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. OPLAH Antibody

OPLAH Antibody

  • 中文名稱：
    OPLAH兔多克隆抗體
  • 貨號：
    CSB-PA016350GA01HU
  • 規(guī)格：
    ￥3,900
  • 其他：

產(chǎn)品詳情

  • Uniprot No.：
  • 基因名：
    OPLAH
  • 別名：
    5 Opase antibody; 5 oxo L prolinase antibody; 5 oxoprolinase (ATP hydrolysing) antibody; 5 oxoprolinase antibody; 5-OPase antibody; 5-oxo-L-prolinase antibody; 5-oxoprolinase antibody; DKFZp434H244 antibody; OPLA antibody; OPLA_HUMAN antibody; oplah antibody; OPLAHD antibody; Pyroglutamase antibody
  • 宿主：
    Rabbit
  • 反應(yīng)種屬：
    Human,Mouse,Rat
  • 免疫原：
    Human OPLAH
  • 免疫原種屬：
    Homo sapiens (Human)
  • 抗體亞型：
    IgG
  • 純化方式：
    Antigen Affinity purified
  • 濃度：
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液：
    PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
  • 產(chǎn)品提供形式：
    Liquid
  • 應(yīng)用范圍：
    ELISA,WB,IHC
  • 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(chǎn)品評價

靶點詳情

  • 功能：
    Catalyzes the cleavage of 5-oxo-L-proline to form L-glutamate coupled to the hydrolysis of ATP to ADP and inorganic phosphate.
  • 基因功能參考文獻：
    1. An autosomal recessive mode of inheritance for 5-oxoprolinase deficiency is further supported by the identification of a single mutation in all 9/14 parent sample sets investigated (except for the father of one patient whose result suggests homozygosity), and the absence of 5-oxoprolinuria in all tested heterozygotes PMID: 27477828
    2. In this study, clinical, biochemical, and genetic aspects of five Chinese 5-oxoprolinuria patients with OPLAH or GSS gene mutations were investigated. PMID: 25851806
    3. the cause of cellular ATP depletion in nephrotic cystinosis may be the futile cycle, formed between two ATP-dependant gamma-glutamyl cycle enzymes, gamma-glutamyl cysteine synthetase and 5-oxoprolinase PMID: 20413906
  • 相關(guān)疾病：
    5-oxoprolinase deficiency (OPLAHD)
  • 蛋白家族：
    Oxoprolinase family
  • 數(shù)據(jù)庫鏈接：

    HGNC: 8149

    OMIM: 260005

    KEGG: hsa:26873

    UniGene: Hs.305882



主站蜘蛛池模板： 在教室伦流澡到高潮hgl视频| 国产美女口爆吞精普通话| 亚洲人成网站18禁止中文字幕 | 日韩丝袜欧美人妻制服| 久久九九精品国产av片国产| 国产免费午夜a无码v视频| 一本色道久久99一综合| 内射国产内射夫妻免费频道| 国产精品成人无码久久久| 2020精品国产视| 2019午夜福利不卡片在线| 51精品国产人成在线观看| 欧美 国产日韩 综合在线| 国产成人18黄网站在线观看| 一区一区三区产品乱码| 无码一区二区三区亚洲人妻| 国产无遮挡裸体免费视频| 中文字幕精品av一区二区五区| 国产av午夜精品一区二区三| 国产自产v一区二区三区c| 成人亚洲a片v一区二区三区日本| 日韩欧美亚洲综合久久影院ds| 永久免费观看国产裸体美女| 中文字幕无线码| 日韩成人无码毛片一区二区| 再深点灬舒服灬太大了在线视频| 亚洲色欲色欲www在线丝| 日本丰满熟妇bbxbbxhd| 婷婷丁香五月天综合东京热| 俄罗斯老熟妇色xxxx| 亚洲国产一区二区三区波多野结衣 | 亚洲无日韩码精品| 亚洲精品鲁一鲁一区二区三区| 欧美黑人添添高潮a片www| 国产亚洲精品久久yy5099| 亚洲综合欧美在线一区在线播放| 天天躁日日躁狠狠躁av麻豆男男| 亚洲无线观看国产精品| 久久人妻国产精品31| 亚 洲 视 频 高 清 无 码| 免费观看又污又黄在线观看|