C1ORF123 抗体 (AA 81-150) (Biotin)
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- 抗原 See all C1ORF123 抗体
- C1ORF123 (Chromosome 1 Open Reading Frame 123 (C1ORF123))
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抗原表位
- AA 81-150
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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 C1ORF123 antibody is conjugated to Biotin
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应用范围
- ELISA, Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C1orf123
- 亚型
- IgG
- Top Product
- Discover our top product C1ORF123 Primary Antibody
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anti-Chromosome 1 Open Reading Frame 123 (C1ORF123) (AA 1-160) antibody
C1ORF123 适用: 人 ELISA, WB, IHC 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.
- 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
- C1ORF123 (Chromosome 1 Open Reading Frame 123 (C1ORF123))
- 别名
- C1orf123 (C1ORF123 产品)
- 别名
- C1orf123 antibody, 1110008H16Rik antibody, chromosome 1 open reading frame 123 antibody, chromosome 3 open reading frame, human C1orf123 antibody, RIKEN cDNA 0610037L13 gene antibody, similar to RIKEN cDNA 0610037L13 antibody, chromosome 1 open reading frame 123 L homeolog antibody, C1orf123 antibody, C3H1orf123 antibody, 0610037L13Rik antibody, RGD1559786 antibody, c1orf123.L antibody
- 背景
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Synonyms: C1orf123, CA123_HUMAN, Chromosome 1 open reading frame 123, RP5-1024G6.3, UPF0587 protein C1orf123.
Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf123 gene product has been provisionally designated C1orf123 pending further characterization.
- 基因ID
- 54987
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