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PROK2 抗体

PROK2 适用: 大鼠, 人, 小鼠 IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7262597
发货至: 中国
  • 抗原 See all PROK2 抗体
    PROK2 (Prokineticin 2 (PROK2))
    适用
    • 23
    • 13
    • 9
    • 3
    • 1
    大鼠, 人, 小鼠
    宿主
    • 36
    • 2
    • 1
    克隆类型
    • 38
    • 1
    多克隆
    标记
    • 15
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PROK2 antibody is un-conjugated
    应用范围
    • 29
    • 17
    • 13
    • 13
    • 10
    • 4
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human PROK2 (NP_001119600.1).
    亚型
    IgG
    Top Product
    Discover our top product PROK2 Primary Antibody
  • 应用备注
    IHC 1:50-1:100
    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
    PROK2 (Prokineticin 2 (PROK2))
    别名
    PROK2 (PROK2 产品)
    别名
    PROK2 antibody, Bv8 antibody, PK2 antibody, Prok1 antibody, BV8 antibody, HH4 antibody, KAL4 antibody, MIT1 antibody, prokineticin 2 antibody, prokineticin 2 S homeolog antibody, prokineticin-2 antibody, PROK2 antibody, prok2 antibody, prok2.S antibody, Prok2 antibody, LOC101104864 antibody
    背景
    This gene encodes a protein expressed in the suprachiasmatic nucleus (SCN) circadian clock that may function as the output component of the circadian clock. The secreted form of the encoded protein may also serve as a chemoattractant for neuronal precursor cells in the olfactory bulb. Proteins from other vertebrates which are similar to this gene product were isolated based on homology to snake venom and secretions from frog skin, and have been shown to have diverse functions. Mutations in this gene are associated with Kallmann syndrome 4. Multiple transcript variants encoding different isoforms have been found for this gene.
    基因ID
    60675
    UniProt
    Q9HC23
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