TMEM147 抗体 (AA 51-150) (AbBy Fluor® 647)
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北京 101111
Quick Overview for TMEM147 抗体 (AA 51-150) (AbBy Fluor® 647) (ABIN1398492)
抗原
适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 51-150
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预测反应
- Human,Mouse,Rat,Cow,Horse,Rabbit,Zebrafish
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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 TMEM147
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亚型
- IgG
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anti-Transmembrane Protein 147 (TMEM147) antibody
TMEM147 适用: 人 WB, IHC (p), ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Protein 147 (TMEM147) (Internal Region) antibodyTMEM147 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC (p), IHC 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Protein 147 (TMEM147) (AA 40-89) antibodyTMEM147 适用: 人, 小鼠, 大鼠, Cow, 犬, 山羊, 马, 兔, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Transmembrane Protein 147 (TMEM147) (N-Term) antibodyTMEM147 适用: 人, 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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- TMEM147 (Transmembrane Protein 147 (TMEM147))
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别名
- TMEM147
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背景
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Synonyms: ransmembrane protein 147, Full=Protein NIE 14, TM147_HUMAN.
Background: TMEM147, also known as , NIFIE 14, is a 224 amino acid protein encoded by a gene mapping to human chromosome 19. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2 % of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc?receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
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基因ID
- 10430
抗原
-
