FTSJ1 抗体 (AA 1-110) (Cy5)
Quick Overview for FTSJ1 抗体 (AA 1-110) (Cy5) (ABIN1704895)
抗原
See all FTSJ1 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 1-110
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交叉反应
- 小鼠, 大鼠
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预测反应
- Human,Dog,Cow,Sheep,Pig,Horse,Rabbit
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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 FTSJ1
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亚型
- IgG
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anti-FtsJ RNA Methyltransferase Homolog 1 (FTSJ1) (AA 1-329) antibody
FTSJ1 适用: 人 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-FtsJ RNA Methyltransferase Homolog 1 (FTSJ1) (AA 1-329) antibodyFTSJ1 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-FtsJ RNA Methyltransferase Homolog 1 (FTSJ1) (AA 1-110) antibodyFTSJ1 适用: 小鼠, 大鼠 ELISA, IF (cc), IF (p), IHC (fro), IHC (p), ICC 宿主: 兔 Polyclonal unconjugated
anti-FtsJ RNA Methyltransferase Homolog 1 (FTSJ1) (N-Term) antibodyFTSJ1 适用: 人, 小鼠, 大鼠, Cow, 犬, 马, Pig, 兔, Bat, Drosophila melanogaster, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-FtsJ RNA Methyltransferase Homolog 1 (FTSJ1) antibodyFTSJ1 适用: 人, 小鼠, 大鼠 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
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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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- FTSJ1 (FtsJ RNA Methyltransferase Homolog 1 (FTSJ1))
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别名
- FTSJ1
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背景
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Synonyms: CDLIV, FTSJ 1, FtsJ homolog 1 E. coli, FtsJ homolog 1, JM23, Mental retardation X linked 44, Mental retardation X linked 9, MRX44, MRX9, Putative ribosomal RNA methyltransferase 1, RRMJ1, SPB1, TRM7, RRMJ1_HUMAN.
Background: FTSJ1 is a 329 amino acid nucleolar protein belonging to the RlmE family and methyltransferase superfamily. Expressed in adult thalamus, hippocampus, amygdala, corpus callosum and caudate nucleus, as well as fetal kidney, lung, liver, brain and lung, FTSJ1 plays a role in rRNA modification and processing. FTSJ1 exists as multiple spliced isoforms which are encoded by a gene located on human chromosome Xp11.23. Notably, defects in the gene encoding FTSJ1 are the cause of mental retardation X-linked type 44 (MRX44) and nonsyndromic X-linked mental retardation (MRX9).
抗原
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