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

AMER1 Antibody

  • 中文名稱:
    AMER1兔多克隆抗體
  • 貨號:
    CSB-PA918886
  • 規格:
    ¥1100
  • 圖片:
    • The image on the left is immunohistochemistry of paraffin-embedded Human gastic cancer tissue using CSB-PA918886(AMER1 Antibody) at dilution 1/40, on the right is treated with synthetic peptide. (Original magnification: ×200)
    • The image on the left is immunohistochemistry of paraffin-embedded Human thyroid cancer tissue using CSB-PA918886(AMER1 Antibody) at dilution 1/40, on the right is treated with synthetic peptide. (Original magnification: ×200)
  • 其他:

產品詳情

  • Uniprot No.:
  • 基因名:
  • 別名:
    AMER1 antibody; FAM123B antibody; WTXAPC membrane recruitment protein 1 antibody; Amer1 antibody; Protein FAM123B antibody; Wilms tumor gene on the X chromosome protein antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human,Mouse
  • 免疫原:
    Synthetic peptide of Human AMER1
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    Non-conjugated
  • 抗體亞型:
    IgG
  • 純化方式:
    Antigen affinity purification
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
  • 產品提供形式:
    Liquid
  • 應用范圍:
    ELISA,IHC
  • 推薦稀釋比:
    Application Recommended Dilution
    ELISA 1:2000-1:5000
    IHC 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:
    Regulator of the canonical Wnt signaling pathway. Acts by specifically binding phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2), translocating to the cell membrane and interacting with key regulators of the canonical Wnt signaling pathway, such as components of the beta-catenin destruction complex. Acts both as a positive and negative regulator of the Wnt signaling pathway, depending on the context: acts as a positive regulator by promoting LRP6 phosphorylation. Also acts as a negative regulator by acting as a scaffold protein for the beta-catenin destruction complex and promoting stabilization of Axin at the cell membrane. Promotes CTNNB1 ubiquitination and degradation. Involved in kidney development.
  • 基因功能參考文獻:
    1. A novel heterozygous frameshift mutation in AMER1 was identified in a patient with osteopathia striata with cranial sclerosis. PMID: 28893644
    2. Losses of AMER1 by other mechanisms apart from mutations. PMID: 26071483
    3. A nonsense mutation (c.1045C>T, p.Glu349*) in the WTX gene. PMID: 24459086
    4. WTX inactivation occurs in a wider variety of tumor types than previously appreciated and point to shared pathogenic mechanisms between a subset of pediatric malignancies. PMID: 24249259
    5. Data indicate that osteopathia striata congenita with cranial sclerosis (OSCS) iscaused by germline deletions of in the X-linked gene WTX (FAM123B, AMER1). PMID: 22670894
    6. Two novel WTX mutations underscore the unpredictability of male survival in osteopathia striata with cranial sclerosis. PMID: 20950377
    7. Stat3 inhibits WTX expression through up-regulation of micro RNA-370 in Wilms tumor. PMID: 23333300
    8. Osteopathia striata with cranial sclerosis or Horan-Beighton syndrome is a rare X-linked dominant inherited bone dysplasia. Genetic analysis allowed the identification of maternally transmitted heterozygous nonsense c.1057C>T (p.R353X) WTX mutation. PMID: 22716240
    9. WTX mutations occur early in Wilms' tumor development, but at a low proportion. There was no evidence that WTX is the main cause of Wilms' tumor. PMID: 22800892
    10. WTX modulates p53 function, in part through regulation of its activator CBP/p300. PMID: 22285752
    11. WTX and NRF2 compete for binding to KEAP1, and thus loss of WTX leads to rapid ubiquitination and degradation of NRF2 and a reduced response to cytotoxic insult. PMID: 22215675
    12. Amer1 exerts its negative regulatory role in Wnt signaling by acting as a scaffold protein for the beta-catenin destruction complex and promoting stabilization of Axin at the plasma membrane. PMID: 21498506
    13. WTX mutations can arise both early and late in Wilms tumour development PMID: 20679664
    14. When gene expression changes mediated by wild-type WTX were compared with those affected by mutant WTX, WTX565 had a 55% overlap in differentially regulated genes, whereas WTX358 regulated only two genes affected by wild-type WTX. PMID: 20956941
    15. Mutations in the WTX-gene are associated with high-grade microsatellite instable colorectal cancers. PMID: 20696052
    16. inactivation of WTX appears to be a late event in tumorigenesis of nephroblastoma in a subgroup of nephroblastomas PMID: 19757195
    17. All investigated families diagnosed with Osteopathia striata with cranial sclerosis had WTX gene defects. PMID: 20209645
    18. WTX, is inactivated in approximately one-third of Wilms tumors; it is inactivated by a monoallelic "single-hit" event targeting the single X chromosome in tumors from males and the active X chromosome in tumors from females PMID: 17204608
    19. findings show that WTX, a protein encoded by a gene mutated in Wilms tumors, forms a complex with beta-catenin, AXIN1, beta-TrCP2 and APC; data provide a possible mechanistic explanation for the tumor suppressor activity of WTX PMID: 17510365
    20. Deletion of the WTX gene is associated with Wilms' tumor with a balanced translocation t(X;18) PMID: 17620295
    21. These data indicate that AMER1 controls the subcellular distribution of APC between membrane- and microtubule-associated pools, and might thereby regulate APC-dependent cellular morphogenesis, cell migration and cell-cell adhesion. PMID: 17925383
    22. Gene has a tumor suppressor function in Wilms tumors, and is involved in beta-catenin destruction. PMID: 18021721
    23. WT1 and WTX mutations occur with similar frequency, that they partially overlap in Wilms tumors, and that mutations in WT1, WTX, and CTNNB1 underlie the genetic basis of about one-third of Wilms tumors PMID: 18311776
    24. Functional inactivation of the WTX gene is not a frequent event in Wilms' tumors. PMID: 18391980
    25. there was not any evidence of WTX mutation in the 143 acute leukemia patients PMID: 18452086
    26. WTX is rarely mutated in acute myeloid leukemia PMID: 18460646
    27. Data indicate that WTX mutation is rare in colorectal, gastric, and hepatocellular carcinomas. PMID: 18720004
    28. The observed phenotypic discordance dependent upon whether a mutation is germline or occurs somatically suggests the existence of temporal or spatial constraints on the action of WTX during tumorigenesis. PMID: 19079258
    29. Mutations in WTX gene is associated with Wilms tumor. PMID: 19137020
    30. WTX binds WT1 and enhances WT1-mediated transcription, suggesting a role for WTX in nuclear pathways implicated in the transcriptional regulation of cellular differentiation programs PMID: 19416806
    31. WTX inactivation is associated with Wilms tumors PMID: 19760609

