Mesp2 抗体 (AA 37-94)
(2 references)-
- 抗原 See all Mesp2 抗体
- Mesp2 (Mesoderm Posterior 2 Homolog (Mesp2))
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抗原表位
- AA 37-94
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适用
- 人
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宿主
- 小鼠
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克隆类型
- 单克隆
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标记
- This Mesp2 antibody is un-conjugated
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应用范围
- ELISA, Western Blotting (WB)
- 纯化方法
- purified
- 免疫原
- Purified recombinant fragment of human MESP2 (AA: 37-94 ) expressed in E. coli.
- 克隆位点
- 1B3F9
- 亚型
- IgG1
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anti-Mesoderm Posterior 2 Homolog (Mesp2) (AA 2-125) antibody
Mesp2 适用: 人 ELISA, IF 宿主: 小鼠 Monoclonal 1C8 unconjugated
anti-Mesoderm Posterior 2 Homolog (Mesp2) (AA 299-348) antibodyMesp2 适用: 小鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Mesoderm Posterior 2 Homolog (Mesp2) (C-Term) antibodyMesp2 适用: 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Mesoderm Posterior 2 Homolog (Mesp2) (Center) antibodyMesp2 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Mesoderm Posterior 2 Homolog (Mesp2) antibodyMesp2 适用: 小鼠 ELISA, WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- ELISA: 1:10000, WB: 1:500 - 1:2000
- 限制
- 仅限研究用
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- 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
- 4°C, -20°C for long term storage
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: "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).
: "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).
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: "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).
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- 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
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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
- 41.8 kDa
- 基因ID
- 145873
- HGNC
- 145873
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