CTTNBP2NL 抗体 (AA 5-110) (AbBy Fluor® 750)
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- 抗原 See all CTTNBP2NL products
- CTTNBP2NL (CTTNBP2 N-terminal Like (CTTNBP2NL))
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抗原表位
- AA 5-110
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适用
- 大鼠
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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 CTTNBP2NL antibody is conjugated to AbBy Fluor® 750
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 大鼠
- 预测反应
- Human,Mouse,Cow,Pig,Horse,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CTTNBP2NL
- 亚型
- IgG
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anti-CTTNBP2 N-terminal Like (CTTNBP2NL) (AA 135-164), (N-Term) antibody
CTTNBP2NL 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB32341 unconjugated
anti-CTTNBP2 N-terminal Like (CTTNBP2NL) (AA 142-172), (N-Term) antibodyCTTNBP2NL 适用: 人 WB, EIA 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
- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- CTTNBP2NL (CTTNBP2 N-terminal Like (CTTNBP2NL))
- 别名
- CTTNBP2NL (CTTNBP2NL 产品)
- 别名
- AA552995 antibody, AA589392 antibody, AU018624 antibody, BC003236 antibody, mKIAA1433 antibody, CTTNBP2 N-terminal like antibody, CTTNBP2NL antibody, Cttnbp2nl antibody
- 背景
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Synonyms: CT2NL_HUMAN, CTTNBP2 N terminal like, CTTNBP2 N terminal like protein, CTTNBP2 N-terminal-like protein, Cttnbp2nl, DKFZp547A023, FLJ13278, KIAA1433.
Background: CTTNBP2NL is a 639 amino acid protein that is encoded by a gene that maps to human chromosome 1p13.2. 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.
- 基因ID
- 55917
- UniProt
- Q9P2B4
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