CHCHD5 抗体 (AA 21-110) (Biotin)
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- 抗原 See all CHCHD5 products
- CHCHD5 (Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 5 (CHCHD5))
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抗原表位
- AA 21-110
- 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 CHCHD5 antibody is conjugated to Biotin
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应用范围
- ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CCDC99
- 亚型
- IgG
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anti-Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 5 (CHCHD5) (AA 1-110) antibody
CHCHD5 适用: 人 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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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.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C for 12 months.
- 有效期
- 12 months
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- 抗原
- CHCHD5 (Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 5 (CHCHD5))
- 别名
- CHCHD5 (CHCHD5 产品)
- 别名
- MGC134601 antibody, MGC85141 antibody, C2orf9 antibody, MIC14 antibody, 1110027L01Rik antibody, AW045710 antibody, coiled-coil-helix-coiled-coil-helix domain containing 5 antibody, coiled-coil-helix-coiled-coil-helix domain containing 5 L homeolog antibody, CHCHD5 antibody, chchd5.L antibody, Chchd5 antibody
- 背景
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Synonyms: C2orf9, CHCH5_HUMAN, CHCHD5, chromosome 2 open reading frame, Coiled coil helix coiled coil helix domain containing 5, Coiled-coil-helix-coiled-coil-helix domain-containing protein 5, FLJ39671, MGC11104.
Background: CHCHD5 is a 110 amino acid protein that contains one CHCH domain. The gene encoding CHCHD5 maps to human chromosome 2, which consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
- 基因ID
- 84269
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