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- 抗原 See all Dynamin 1-Like (DNM1L) 抗体
- Dynamin 1-Like (DNM1L)
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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 Dynamin 1-Like antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (IF)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of human DRP1
- 亚型
- IgG
- Top Product
- Discover our top product DNM1L Primary Antibody
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anti-Dynamin 1-Like (DNM1L) (AA 69-213) antibody
DNM1L 适用: 人 WB, ELISA, IHC 宿主: 小鼠 Monoclonal 4E11B11 unconjugated
anti-Dynamin 1-Like (DNM1L) (AA 69-213) antibodyDNM1L 适用: 人 WB, ELISA, ICC, FACS 宿主: 小鼠 Monoclonal 4A4C7 unconjugated
anti-Dynamin 1-Like (DNM1L) (AA 1-710) antibodyDNM1L 适用: 人 WB, ELISA, IHC (p) 宿主: 小鼠 Monoclonal 3B5 unconjugated
anti-Dynamin 1-Like (DNM1L) antibodyDNM1L 适用: 人, 小鼠, 大鼠 WB, ELISA, IF, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Dynamin 1-Like (DNM1L) antibodyDNM1L 适用: 人 WB, IHC, IF, IHC (p) 宿主: 小鼠 Monoclonal 3F3 unconjugated
anti-Dynamin 1-Like (DNM1L) antibodyDNM1L 适用: 人, 小鼠, 大鼠, 猴 WB, IHC, IHC (p) 宿主: 小鼠 Monoclonal 2E7 unconjugated
anti-Dynamin 1-Like (DNM1L) antibodyDNM1L 适用: 人, 小鼠, 大鼠, 猴, 犬 WB, IHC, IHC (p) 宿主: 小鼠 Monoclonal 4F6 unconjugated
anti-Dynamin 1-Like (DNM1L) (AA 411-710) antibodyDNM1L 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Dynamin 1-Like (DNM1L) (AA 496-710) antibodyDNM1L 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Dynamin 1-Like (DNM1L) (C-Term) antibodyDNM1L 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB 1:500-1:2000 IF 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
- Dynamin 1-Like (DNM1L)
- 别名
- DRP1 (DNM1L 产品)
- 背景
- This gene encodes a member of the dynamin superfamily of GTPases. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer's disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF). Alternative splicing results in multiple transcript variants encoding different isoforms.
- 分子量
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Observed_MW: 82 kDa
Calculated_MW: 60 kDa/78 kDa/79 kDa/80 kDa/81 kDa/82 kDa/83 kDa
- 基因ID
- 10059
- UniProt
- O00429
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