C21orf91 抗体 (FITC)
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- 抗原 See all C21orf91 products
- C21orf91 (Chromosome 21 Open Reading Frame 91 (C21orf91))
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适用
- 人, 小鼠, 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 C21orf91 antibody is conjugated to FITC
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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 EURL/C21orf91
- 亚型
- IgG
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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
- C21orf91 (Chromosome 21 Open Reading Frame 91 (C21orf91))
- 别名
- C21orf91 (C21orf91 产品)
- 别名
- C21orf14 antibody, C21orf38 antibody, CSSG1 antibody, EURL antibody, YG81 antibody, C21orf91 antibody, 1700010I10Rik antibody, 2310009O17Rik antibody, E330003K22Rik antibody, Eurl antibody, eurl antibody, chromosome 21 open reading frame 91 antibody, chromosome 1 open reading frame, human C21orf91 antibody, chromosome 3 open reading frame, human C21orf91 antibody, chromosome 21 open reading frame 91 L homeolog antibody, DNA segment, Chr 16, ERATO Doi 472, expressed antibody, zgc:110006 antibody, C21orf91 antibody, C1H21ORF91 antibody, C3H21orf91 antibody, c21orf91.L antibody, c21orf91 antibody, C1H21orf91 antibody, D16Ertd472e antibody, zgc:110006 antibody
- 背景
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Synonyms: C21orf14, C21orf38, C21orf7, Chromosome 21 open reading frame 38, Chromosome 21 open reading frame 91, Early undferentiated retina and lens, EURL, Protein EURL homolog, YG81, EURL_HUMAN.
Background: First is a 297 amino acid protein that contains a putative carboxy-terminal coiled-coil domain. With highest expression in embryonic dorsal retina and, during later embryonic stages, the anterior epithelial cells of the lens, it is suspected that EURL may play a role in cell determination and differentiation. The gene encoding EURL maps to the long arm of chromosome 21, which houses approximately 300 genes and comprises nearly 1.5 % of the human genome. Chromosome 21-associated disorders include Alzheimer's Disease, amyotrophic lateral sclerosis and, most notably, Down Syndrome (also known as trisomy 21).
- 基因ID
- 54149
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