日韩在线视频不卡-日一区二区三区-天堂国产+人+综合+亚洲欧美-精品国产一区二区三区久久狼-国产成人无码18禁午夜福利网址-国产在线拍偷自揄拍精品-九色91丨porny丨丝袜-久久天天躁狠狠躁夜夜av-99蜜桃臀久久久欧美精品-成人一区二区视频-狠狠操人人干-40岁干柴烈火少妇高潮不断-国产福利不卡-伊人98-丰满多毛的陰户视频-日韩一二三四五区-国产专区一线二线三线码-好男人社区影院www-国产精品2019-欧美三级一区

Your Good Partner in Biology Research

PYGL Antibody

  • 中文名稱(chēng):
    PYGL兔多克隆抗體
  • 貨號(hào):
    CSB-PA019122GA01HU
  • 規(guī)格:
    ¥3,900
  • 其他:

產(chǎn)品詳情

  • Uniprot No.:
  • 基因名:
  • 別名:
    Glycogen phosphorylase antibody; Glycogen phosphorylase L antibody; Glycogen phosphorylase liver antibody; Glycogen phosphorylase liver form antibody; GSD6 antibody; Hers disease; glycogen storage disease type VI antibody; liver form antibody; OTTHUMP00000233649 antibody; OTTHUMP00000233651 antibody; Phosphorylase glycogen liver antibody; Pygl antibody; PYGL_HUMAN antibody
  • 宿主:
    Rabbit
  • 反應(yīng)種屬:
    Human,Mouse,Rat
  • 免疫原:
    Human PYGL
  • 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 0.1% 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(chǔ)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(píng)價(jià)

靶點(diǎn)詳情

  • 功能:
    Allosteric enzyme that catalyzes the rate-limiting step in glycogen catabolism, the phosphorolytic cleavage of glycogen to produce glucose-1-phosphate, and plays a central role in maintaining cellular and organismal glucose homeostasis.
  • 基因功能參考文獻(xiàn):
    1. Susceptibility to excessive liver glycogen storage in patients with type 1 diabetes. PMID: 15223230
    2. Deficiency of liver glycogen phosphorylase is predominantly the result of missense mutations affecting enzyme activity. There are no common mutations and the severity of clinical symptoms varies significantly. PMID: 17705025
  • 相關(guān)疾?。?/div>
    Glycogen storage disease 6 (GSD6)
  • 亞細(xì)胞定位:
    Cytoplasm, cytosol.
  • 蛋白家族:
    Glycogen phosphorylase family
  • 數(shù)據(jù)庫(kù)鏈接:

    HGNC: 9725

    OMIM: 232700

    KEGG: hsa:5836

    STRING: 9606.ENSP00000216392

    UniGene: Hs.282417