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- 抗原 See all Septin 9 (SEPT9) 抗体
- Septin 9 (SEPT9)
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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 Septin 9 antibody is un-conjugated
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应用范围
- Immunofluorescence (IF)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant fusion protein of human 44083 (NP_001106964.1).
- 亚型
- IgG
- Top Product
- Discover our top product SEPT9 Primary Antibody
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anti-Septin 9 (SEPT9) (AA 57-85), (C-Term) antibody
SEPT9 适用: 人 WB, IHC (p), FACS 宿主: 兔 Polyclonal RB1931 unconjugated
anti-Septin 9 (SEPT9) (AA 26-125) antibodySEPT9 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Septin 9 (SEPT9) (C-Term) antibodySEPT9 适用: 人, 小鼠, 大鼠, 斑马鱼, 豚鼠, 猴, 小鸡, Hamster WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Septin 9 (SEPT9) antibodySEPT9 适用: 人 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Septin 9 (SEPT9) (AA 1-568) antibodySEPT9 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Septin 9 (SEPT9) (AA 26-125) antibodySEPT9 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 2C6 unconjugated
anti-Septin 9 (SEPT9) (AA 1-110) antibodySEPT9 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Septin 9 (SEPT9) (C-Term) antibodySEPT9 适用: 人, 小鼠, 大鼠 WB, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Septin 9 (SEPT9) (Middle Region) antibodySEPT9 适用: 人, 小鼠, 大鼠, 斑马鱼, 豚鼠, 兔, Cow, 犬, 马 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Septin 9 (SEPT9) (C-Term) antibodySEPT9 适用: 人, 小鼠, 大鼠, 斑马鱼, 豚鼠, 兔, Cow, 犬, 马 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- 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
- Septin 9 (SEPT9)
- 别名
- SEPT9 (SEPT9 产品)
- 背景
- This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.
- 基因ID
- 10801
- UniProt
- Q9UHD8
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