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- 抗原 See all NDE1 抗体
- NDE1
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适用
- 人, 小鼠, 大鼠
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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 NDE1 antibody is un-conjugated
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应用范围
- Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein of human NDE1 (NP_060138.1).
- 亚型
- IgG
- Top Product
- Discover our top product NDE1 Primary Antibody
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anti-NDE1 (NDE1) (AA 1-335) antibody
NDE1 适用: 人 WB, ELISA, IF 宿主: 小鼠 Monoclonal 2G11-1C11 unconjugated
anti-NDE1 (NDE1) (AA 1-110) antibodyNDE1 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-NDE1 (NDE1) (N-Term) antibodyNDE1 适用: 人, 小鼠, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-NDE1 (NDE1) antibodyNDE1 适用: 人, 小鼠, 大鼠 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-NDE1 (NDE1) (AA 1-110) antibodyNDE1 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-NDE1 (NDE1) (AA 1-110) antibodyNDE1 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-NDE1 (NDE1) (Middle Region) antibodyNDE1 适用: 人, 小鼠, 大鼠, 兔, Cow, 斑马鱼, 犬, 豚鼠, 马 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IHC 1:50-1:200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: 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. Avoid freeze / thaw cycles.
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- 抗原
- NDE1
- 别名
- NDE1 (NDE1 产品)
- 别名
- 2810027M15Rik antibody, AU042936 antibody, AW822251 antibody, Nude antibody, mNudE antibody, HOM-TES-87 antibody, LIS4 antibody, NDE antibody, NUDE antibody, NUDE1 antibody, fb82g01 antibody, im:7141877 antibody, wu:fb82g01 antibody, zgc:114109 antibody, nudE neurodevelopment protein 1 antibody, Nde1 antibody, NDE1 antibody, nde1 antibody
- 背景
- This gene encodes a member of the nuclear distribution E (NudE) family of proteins. The encoded protein is localized at the centrosome and interacts with other centrosome components as part of a multiprotein complex that regulates dynein function. This protein plays an essential role in microtubule organization, mitosis and neuronal migration. Mutations in this gene cause lissencephaly 4, a disorder characterized by lissencephaly, severe brain atrophy, microcephaly, and severe mental retardation. Alternative splicing results in multiple transcript variants.
- 基因ID
- 54820
- UniProt
- Q9NXR1
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