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| Product Name | Recombinant Human MAGE-like protein 2 (MAGEL2) |
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| Description | 1-529aa, full length protein. MW: 132,822 Da. Purity >85% (SDS-PAGE). Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally sim |
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| Size | 0.05 mg (E-Coli), 0.05 mg (Baculovirus), 0.2 mg (E-Coli), 0.2 mg (Yeast), 0.05 mg (Mammalian-Cell) |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | [MAGE-like protein 2; MAGE-like protein 2; MAGE-like protein 2; MAGE family member L2; Necdin-like protein 1; Protein nM15] |
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| Gene, Accession, CAS # | MAGEL2, Gene ID: 54551, Accession: NP_061939.3 |
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| Catalog # | MBS1313753 |
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| Price | |
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| Order / More Info | Recombinant Human MAGE-like protein 2 (MAGEL2) from MYBIOSOURCE INC. |
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| Product Specific References | n/a |
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