KIAA0562 抗体 (AA 451-550) (Biotin)
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- 抗原 See all KIAA0562 products
- KIAA0562
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抗原表位
- AA 451-550
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适用
- 人, 小鼠
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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 KIAA0562 antibody is conjugated to Biotin
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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, 小鼠
- 预测反应
- Rat,Dog,Cow,Sheep,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CEP104/KIAA0562
- 亚型
- IgG
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anti-KIAA0562 (KIAA0562) (AA 1-554) antibody
KIAA0562 适用: 人 WB, IF 宿主: 小鼠 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
- KIAA0562
- 别名
- CEP104/KIAA0562 (KIAA0562 产品)
- 别名
- KIAA0562 antibody, glybp antibody, kiaa0562 antibody, A930027E11 antibody, AI115523 antibody, Kiaa0562 antibody, mKIAA0562 antibody, GlyBP antibody, centrosomal protein 104 antibody, centrosomal protein 104kDa antibody, CEP104 antibody, cep104 antibody, Cep104 antibody
- 背景
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Synonyms: CE104_HUMAN, Centrosomal protein of 104 kDa, Cep104, GlyBP, Glycine Binding Protein, glycine-, glutamate- and thienylcyclohexylpiperidine-binding protein, KIAA0562, LOC246295.
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 KIAA0562 gene product has been provisionally designated KIAA0562 pending further characterization.
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