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| Product Name | Recombinant Mouse Phosphatidate phosphatase LPIN3 (Lpin3) , partial |
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| Description | MW: 94,316 Da. Purity >85% (SDS-PAGE). Humans lipodystrophy is characterized by loss of body fat, fatty liver, hypertriglyceridemia, and insulin resistance. Mice carrying mutations in the fatty liver dystrophy (fld) gene have similar phenotypes. Through positional cloning, the mouse gene responsible for fatty liver dystrophy was isolated and designated Lpin1. The nuclear protein encoded by Lpin1 was named lipin. Lpin1 mRNA was expressed at high levels in adipose tissue and was induced during dif |
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| Size | 0.5 mg (E-Coli), 0.05 mg (Baculovirus), 0.5 mg (Yeast), 0.05 mg (Mammalian-Cell), 1 mg (E-Coli) |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | [phosphatidate phosphatase LPIN3; Phosphatidate phosphatase LPIN3; phosphatidate phosphatase LPIN3; lipin 3; Lipin-3] |
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| Gene, Accession, CAS # | Lpin3, Gene ID: 64899, Accession: NP_001186047.1 |
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| Catalog # | MBS1362522 |
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| Price | |
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| Order / More Info | Recombinant Mouse Phosphatidate phosphatase LPIN3 (Lpin3) , partial from MYBIOSOURCE INC. |
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| Product Specific References | n/a |
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