NRARP 抗体 (AA 41-114) (Biotin)
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- 抗原 See all NRARP 抗体
- NRARP (NOTCH-Regulated Ankyrin Repeat Protein (NRARP))
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抗原表位
- AA 41-114
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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 NRARP antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 预测反应
- Human,Mouse,Rat,Cow,Sheep,Pig,Chicken
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human NRARP
- 亚型
- IgG
- Top Product
- Discover our top product NRARP 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
- NRARP (NOTCH-Regulated Ankyrin Repeat Protein (NRARP))
- 别名
- NRARP (NRARP 产品)
- 别名
- 2700054M22Rik antibody, Nrarp-a antibody, fc89b12 antibody, id:ibd2282 antibody, wu:fa14d10 antibody, wu:fc89b12 antibody, zgc:100826 antibody, Nrarp-b antibody, zgc:101875 antibody, Notch-regulated ankyrin repeat protein antibody, NOTCH regulated ankyrin repeat protein antibody, NOTCH regulated ankyrin repeat protein S homeolog antibody, NOTCH-regulated ankyrin repeat protein antibody, NOTCH regulated ankyrin repeat protein a antibody, NOTCH regulated ankyrin repeat protein b antibody, Nrarp antibody, NRARP antibody, nrarp.S antibody, nrarpa antibody, nrarpb antibody
- 背景
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Synonyms: MGC61598, Notch regulated ankyrin repeat containing protein, NOTCH regulated ankyrin repeat protein, Notch-regulated ankyrin repeat-containing protein, nrarp, NRARP_HUMAN.
Background: Nrarp (NOTCH-regulated ankyrin repeat protein) is a 114 amino acid protein that contains two ANK repeats and is thought to play a role in the formation of somites. The gene encoding Nrarp maps to human chromosome 9, which contains 145 million base pairs and comprises 4 % of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia and Familial dysautonomia are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in translocations that lead to the aberrant production of a BCR-ABL fusion protein often found in leukemias.
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