SLC1A1 Antibody Blocking Peptide(bs-21312P)-500ug

SLC1A1 Antibody Blocking Pepti

de(bs-21312P)-500ug
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  • bs-21312P
  • 2025年10月16日
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      500ug

    产品编号bs-21312P
    英文名称SLC1A1 Antibody Blocking Peptide
    中文名称胶质细胞谷氨酸运载蛋白3/神经/上皮细胞谷氨酸运载蛋白封闭多肽
    英文别名Excitatory amino acid transporters 3; Slc1a1; Eaac1; Eaat3; SLC1A1; EAAC1; EAAT3; solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1; EAAC 2; Excitatory amino acid carrier 1; Excitatory amino acid carrier 2; Excitatory amino acid carrier1; MEAAC 1; MEAAC1; Neuronal and epithelial glutamate transporter; REAAC 1; REAAC1; Slc1 a1; Slc1a 1; Slc1a1; Sodium dependent glutamate/aspartate transporter 3; Solute carrier family 1, member 1; EAA3_HUMAN.
    纯化方法HPLC
    研究领域

    Neuroscience > Neurotransmitter > Amino Acids > Aspartate

    Neuroscience > Neurotransmitter > Amino Acids > Glutamate

    Neuroscience > Neurotransmitter > Transporters > Glutamate

    亚基Interacts with ARL6IP5/PRAF3.
    亚细胞定位Membrane; Multi-pass membrane protein.
    组织特异性Expressed in all tissues tested including liver, muscle, testis, ovary, retinoblastoma cell line, neurons and brain (in which there was dense expression in substantia nigra, red nucleus, hippocampus and in cerebral cortical layers).
    翻译后修饰Glycosylated.
    相似性Belongs to the sodium:dicarboxylate (SDF) symporter (TC 2.A.23) family. SLC1A1 subfamily.
    功能Transports L-glutamate and also L- and D-aspartate. Essential for terminating the postsynaptic action of glutamate by rapidly removing released glutamate from the synaptic cleft. Acts as a symport by cotransporting sodium. Negatively regulated by ARL6IP5 (By similarity).
    保存条件Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料This gene encodes a member of the high-affinity glutamate transporters that play an essential role in transporting glutamate across plasma membranes. In brain, these transporters are crucial in terminating the postsynaptic action of the neurotransmitter glutamate, and in maintaining extracellular glutamate concentrations below neurotoxic levels. This transporter also transports aspartate, and mutations in this gene are thought to cause dicarboxylicamino aciduria, also known as glutamate-aspartate transport defect.

     

     

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