C21ORF56 抗体 (Biotin)
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- 抗原 See all C21ORF56 (C21orf56) products
- C21ORF56 (C21orf56) (Chromosome 21 Open Reading Frame 56 (C21orf56))
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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 C21ORF56 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (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 C21ORF56
- 亚型
- IgG
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anti-Chromosome 21 Open Reading Frame 56 (C21orf56) antibody
C21orf56 适用: 人, 犬 WB, IHC, IHC (p), FACS 宿主: 小鼠 Monoclonal 1H6 unconjugated
anti-Chromosome 21 Open Reading Frame 56 (C21orf56) (AA 1-186) antibodyC21orf56 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 21 Open Reading Frame 56 (C21orf56) (AA 108-157) antibodyC21orf56 适用: 人, 小鼠, 大鼠, Cow, 豚鼠, 马, Bat, Hamster, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 21 Open Reading Frame 56 (C21orf56) (N-Term) antibodyC21orf56 适用: 人, 小鼠, 大鼠, Cow, 豚鼠, 马, 犬, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 21 Open Reading Frame 56 (C21orf56) (Middle Region) antibodyC21orf56 适用: 人, 小鼠, 大鼠, Cow, 豚鼠, 马 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400 - 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 for 12 months.
- 有效期
- 12 months
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- 抗原
- C21ORF56 (C21orf56) (Chromosome 21 Open Reading Frame 56 (C21orf56))
- 别名
- C21ORF56 (C21orf56 产品)
- 别名
- C21orf56 antibody, spermatogenesis and centriole associated 1 like antibody, SPATC1L antibody
- 背景
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Synonyms: Chromosome 21 open reading frame 56, DKFZp434N0650, MGC99490, Uncharacterized protein C21orf56, SPC1L_HUMAN.
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. The C21orf56 gene product has been provisionally designated C21orf56 pending further characterization.
- 基因ID
- 84221
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