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PRMT7 抗体 (AA 121-526)

The 兔 多克隆 anti-PRMT7 antibody (ABIN7870321) specifically detects PRMT7 in WB, ELISA, IF, FACS 和 IHC (p). The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN7870321
发货至: 中国
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Quick Overview for PRMT7 抗体 (AA 121-526) (ABIN7870321)

抗原

See all PRMT7 抗体
PRMT7 (Protein Arginine Methyltransferase 7 (PRMT7))

适用

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  • 19
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  • 2
  • 1
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  • 1
人, 小鼠, 大鼠

宿主

  • 49
  • 10
  • 1

克隆类型

  • 38
  • 22
多克隆

标记

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  • 2
  • 2
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  • 1
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This PRMT7 antibody is un-conjugated

应用范围

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  • 17
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  • 9
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  • 1
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Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 6
    • 6
    • 4
    • 4
    • 4
    • 2
    • 2
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    • 1
    • 1
    • 1
    • 1
    • 1
    AA 121-526

    原理

    PRMT7 Antibody / Protein arginine N-methyltransferase 7

    纯化方法

    Antigen affinity purified

    免疫原

    E. coli-derived recombinant human protein (amino acids K121-D526) was used as the immunogen for the PRMT7 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the PRMT7 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 PRMT7 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

    PRMT7 (Protein Arginine Methyltransferase 7 (PRMT7))

    别名

    PRMT7

    背景

    Protein arginine methyltransferase 7 is a protein that in humans is encoded by the PRMT7 gene. This gene encodes a member of the protein arginine N-methyltransferase family of proteins. The encoded enzyme transfers single methyl groups to arginine residues to generate monomethylarginines on histone proteins as well as other protein substrates. This enzyme plays a role in a wide range of biological processes, including neuronal differentiation, male germ line imprinting, small nuclear ribonucleoprotein biogenesis, and regulation of the Wnt signaling pathway. Mutations in this gene underlie multiple related syndromes in human patients characterized by intellectual disability, short stature and other features. The encoded protein may promote breast cancer cell invasion and metastasis in human patients.

    UniProt

    Q9NVM4

    途径

    Ribonucleoprotein Complex Subunit Organization
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