NGRN 抗体 (AA 96-200) (Biotin)
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- 抗原 See all NGRN 抗体
- NGRN (Neugrin, Neurite Outgrowth Associated (NGRN))
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抗原表位
- AA 96-200
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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 NGRN 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,Dog,Cow,Sheep,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human Neugrin
- 亚型
- IgG
- Top Product
- Discover our top product NGRN Primary Antibody
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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
- NGRN (Neugrin, Neurite Outgrowth Associated (NGRN))
- 别名
- Neugrin (NGRN 产品)
- 别名
- Ngrn antibody, zgc:136784 antibody, dsc92 antibody, Neugrin antibody, DKFZp469B131 antibody, DSC92 antibody, AW552001 antibody, neugrin, neurite outgrowth associated antibody, ngrn antibody, NGRN antibody, Ngrn antibody
- 背景
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Synonyms: DSC92, FI58Gm, Mesenchymal stem cell protein DSC92, Neugrin, Neugrin neurite outgrowth associated, Neurite outgrowth associated protein, Neurite outgrowth-associated protein, Ngrn, NGRN_HUMAN, Spinal cord-derived protein FI58G.
Background: Neugrin, also known as NGRN, mesenchymal stem cell protein DSC92, neurite outgrowth-associated protein or spinal cord-derived protein FI58G, is a 291 amino acid protein that plays a role in neuronal differentiation and belongs to the neugrin family. As both a secreted and nuclear protein, neugrin exists as two alternatively spliced isoforms and is highly expressed in skeletal muscle, brain and heart. Neugrin is upregulated in neuroblastostoma cells by retinoic acid treatment and is encoded by a gene that maps to human chromosome 15q26.1. Chromosome 15 houses over 700 genes and comprises nearly 3 % of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
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