GARS 抗体 (AA 43-289)
Quick Overview for GARS 抗体 (AA 43-289) (ABIN7596061)
抗原
See all GARS 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 43-289
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原理
- Human GARS antibody
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纯化方法
- protein-A affinity chromatography
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免疫原
- Recombinant human GARS (43-289aa) purified from E. coli
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亚型
- IgG1 kappa
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anti-Glycyl-tRNA Synthetase (GARS) (AA 567-735) antibody
GARS 适用: 人 WB, IHC, IF, FACS, ICC 宿主: 兔 Polyclonal unconjugated
anti-Glycyl-tRNA Synthetase (GARS) (AA 60-370) antibodyGARS 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Glycyl-tRNA Synthetase (GARS) antibodyGARS 适用: 人, 小鼠, 大鼠 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Glycyl-tRNA Synthetase (GARS) (AA 1-389) antibodyGARS 适用: 人 WB, IHC, IF, ELISA, IP 宿主: 兔 Polyclonal unconjugated
anti-Glycyl-tRNA Synthetase (GARS) (C-Term) antibodyGARS 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Glycyl-tRNA Synthetase (GARS) (AA 15-305) antibodyGARS 适用: 人 WB, IF, FACS 宿主: 小鼠 Monoclonal 1641CT837-23-96 unconjugated
anti-Glycyl-tRNA Synthetase (GARS) (AA 35-305) antibodyGARS 适用: 人 WB, FACS 宿主: 小鼠 Monoclonal 1641CT125-1-1 unconjugated
anti-Glycyl-tRNA Synthetase (GARS) (AA 1-685) antibodyGARS 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Glycyl-tRNA Synthetase (GARS) (AA 1-685) antibodyGARS 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Glycyl-tRNA Synthetase (GARS) antibodyGARS 适用: 人 WB, IF, FACS 宿主: 小鼠 Monoclonal 1C6 unconjugated
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应用备注
- Optimal working dilution should be determined by the investigator.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% glycero
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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,-80 °C
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储存方法
- Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C. Avoid repeated freezing and thawing cycles.
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- GARS (Glycyl-tRNA Synthetase (GARS))
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别名
- GARS
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背景
- GARS, also known as glycyl-tRNA synthetase, is one of the aminoacyl-tRNA synthetase that charge tRNAswith their cognate amino acids. Defects in the gene encoding GlyRS is the cause of Charcot-Marie-Toothdisease type 2D (CMT2D), which is an autosomal dominant inherited disease characterized by severe weakness,atrophy and absence of deep tendon reflexes in the upper extremities. Defects in the GlyRS gene is also thecause of distal hereditary muscular neuropathy type V (HMN5), a disease similar to CMT2D, though the distalsensory involvement is less severe in HMN5 patients.
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NCBI登录号
- NP_002038
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途径
- Ribonucleoside Biosynthetic Process
抗原
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