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ZFP36L1 抗体 (AA 28-502)

The 兔 多克隆 anti-ZFP36L1 antibody (ABIN7873270) specifically detects ZFP36L1 in WB, ELISA, IHC (p) 和 FACS. The antibody is reactive with 人, 小鼠, 大鼠 和 猴 samples.
产品编号 ABIN7873270
发货至: 中国
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Quick Overview for ZFP36L1 抗体 (AA 28-502) (ABIN7873270)

抗原

See all ZFP36L1 抗体
ZFP36L1 (ZFP36 Ring Finger Protein-Like 1 (ZFP36L1))

适用

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人, 小鼠, 大鼠, 猴

宿主

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  • 3

克隆类型

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多克隆

标记

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This ZFP36L1 antibody is un-conjugated

应用范围

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

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    AA 28-502

    原理

    CMG-1 Antibody / Capillary morphogenesis gene 1 / IFT74

    纯化方法

    Antigen affinity purified

    免疫原

    An E.coli-derived human recombinant protein (amino acids I28-H502) was used as the immunogen for the CMG-1 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the CMG-1 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 CMG-1 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

    ZFP36L1 (ZFP36 Ring Finger Protein-Like 1 (ZFP36L1))

    别名

    CMG-1

    背景

    Intraflagellar transport protein 74 homolog (IFT74), also known as coiled-coil domain-containing protein 2 (CCDC2) and capillary morphogenesis gene 1 protein (CMG1), is a protein that in humans is encoded by the IFT74 gene. This gene encodes a core intraflagellar transport (IFT) protein which belongs to a multi-protein complex involved in the transport of ciliary proteins along axonemal microtubules. IFT proteins are found at the base of the cilium as well as inside the cilium, where they assemble into long arrays between the ciliary base and tip. This protein, together with intraflagellar transport protein 81, binds and transports tubulin within cilia and is required for ciliogenesis. Naturally occurring mutations in this gene are associated with amyotrophic lateral sclerosis--frontotemporal dementia and Bardet-Biedl Syndrome.

    UniProt

    Q96LB3
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