C9ORF57 抗体 (AA 61-160) (Cy7)
Quick Overview for C9ORF57 抗体 (AA 61-160) (Cy7) (ABIN1707342)
抗原
适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 61-160
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预测反应
- Human
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human C9orf57
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亚型
- IgG
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anti-Chromosome 9 Open Reading Frame 57 (C9ORF57) (AA 51-127) antibody
C9ORF57 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
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应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- C9ORF57 (Chromosome 9 Open Reading Frame 57 (C9ORF57))
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别名
- C9orf57
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背景
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Synonyms: C9orf57, Chromosome 9 open reading frame 57, CI057_HUMAN, RP11-346E17.3, Uncharacterized protein C9orf57.
Background: Chromosome 9 consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf57 gene product has been provisionally designated C9orf57 pending further characterization.
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基因ID
- 138240
抗原
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