NCKAP1L 抗体 (AA 1-100) (Biotin)
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- 抗原 See all NCKAP1L 抗体
- NCKAP1L (NCK-Associated Protein 1-Like (NCKAP1L))
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抗原表位
- AA 1-100
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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 NCKAP1L antibody is conjugated to Biotin
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应用范围
- Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human NCKAP1L/HEM1
- 亚型
- IgG
- Top Product
- Discover our top product NCKAP1L Primary Antibody
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- 应用备注
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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
- NCKAP1L (NCK-Associated Protein 1-Like (NCKAP1L))
- 别名
- NCKAP1L/HEM1 (NCKAP1L 产品)
- 别名
- HEM1 antibody, 4930568P13Rik antibody, AI463083 antibody, Hem1 antibody, Hemp1 antibody, NCK associated protein 1 like antibody, zgc:172352 antibody, nck-associated protein 1-like antibody, NCK-associated protein 1-like antibody, NCKAP1L antibody, zgc:172352 antibody, LOC100030968 antibody, nckap1l antibody, LOC100618382 antibody, LOC100639088 antibody, Nckap1l antibody
- 背景
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Synonyms: 4930568P13Rik, AI463083, HEM1, Hematopoietic protein 1, HEMATOPOIETIC PROTEIN HEM-1, Hemp1, Membrane associated protein hem1, Membrane-associated protein HEM-1, NCK associated protein 1 like, Nck-associated protein 1-like, NCKAP1L, NCKPL_HUMAN.
Background: HEM1 is a 1,127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5 % of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
- 基因ID
- 3071
- 途径
- Regulation of Actin Filament Polymerization
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