CTU2 抗体 (AA 301-400) (FITC)
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- 抗原 See all CTU2 抗体
- CTU2 (Cytosolic Thiouridylase Subunit 2 (CTU2))
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抗原表位
- AA 301-400
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适用
- 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 CTU2 antibody is conjugated to FITC
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Cow,Sheep,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CTU2/C16orf84
- 亚型
- IgG
- Top Product
- Discover our top product CTU2 Primary Antibody
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anti-Cytosolic Thiouridylase Subunit 2 (CTU2) antibody
CTU2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Cytosolic Thiouridylase Subunit 2 (CTU2) (AA 186-515) antibodyCTU2 适用: 人 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
- CTU2 (Cytosolic Thiouridylase Subunit 2 (CTU2))
- 别名
- CTU2 (CTU2 产品)
- 别名
- C16orf84 antibody, NCS2 antibody, UPF0432 antibody, Ncs2 antibody, 2310061F22Rik antibody, cytosolic thiouridylase subunit 2 antibody, CTU2 antibody, Ctu2 antibody
- 背景
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Synonyms: C16orf84, ctu2, CTU2_HUMAN, Cytoplasmic tRNA 2-thiolation protein 2, cytosolic thiouridylase subunit 2 homolog (S. pombe), NCS2, PF0432.
Background: CTU2 is a 515 amino acid cytoplasmic protein that plays a role in the 2-thiolation of mcm(5)S(2)U at wobble positions of tRNA. CTU2 forms a complex with CTU1 and Urm1, and may also form a separate heterodimer with CTU1 to ligate sulfur from thiocarboxylated Urm1 onto tRNA. Existing as three alternatively spliced isoforms, the gene encoding CTU2 maps to human chromosome 16q24.3. Chromosome 16 encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
- 基因ID
- 348180
- UniProt
- Q2VPK5
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