PGBD3 抗体 (AA 410-460)
Quick Overview for PGBD3 抗体 (AA 410-460) (ABIN1385394)
抗原
See all PGBD3 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 410-460
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交叉反应
- 人
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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 PGBD3
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亚型
- IgG
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anti-PiggyBac Transposable Element Derived 3 (PGBD3) (AA 21-49), (N-Term) antibody
PGBD3 适用: 人 WB 宿主: 兔 Polyclonal RB42444 unconjugated
anti-PiggyBac Transposable Element Derived 3 (PGBD3) (AA 52-101) antibodyPGBD3 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-PiggyBac Transposable Element Derived 3 (PGBD3) (AA 71-120) antibodyPGBD3 适用: 人 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
IF(IHC-P) 1:50-200 -
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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- PGBD3 (PiggyBac Transposable Element Derived 3 (PGBD3))
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别名
- PGBD3
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背景
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Synonyms: PGBD 3, PiggyBac transposable element derived 3, PiggyBac transposable element derived protein 3, PGBD3_HUMAN.
Background: PiggyBac transposable element derived 3, also known as PGBD3, encodes a 593 amino acid transposase and is a member of the piggyBac transposable element derived (PGBD) gene family, which includes several genes that are derived from piggyBac transposons. Initially characterized in the cabbacge looper moth, Trichoplusia ni, the PGBD family is conserved in a wide variety of species, including protozoa and primates. More specifically, while PGBD3 and PGBD4 are primate-specific genes, the other three members of the PGBD family (namely PGBD1, PGBD2 and PGBD5) are conserved among a variety of vertebrates. PGBD3 appears to be novel, with no clear relationship to other transposases or other known protein families. However, the PGBD3 gene overlaps with the CSB gene on chromosome 10 and, with the CSB gene, plays a role in Cockayne syndrome, a rare disorder characterized by premature aging, microcephaly, photosensitivity and severe neurologic degeneration.
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基因ID
- 267004
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UniProt
- Q8N328
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途径
- Chromatin Binding
抗原
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