GLRA1 抗体 (AA 29-154)
Quick Overview for GLRA1 抗体 (AA 29-154) (ABIN5611339)
抗原
See all GLRA1 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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抗原表位
- AA 29-154
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原理
- GLRA1 Antibody
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纯化方法
- Purified antibody
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免疫原
- Purified recombinant fragment of human GLRA1 (AA: 29-154) expressed in E. Coli.
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亚型
- IgG1
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anti-Glycine Receptor, alpha 1 (GLRA1) (AA 23-113) antibody
GLRA1 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Glycine Receptor, alpha 1 (GLRA1) (AA 121-220) antibodyGLRA1 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 2E6 unconjugated
anti-Glycine Receptor, alpha 1 (GLRA1) antibodyGLRA1 适用: 人, 大鼠, 小鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Glycine Receptor, alpha 1 (GLRA1) (Internal Region) antibodyVerified GLRA1 适用: 人, 大鼠, 小鼠 WB, ELISA, IHC 宿主: 山羊 Polyclonal unconjugated
anti-Glycine Receptor, alpha 1 (GLRA1) (AA 121-220) antibodyGLRA1 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 4D9 unconjugated
anti-Glycine Receptor, alpha 1 (GLRA1) (Internal Region) antibodyGLRA1 适用: 人, 大鼠, 小鼠 WB, ELISA, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Glycine Receptor, alpha 1 (GLRA1) antibodyGLRA1 适用: 人 WB, IF, ICC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Glycine Receptor, alpha 1 (GLRA1) (N-Term) antibodyGLRA1 适用: 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Glycine Receptor, alpha 1 (GLRA1) (AA 1-449) antibodyGLRA1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Glycine Receptor, alpha 1 (GLRA1) (Middle Region) antibodyGLRA1 适用: 人, 大鼠, 小鼠, 犬, Cow, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- ELISA: 1/10000
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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
- Purified antibody in PBS with 0.05 % sodium azide.
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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
- 4 °C,-20 °C
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储存方法
- Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
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- GLRA1 (Glycine Receptor, alpha 1 (GLRA1))
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别名
- GLRA1
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背景
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The protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor, which mediates postsynaptic inhibition in the central nervous system. Defects in this gene are a cause of startle disease (STHE), also known as hereditary hyperekplexia or congenital stiff-person syndrome. Multiple transcript variants encoding different isoforms have been found.
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分子量
- 52.6 kDa
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基因ID
- 2741
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途径
- Synaptic Membrane
抗原
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