SLC6A5 抗体
Quick Overview for SLC6A5 抗体 (ABIN7270475)
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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原理
- Glyt2 Rabbit mAb
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交叉反应
- 人, 小鼠, 大鼠
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产品特性
- Monoclonal Antibodies
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纯化方法
- Affinity purification
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免疫原
- Recombinant protein of Human Glyt2.
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亚型
- IgG
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anti-Solute Carrier Family 6 (Neurotransmitter Transporter, Glycine), Member 5 (SLC6A5) (AA 1-229) antibody
SLC6A5 适用: 大鼠, 小鼠 WB, IHC, IP 宿主: 兔 Polyclonal unconjugated
anti-Solute Carrier Family 6 (Neurotransmitter Transporter, Glycine), Member 5 (SLC6A5) (N-Term) antibodySLC6A5 适用: 人, 大鼠, 小鼠, 犬, 豚鼠, 马, 兔, Cow, 斑马鱼 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Solute Carrier Family 6 (Neurotransmitter Transporter, Glycine), Member 5 (SLC6A5) (AA 294-393) antibodySLC6A5 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 3B3 unconjugated
anti-Solute Carrier Family 6 (Neurotransmitter Transporter, Glycine), Member 5 (SLC6A5) (AA 503-552) antibodySLC6A5 适用: 人, 大鼠, 小鼠, 犬, 豚鼠, 马, 兔, Cow, 斑马鱼, Bat, 猴, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Solute Carrier Family 6 (Neurotransmitter Transporter, Glycine), Member 5 (SLC6A5) (AA 1-200) antibodySLC6A5 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Solute Carrier Family 6 (Neurotransmitter Transporter, Glycine), Member 5 (SLC6A5) (Middle Region) antibodySLC6A5 适用: 人, 大鼠, 小鼠, 犬, 豚鼠, 马, 兔, Cow, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB,1:500 - 1:2000
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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,0.05 % BSA,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
- Glyt2
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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,Glyt2
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分子量
- 87kDa
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基因ID
- 9152
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UniProt
- Q9Y345
抗原
-
