TMEM147 抗体 (AA 51-150) (Biotin)
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- 抗原 See all TMEM147 products
- TMEM147 (Transmembrane Protein 147 (TMEM147))
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抗原表位
- AA 51-150
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适用
- 人
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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 TMEM147 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Cow,Horse,Rabbit,Zebrafish
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human TMEM147
- 亚型
- IgG
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 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 for 12 months.
- 有效期
- 12 months
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- 抗原
- TMEM147 (Transmembrane Protein 147 (TMEM147))
- 别名
- TMEM147 (TMEM147 产品)
- 别名
- 2010004E11Rik antibody, 5033425B17Rik antibody, Nifie14 antibody, RGD1304706 antibody, NIFIE14 antibody, nifie14 antibody, zgc:92863 antibody, Transmembrane protein 147 antibody, transmembrane protein 147 antibody, transmembrane protein 147 S homeolog antibody, tm147 antibody, tmem147 antibody, Tmem147 antibody, TMEM147 antibody, tmem147.S antibody
- 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.
- 基因ID
- 10430
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