C9orf64 抗体 (AA 161-260) (HRP)
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- 抗原 See all C9orf64 products
- C9orf64 (Chromosome 9 Open Reading Frame 64 (C9orf64))
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抗原表位
- AA 161-260
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This C9orf64 antibody is conjugated to HRP
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人
- 预测反应
- Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C9orf64
- 亚型
- IgG
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anti-Chromosome 9 Open Reading Frame 64 (C9orf64) (AA 182-341) antibody
C9orf64 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 9 Open Reading Frame 64 (C9orf64) (AA 45-94) antibodyC9orf64 适用: 人, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 9 Open Reading Frame 64 (C9orf64) (AA 266-315) antibodyC9orf64 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 注意事项
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- C9orf64 (Chromosome 9 Open Reading Frame 64 (C9orf64))
- 别名
- C9orf64 (C9orf64 产品)
- 别名
- C9orf64 antibody, MGC84745 antibody, MGC97544 antibody, chromosome Z C9orf64 homolog antibody, chromosome 9 open reading frame 64 L homeolog antibody, chromosome 9 open reading frame 64 antibody, chromosome 15 open reading frame, human C9orf64 antibody, queuosine salvage protein antibody, CZH9orf64 antibody, c9orf64.L antibody, c9orf64 antibody, C15H9orf64 antibody, C8H9orf64 antibody, C9orf64 antibody
- 背景
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Synonyms: C9orf64, CI064_HUMAN, UPF0553 protein C9orf64.
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 C9orf64 gene product has been provisionally designated C9orf64 pending further characterization.
- 基因ID
- 84267
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