RPUSD2 抗体 (AbBy Fluor® 680)
Quick Overview for RPUSD2 抗体 (AbBy Fluor® 680) (ABIN5010096)
抗原
适用
宿主
克隆类型
标记
应用范围
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交叉反应
- 人, 小鼠, 大鼠
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human RPUSD2
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亚型
- IgG
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anti-RNA Pseudouridylate Synthase Domain Containing 2 (RPUSD2) (AA 201-250) antibody
RPUSD2 适用: 人, 小鼠, 大鼠, Cow, 马, 豚鼠, 兔, Bat, 猴 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-RNA Pseudouridylate Synthase Domain Containing 2 (RPUSD2) (N-Term) antibodyRPUSD2 适用: 人, 小鼠, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-RNA Pseudouridylate Synthase Domain Containing 2 (RPUSD2) (AA 417-466) antibodyRPUSD2 适用: 人, Cow, 犬 WB 宿主: 兔 Polyclonal unconjugated
anti-RNA Pseudouridylate Synthase Domain Containing 2 (RPUSD2) (C-Term) antibodyRPUSD2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-RNA Pseudouridylate Synthase Domain Containing 2 (RPUSD2) (N-Term) antibodyRPUSD2 适用: 人, 小鼠, 大鼠, Cow, 犬, 马, 豚鼠, 兔, 斑马鱼 WB, IHC 宿主: 兔 Polyclonal unconjugated
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应用备注
- IF(IHC-P) 1:50-200
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- RPUSD2 (RNA Pseudouridylate Synthase Domain Containing 2 (RPUSD2))
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别名
- RPUSD2
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背景
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Synonyms: C15orf19, C18B11, C18B11 homolog, RNA pseudouridylate synthase domain containing 2, RNA pseudouridylate synthase domain containing protein 2, RNA pseudouridylate synthase domain-containing protein 2, RPUSD 2, RPUSD-2, RUSD2_HUMAN.
Background: RPUSD2, is a 545 amino acid member of the pseudouridine synthase rluA family and is encoded by a gene that is located on chromosome 15. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
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基因ID
- 27079
抗原
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