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MSX1 抗体 (AA 111-138)

This 兔 多克隆 antibody specifically detects MSX1 in WB 和 IF. It exhibits reactivity toward 人 和 小鼠.
产品编号 ABIN7870112
发货至: 中国
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Quick Overview for MSX1 抗体 (AA 111-138) (ABIN7870112)

抗原

See all MSX1 抗体
MSX1 (Msh Homeobox 1 (MSX1))

适用

  • 56
  • 34
  • 16
  • 9
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
人, 小鼠

宿主

  • 45
  • 11
  • 1

克隆类型

  • 47
  • 10
多克隆

标记

  • 24
  • 5
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MSX1 antibody is un-conjugated

应用范围

  • 42
  • 24
  • 14
  • 13
  • 13
  • 11
  • 5
  • 5
  • 4
  • 3
Western Blotting (WB), Immunofluorescence (IF)
  • 抗原表位

    • 16
    • 7
    • 5
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 111-138

    原理

    MSX1 Antibody

    纯化方法

    Antigen affinity purified

    免疫原

    A portion of amino acids 111-138 from the human protein was used as the immunogen for the MSX1 antibody.

    亚型

    Ig Fraction
  • 应用备注

    The stated application concentrations are suggested starting points. Titration of the MSX1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    In 1X PBS, pH 7.4, with 0.09 % sodium azide

    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

    Aliquot the MSX1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • 抗原

    MSX1 (Msh Homeobox 1 (MSX1))

    别名

    MSX1

    背景

    Homeobox protein MSX-1 is a member of the muscle segment homeobox gene family. The protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia.

    UniProt

    P28360

    途径

    Regulation of Muscle Cell Differentiation, Positive Regulation of Response to DNA Damage Stimulus
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