial therapy based on splice correction of SMN2 and endocytosis improvement to efficiently treat SMA PMID: 27499521
    9. t is beyond doubt that PL S3 must be further investigated to determine its role in diagnostics, prediction, treatment and monitoring of treatment of colorectal cancer. PMID: 26146096
    10. PLS3 is a genuine spinal muscular atrophy protective modifier in SMN1-deleted individuals PMID: 26573968
    11. Measurements of SMN and PLS3 transcript and protein levels in induced pluripotent stem cell-derived motor neurons show limited value as Spinal muscular atrophy biomarkers. PMID: 26114395
    12. High levels of recombinant hPLS3 mRNA were expressed in motor neurons of SMA mice and an increased level of PLS3 protein in total spinal cord, yet neither survival nor the fundamental electrophysiological aspects of the neuromuscular junction improved. PMID: 26134627
    13. results confirm the role of PLS3 mutations in early onset osteoporosis. The mechanism whereby PLS3 affects bone health is unclear, but it may be linked to osteocyte dendrite function and skeletal mechanosensing PMID: 25209159
    14. plastin 3 is a regulator of actin microfilament bundles at the ES in which it dictates the configuration of the filamentous actin network PMID: 26048141
    15. PLS3 was expressed in circulating tumor cells undergoing the epithelial-mesenchymal transition in patients with breast cancer; an excellent biomarker for identifying groups at risk of recurrence or with a poor prognosis PMID: 25880010
    16. PLS3 overexpression is associated with colorectal cancer. PMID: 24217791
    17. T-plastin expression downstream to the calcineurin/NFAT pathway is involved in keratinocyte migration. PMID: 25226517
    18. Data suggest that several single-nucleotide polymorphisms (SNPs) of the plastin genes PLS3 and LCP1 could serve as gender- and/or stage-specific molecular predictors of tumor recurrence in stage II/III colorectal cancer as well as therapeutic targets. PMID: 24170770
    19. Loss of PLS3 is associated with spinal muscular atrophy. PMID: 24271012
    20. PLS3 expression and SMA phenotype: a commentary on correlation of PLS3 expression with disease severity in children with spinal muscular atrophy. PMID: 24284364
    21. PLS3 gene may have an age- and gender-specific role in the clinical severity of SMA in children afflicted with this condition. PMID: 24172247
    22. Plastin 3 (PLS3) appears to be important in human bone health, on the basis of pathogenic variants in PLS3 in five families with X-linked osteoporosis and osteoporotic fractures that we report here. PMID: 24088043
    23. study identified a common gene variant in PLS3 as an independent prognostic marker in female patients with stage II and III colon cancer PMID: 23549633
    24. PLS3 over-expression led to a stabilization of axons which, in turn, results in a significant delay of axon pruning, counteracting poor axonal connectivity in spinal muscular atrophy neuromuscular junctions. PMID: 23263861
    25. Overexpression of PLS3 is associated with epithelial-mesenchymal transition and is associated with metastasis in colorectal cancer PMID: 23378342
    26. PLS3, Twist, KIR3DL2 and NKp46 gene expression can model efficient molecular Sezary syndrome diagnosis. PMID: 23429988
    27. PLS3 is expressed in the majority of SS patients and provide insight into the molecular regulation of PLS3 expression in CTCL PMID: 22495182
    28. T-plastin is a marker restricted to malignant lymphocytes from Sezary syndrome patients and plays a role for cell survival and migration. PMID: 22627769
    29. The PLS3 gene may be an age- and/or puberty-specific and sex-specific modifier of spinal muscular atrophy. PMID: 20937953
    30. expression of T-plastin in the placental context may indeed be associated with the enhanced replicative potential of placental trophoblasts. PMID: 14567899
    31. T-plastin has the potential to be a Sezary cell-specific marker valuable for diagnostic and treatment of Sezary syndrome. PMID: 14612505
    32. T-plastin increases Arp2/3-mediated actin-based movement PMID: 15741236
    33. T-fimbrin has a role in the response to DNA damage PMID: 16142308
    34. unaffected SMN1-deleted females exhibit significantly higher expression of PLS3 than their spinal muscular atrophy-affected counterparts PMID: 18440926
    35. Increased T-plastin is associated with leukemic cutaneous T-cell lymphoma PMID: 18569641

    顯示更多

    收起更多

  • 相關疾病:
    Osteoporosis (OSTEOP)
  • 亞細胞定位:
    Cytoplasm.
  • 組織特異性:
    Expressed in a variety of organs, including muscle, brain, uterus and esophagus.
  • 數據庫鏈接:

    HGNC: 9091

    OMIM: 166710

    KEGG: hsa:5358

    STRING: 9606.ENSP00000348163

    UniGene: Hs.496622



主站蜘蛛池模板: 亚洲爱婷婷色婷婷五月| 久久久久九九精品影院| 日本一卡2卡3卡4卡免费乱码网站| 午夜福利精品亚洲不卡| 精品夜夜澡人妻无码av蜜桃| 国产精品久久久久久久久久| 亚洲精品国产一二三无码av| 在线岛国片免费无码av| 久久久亚洲欧洲日产国码农村| 无码一卡二卡三卡四卡| 日本久久高清一区二区三区毛片| 日韩精品久久久久久久电影蜜臀| 欧美激情视频一区二区三区免费| 亚洲日韩欧美在线成人| 亚洲欧美综合精品久久成人网| 精品夜夜澡人妻无码av| 国产精品麻豆欧美日韩ww| 成人亚洲国产精品一区不卡| 国产亚洲精品岁国产微拍精品| 中文字幕日产熟女乱码| 人人色在线视频播放| 奇米影视第四色首页| 欧美顶级少妇做爰hd| 在线天堂中文官网| 亚洲va久久久噜噜噜久久无码| 欧美性色大片在线观看| 人与动人物xxxx毛片人与狍| 成人性生交大片免费看r链接| 亚洲一区二区三区乱码在线欧洲| 无码精品人妻一区二区三区av | 女同亚洲一区二区无线码| 伊人蕉久中文字幕无码专区| 无码成人aaaaa毛片| 国产福利视频在线观看| 国产精品久久久久久久久绿色| 精品亚洲aⅴ在线无码播放| 国产国拍亚洲精品av| 国产在线无码一区二区三区| 亚洲最大无码中文字幕| 成人伊人精品色xxxx视频| 再深点灬舒服灬太大了网站 |