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

  1. Home
  2. 抗體
  3. 單克隆抗體
  4. KIF7 Monoclonal Antibody

KIF7 Monoclonal Antibody

  • 中文名稱：
    KIF7鼠單克隆抗體
  • 貨號：
    CSB-MA000220
  • 規格：
    ￥1090
  • 圖片：
    • IHC staining of Mouse Kidney tissue, diluted at 1:200.
  • 其他：

產品詳情

  • 產品描述：
    CUSABIO貨號：CSB-MA000220 KIF7單克隆抗體是一款針對Hedgehog信號通路關鍵調控因子KIF7蛋白的高特異性科研試劑，適用于人、小鼠、大鼠等多物種研究。KIF7作為纖毛運動相關驅動蛋白，在胚胎發育調控、細胞極性建立及腫瘤發生等生命過程中發揮重要作用，其異常表達與多種發育障礙及腫瘤疾病密切相關。本產品采用高純度重組蛋白免疫制備，經嚴格質控驗證其特異性識別天然及變性狀態下的KIF7抗原表位，在ELISA和免疫組化（IHC）實驗中展現優異性能。克隆號為4C7的鼠源單抗經Protein G純化工藝處理，純度達95%以上，提供1mg/mL濃度規格，建議-20℃長期保存并避免反復凍融。該抗體特別適用于腫瘤微環境研究、發育生物學機制探索、信號通路交互作用分析等基礎科研領域，為揭示KIF7在神經管發育、骨骼形成及腫瘤轉移中的分子機制提供可靠工具。關鍵詞：KIF7單克隆抗體、Hedgehog信號通路、纖毛運動蛋白、腫瘤機制研究、科研抗體。
  • Uniprot No.：
  • 基因名：
  • 別名：
    EQYK340 antibody; kif7 antibody; KIF7_HUMAN antibody; kinesin family member 7 antibody; kinesin like protein KIF7 antibody; Kinesin-like protein kif7 antibody; UNQ340 antibody
  • 宿主：
    Mouse
  • 反應種屬：
    Human,Mouse,Rat
  • 免疫原：
    Synthetic Peptide
  • 免疫原種屬：
    H, M, R
  • 標記方式：
    Non-conjugated
  • 抗體亞型：
    IgG
  • 克隆號：
    14B6
  • 濃度：
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液：
    PBS, pH 7.4, containing 0.5%BSA, 0.02% sodium azide as Preservative and 50% Glycerol.
  • 產品提供形式：
    Liquid
  • 應用范圍：
    ELISA,IHC
  • 推薦稀釋比：
    Application Recommended Dilution
    IHC 1:100-1:200
  • 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：
    Essential for hedgehog signaling regulation: acts as both a negative and positive regulator of sonic hedgehog (Shh) and Indian hedgehog (Ihh) pathways, acting downstream of SMO, through both SUFU-dependent and -independent mechanisms. Involved in the regulation of microtubular dynamics. Required for proper organization of the ciliary tip and control of ciliary localization of SUFU-GLI2 complexes. Required for localization of GLI3 to cilia in response to Shh. Negatively regulates Shh signaling by preventing inappropriate activation of the transcriptional activator GLI2 in the absence of ligand. Positively regulates Shh signaling by preventing the processing of the transcription factor GLI3 into its repressor form. In keratinocytes, promotes the dissociation of SUFU-GLI2 complexes, GLI2 nuclear translocation and Shh signaling activation. Involved in the regulation of epidermal differentiation and chondrocyte development.
  • 基因功能參考文獻：
    1. two children who both had two missense mutations in the Kinesin Family Member 7 (KIF7) gene, are reported. PMID: 26174511
    2. Kif7 may contribute to pathogenesis of gestational trophoblastic disease through enhancing survival and promoting dissemination of trophoblasts. PMID: 25265279
    3. We identified a Turkish family who had a novel homozygous sequence change, c.2593-2A>C, located at the acceptor splice site of intron 12 of KIF7 (IVS12-2A>C). PMID: 25714560
    4. results suggested that PPFIA1 functioned with PP2A to promote the dephosphorylation of Kif7, triggering Kif7 localization to the tips of primary cilia and promoting Gli transcriptional activity. PMID: 25492966
    5. Studied the ExoS to identify unknown cellular targets associated with ExoS-induced cytotoxicity in a P. aeruginosa infection model.A pull-down assay revealed that ExoS bound the truncated KIF7 gene encoding the N-terminal domain (residues 1-109) of KIF7. PMID: 24462444
    6. six novel mutations were identified at the KIF7 locus in five suspected Acrocallosal syndrome cases PMID: 23125460
    7. This study confirms that KIF7 mutations can cause acrocallosal syndrome. PMID: 23142271
    8. report the first missense homozygous disease-causing mutation in KIF7 and expand the clinical spectrum associated with mutations in this gene to include multiple epiphyseal dysplasia PMID: 22587682
    9. The high-resolution structure of the human KIF7 motor domain is reported and is compared with that of conventional kinesin, the founding member of the kinesin superfamily. PMID: 22281744
    10. Data report mutations in the KIF7 gene, a known regulator of sonic hedgehog signaling and a putative ciliary motor protein, in Joubert syndrome patients. PMID: 21633164
    11. Our data show the role of KIF7 in human primary cilia, especially in the Hedgehog pathway through the regulation of GLI targets, and expand the clinical spectrum of ciliopathies. PMID: 21552264

