电话:
+86 (0512) 65829739
传真:
+86 (010) 6788 5057
电子邮件:
orders@antibodies-online.cn

Mesp2 抗体 (AA 37-94)

This anti-Mesp2 antibody is a 小鼠 单克隆 antibody detecting Mesp2 in ELISA. Suitable for 人. This Primary Antibody has been cited in 2+ publications.
产品编号 ABIN1098148
发货至: 中国

Quick Overview for Mesp2 抗体 (AA 37-94) (ABIN1098148)

抗原

See all Mesp2 抗体
Mesp2 (Mesoderm Posterior 2 Homolog (Mesp2))

适用

  • 6
  • 4
  • 2

宿主

  • 7
  • 3
小鼠

克隆类型

  • 7
  • 3
单克隆

标记

  • 10
This Mesp2 antibody is un-conjugated

应用范围

  • 8
  • 7
  • 2
  • 1
  • 1
  • 1
ELISA

克隆位点

1B3F9
  • 抗原表位

    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 37-94

    原理

    MESP2 Antibody

    纯化方法

    Purified antibody

    免疫原

    Purified recombinant fragment of human MESP2 (AA: 37-94 ) expressed in E. Coli.

    亚型

    IgG1
  • 应用备注

    ELISA: 1/10000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified antibody in PBS with 0.05 % 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

    4 °C,-20 °C

    储存方法

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Qiu, Zhou, Jiang, Ji, Ding, Lv, Liu, Tang, Cheng, Qiu: "Mutation analysis of MESP2, HES7 and DUSP6 gene exons in patients with congenital scoliosis." in: Studies in health technology and informatics, Vol. 176, pp. 52-5, (2012) (PubMed).

    Cornier, Staehling-Hampton, Delventhal, Saga, Caubet, Sasaki, Ellard, Young, Ramirez, Carlo, Torres, Emans, Turnpenny, Pourquié: "Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndrome." in: American journal of human genetics, Vol. 82, Issue 6, pp. 1334-41, (2008) (PubMed).

  • 抗原

    Mesp2 (Mesoderm Posterior 2 Homolog (Mesp2))

    别名

    MESP2

    背景

    This gene encodes a member of the bHLH family of transcription factors and plays a key role in defining the rostrocaudal patterning of somites via interactions with multiple Notch signaling pathways. This gene is expressed in the anterior presomitic mesoderm and is downregulated immediately after the formation of segmented somites. This gene also plays a role in the formation of epithelial somitic mesoderm and cardiac mesoderm. Mutations in the MESP2 gene cause autosomal recessive spondylocostal dystosis 2 (SCD02).

    分子量

    41.8 kDa

    基因ID

    145873

    UniProt

    Q0VG99
You are here:
Chat with us!