C9ORF72 抗体 (AA 400-450)
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北京 101111
Quick Overview for C9ORF72 抗体 (AA 400-450) (ABIN5688963)
抗原
See all C9ORF72 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 400-450
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特异性
- ALSFTD antibody is human, mouse and rat reactive. At least two isoforms are known to exist.
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纯化方法
- ALSFTD Antibody is affinity chromatography purified via peptide column.
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免疫原
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ALSFTD antibody was raised against a 19 amino acid peptide from near the carboxy terminus of human ALSFTD.
The immunogen is located within amino acids 400 - 450 of ALSFTD. -
亚型
- IgG
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anti-Chromosome 9 Open Reading Frame 72 (C9ORF72) (AA 1-230) antibody
C9ORF72 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 9 Open Reading Frame 72 (C9ORF72) (AA 391-481) antibodyC9ORF72 适用: 人, 大鼠, 小鼠 WB, ELISA, FACS, IF (cc), IF (p), ICC, IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 9 Open Reading Frame 72 (C9ORF72) (AA 138-430) antibodyC9ORF72 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 9 Open Reading Frame 72 (C9ORF72) (AA 396-424), (C-Term) antibodyC9ORF72 适用: 人 WB 宿主: 兔 Polyclonal RB27382 unconjugated
anti-Chromosome 9 Open Reading Frame 72 (C9ORF72) (AA 1-481) antibodyC9ORF72 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Chromosome 9 Open Reading Frame 72 (C9ORF72) (AA 396-424) antibodyC9ORF72 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
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应用备注
- ALSFTD antibody can be used for the detection of ALSFTD by Western blot at 1 - 2 μ,g/mL. Antibody can also be used for immunocytochemistry at 10 μ,g/mL.
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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
- ALSFTD Antibody is supplied in PBS containing 0.02 % 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
- ALSFTD antibody can be stored at 4°C for three months and -20°C, stable for up to one year.
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- C9ORF72 (Chromosome 9 Open Reading Frame 72 (C9ORF72))
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别名
- ALSFTD
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背景
- ALSFTD (C9orf72) is considered to play a role in gender determination (1). Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG (2). Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster (3,4).
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分子量
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Predicted: 53 kDa
Observed: 52 kDa -
基因ID
- 203228
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NCBI登录号
- NP_060795
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UniProt
- Q96LT7
抗原
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