    顯示更多

    收起更多

  • 相關疾病：
    Bardet-Biedl syndrome (BBS); Hydrolethalus syndrome 2 (HLS2); Acrocallosal syndrome (ACLS); Joubert syndrome 12 (JBTS12); Al-Gazali-Bakalinova syndrome (AGBK)
  • 亞細胞定位：
    Cell projection, cilium. Cytoplasm, cytoskeleton, cilium basal body. Note=Localizes to the cilium tip.
  • 蛋白家族：
    TRAFAC class myosin-kinesin ATPase superfamily, Kinesin family, KIF27 subfamily
  • 組織特異性：
    Embryonic stem cells, melanotic melanoma and Jurkat T-cells. Expressed in heart, lung, liver, kidney, testis, retina, placenta, pancreas, colon, small intestin, prostate and thymus.
  • 數據庫鏈接：

    HGNC: 30497

    OMIM: 200990

    KEGG: hsa:374654

    STRING: 9606.ENSP00000377934

    UniGene: Hs.513134



主站蜘蛛池模板： 日韩精品一卡2卡3卡4卡新区| 欧美精品1卡二卡三卡四卡| 国产成人美女裸体片免费看| 国产99视频精品免费观看9| 少妇大胆瓣开下部自慰| 无码专区—va亚洲v专区| 性欧美大战久久久久久久| 亚洲一卡二卡三卡四卡| 国产老熟女网站| 人人澡人摸人人添| 日韩亚洲中字无码一区二区三区| 夜夜高潮夜夜爽高清视频| av色综合久久天堂av色综合| 日本饥渴人妻欲求不满| 亚洲精品乱码久久久久久不卡| 欧美性黑人极品hd另类| 55夜色66夜色国产精品视频| 精品国产卡一卡2卡3卡| 国产精品福利一区二区| 无码人妻丰满熟妇啪啪| 人人鲁人人莫人人爱精品| 国产粗话肉麻对白在线播放| 69堂人成无码免费视频果冻传媒 | 玩弄人妻少妇老师美妇厨房| 奇米777四色影视在线看| 区二区欧美性插b在线视频网站| 亚洲一区二区三区av无码| 国产国产久热这里只有精品| 亚洲成在人网站无码天堂| 精品国产一区二区三区免费| 人妻丰满熟妇av无码区免| 99热在线精品国产观看| 国产精品色情国产三级在| 久久天天躁夜夜躁狠狠85麻豆| 99国产精品白浆在线观看免费| 欧美人与动牲交zooz男人| 丝袜老师高潮呻吟高潮| 色综合视频一区二区三区44| 精品亚洲国产成人av| 曰本女人与公拘交酡免费视频| 久热在线这里只有精品国产|