AKD1 抗体 (Alexa Fluor 488)
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- 抗原 See all AKD1 (ADK1) products
- AKD1 (ADK1) (Adenylate Kinase Domain Containing 1 (ADK1))
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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 AKD1 antibody is conjugated to Alexa Fluor 488
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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 AKD1
- 亚型
- IgG
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anti-Adenylate Kinase Domain Containing 1 (ADK1) (AA 321-421) antibody
ADK1 适用: 人 IHC (p), ELISA, IF 宿主: 小鼠 Monoclonal 1H8 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
- AKD1 (ADK1) (Adenylate Kinase Domain Containing 1 (ADK1))
- 别名
- AKD1 (ADK1 产品)
- 背景
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Synonyms: adenylate kinase domain containing 1, adenylate kinase domain containing 2, Adenylate kinase domain-containing protein 1, Adenylate kinase domain-containing protein 2, AKD1, AKD1_HUMAN, AKD2 , C6orf224, chromosome 6 open reading frame 199, chromosome 6 open reading frame 224 Gm234, Gm7127, RP1-70A9.
Background: AKD1 is a 1,911 amino acid coiled-coil protein belonging to the adenylate kinase family. AKD1 exists as six alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 6q21. Chromosome 6 makes up nearly 6 % of the human genome and contains 170 million base pairs, which encode 1,200 genes. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting the presence of a cancer susceptibility locus. A bipolar disorder susceptibility locus is also linked to the q arm of chromosome 6. The PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins are located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6.
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