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. 多克隆抗體
  4. AMN Antibody

AMN Antibody

  • 中文名稱：
    AMN兔多克隆抗體
  • 貨號：
    CSB-PA880128LA01HU
  • 規格：
    ￥440
  • 圖片：
    • IHC image of CSB-PA880128LA01HU diluted at 1:600 and staining in paraffin-embedded human gastric cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
    • Immunofluorescence staining of Hela cells with CSB-PA880128LA01HU at 1:200, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was 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) AMN Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    AMN
  • 別名：
    5033428N14Rik antibody; amn antibody; Amnion associated transmembrane protein antibody; Amnionless antibody; Amnionless homolog antibody; AMNLS_HUMAN antibody; AV002116 antibody; PRO1028 antibody; Protein amnionless antibody; Type I transmembrane protein antibody; UNQ513/PRO1028 antibody; Visceral endoderm specific type 1 transmembrane protein antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Recombinant Human Protein amnionless protein (25-163AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標記方式：
    Non-conjugated

    本頁面中的產品，AMN Antibody (CSB-PA880128LA01HU)，的標記方式是Non-conjugated。對于AMN Antibody，我們還提供其他標記。見下表：

    可提供標記
    標記方式 貨號 產品名稱 應用
    HRP CSB-PA880128LB01HU AMN Antibody, HRP conjugated ELISA
    FITC CSB-PA880128LC01HU AMN Antibody, FITC conjugated
    Biotin CSB-PA880128LD01HU AMN Antibody, Biotin conjugated ELISA
  • 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, IHC, IF
  • 推薦稀釋比：
    Application Recommended Dilution
    IHC 1:500-1:1000
    IF 1:200-1:500
  • 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：
    Membrane-bound component of the endocytic receptor formed by AMN and CUBN. Required for normal CUBN glycosylation and trafficking to the cell surface. The complex formed by AMN and CUBN is required for efficient absorption of vitamin B12. Required for normal CUBN-mediated protein transport in the kidney (Probable).
  • 基因功能參考文獻：
    1. Study shows that cubilin mutations (novel and some previously reported) and all previously reported amnionless missense mutations resulted in endoplasmic reticulum retention and completely inhibited amnionless-dependent plasma membrane expression of cubilin. PMID: 29402915
    2. heterozygous mutations in AMN in a family from the United Kingdom with clinical features of Imerslund-Grasbeck Syndrome PMID: 26040326
    3. Our genetic screening of 154 families of patients with inherited cobalamin malabsorption revealed population-specific mutations, mutational hotspots, and functionally distinct regions in the three causal genes: CUBN, AMN, and GIF. PMID: 22929189
    4. We present evidence that this founder mutation causes over 50% of the Imerslund-Grasbeck syndrome (IGS) cases among Arabic, Turkish, and Sephardic Jewish families, and the mutation is as old as human civvlization. PMID: 22078000
    5. amnionless is essential for the correct luminal expression of cubilin in humans. PMID: 21750092
    6. homozygous mutations affecting exons 1-4 of human AMN lead to megaloblastic anemia 1 PMID: 12590260
    7. cubilin and amnionless are subunits of a novel cubilin/amnionless (cubam) complex PMID: 14576052
    8. Recurrent spontaneous abortions may be caused by mutations in the Amnionless gene. PMID: 16403802
    9. This review summarizes recent data on the biological function of amnionless and focuses on its implication in embryonic nutrition and central nervous system malformations. PMID: 17979745

    顯示更多

    收起更多

  • 相關疾病：
    Recessive hereditary megaloblastic anemia 1 (RH-MGA1)
  • 亞細胞定位：
    [Isoform 1]: Apical cell membrane; Single-pass type I membrane protein. Cell membrane; Single-pass type I membrane protein. Endosome membrane. Membrane, coated pit.; [Soluble protein amnionless]: Secreted.
  • 組織特異性：
    Detected in proximal tubules in the kidney cortex (at protein level). Long isoforms are highly expressed in small intestine, colon and kidney (renal proximal tubule epithelial cells). Shorter isoforms are detected at lower levels in testis, thymus and per
  • 數據庫鏈接：

    HGNC: 14604

    OMIM: 261100

    KEGG: hsa:81693

    STRING: 9606.ENSP00000299155

    UniGene: Hs.534494



主站蜘蛛池模板： 国产成年无码v片在线| 97久久婷婷五月综合色d啪蜜芽 | 内射人妻少妇无码一本一道| 久久成人麻豆午夜电影| 猫咪av成人永久网站在线观看| 国产精品久久自在自线不卡| 在线天堂中文官网| 久久棈精品久久久久久噜噜 | 国产人妖xxxx做受视频| 狠狠人妻久久久久久综合| 色欲久久综合亚洲精品蜜桃 | 欧美99久久无码一区人妻a片| 任我爽橹在线精品视频| 人妻va精品va欧美va| 妺妺窝人体色www聚色窝仙踪| 色九月亚洲综合网| 色欲综合久久中文字幕网| 水蜜桃亚洲一二三四在线| 日本亚洲色大成网站www| 无码国产一区二区三区四区| 欧美人禽zozo动人物杂交| 亚洲中文字幕无码中字| 97免费公开在线视频| 人妻无码少妇一区二区| 婷婷射精av这里只有精品| av怡红院一区二区三区| 真人做人60分钟啪啪免费看| 亚洲国产精品无码专区影院| 亚洲午夜成人片| 色婷婷久久综合中文久久一本| 奇米777狠狠色噜噜狠狠狠| 中国老熟女重囗味hdxx| 国产成人精品无码专区| 日本熟妇色一本在线观看| 国产精品无码a∨麻豆| 人妻少妇中文字幕久久| 欧美又大又粗午夜剧场免费| 天堂va欧美ⅴa亚洲va| 潮喷失禁大喷水aⅴ无码| 久久aⅴ无码av高潮av喷吹| 少妇人妻陈艳和黑人教练|