PDZD9 抗体 (AA 50-100) (Alexa Fluor 350)
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- 抗原 See all PDZD9 抗体
- PDZD9 (PDZ Domain Containing 9 (PDZD9))
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抗原表位
- AA 50-100
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适用
- 人, 大鼠, 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 PDZD9 antibody is conjugated to Alexa Fluor 350
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human PDZD9
- 亚型
- IgG
- Top Product
- Discover our top product PDZD9 Primary Antibody
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anti-PDZ Domain Containing 9 (PDZD9) (AA 50-100) antibody
PDZD9 适用: 人, 大鼠, 小鼠 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-PDZ Domain Containing 9 (PDZD9) (AA 73-122) antibodyPDZD9 适用: 人, 犬 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IF(IHC-P) 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
- PDZD9 (PDZ Domain Containing 9 (PDZD9))
- 别名
- PDZD9 (PDZD9 产品)
- 别名
- C16orf65 antibody, C25H16orf65 antibody, 4930408O21Rik antibody, LRRGT00105 antibody, PDZ domain containing 9 antibody, PDZD9 antibody, Pdzd9 antibody
- 背景
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Synonyms: PDZ domain containing 9, PDZ domain containing protein 9, PDZD 9, PDZK-9.\, PDZD9_HUMAN.
Background: PDZD9 (PDZ domain containing 9) is a 264 amino acid protein that contains one PDZ (DHR) domain and participates in protein binding. Conserved in chimpanzee, dog, cow, mouse and rat, PDZD9 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 16p12.1. Chromosome 16 encodes over 900 genes, approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. Giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth, and the rare disorder Rubinstein-Taybi syndrome, characterized by mental retardation and predisposition to tumor growth and white blood cell neoplasias, are associated with chromosome 16. Crohn's disease, a gastrointestinal inflammatory condition, and systemic lupus erythematosis are also associated with chromosome 16.
- 基因ID
- 255762
- UniProt
- Q8IXQ8
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