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PQBP1 (polyglutamine binding protein-1) is a highly conserved nuclear protein expressed in mesoderm and nuclear tissue. The PQBP1 gene that encodes this protein belongs to a disease-causing gene of mental disability, which is involved in the transcriptional and post-transcriptional regulation of gene expression in animals and even plants. This gene mutation can lead to X-linked mental retardation (XLID), is often referred to as Lempenning's syndrome. People with these disabilities have a series of common symptoms, including microcephaly, short stature and impaired intellectual development.
|Cat.No.||Product Name||Source||Species||Tag||Molecular Weight|
|BP-801492||Recombinant Human PQBP1, His-tagged||E.coli||Human||His|
|BP-801493||Recombinant Rhesus monkey PQBP1 Protein, His-tagged||Mammalian Cells||Rhesus monkey||His|
|BP-801494||Recombinant Rat PQBP1 Protein||Mammalian Cells||Rat||His|
|BP-801495||Recombinant Zebrafish PQBP1||Mammalian Cells||Zebrafish||His|
|BP-801496||Recombinant Human Polyglutamine Binding Protein 1, His-tagged|
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