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METTL7A 抗体

This anti-METTL7A antibody is a 兔 多克隆 antibody detecting METTL7A in WB 和 IHC. Suitable for 人 和 大鼠.
产品编号 ABIN7264251
发货至: 中国
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北京 101111
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Room 801-803
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for METTL7A 抗体 (ABIN7264251)

抗原

See all METTL7A 抗体
METTL7A (Methyltransferase Like 7A (METTL7A))

适用

  • 28
  • 6
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
人, 大鼠

宿主

  • 27
  • 1

克隆类型

  • 28
多克隆

标记

  • 13
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This METTL7A antibody is un-conjugated

应用范围

  • 15
  • 12
  • 9
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • 产品特性

    Polyclonal Antibody

    纯化方法

    Affinity purification

    免疫原

    Recombinant fusion protein of human METTL7A (NP_054752.3).

    亚型

    IgG
  • 应用备注

    WB 1:500-1:2000 IHC 1:50-1:200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    METTL7A (Methyltransferase Like 7A (METTL7A))

    别名

    METTL7A

    背景

    METTL7A (methyltransferase like 7A), also known as AAM-B, is a 244 amino acid protein that is thought to function as a methyltransferase and is encoded by a gene which maps to chromosome 12. Encoding over 1,100 genes, chromosome 12 comprises nearly 4.5 % of the human genome and is associated with a number of skeletal deformaties, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Chromosome 12 is also home to both a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and a natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Additionally, Trisomy 12p (three copies of the p arm of chromosome 12) leads to facial developmental defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism.

    分子量

    Observed_MW: 28 kDa

    Calculated_MW: 28 kDa

    基因ID

    25840

    UniProt

    Q9H8H3
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