Septin 9 抗体 (AA 203-253)
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北京 101111
Quick Overview for Septin 9 抗体 (AA 203-253) (ABIN8124587)
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 203-253
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原理
- SEPT9 Antibody
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特异性
- SEPT9 Polyclonal Antibody detects endogenous levels of protein.
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纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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免疫原
- Synthesized peptide derived from part region of human protein AA range: 203-253
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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 15-282) antibodySEPT9 适用: 人, 小鼠 WB, IHC, IF, ELISA, FACS 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) (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) (AA 26-125) antibodySEPT9 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Septin 9 (SEPT9) (AA 536-586) antibodySEPT9 适用: 人 IHC, IF (p) 宿主: 兔 Polyclonal unconjugated
anti-Septin 9 (SEPT9) (AA 1-110) antibodySEPT9 适用: 人 WB, IF 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 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
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应用备注
- WB 1:500-2000 ELISA 1:5000-20000
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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
- Liquid in PBS containing 50 % glycerol, and 0.02 % sodium azide.
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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/1 year
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有效期
- 12 months
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- Septin 9 (SEPT9)
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别名
- SEPT9
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背景
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Background: septin 9(SEPT9) Homo sapiens 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.[provided by RefSeq, Mar 2009],
Gene Name: SEPT9 KIAA0991 MSF
Protein Name: Septin-9 (MLL septin-like fusion protein MSF-A) (MLL septin-like fusion protein) (Ovarian/Breast septin) (Ov/Br septin) (Septin D1)
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基因ID
- 10801
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UniProt
- Q9UHD8
抗原
-
