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OCRL 抗体

OCRL 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7264779
发货至: 中国
  • 抗原 See all OCRL 抗体
    OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))
    适用
    • 27
    • 11
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 21
    • 6
    克隆类型
    • 24
    • 3
    多克隆
    标记
    • 16
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This OCRL antibody is un-conjugated
    应用范围
    • 15
    • 11
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human OCRL (NP_001578.2).
    亚型
    IgG
    Top Product
    Discover our top product OCRL Primary Antibody
  • 应用备注
    WB 1:500-1:2000
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))
    别名
    OCRL (OCRL 产品)
    别名
    OCRL antibody, wu:fi09g03 antibody, zgc:152864 antibody, locr antibody, nphl2 antibody, ocrl1 antibody, inpp5f antibody, INPP5F antibody, LOCR antibody, NPHL2 antibody, OCRL-1 antibody, OCRL1 antibody, 9530014D17Rik antibody, BB143339 antibody, OCRL, inositol polyphosphate-5-phosphatase antibody, phosphatidylinositol polyphosphate 5-phosphatase antibody, oculocerebrorenal syndrome of Lowe antibody, Ocrl antibody, NAEGRDRAFT_58601 antibody, OCRL antibody, ocrl antibody
    背景
    This gene encodes an inositol polyphosphate 5-phosphatase. This protein is involved in regulating membrane trafficking and is located in numerous subcellular locations including the trans-Golgi network, clathrin-coated vesicles and, endosomes and the plasma membrane. This protein may also play a role in primary cilium formation. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. Alternate splicing results in multiple transcript variants.
    分子量

    Observed_MW: 110 kDa

    Calculated_MW: 103 kDa/104 kDa

    基因ID
    4952
    UniProt
    Q01968
    途径
    Inositol Metabolic Process
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