Septin 9 抗体 (AA 1-110)
Quick Overview for Septin 9 抗体 (AA 1-110) (ABIN6147560)
抗原
See all Septin 9 (SEPT9) 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 1-110
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序列
- MEPPASKVPE VPTAPATDAA PKRVEIQMPK PAEAPTAPSP AQTLENSEPA PVSQLQSRLE PKPQPPVAEA TPRSQEATEA APSCVGDMAD TPRDAGLKQA PASRNEKAPV
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交叉反应
- 人, 小鼠, 大鼠
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产品特性
- Polyclonal Antibodies
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纯化方法
- Affinity purification
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免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-110 of human Septin 9 (NP_001106964.1).
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亚型
- IgG
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anti-Septin 9 (SEPT9) (AA 57-85), (C-Term) antibody
SEPT9 适用: 人 WB, FACS, IHC (p) 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, 豚鼠, 斑马鱼, 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 26-125) antibodySEPT9 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 2C6 unconjugated
anti-Septin 9 (SEPT9) (AA 1-568) antibodySEPT9 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Septin 9 (SEPT9) antibodySEPT9 适用: 人, 小鼠, 大鼠 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, 豚鼠, 斑马鱼, Cow, 犬, 马, 兔 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Septin 9 (SEPT9) (C-Term) antibodySEPT9 适用: 人, 小鼠, 大鼠, 豚鼠, 斑马鱼, Cow, 犬, 马, 兔 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB,1:500 - 1:2000,IF,1:50 - 1:200
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说明
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HIGH QUALITY
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- Septin 9 (SEPT9)
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别名
- 9-Sep
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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.,SEPT9,AF17q25,MSF,MSF1,NAPB,PNUTL4,SINT1,SeptD1,septin-9,Cell Biology & Developmental Biology,Cell Cycle,Immunology & Inflammation,Cytokines,9-Sep
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分子量
- 38 kDa/41 kDa/47 kDa/52 kDa/63 kDa/64 kDa/65 kDa
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基因ID
- 10801
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UniProt
- Q9UHD8
抗原
-
