| 产品详情 |
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| Product Name | Recombinant Human Putative NOL1/NOP2/Sun domain family member 5B (NSUN5P1) |
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| Description | 1-163aa, full length protein. MW: 16,485 Da. Purity >85% (SDS-PAGE). This gene shares high sequence similarity with the genes WBSCR20A and WBSCR20C; these three genes are the products of gene duplication during evolution. This protein is smaller than the proteins encoded by WBSCR20A and WBSCR20C. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Multiple transcript variants encoding the same protein have been fo |
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| Size | 0.05 mg (E-Coli), 0.2 mg (E-Coli), 0.5 mg (E-Coli), 0.05 mg (Baculovirus), 0.2 mg (Yeast) |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | [Putative NOL1/NOP2/Sun domain family member 5B; Putative NOL1/NOP2/Sun domain family member 5B; Williams-Beuren syndrome chromosomal region 20B protein] |
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| Gene, Accession, CAS # | NSUN5P1, Accession: Q3KNT7.1 |
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| Catalog # | MBS1377348 |
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| Price | |
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| Order / More Info | Recombinant Human Putative NOL1/NOP2/Sun domain family member 5B (NSUN5P1) from MYBIOSOURCE INC. |
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| Product Specific References | n/a |
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