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FIP1L1 抗体 (AA 23-558)

This 兔 多克隆 antibody specifically detects FIP1L1 in WB, IF, ELISA, IHC (p) 和 FACS. It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN7872545
发货至: 中国
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Quick Overview for FIP1L1 抗体 (AA 23-558) (ABIN7872545)

抗原

See all FIP1L1 抗体
FIP1L1 (FIP1 Like 1 (FIP1L1))

适用

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人, 小鼠, 大鼠

宿主

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克隆类型

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多克隆

标记

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This FIP1L1 antibody is un-conjugated

应用范围

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

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    AA 23-558

    原理

    FIP1L1 Antibody / Pre-mRNA 3'-end-processing factor FIP1

    纯化方法

    Antigen affinity purified

    免疫原

    Recombinant human protein (amino acids E23-E558) was used as the immunogen for the FIP1L1 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the FIP1L1 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 FIP1L1 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

    FIP1L1 (FIP1 Like 1 (FIP1L1))

    别名

    FIP1L1

    背景

    Factor interacting with PAPOLA and CPSF1 (i.e, FIP1L1, also termed Pre-mRNA 3'-end-processing factor FIP1) is a protein that in humans is encoded by the FIP1L1 gene (also known as Rhe, FIP1, and hFip1). This gene encodes a subunit of the CPSF (cleavage and polyadenylation specificity factor) complex that polyadenylates the 3' end of mRNA precursors. This gene, the homolog of yeast Fip1 (factor interacting with PAP), binds to U-rich sequences of pre-mRNA and stimulates poly(A) polymerase activity. Its N-terminus contains a PAP-binding site and its C-terminus an RNA-binding domain. An interstitial chromosomal deletion on 4q12 creates an in-frame fusion of human genes FIP1L1 and PDGFRA (platelet-derived growth factor receptor, alpha). The FIP1L1-PDGFRA fusion gene encodes a constitutively activated tyrosine kinase that joins the first 233 amino acids of FIP1L1 to the last 523 amino acids of PDGFRA. This gene fusion and chromosomal deletion is the cause of some forms of idiopathic hypereosinophilic syndrome (HES). This syndrome, recently reclassified as chronic eosinophilic leukemia (CEL), is responsive to treatment with tyrosine kinase inhibitors. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

    UniProt

    Q6UN15
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