Septin 9 抗体 (AA 15-282) (APC)
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北京 101111
Quick Overview for Septin 9 抗体 (AA 15-282) (APC) (ABIN8035766)
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 15-282
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原理
- Anti-MSF/SEPTIN9 Antibody APC Conjugated
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交叉反应 （详细）
- No cross-reactivity with other proteins.
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纯化方法
- Immunogen affinity purified.
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免疫原
- E.coli-derived human MSF/SEPTIN9 recombinant protein (Position: R15-D282).
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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) (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) (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 536-586) antibodySEPT9 适用: 人 IHC, IF (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 1-110) antibodySEPT9 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Septin 9 (SEPT9) antibodySEPT9 适用: 人, 小鼠, 大鼠 IF 宿主: 兔 Polyclonal unconjugated
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应用备注
- Flow Cytometry, Optimal dilutions should be determined by end users.
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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
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 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
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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有效期
- 12 months
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- Septin 9 (SEPT9)
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别名
- SEPTIN9
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背景
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Background: 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.
Gene Full Name: septin 9
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基因ID
- 10801
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UniProt
- Q9UHD8
抗原
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