Anti-MNX1 antibody
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概述
- 产品描述Motor neuron and pancreas homeobox 1(MNX1) Homo sapiens This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. Defects in MNX1 are a cause of Currarino syndrome. The triad of a presacral tumor, sacral agenesis and anorectal malformation constitutes the Currarino syndrome which is caused by dorsal-ventral patterning defects during embryonic development. The syndrome occurs in the majority of patients as an autosomal dominant trait. Function:Putative transcription factor involved in pancreas development and function. Similarity: Contains 1 homeobox DNA-binding domain. Tissue specificity:Expressed in lymphoid and pancreatic tissues.
- 产品名称Anti-MNX1 antibody
- 分子量44 kDa
- 种属反应性Human, Mouse
- 验证应用WB
- 抗体类型兔多抗
- 免疫原Synthesized peptide derived from human protein . at AA range: 260-340
- 偶联Non-conjugated
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性能
- 形态Liquid
- 浓度1 mg/mL.
- 存放说明Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.
- 存储缓冲液Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
- 亚型IgG
- 纯化方式Immunogen affinity purified.
- 亚细胞定位Nucleus.
- 其它名称HB 9 antibody
HB9 antibody
HLXB 9 antibody
HLXB9 antibody
Homeo box HB9 antibody
Homeobox HB9 antibody
Homeobox protein HB9 antibody
HOXHB9 antibody
MNX1 antibody
MNX1_HUMAN antibody
Motor neuron and pancreas homeobox 1 antibody
Motor neuron and pancreas homeobox protein 1 antibody
Sacral agenesis autosomal dominant (Currarino triad) antibody
SCRA 1 antibody
SCRA1 antibody
more
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特别提示：本公司的所有产品仅可用于科研实验，严禁用于临床医疗及其他非科研用途！
