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Septin 9 抗体

This anti-Septin 9 antibody is a 兔 多克隆 antibody detecting Septin 9 in WB 和 ELISA. Suitable for 人.
产品编号 ABIN7231314
发货至: 中国
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Quick Overview for Septin 9 抗体 (ABIN7231314)

抗原

See all Septin 9 (SEPT9) 抗体
Septin 9 (SEPT9)

适用

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宿主

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克隆类型

  • 30
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多克隆

标记

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This Septin 9 antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA
  • 原理

    SEPT9 Polyclonal Antibody

    特异性

    The antibody detects endogenous levels of SEPT9 protein

    纯化方法

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    免疫原

    Synthesized peptide derived from part region of human SEPT9 protein

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

    说明

    Primary Antibody

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    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

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • 抗原

    Septin 9 (SEPT9)

    别名

    SEPT9

    背景

    Rabbit Anti-SEPT9 Polyclonal Antibody,Septin-9, MLL septin-like fusion protein MSF-A, MLL septin-like fusion protein, Ovarian/Breast septin, Ov/Br septin, Septin D1,SEPT9 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

    分子量

    observerd band 64kDa

    基因ID

    10801

    UniProt

    Q9UHD8
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