    顯示更多

    收起更多

  • 相關疾病:
    Osteopathia striata with cranial sclerosis (OSCS)
  • 亞細胞定位:
    Cytoplasm. Cell membrane; Peripheral membrane protein; Cytoplasmic side. Nucleus. Note=Shuttles between nucleus and cytoplasm. Detected in nuclear paraspeckles that are found close to splicing speckles. Translocates to the cell membrane following binding to PtdIns(4,5)P2.
  • 蛋白家族:
    Amer family
  • 組織特異性:
    Detected in fetal and adult kidney, brain and spleen.
  • 數據庫鏈接:

    HGNC: 26837

    OMIM: 300373

    KEGG: hsa:139285

    STRING: 9606.ENSP00000329117

    UniGene: Hs.314225



主站蜘蛛池模板: 中文字幕在线观看亚洲视频| 精品国产一区二区三区免费| 人妻少妇精品中文字幕av蜜桃| 亚洲毛片不卡av在线播放一区| 色一情一乱一伦一区二区三区小说 | 女人扒开屁股桶爽30分钟| 精品久久久久久无码专区不卡| 国产又粗又硬又大爽黄老大爷视| 国产精品毛片完整版视频| 国产男女嘿咻视频在线观看| 小泽玛利亚一区二区在线观看| 欧美黑人添添高潮a片www| 国产精品免费无遮挡无码永久视频| 欧美片内射欧美美美妇| 天堂av无码av在线a√| 欧美人与性动交ccoo| 久久久久女人精品毛片| 久久久喷潮一区二区三区| av国産精品毛片一区二区视频 | 在线观看国产亚洲视频免费| 高级会所人妻互换94部分| 久章草在线精品视频免费观看 | 日本熟日本熟妇在线视频| 成人女人黄网站免费视频| 精品国偷自产在线视频| 天天爽天天爽夜夜爽毛片| 亚洲人成人伊人成综合网无码 | 人妻人人做人做人人爱| 超级av在线天堂东京热| 韩国无码av片在线观看网站 | 日本护士毛茸茸高潮| 亚洲色无码专线精品观看| 精品国际久久久久999波多野| 欧美一区二区三区| 日韩亚洲欧美中文在线| 最新国产精品好看的精品| 久久久中日ab精品综合| 少妇被粗大猛进进出出s小说| 成人乱人伦视频在线观看| 无人区一线二线三线乱码| 亚洲加勒比无码一区二区|