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Aurora A 抗体 (AA 1-97)

This 兔 多克隆 antibody specifically detects Aurora A in WB, ELISA, IF, IHC (p) 和 FACS. It exhibits reactivity toward 人.
产品编号 ABIN7869653
发货至: 中国
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Quick Overview for Aurora A 抗体 (AA 1-97) (ABIN7869653)

抗原

See all Aurora A (AURKA) 抗体
Aurora A (AURKA) (Aurora Kinase A (AURKA))

适用

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宿主

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克隆类型

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多克隆

标记

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This Aurora A antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • 抗原表位

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    AA 1-97

    原理

    Aurora A Antibody / AURKA

    纯化方法

    Antigen affinity purified

    免疫原

    Recombinant human protein (amino acids M1-K97) was used as the immunogen for the Aurora A antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the Aurora A antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the Aurora A antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    Aurora A (AURKA) (Aurora Kinase A (AURKA))

    别名

    Aurora A

    背景

    AURKA (aurora kinase A), also called ARK1, AurA, AIK, AURORA2, BTAK, PPP1R47, STK7, STK15 and STK6 is a mitotic centrosomal protein kinase. The main role of AURKA in tumor development is in controlling chromosome segregation during mitosis. Aurora A is a member of a family of mitotic serine/threonine kinases. Cell cycle and Northern blot analyses showed that peak expression of AURKA occurs during the G2/M phase and then decreases. By fluorescence in situ hybridization, AURKA gene is represented by 2 signals in chromosome bands 20q13.2-q13.3 and 1q41-q42. The AURKA gene is overexpressed in many human cancers. Ectopic overexpression of Aurora kinase A in mammalian cells induces centrosome amplification, chromosome instability, and oncogenic transformation, a phenotype characteristic of loss-of-function mutations of p53. Depletion of Ajuba prevented activation of AURKA at centrosomes in late G2 phase and inhibited mitotic entry. Activation of AURKA was independently sufficient to induce rapid ciliary resorption, and AURKA acted in this process through phosphorylation of HDAC6, leading to HDAC6-dependent tubulin deacetylation and destabilization of the ciliary axoneme. Small molecule inhibitors of AURKA and HDAC6 reduced regulated disassembly of cilia.

    UniProt

    O14965

    途径

    Cell Division Cycle, Asymmetric Protein Localization
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