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Mesp2 抗体 (AA 37-94)

Mesp2 适用: 人 ELISA 宿主: 小鼠 Monoclonal 1B3F9 unconjugated
产品编号 ABIN1098148
发货至: 中国
  • 抗原 See all Mesp2 抗体
    Mesp2 (Mesoderm Posterior 2 Homolog (Mesp2))
    抗原表位
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 37-94
    适用
    • 4
    • 3
    • 2
    宿主
    • 6
    • 1
    小鼠
    克隆类型
    • 6
    • 1
    单克隆
    标记
    • 7
    This Mesp2 antibody is un-conjugated
    应用范围
    • 5
    • 4
    • 1
    ELISA
    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.
    克隆位点
    1B3F9
    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 (Mesp2 产品)
    别名
    bHLHc6 antibody, SCDO2 antibody, mesoderm posterior 2 antibody, mesoderm posterior bHLH transcription factor 2 antibody, Mesp2 antibody, MESP2 antibody
    背景

    Description: 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).

    Aliases: SCDO2, bHLHc6

    分子量
    41.8kDa
    基因ID
    145873
    HGNC
    145873
    UniProt
    Q0VG99
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