SLC6A5 抗体 (AA 1-200)
Quick Overview for SLC6A5 抗体 (AA 1-200) (ABIN6148044)
抗原
See all SLC6A5 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
 - AA 1-200
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序列
 - MDCSAPKEMN KLPANSPEAA AAQGHPDGPC APRTSPEQEL PAAAAPPPPR VPRSASTGAQ TFQSADARAC EAERPGVGSC KLSSPRAQAA SAALRDLREA QGAQASPPPG SSGPGNALHC KIPFLRGPEG DANVSVGKGT LERNNTPVVG WVNMSQSTVV LGTDGITSVL PGSVATVATQ EDEQGDENKA RGNWSSKLDF
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交叉反应
 - 人, 小鼠, 大鼠
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产品特性
 - Polyclonal Antibodies
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免疫原
 - Recombinant fusion protein containing a sequence corresponding to amino acids 1-200 of human SLC6A5 (NP_004202.3).
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亚型
 - IgG
 
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应用备注
 - WB,1:500 - 1:2000
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说明
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HIGH QUALITY
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限制
 - 仅限研究用
 
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状态
 - Liquid
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缓冲液
 - PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
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储存液
 - Sodium azide
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注意事项
 - This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
 - -20 °C
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储存方法
 - Store at -20°C. Avoid freeze / thaw cycles.
 
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- SLC6A5 (Solute Carrier Family 6 (Neurotransmitter Transporter, Glycine), Member 5 (SLC6A5))
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别名
 - SLC6A5
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背景
 - This gene encodes a sodium- and chloride-dependent glycine neurotransmitter transporter. This integral membrane glycoprotein is responsible for the clearance of extracellular glycine during glycine-mediated neurotransmission. This protein is found in glycinergic axons and maintains a high presynaptic pool of neurotransmitter at glycinergic synapses. Mutations in this gene cause hyperekplexia, a heterogenous neurological disorder characterized by exaggerated startle responses and neonatal apnea. Two transcript variants encoding different isoforms have been found for this gene.,SLC6A5,GLYT-2,GLYT2,HKPX3,NET1,Neuroscience,Cell Type Marker,Neuron marker,Synapse marker,SLC6A5
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分子量
 - 87 kDa
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基因ID
 - 9152
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UniProt
 - Q9Y345
 
抗原
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