C21orf59 抗体 (AA 151-250) (Cy5)
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- 抗原 See all C21orf59 products
- C21orf59 (Chromosome 21 Open Reading Frame 59 (C21orf59))
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抗原表位
- AA 151-250
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适用
- 人
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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 C21orf59 antibody is conjugated to Cy5
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- 预测反应
- Human,Mouse,Rat,Cow,Sheep,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C21orf59
- 亚型
- IgG
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anti-Chromosome 21 Open Reading Frame 59 (C21orf59) (N-Term) antibody
C21orf59 适用: 人, 小鼠, 大鼠, 豚鼠, 马, 兔, Cow, 犬 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 21 Open Reading Frame 59 (C21orf59) (AA 1-290) antibodyC21orf59 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Chromosome 21 Open Reading Frame 59 (C21orf59) (N-Term) antibodyC21orf59 适用: 人, 小鼠, 大鼠, 豚鼠, 马, 猴, Pig WB 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
- C21orf59 (Chromosome 21 Open Reading Frame 59 (C21orf59))
- 别名
- C21orf59 (C21orf59 产品)
- 别名
- C21orf59 antibody, MGC83493 antibody, C3H21orf59 antibody, C21orf48 antibody, RA_m005_jsm24C07r antibody, chromosome 1 open reading frame, human C21orf59 antibody, chromosome 21 open reading frame 59 L homeolog antibody, chromosome 3 C21orf59 homolog antibody, chromosome 21 open reading frame 59 antibody, chromosome 3 open reading frame, human C21orf59 antibody, chromosome 14 open reading frame, human C21orf59 antibody, C1H21ORF59 antibody, c21orf59.L antibody, C3H21orf59 antibody, c21orf59 antibody, C21orf59 antibody, C14H21orf59 antibody
- 背景
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Synonyms: C21orf48, C21orf59, Chromosome 21 open reading frame 59, CU059_HUMAN, FLJ20467, FLJ37137, FLJ40247, Uncharacterized protein C21orf59.
Background: The smallest of the human chromosomes, 21 makes up about 1.5 % of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C21orf59, also known as C21orf48, is a 290 amino acid protein and its gene product has been provisionally designated C21orf59 pending further characterization.
- 基因ID
- 56683
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