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Rabbit Polyclonal Anti-Excitat

ory Amino Acid Transporter 2 (extracellular)
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  • ¥11000
  • OriGene已认证
  • TA328838
  • 美国
  • 2026年04月01日
  • IHC, WB
  • Rabbit
  • Human, Mouse, Rat
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体名

      Rabbit Polyclonal Anti-Excitatory Amino Acid Transporter 2 (extracellular)

    • 抗体英文名

      Rabbit Polyclonal Anti-Excitatory Amino Acid Transporter 2 (extracellular)

    • 靶点

      Slc1a2

    • 应用范围

      IHC, WB

    • 宿主

      Rabbit

    • 适应物种

      Human, Mouse, Rat

    • 保质期

      Stable for 12 months from date of receipt.

    • 目录编号

      TA328838

    • 级别

      科研级

    • 库存

      7周

    • 供应商

      OriGene

    • 克隆性

      Polyclonal

    • 保存条件

      Store at -20°C as received.

    • 形态

      Lyophilized. Concentration before lyophilization ~0.8mg/ml (lot dependent, please refer to CoA along with shipment for actual concentration). Buffer before lyophilization: Phosphate buffered saline (PBS), pH 7.4, 1% BSA, 0.025% NaN3.

    • 免疫原

      Peptide (C)KQLGPGKKNDEVS, corresponding to amino acid residues 151-163 of rat EAAT2. 2nd extracellular loop.

    • 规格

      50 ul

    Rabbit Polyclonal Anti-Excitatory Amino Acid Transporter 2 (extracellular).更多抗体产品详情信息,请到OriGene 官网网站进行查看了解,有任何问题欢迎随时联系我们。

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    图标文献和实验
    相关实验
    • Characterization of Wild‐Type Excitatory Amino Acid Ion Channel Receptors

      . Described in this unit are receptor binding assays for studying ion?channel forming excitatory amino acid (EAA) receptors in the mammalian central nervous system. One of the three major types of ionotropic (channel?forming) EAA receptors are the AMPA

    • Methods for the Detection of D-Amino-Acid Oxidase

      then twice for 5 min. It was incubated for 1 hr in TBS-T containing rabbit anti-hog D-amino-acid oxidase IgG (1/3,000 dilution) and quickly rinsed twice with TBS-T and further washed in TBS-T once for 15 min then twice for 5 min. The membrane was incubated

    • Products of Arachidonic Acid Metabolism

      of rabbit polyclonal antibodies directed to the major sodium transporters and water channels expressed in each renal tubule segment.” It allows and facilitates characterization and analysis of tubular functional differences that define individual nephron

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