GLRB 抗体 (AA 23-160)
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- 抗原 See all GLRB 抗体
- GLRB (Glycine Receptor, beta (GLRB))
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抗原表位
- AA 23-160
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适用
- 人
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宿主
- 小鼠
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克隆类型
- 单克隆
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标记
- This GLRB antibody is un-conjugated
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应用范围
- ELISA, Immunocytochemistry (ICC), Flow Cytometry (FACS)
- 原理
- GLRB Antibody
- 纯化方法
- Purified antibody
- 免疫原
- Purified recombinant fragment of human GLRB (AA: 23-160) expressed in E. Coli.
- 克隆位点
- 3B8A8
- 亚型
- IgG2b
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anti-Glycine Receptor, beta (GLRB) (AA 51-150) antibody
GLRB 适用: 人, 小鼠, 大鼠 WB, ELISA, IF (cc), IF (p), ICC, IHC (fro), IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Glycine Receptor, beta (GLRB) (AA 355-472) antibodyGLRB 适用: 人 ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Glycine Receptor, beta (GLRB) (AA 336-355), (AA 336-455) antibodyGLRB 适用: 小鼠, 大鼠, 猴 ICC, IHC 宿主: 小鼠 Monoclonal 299E7 unconjugated
anti-Glycine Receptor, beta (GLRB) (AA 102-132), (N-Term) antibodyGLRB 适用: 人, 小鼠 WB, EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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ELISA: 1/10000
FCM: 1/200 - 1/400
ICC: 1/200 - 1/1000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- Purified antibody in PBS with 0.05 % sodium azide.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 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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- 抗原
- GLRB (Glycine Receptor, beta (GLRB))
- 别名
- GLRB (GLRB 产品)
- 别名
- HKPX2 antibody, glrb antibody, MGC145156 antibody, AI853901 antibody, Glyrb antibody, spa antibody, spastic antibody, glrb2 antibody, zgc:101041 antibody, glycine receptor beta antibody, glycine receptor, beta antibody, glycine receptor, beta subunit antibody, glycine receptor, beta b antibody, GLRB antibody, Glrb antibody, glrb antibody, glrbb antibody
- 背景
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Description: This gene encodes the beta subunit of the glycine receptor, which is a pentamer composed of alpha and beta subunits. The receptor functions as a neurotransmitter-gated ion channel, which produces hyperpolarization via increased chloride conductance due to the binding of glycine to the receptor. Mutations in this gene cause startle disease, also known as hereditary hyperekplexia or congenital stiff-person syndrome, a disease characterized by muscular rigidity. Alternative splicing results in multiple transcript variants.
Aliases: HKPX2
- 分子量
- 56.1kDa
- 基因ID
- 2743
- HGNC
- 2743
- UniProt
- P48167
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